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Get PDF Full Texts from EurekaMag Chapter 55371

Chapter 55371 provides scholary research titles of which PDF Full Texts are available through EurekaMag.

Urbán, E.; Terhes, G.; Markotics, A.; Sóki, József.; Nagy, E., 2010:
Rare extraintestinal infection caused by toxin-producing Clostridium difficile

Zamurovic, M., 2014:
Rare extrapelvic endometriosis on iliac vein wall--diagnosis and treatment

Medhat, M.A.; Abdel Malek, M.A.Y.; Zaki, S.; Helmy, A.; Driscoll, J.J., 2014:
Rare extraperitoneal involvement with fatal outcome in a case of bilateral luteinized thecoma of the ovaries with sclerosing peritonitis

Walczak, B.E.; Peterson, J.S.; Irwin, R.B., 2009:
Rare extraskeletal osteosarcoma in the anterolateral right leg of a 37-year-old man

Kapoor, S., 2012:
Rare facial dermatological lesions associated with Demodex infection, besides acne vulgaris

Hsieh, L.; Nugent, D., 2012:
Rare factor deficiencies

Baselga, Aés.; Gómez-Rodríguez, C.; Novoa, F.; Vogler, A.P., 2014:
Rare failures of DNA barcodes [corrected] to separate morphologically distinct species in a biodiversity survey of Iberian leaf beetles

Pagnamenta, A.T.; Khan, H.; Walker, S.; Gerrelli, D.; Wing, K.; Bonaglia, M.Clara.; Giorda, R.; Berney, T.; Mani, E.; Molteni, M.; Pinto, D.; L.C.uteur, A.; Hallmayer, J.; Sutcliffe, J.S.; Szatmari, P.; Paterson, A.D.; Scherer, S.W.; Vieland, V.J.; Monaco, A.P., 2011:
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

Jimbo, T.; Fujita, Y.; Yumoto, Y.; Fukushima, K.; Kato, K., 2016:
Rare fetal complications associated with placental mesenchymal dysplasia: a report of two cases

Damodaran, S.; Jones, M.; Mahmood, T.A., 2011:
Rare finding in a common procedure: unsuspected pregnancy during hysterosalpingography

Sharma, A.; Paliwal, P.; Dadhwal, V.; Sharma, Y.; Deka, D., 2009:
Rare finding of 2n/4n mixoploidy in mother and fetus with severe immune hydrops

Narayanan, C.Dhanasekaran.; Bhaskarapprakash, A.Ranganath.; Vijay, B.; Vijayaraghavan, S.; Srinivasan, V., 2007:
Rare finding of a gastrojejuno appendicular fistula during a laparotomy for roux-en-y conversion

Assaf, M.; Angheluta, L.; Goldenfeld, N., 2011:
Rare fluctuations and large-scale circulation cessations in turbulent convection

Bandelier, C.; Leimgruber, A.; Wassenberg, J.; Bart, P.A.; Spertini, F., 2008:
Rare food allergies

Mohanavalli, S.; David, J.Jasline.; Gnanam, A., 2012:
Rare foreign bodies in oro-facial regions

Al-Hamdany, S.; Holm, I.Elisabeth., 2010:
Rare form of Creutzfeldt-Jakob disease

Nair, S.; Eldjerou, L.K.; Harris, N.S.; Dunbar, L.N., 2015:
Rare form of autosomal dominant thalassemia--hemoglobin Hakkari

Lazarov, N.; Lazarov, L.; Lazarov, S., 2010:
Rare form of cervix carcinoma, infiltrating cervical myoma

Mani, S.; Natarajan, B.; Rajaram, K.; Sahuthullah, Y.Ahmed.; Gokulanathan, S.; Sitra, G., 2013:
Rare form of cherubism: Case report with review of literature

Limanskiĭ, S.S., 2012:
Rare form of epilepsy

Matsuura, T.; Sugihara, K.; Kohmura, Y.; Sugimura, H.; Kanayama, N., 2010:
Rare form of extraovarian peritoneal serous papillary carcinoma with solitary tumor in the abdominal wall: a case report and literature review

Massin, M.M.; Malekzadeh-Milani, S-Guiti.; Dessy, H., 2008:
Rare form of protection against ventricular deconditioning in transposition of the great arteries

Croitoru, A.; Melloni, B.; Dupuy-Grasset, M.; Darde, M.L.; Delage, M.; Bonnaud, F., 2012:
Rare form of semi-invasive aspergillosis in immunocompetent patient: case report

Marquard, J.; Palladino, A.A.; Stanley, C.A.; Mayatepek, E.; Meissner, T., 2011:
Rare forms of congenital hyperinsulinism

Unc, O.D.; Steriu, L.; Iordache, I.; Kabtour, B.; Ples, D.; Calin, I.; Grasa, C., 2010:
Rare forms of hydatid cyst. Case reports

Koneru, J.N.; Wood, M.A.; Ellenbogen, K.A., 2012:
Rare forms of preexcitation: a case study and brief overview of familial forms of preexcitation

Shishov, A.S.; Blank, I.A.; Petrova, I.S.; Kulagina, M.V.; Rusanova, S.A., 2014 :
Rare forms of segmental exanthema in patients with Herpes zoster

Setdikova, G.R.; Filippova, E.M.; Paklina, O.V.; Kriger, A.G.; Chekmareva, I.A.; Gorin, D.S.; Berelavichus, S.V.; Bedin, V.V.; Tavobilov, M.M., 2013:
Rare forms of the ductal carcinoma of the pancreas

Park, S.Hyuk.; Chi, H-Sook.; Kwon, M-Ryang.; Cho, Y-Uk.; Jang, S.; Park, C-Jeoung., 2013:
Rare frameshift mutation Cys475Tyrfs(*)11 in the BCR/ABL kinase domain contributes to imatinib mesylate resistance in 2 Korean patients with chronic myelogenous leukemia

Iolascon, A.; Badiali, M.; Pession, A.; Basso, G.; Losi, L.; Delgiudice, E.; Perrotta, S.; Cutillo, S.; Tonini, G., 1993:
Rare frequencey of point mutations for codon 12, 13 and 61 of ras gene in italian neuroblastoma

Lian, K.; Schwartz, M.L.; Bilbao, J.; Perry, J.; Aviv, R.I.; Symons, S.P., 2012:
Rare frontal lobe intraparenchymal epidermoid cyst with atypical imaging

Butali, A.; Mossey, P.; Adeyemo, W.; Eshete, M.; Gaines, L.; Braimah, R.; Aregbesola, B.; Rigdon, J.; Emeka, C.; Olutayo, J.; Ogunlewe, O.; Ladeinde, A.; Abate, F.; Hailu, T.; Mohammed, I.; Gravem, P.; Deribew, M.; Gesses, M.; Adeyemo, A.; Marazita, M.; Murray, J., 2015:
Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population

Weinhold, B., 2013:
Rare fungal illness follows tornado

Lin, S-Hong.; Chang, F-Yee.; Yang, Y-Sung.; Jin, J-Shiaw.; Chen, T-Wei., 2012:
Rare gallbladder adenomyomatosis presenting as atypical cholecystitis: case report

Liu, Z-Bo.; Li, Z-Ru.; Zuo, M-Hui.; Li, Q-Zhong.; Ma, F.; Li, Z-Jun.; Chen, G-hui.; Sun, C-Chung., 2009:
Rare gas atomic number dependence of the hyperpolarizability for rare gas inserted fluorohydrides, HRgF (Rg = He, Ar, and Kr)

Hayes, W.W.; Manson, J.R., 2007:
Rare gas collisions with molten metal surfaces

Albertí, M., 2010:
Rare gas-benzene-rare gas interactions: structural properties and dynamic behavior

Kirsten, T.; Steinbrunn, F.; Zähringer, J., 1970:
Rare gases in lunar samples: study of distribution and variafions by a microprobe technique

Ribeiro, M.Capsy.Boga.; Lopes, L.Roberto.; de Souza Neto, Jão.Coelho.; Meirelles, L.Rodrigues.; de Carvalho, R.Barbosa.; Andreollo, N.Adami., 2012:
Rare gastric inflammatory myofibroblastic tumor in an adult woman: a case report with review of the literature

Drake, M.G.; Nasseri, J.; Mills, M.R., 2007:
Rare gastric metastasis of testicular choriocarcinoma

Flegel, W.A., 2010:
Rare gems: null phenotypes of blood groups

Soutar, A.K., 2010:
Rare genetic causes of autosomal dominant or recessive hypercholesterolaemia

Harosh, I., 2015:
Rare genetic diseases with human lean and/or starvation phenotype open new avenues for obesity and type II diabetes treatment

Lacombe, D.; Morice-Picard, F., 2015:
Rare genetic diseases, signalling pathways, and keloid scar formation

Emery, A., 2009:
Rare genetic disorders in certain populations

Bodmer, W.; Tomlinson, I., 2010:
Rare genetic variants and the risk of cancer

Witte, J.S., 2013:
Rare genetic variants and treatment response: sample size and analysis issues

Roy, S.William.; Irimia, M., 2008:
Rare genomic characters do not support Coelomata: RGC_CAMs

Glessner, J.T.; Connolly, J.J.M.; Hakonarson, H., 2015:
Rare genomic deletions and duplications and their role in neurodevelopmental disorders

Walters, R.G.; Coin, L.J.M.; Ruokonen, A.; de Smith, A.J.; El-Sayed Moustafa, J.S.; Jacquemont, S.; Elliott, P.; Esko, Tõnu.; Hartikainen, A-Liisa.; Laitinen, J.; Männik, K.; Martinet, D.; Meyre, D.; Nauck, M.; Schurmann, C.; Sladek, R.; Thorleifsson, G.; Thorsteinsdóttir, U.; Valsesia, A.; Waeber, G.; Zufferey, F.; Balkau, B.; Pattou, Fçois.; Metspalu, A.; Völzke, H.; Vollenweider, P.; Stefansson, Kári.; Järvelin, M-Riitta.; Beckmann, J.S.; Froguel, P.; Blakemore, A.I.F., 2013:
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity

Anglani, F.; Fabris, A.; Torregrossa, R.; Cristofaro, R.; Gambaro, G.; D'Angelo, A., 2011:
Rare genomic variants and susceptibility to multifactorial diseases. The example of medullary sponge kidney

Perroud, N.; Salzmann, A.; Saiz, P.A.; Baca-Garcia, E.; Sarchiapone, M.; Garcia-Portilla, M.P.; Carli, V.; Vaquero-Lorenzo, Cón.; Jaussent, I.; Mouthon, D.; Vessaz, M.; Huguelet, P.; Courtet, P.; Malafosse, A.; Perroud, N.; Saiz, P.A.; Baca-Garcia, E.; Sarchiapone, M.; Carli, V.; Courtet, P.; Malafosse, A., 2011:
Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder

L.C.m-Duchez, Véronique.; Soria, C.; Dit Sollier, C.Bal.; Borg, J-Yvonne.; Coudert, M.; Montalescot, G.; Esposito, Gétan.; Drouet, L.; Collet, J-Philippe., 2009:
Rare genotypes of protein Z gene are a risk factor for premature myocardial infarction but not protein Z plasma level

Moir-Meyer, G.L.; Pearson, J.F.; Lose, F.; Scott, R.J.; McEvoy, M.; Attia, J.; Holliday, E.G.; Pharoah, P.D.; Dunning, A.M.; Thompson, D.J.; Easton, D.F.; Spurdle, A.B.; Walker, L.C., 2015:
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition

Welander, J.; Andreasson, A.; Juhlin, C.Christofer.; Wiseman, R.W.; Bäckdahl, M.; Höög, A.; Larsson, C.; Gimm, O.; Söderkvist, P., 2014:
Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma

Agarwal, S.K.; Mateo, C.M.; Marx, S.J., 2009:
Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states

Yue-Chun, L.; Lin, J-Feng., 2014:
Rare giant T-wave inversions associated with myocardial stunning: report of 2 cases

Zhang, H.; Zhang, N.; Dong, L.; She, L.; Wang, X.; Xu, E.; Yan, Z.; Zhang, X., 2014:
Rare giant bilateral calvarial hyperostosis across the superior sagittal sinus secondary to brain meningioma: A case report

Cooper, P.B.; Katus, M.; Moores, L.; Geyer, D.; Smirniotopoulos, J.G.; Sandberg, G.D.; Rushing, E.J., 2007:
Rare giant cell ependymoma in an octogenarian. Case report and review of the literature

Yang, C.; Gong, Y.; Liu, J.; Qi, X., 2014:
Rare giant cell tumor involvement of the olecranon bone

Yang, T.; Zhang, L.; Bao, H.; Hua, Z., 2013:
Rare giant epidermal cyst in the infratemporal fossa and middle cranial fossa

Shi, D.; Li, Q., 2014:
Rare giant salivary gland pleomorphic adenoma on the neck

Zhang, M-Jing.; Sun, Z-Yong.; Liu, Y.; Wu, S-Min.; Lu, K-Hua., 2012:
Rare giant secondary cutis verticis gyrata

Hughes, D.G.; Alleyne, C.H., 2014:
Rare giant traumatic cervical arteriovenous fistula in neurofibromatosis type 1 patient

Abbaszadegan, M.R.; Modarresi, A.; Khadivi-Zand, F.; Velayati, A., 2008:
Rare gross deletion in T-cell immune regulator-1 gene in Iranian family with infantile malignant osteopetrosis

Mandal, S.; Dhingra, K.; Gupta, P.; Khurana, N., 2010:
Rare growth of a psammomatous meningioma in a mature ovarian teratoma: a case report

Opolski, G., 2013:
Rare heart disease - unity is strength

Guzeeva, M.V.; Guzeeva, T.M., 2011:
Rare helminthiases

Arya, V.; Kumar, R.; Yadav, R.S.; Dabadghao, P.; Agarwal, S., 2009:
Rare hemoglobin variant Hb I Philadelphia in North Indian family

Atalay, E.Omer.; Atalay, A.; Koyuncu, H.; Oztürk, O.; Köseler, A.; Ozkan, A.; Demirtepe, S., 2008:
Rare hemoglobin variant Hb Yaizu observed in Turkey

Zorai, A.; Moumni, I.; Mosbahi, I.; Douzi, K.; Chaouachi, D.; Guemira, F.; Abbes, S., 2015:
Rare hemoglobin variants in Tunisian population

Bain, B.J., 2012:
Rare hemoglobinopathy presenting as progressive dyspnea

Kueviakoe, M.D.I.; Agbétiafa, K.; Padaro, E.; Fétéké, L.; Layibo, Y.; Amavi, T.; Egnondou, K.; Vovor, A.; Ségbéna, A.Y., 2014:
Rare hemoglobins in Togo: a 15-year study at the Lomé University Campus Hospital Center

Ramanadham, S.; Toomay, S.M.; Yopp, A.C.; Balch, G.C.; Sharma, R.; Schwarz, R.E.; Mansour, J.C., 2012:
Rare hepatic arterial anatomic variants in patients requiring pancreatoduodenectomy and review of the literature

Tan, Y.; Xiao, E-hua., 2014:
Rare hepatic malignant tumors: dynamic CT, MRI, and clinicopathologic features: with analysis of 54 cases and review of the literature

L.D.stri, G.; Castaing, M.; Ferlito, F.; Minutolo, V.; D.C.taldo, A.; Puleo, S., 2014:
Rare hepatic metastases of colorectal cancer in livers with symptomatic HBV and HCV hepatitis

Kanazawa, N., 2012:
Rare hereditary autoinflammatory disorders: towards an understanding of critical in vivo inflammatory pathways

Kaziulin, A.N.; Kucheriavyĭ, I.A., 2008:
Rare hereditary diseases of the pancreas

Knoch, J.; Kamenisch, Y.; Kubisch, C.; Berneburg, M., 2013:
Rare hereditary diseases with defects in DNA-repair

Koralkova, P.; van Solinge, W.W.; van Wijk, R., 2014:
Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis

Nagy, Péter.; Lahm, E.; Pápai, Z., 2014:
Rare hereditary tumours

Knobe, K.; Astermark, J.; Berntorp, E.; Hillarp, A.; Strandberg, K.; Svensson, P.J., 2011:
Rare hereditary types of hemophilia. Bleeding symptoms, family history and laboratory analyses indicates diagnosis

Lee, T.K.; Miller, J.S.; Epstein, J.I., 2010:
Rare histological patterns of prostatic ductal adenocarcinoma

Navarro-Núñez, L.; Teruel, R.; Antón, A.I.; Nurden, P.; Martínez-Martínez, I.; Lozano, M.L.; Rivera, J.; Corral, J.; Mezzano, D.; Vicente, V.; Martinez, C., 2011:
Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure

Thye, T.; Ehmen, C.; Intemann, C.D.; Chinbuah, M.Amanua.; Ziegler, A.; Horstmann, R.D.; Meyer, C.G., 2010:
Rare human IFNG variants

McClure-Begley, T.D.; Papke, R.L.; Stone, K.L.; Stokes, C.; Levy, A.D.; Gelernter, J.; Xie, P.; Lindstrom, J.; Picciotto, M.R., 2014:
Rare human nicotinic acetylcholine receptor α4 subunit (CHRNA4) variants affect expression and function of high-affinity nicotinic acetylcholine receptors

Soares, E.Costa.Studart.; Costa, Fábio.Wildson.Gurgel.; Neto, I.Cavalcante.Pita.; Bezerra, Tácio.Pinheiro.; do Socorro Vidal Patrocínio, Régia.Maria.; Alves, A.Paula.Negreiros.Nunes., 2011:
Rare hybrid odontogenic tumor in a 2-year-old child

Wang, W.; Fu, J-Fen.; Gong, F-Qi.; Zhu, W-Hua.; Shen, Z., 2011:
Rare hypertension as a result of 17alpha-hydroxylase deficiency

Jain, A.; Naithani, M.; Chaudhary, Z.; Sharma, P., 2012:
Rare iatrogenic airway foreign body: The rivet from the fulcrum of the McCoy laryngoscope blade

Della Volpe, N.; Bianco, L.; Bonuso, C.; Annecchiarico, M.; D.S.lverio, P.; Caiazza, A., 2008:
Rare ileal localisation of angiolipoma presenting as chronic haemorrhage and severe anaemia: a case report

Tanyeli, O.; Dereli, Y.; Gormus, N., 2014:
Rare images of tuberculous pericarditis causing constrictive pericarditis

Farah, N.; Williams, A.; Joyce, M.; Bothamley, G.H.; Rajakulasingam, K., 2013:
Rare immediate hypersensitivity to rifampicin in a patient with tuberculosis requiring drug discontinuation

Kapila, R.Kumar.; Singal, P.; Gupta, S.Kumar.; Samdhani, S.; Sharma, S.D.; Srivastava, S.P., 2010:
Rare impacted foreign bodies of larynx

Eyskens, F., 2010:
Rare inborn errors of metabolism in adults: the lysosomal storage disorders

Eggink, H.; Kuiper, A.; Peall, K.J.; Contarino, M.Fiorella.; Bosch, A.M.; Post, B.; Sival, D.A.; Tijssen, M.A.J.; de Koning, T.J., 2015:
Rare inborn errors of metabolism with movement disorders: a case study to evaluate the impact upon quality of life and adaptive functioning

Mathur, P.; Saxena, A.K., 2010:
Rare incarcerated giant scrotal hernia associated with congenital pouch colon

Sun, X.; Chen, Z.; Yang, W.; Yu, F.; Zhao, J.; He, P.; Wang, Z., 2014:
Rare incidence of a diffuse brain metastatic carcinoma: A case report

Trent, J.C.; Patel, S.S.; Zhang, J.; Araujo, D.M.; Plana, J-Carlos.; Lenihan, D.J.; Fan, D.; Patel, S.R.; Benjamin, R.S.; Khakoo, A.Y., 2010:
Rare incidence of congestive heart failure in gastrointestinal stromal tumor and other sarcoma patients receiving imatinib mesylate

Quintin, E.; Scoazec, J-Yves.; Marotte, H.; Miossec, P., 2011:
Rare incidence of methotrexate-specific lesions in liver biopsy of patients with arthritis and elevated liver enzymes

Hoang, C., 2008:
Rare incidentalomas: diagnostic procedure

Stănciulea, O.; Preda, C.; Herlea, V.; Popa, M.; Ulmeanu, D.; Vasilescu, C., 2007:
Rare indication of cephalic duodenopancreatectomy with total gastrectomy--periampullary carcinoma in moderate form of familial adenomatous polyposis

Narayan, P.; Holmström, K.M.; Kim, D-Hyun.; Whitcomb, D.J.; Wilson, M.R.; St George-Hyslop, P.; Wood, N.W.; Dobson, C.M.; Cho, K.; Abramov, A.Y.; Klenerman, D., 2014:
Rare individual amyloid-β oligomers act on astrocytes to initiate neuronal damage

Pauli, G.; Bessot, J.C., 2009:
Rare indoor allergens

Rivera, N.Thakkar.; Bray, N.; Wang, H.; Zelnick, K.; Osman, A.; Vicuña, R., 2015:
Rare infection of implantable cardioverter-defibrillator lead with Candida albicans: case report and literature review

Abozaid, S.; Peretz, A.; Nasser, W.; Zarfin, Y., 2013:
Rare infection--prolonged A. naeslundii bacteremia caused by severe caries

Brinar, V.V.; Habek, M., 2010:
Rare infections mimicking MS

Schöneberg, I., 2008:
Rare infectious diseases in Germany. Obligatory notification results

Dapat, C.; Suzuki, Y.; Saito, R.; Kyaw, Y.; Myint, Y.Yi.; Lin, N.; Oo, H.Naing.; Oo, K.Yi.; Win, N.; Naito, M.; Hasegawa, G.; Dapat, I.C.; Zaraket, H.; Baranovich, T.; Nishikawa, M.; Saito, T.; Suzuki, H., 2010:
Rare influenza A (H3N2) variants with reduced sensitivity to antiviral drugs

Błasiak-Kołacińska, N.; Pietruszewska, W.; Grzelak, P.; Raźniewski, M.; Stefańczyk, L.; Majos, A., 2014:
Rare infraglottic lesions in magnetic resonance imaging

Censani, M.; Anyane-Yeboa, K.; Wapner, R.; Spiegel, E.; Guzman, E.; Oberfield, S.E., 2013:
Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report

Davis, L.K.; Maltman, N.; Mosconi, M.W.; Macmillan, C.; Schmitt, L.; Moore, K.; Francis, S.M.; Jacob, S.; Sweeney, J.A.; Cook, E.H., 2012:
Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis

Acharya, S.S.; Dimichele, D.M., 2009:
Rare inherited disorders of fibrinogen

Devuyst, O.; Knoers, N.V.A.M.; Remuzzi, G.; Schaefer, F.; Antignac, C.; Bindels, Ré.; Chauveau, D.; Devuyst, O.; Emma, F.; Gansevoort, R.T.; Maxwell, P.H.; Ong, A.; Remuzzi, G.; Ronco, P.; Schaefer, F., 2014:
Rare inherited kidney diseases: challenges, opportunities, and perspectives

Stein, J.L.; Parikshak, N.N.; Geschwind, D.H., 2013:
Rare inherited variation in autism: beginning to see the forest and a few trees

Sirker, A.A.; Scott, P.; Melikian, N., 2014:
Rare insight into the rapid evolution of a coronary aneurysm and fistula

Schoenberger, C., 2009:
Rare instance of organ donation in Japan highlights shortage of donors

Hames, K.; Athreya, S., 2014:
Rare instance of small bowel obstruction following unilateral uterine artery embolization

Cagaš, J.; Vlček, P.; Jeřábek, J., 2013:
Rare internal hernia in the falciform ligament as a rare course of abdominal emergency and infrequent cause of ileus

Premanayagam, V.; Gnanaprakasam; Jamila, A., 2010:
Rare intra-abdominal tumor in a young male

Okeahialam, B.N.; Anya, T.S.; Chundusu, C.; Isiguzo, G., 2014:
Rare intracardiac aneurysms seen in Jos, Nigeria: a report of two cases

Aoyama, T.; Hida, K.; Yano, S.; Yamauchi, T.; Iwasaki, Y., 2008:
Rare intramedullary tandem lesion on MRI due to spinal arteriovenous fistula

Pistor, C.; Mariss, G.; Meyer, W.; Middel, P., 2012:
Rare intramuscular haemangioma of the sternocleidomastoid muscle

Hunsaker, M.R.; Greco, C.M.; Tassone, F.; Berman, R.F.; Willemsen, R.; Hagerman, R.J.; Hagerman, P.J., 2011:
Rare intranuclear inclusions in the brains of 3 older adult males with fragile x syndrome: implications for the spectrum of fragile x-associated disorders

Stevens, E.Andrew.; Stanton, C.A.; Nichols, K.; Ellis, T.L., 2009:
Rare intraparenchymal choroid plexus carcinoma resembling atypical teratoid/rhabdoid tumor diagnosed by immunostaining for INI1 protein

Keskinruzgar, A.; Demirkol, M.; Ege, B.; Aras, M.Hamdi.; Ay, S., 2016:
Rare involvement of herpes zoster in the mandibular branch of the trigeminal nerve: A case report and review of the literature

Chen, T-Cheng.; Lo, W-Chia.; Ko, J-Yuh.; Lou, P-Jen.; Yang, T-Lin.; Wang, C-Ping., 2009:
Rare involvement of submandibular gland by oral squamous cell carcinoma

Milan, D.J.; Melman, Y.F.; Ellinor, P.T., 2010:
Rare ion channel polymorphisms: separating signal from noise

Jordan, B., 2013:
Rare is frequent

Graf von der Schulenburg, J-Matthias.; Frank, M., 2015:
Rare is frequent and frequent is costly: rare diseases as a challenge for health care systems

Sadowski, R.M.; Montilla, R.D., 2008:
Rare isolated trapezoid fracture: a case report

Sahai, S.; Mishra, D.; Tripathi, P., 2011:
Rare isolation of Trichophyton soudanense from three cases of superficial mycoses in Lucknow, India

Damiola, F.; Pertesi, M.; Oliver, J.; L.C.lvez-Kelm, F.; Voegele, C.; Young, E.L.; Robinot, N.; Forey, N.; Durand, G.; Vallée, M.P.; Tao, K.; Roane, T.C.; Williams, G.J.; Hopper, J.L.; Southey, M.C.; Andrulis, I.L.; John, E.M.; Goldgar, D.E.; Lesueur, F.; Tavtigian, S.V., 2015:
Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

Grases, F.; Costa-Bauza, A.; Prieto, R.M.; Servera, A.; Pieras, E.; Ferrutxe, J., 2012:
Rare kidney stones

Compérat, E.M.; Camparo, P., 2009:
Rare kidney tumors and the role of molecular medicine

Farag, A.; Anan, E., 2012:
Rare knee tumor masked by spasticity in patient with spinal cord injury

Tang, M.; Luo, Y.; Chen, L.; Zhang, J.; Deng, L.; An, Q.; Ling, Y., 2015:
Rare knot formation during insertion of a peripherally inserted central catheter

Nguyen, M-Linh.T.; Han, L.; Minors, A.M.; Bentley-Hibbert, S.; Pradhan, T.S.; Pua, T.L.; Tedjarati, S.S., 2013:
Rare large cell neuroendocrine tumor of the endometrium: A case report and review of the literature

Farjadian, S.; Moghtaderi, M.; Zuntini, R.; Ferrari, S., 2014:
Rare large homozygous CFTR gene deletion in an Iranian patient with cystic fibrosis

Bajin, Münir.Demir.; Yılmaz, T.; Yilmaz, G., 2011:
Rare laryngeal anomaly or spontaneously drained bilateral saccular cyst?

Obert, L.; Munyon, R.; Choe, A.; Rubenstein, J.; Azizkhan, R., 2012:
Rare late complication of the Nuss procedure: a case report

Lopez-Beltran, A., 2012:
Rare lesions and tumors of the urinary bladder. Selected issues

Yilmaz, C.; Altinors, N.; Sonmez, E.; Gulsen, S.; Caner, H., 2010:
Rare lesions of the cerebellopontine angle

Chan, A.Pak-Hin.; Wong, T.Cheung.; Sieh, K-Man.; Leung, S.Siu-Man.; Cheung, K-Yin.; Fung, K-Yau., 2010:
Rare ligamentum flavum cyst causing incapacitating lumbar spinal stenosis: Experience with 3 Chinese patients

Anonymous, 2007:
Rare liver treatment allowed for HIV-positive man

Berends, M.; Bodewes, H.W.; Netten, P.M., 2007:
Rare localisation of air

Kolarević, D.; Tomasević, Z.; Marković, I.; Zegarac, M.; Pupić, G., 2013:
Rare localisation of breast cancer metastasis to thyroid gland

Koffi, K.Gustave.; N'dathz, E.; Tolo, A.; Nanho, D.Clotaire.; Meite, N'dogomo.; Ayemou, R.; Kouehion, P.; Sanogo, I., 2010:
Rare localisations of endemic Burkitt lymphoma: about 21 cases observed in the Haematology Department of the University Hospital of Yopougon Abidjan

Grabchenko, I.M., 1946:
Rare localization of an accessory mammary gland

E.B.uanani, A.; Saidi, H.; Fikry, T., 2011:
Rare localization of an aggressive epithelioid sarcoma in an adolescent

Chojnacka, H.; Giżewska-Kacprzak, K.; Grodzki, T.; Rybkiewicz, M.; Nowakowski, P.; Gawrych, E., 2016:
Rare localization of an extralobar pulmonary sequestration in a child as a diagnostic challenge: a case report and review of the literature

Armanda, Všnja.; Culić, Sđana.; Pogorelić, Z.; Kuljiš, D.; Budimir, Džen.; Kuzmić-Prusac, I., 2013:
Rare localization of extrarenal nephroblastoma in 1-month-old female infant

E.F.kih, L.; Hassene, H.; Abdelghaffar, H.; Fenniche, S.; Belhabib, D.; Ben Miled, K.; Mezni, F.; Megdiche, M.Lamine., 2010:
Rare localization of sarcoma in an adolescent: thoracic Ewing sarcoma

Bogdanova, E.V.; Batyrov, F.A.; Kiselevich, O.K.; Iusubova, A.N., 2009:
Rare localization of tuberculosis in a generalized process in an infant

Ben Abdelghani, K.; Maatallah, K.; Ajili, F.; Souabni, L.; Laatar, A.; Zakraoui, L., 2015:
Rare localization of tuberculosis: tenosynovitis of the fingers

Bargagli, E.; Olivieri, C.; Penza, F.; Bertelli, P.; Gonnelli, S.; Volterrani, L.; Rottoli, P., 2012:
Rare localizations of bone sarcoidosis: two case reports and review of the literature

Delis, S.G.; Bakoyiannis, A.; Exintabelones, T.; Triantopoulou, C.; Papailiou, J.; Dervenis, C., 2007:
Rare localizations of the hydatid disease. Experience from a single center

Kang, N.; Chung, J-Wook.; Jung, S-No., 2009:
Rare location of Castleman disease in the temporal region

Jerbi Omezzine, S.; Hafsa, C.; Ben Ghozlan, H.; Sassi, N.; Hamza, H.A.; Gannouni, A., 2008:
Rare location of a chondromyxoid fibroma: the os calcis

Louati, Héla.; Dhouib, A.; Douira, W.; Ben Hassine, L.; Lahmar, L.; Nouira, F.; Fdhila, F.; Ghorbel, Sène.; Chaouachi, Béji.; Bellagha, I., 2011:
Rare location of a rhabdomyosarcoma

Shakya, V.Chandra.; Agrawal, C.Shekhar.; Sah, P.; Pradhan, A.; Adhikary, S., 2015:
Rare location of primary non-Hodgkin's lymphoma in the rectum

Neuzillet, Y.; Méjean, A.; Lebret, T., 2009:
Rare locations of metastases from germ cell cancers

Neuzillet, Y.; Méjean, A.; Lebret, T., 2009:
Rare locations of metastases from penile cancer

Lebret, T.; Méjean, A., 2009:
Rare locations of metastases from prostate cancer

Méjean, A.; Lebret, T., 2009:
Rare locations of metastases from renal carcinoma

Lebret, T.; Méjean, A., 2009:
Rare locations of metastases from urothelial carcinoma

Milović, N.; Lazić, M.; Aleksić, P.; Radovanović, D.; Bancević, V.; Savić, S.; Stamenković, D.; Spasić, D.; Kosević, B.; Perović, D.; Jovanović, M., 2014:
Rare locations of metastastatic renal cell carcinoma: a presentation of three cases

Romeo, S.; Yin, W.; Kozlitina, J.; Pennacchio, L.A.; Boerwinkle, E.; Hobbs, H.H.; Cohen, J.C., 2009:
Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans

E.H.ddad, A.; Bassou, D.; Chaouir, S.; Amil, T.; Hanine, A., 2012:
Rare lumbar spine localization of a giant cell tumor

Juvet, S.C.; Hwang, D.; Waddell, T.K.; Downey, G.P., 2008:
Rare lung disease II: pulmonary alveolar proteinosis

Gupta, S.; Bayoumi, A.M.; Faughnan, M.E., 2011:
Rare lung disease research: strategies for improving identification and recruitment of research participants

Paone, G.; Toti, S.; Salvati, F., 2015:
Rare lung diseases

Juvet, S.C.; Hwang, D.; Downey, G.P., 2011:
Rare lung diseases III: pulmonary Langerhans' cell histiocytosis

Farkash, E.A.; Ferry, J.A.; Harris, N.Lee.; Hochberg, E.P.; Takvorian, R.W.; Zuckerman, D.S.; Sohani, A.R., 2009:
Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls

Schillaci, O.; Travascio, L.; Lacanfora, A.; Ceccarelli, S.; Simonetti, G., 2013:
Rare lymphoid malignancies of the breast: report of two cases illustrating potential diagnostic techniques

Lazzi, S.; Bellan, C.; Onnis, A.; D.F.lco, G.; Sayed, S.; Kostopoulos, I.; Onorati, M.; D'Amuri, A.; Santopietro, R.; Vindigni, C.; Fabbri, A.; Righi, S.; Pileri, S.; Tosi, P.; Leoncini, L., 2009:
Rare lymphoid neoplasms coexpressing B- and T-cell antigens. The role of PAX-5 gene methylation in their pathogenesis

Foo, J-Nee.; Liany, H.; Bei, J-Xin.; Yu, X-Qing.; Liu, J.; Au, W-Lok.; Prakash, K.M.; Tan, L.C.; Tan, E-King., 2014:
Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease

Lynn, K., 2011:
Rare male breast cancer has similarities to female disease

Akin, Y.; Sarac, M.; Yucel, S., 2013:
Rare malformation of glans penis: arteriovenous malformation

Marcus, L.; Carlin, N.; Carlin, R., 2011:
Rare malignant neoplasm of the leg: diagnosis and management dilemma

Pendlimari, R.; Leonard, D.; Dozois, E.J., 2011:
Rare malignant neuroendocrine transformation of a presacral teratoma in patient with Currarino syndrome

Brecht, I.B.; Bremensdorfer, C.; Schneider, D.T.; Frühwald, M.C.; Offenmüller, S.; Mertens, R.; Vorwerk, P.; Koscielniak, E.; Bielack, S.S.; Benesch, M.; Hero, B.; Graf, N.; von Schweinitz, D.; Kaatsch, P., 2014:
Rare malignant pediatric tumors registered in the German Childhood Cancer Registry 2001-2010

Haubner, F.; Gassner, H.G.; Eder, F.; Müller-Vogt, U., 2011:
Rare malignant tumor of the parotid gland. Myoepithelial carcinoma

HARTZ.P.H.; VAN der SAR.A., 2014:
Rare malignant tumors in children

Greco, M.; Vitagliano, T.; Fiorillo, M.A.; Atzeni, M.; Corona, A.; Ribuffo, D., 2011:
Rare malignant tumors of the scalp: a report of four cases, their treatment and a review of the literature

Liao, H-Rong.; Li, T-Shih.; Chen, K-Bao.; Li, C-Yuan.; Jeng, L-Bin.; Yang, H-Ren.; Poon, K-Shing., 2011:
Rare malposition of a central venous catheter into the left internal mammary vein in a liver transplantation patient

Li, C-Cheng.; Feinerman, D.M.; MacCarthy, K.D.; Woo, S-Bin., 2014:
Rare mandibular surgical ciliated cysts: report of two new cases

Malik, A.Ali.; Halabi, A.Munem.; Jamil, G.; Qureshi, A., 2013:
Rare manifestation of Behcet's syndrome: insight from multimodality cardiovascular imaging

Udayakumaran, S., 2015:
Rare manifestation of a craniovertebral junction anomaly: is blue breath holding always benign?

Soeiro, A.de.Matos.; Bergamin, Fício.Sanchez.; Almeida, M.Carolina.Feres.de.; Serrano, C.Vicente.; Falcão, B.Alencar.de.Araripe.; Ganem, F., 2013:
Rare manifestation of acute pulmonary edema associated with acute lupus myocarditis

Kim, H.Kyu.; Jang, W.Sun.; Kim, B.Joon.; Kim, M.Nam., 2013:
Rare manifestation of giant molluscum contagiosum on the scalp in old age

Birla, S.; Singla, R.; Sharma, A.; Tandon, N., 2015:
Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation

Adams, W.Brodie.; Becknell, C.A., 2007:
Rare manifestation of scalp necrosis in temporal arteritis

Ekart, R.; Grobelšek, V.Kovačič.; Dai, K.; Cernelč, P.; Hojs, R., 2014:
Rare manifestation of the thrombotic microangiopathy in a patient with sarcoidosis, common variable immunodeficiency and large B-cell non-hodgkin lymphoma: case report

Buhaescu, I.; Williams, A.; Yood, R., 2008:
Rare manifestations of Churg-Strauss syndrome: coronary artery vasospasm, temporal artery vasculitis, and reversible monocular blindness-a case report

Badakali, M.; Badakali, A.; Dombale, V., 2012:
Rare manifestations of Neu-Laxova syndrome

Rajai, M., 2007:
Rare manifestations of Wegener's granulomatosis

Angelo, K.M.; Nnedu, O.N., 2013:
Rare manifestations of coccidioidomycosis

Sharma, S.K.; Soneja, M.; Sharma, A.; Sharma, M.C.; Hari, S., 2013:
Rare manifestations of sarcoidosis in modern era of new diagnostic tools

Cheng, S.; Lu, S-Cen.; Zhang, B.; Xue, Z.; Wang, H-Wei., 2013:
Rare massive osteolipoma in the upper part of the knee in a young adult

Akcay, M.; Senkaya, E.B.; Bilge, M.; Yeter, E.; Misra, M.C.; Kurt, M.; Davutoglu, V., 2011:
Rare mechanical complication of myocardial infarction: isolated right ventricle free wall rupture

Onrubia, X.; Armero, R.; Roca de Togores, A.; Higueras, J., 2007:
Rare mechanical guidewire complication during central venous catheterization

Khokhlov, V.D.; Krut', M.I.; Sashko, S.Iu., 2008 :
Rare mechanism of the renal artery injury

Guder, E.; Dommerich, S.; Guthoff, R.; Pau, H.N., 2011:
Rare mechanisms of blowout fractures. Discussion of two case reports

Lucchetti, G.; dos Santos Camargo, L.; Lucchetti, A.L.G.; Schwartz, G.E.; Nasri, F., 2015:
Rare medical conditions and suggestive past-life memories: a case report and literature review

Bhattacharya, P.C.; Muzumder, R.; Dev Sarmah, G.C., 1991:
Rare medicinal plants of assam

Mencarelli, M.; Dubern, B.; Alili, R.; Maestrini, S.; Benajiba, L.; Tagliaferri, M.; Galan, P.; Rinaldi, M.; Simon, C.; Tounian, P.; Hercberg, S.; Liuzzi, A.; D.B.asio, A.Maria.; Clement, K., 2011:
Rare melanocortin-3 receptor mutations with in vitro functional consequences are associated with human obesity

Zhang, L.; Shen, Y.; Wang, F.; Leng, Y.; Liu, J-Kai., 2010:
Rare merosesquiterpenoids from basidiomycete Craterellus odoratus and their inhibition of 11beta-hydroxysteroid dehydrogenases

Wendel, U.; Burgard, P., 2007:
Rare metabolic diseases

Prytz, H.; Lindgren, S., 2013:
Rare metabolic diseases can be manifested as liver disease

Hollander, E., 2008:
Rare metabolic syndromes, a vascular hypotheses of Alzheimer's disease, and drug developments for attention and trauma

Carreras, C.; Kulkarni, H.R.; Baum, R.P., 2013:
Rare metastases detected by (68)Ga-somatostatin receptor PET/CT in patients with neuroendocrine tumors

Zamurovic, M.; Pesic-Stevanovic, I.; Perisic, Z., 2011:
Rare metastases of carcinoma of uterine cervix

Zamurovic, M.; Pesic-Stevanovic, I., 2012:
Rare metastases of pancreatic tail carcinoma in female genital organs

Kim, H.Seung.; Park, N-Hyun.; Kang, S-Beom., 2008:
Rare metastases of recurrent cervical cancer to the pericardium and abdominal muscle

Madani, A.; Jozaghi, Y.; Tabah, R.; How, J.; Mitmaker, E., 2015:
Rare metastases of well-differentiated thyroid cancers: a systematic review

Pawar, A.; Schlader, E.; Mac-Thiong, J-Marc.; Maurais, G.; Dion, D.; Bédard, D., 2011:
Rare metastatic adenocarcinoma to the spine infiltrating three adjacent foramen in lumbar vertebrae

Krishna, M.Vamshi.; Prabhash, K.; Noronha, V.; Menon, S.; Dua, S.G.; Rangarajan, V.; Tangaonkar, H.B., 2012:
Rare metastatic prostatic malignancy: A case report and approach to management

Athanasoulia, A.P.; Auer, M.; Riepe, F.G.; Stalla, G.K., 2014:
Rare missense P450c17 (CYP17A1) mutation in exon 1 as a cause of 46,XY disorder of sexual development: implications of breast tissue 'unresponsiveness' despite adequate estradiol substitution

Haller, G.; Kapoor, M.; Budde, J.; Xuei, X.; Edenberg, H.; Nurnberger, J.; Kramer, J.; Brooks, A.; Tischfield, J.; Almasy, L.; Agrawal, A.; Bucholz, K.; Rice, J.; Saccone, N.; Bierut, L.; Goate, A., 2014:
Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence

Sabatelli, M.; Eusebi, F.; Al-Chalabi, A.; Conte, A.; Madia, F.; Luigetti, M.; Mancuso, I.; Limatola, C.; Trettel, F.; Sobrero, F.; D.A.gelantonio, S.; Grassi, F.; D.C.stro, A.; Moriconi, C.; Fucile, S.; Lattante, S.; Marangi, G.; Murdolo, M.; Orteschi, D.; Del Grande, A.; Tonali, P.; Neri, G.; Zollino, M., 2010 :
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis

Khanna, A.; Khanna, A.; Parker, M., 2008:
Rare mode of dynamic hip screw failure

Wylie, L., 2010:
Rare models: Roger Casement, the Amazon, and the ethnographic picturesque

Manger, K.; Nüsslein, H.; Schett, G.; Manger, B., 2009:
Rare monogenetic syndromes in rheumatology practice

Kuscher, S.; Kronberger, I.; Oberwalder, M.; Biebl, M.; Pratschke, J.; Bruder, E.; Aigner, F., 2015:
Rare morphological disorder in therapy refractory chronic constipation

Carlomagno, N.; Santangelo, M.L.; Mastromarino, R.; Calogero, A.; Dodaro, C.; Renda, A., 2014:
Rare multiple primary malignancies among surgical patients-a single surgical unit experience

Ebenezer, D.A.; Rathinam, B.A.D., 2013:
Rare multiple variations in brachial plexus and related structures in the left upper limb of a Dravidian male cadaver

Ingelsson, M.; Basun, H.; Pettersson, F.Ekholm.; Kilander, L.; Nilsson, L.N.G.; Lannfelt, L., 2009:
Rare mutations aim toward future treatment

Sveinbjornsson, G.; Mikaelsdottir, E.; Palsson, R.; Indridason, O.S.; Holm, H.; Jonasdottir, A.; Helgason, A.; Sigurdsson, S.; Jonasdottir, A.; Sigurdsson, A.; Eyjolfsson, G.Ingi.; Sigurdardottir, O.; Magnusson, O.Th.; Kong, A.; Masson, G.; Sulem, P.; Olafsson, I.; Thorsteinsdottir, U.; Gudbjartsson, D.F.; Stefansson, K., 2015:
Rare mutations associating with serum creatinine and chronic kidney disease

Park, D.J.; Tao, K.; Le Calvez-Kelm, F.; Nguyen-Dumont, T.; Robinot, N.; Hammet, F.; Odefrey, F.; Tsimiklis, H.; Teo, Z.L.; Thingholm, L.B.; Young, E.L.; Voegele, C.; Lonie, A.; Pope, B.J.; Roane, T.C.; Bell, R.; Hu, H.; Shankaracharya; Huff, C.D.; Ellis, J.; Li, J.; Makunin, I.V.; John, E.M.; Andrulis, I.L.; Terry, M.B.; Daly, M.; Buys, S.S.; Snyder, C.; Lynch, H.T.; Devilee, P.; Giles, G.G.; Hopper, J.L.; Feng, B-Jian.; Lesueur, F.; Tavtigian, S.V.; Southey, M.C.; Goldgar, D.E., 2015:
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers

Acuña, Río.; Martínez-de-la-Maza, L.; Ponce-Coria, Jé.; Vázquez, N.; Ortal-Vite, Pélope.; Pacheco-Alvarez, D.; Bobadilla, N.A.; Gamba, G., 2011:
Rare mutations in SLC12A1 and SLC12A3 protect against hypertension by reducing the activity of renal salt cotransporters

van der Zee, J.; Van Langenhove, T.; Kovacs, G.G.; Dillen, L.; Deschamps, W.; Engelborghs, S.; Matěj, R.; Vandenbulcke, M.; Sieben, A.; Dermaut, B.; Smets, K.; Van Damme, P.; Merlin, Céline.; Laureys, A.; Van Den Broeck, M.; Mattheijssens, M.; Peeters, K.; Benussi, L.; Binetti, G.; Ghidoni, R.; Borroni, B.; Padovani, A.; Archetti, S.; Pastor, P.; Razquin, C.; Ortega-Cubero, S.; Hernández, I.; Boada, Mè.; Ruiz, Aín.; de Mendonça, A.; Miltenberger-Miltényi, G.; do Couto, F.Simões.; Sorbi,, 2015:
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Park, D.J.; Lesueur, F.; Nguyen-Dumont, T.; Pertesi, M.; Odefrey, F.; Hammet, F.; Neuhausen, S.L.; John, E.M.; Andrulis, I.L.; Terry, M.B.; Daly, M.; Buys, S.; L.C.lvez-Kelm, F.; Lonie, A.; Pope, B.J.; Tsimiklis, H.; Voegele, C.; Hilbers, F.M.; Hoogerbrugge, N.; Barroso, A.; Osorio, A.; Giles, G.G.; Devilee, P.; Benitez, J.; Hopper, J.L.; Tavtigian, S.V.; Goldgar, D.E.; Southey, M.C., 2012:
Rare mutations in XRCC2 increase the risk of breast cancer

D'Arcangelo, M.; D'Incecco, A.; Cappuzzo, F., 2013:
Rare mutations in non-small-cell lung cancer

Welling, P.A., 2014:
Rare mutations in renal sodium and potassium transporter genes exhibit impaired transport function

Neocleous, V.; Ioannou, Y.S.; Bartsota, M.; Costi, C.; Skordis, N.; Phylactou, L.A., 2010:
Rare mutations in the CYP21A2 gene detected in congenital adrenal hyperplasia

Konstantinova, D.; Kaneva, R.; Dimitrov, R.; Savov, A.; Ivanov, S.; Dyankova, T.; Kremensky, I.; Mitev, V., 2010:
Rare mutations in the PIK3CA gene contribute to aggressive endometrial cancer

Monette, M.Y.; Rinehart, J.; Lifton, R.P.; Forbush, B., 2011:
Rare mutations in the human Na-K-Cl cotransporter (NKCC2) associated with lower blood pressure exhibit impaired processing and transport function

Breitenkamp, A.F.S.; Matthes, J.; Nass, R.Daniel.; Sinzig, J.; Lehmkuhl, G.; Nürnberg, P.; Herzig, S., 2015:
Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function

Vergotine, Z.; Kengne, A.P.; Erasmus, R.T.; Yako, Y.Y.; Matsha, T.E., 2014:
Rare mutations of peroxisome proliferator-activated receptor gamma: frequencies and relationship with insulin resistance and diabetes risk in the mixed ancestry population from South Africa

Nakanishi, H.; Uzawa, K.; Yokoe, H.; Miya, T.; Wang, X.; Watanabe, T.; Miyakawa, A.; Shiiba, M.; Sato, T.; Imai, Y.; Tanzawa, H., 1997:
Rare mutations of the growth suppressor genes involved in negative regulation of the cell cycle

Iatta, R.; Napoli, C.; Borghi, E.; Montagna, M.Teresa., 2010:
Rare mycoses of the oral cavity: a literature epidemiologic review

Wang, Y-Fei.; Li, Q.; Xu, W-Gui.; Xiao, J-Yu.; Pang, Q-Song.; Yang, Q.; Zhang, Y-Zuo., 2013:
Rare myeloid sarcoma/acute myeloid leukemia with adrenal mass after allogeneic mobilization peripheral blood stem cell transplantation

Gentili, S.; Lonial, S., 2016:
Rare myelomas: sometimes when you hear hooves, it's a zebra..

Cikes, N.; Baresić, M., 2013:
Rare myositides and myopathies

Savastano, C.Pagani.; Bernardi, P.; Seuánez, H.N.; Moreira, M.Ângelo.Martins.; Orioli, Iêda.Maria., 2014:
Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene

Araújo, R.de.Paula.; Gomes, E.Ferreira.; Menezes, D.Beserra.de.; Ferreira, L.Maria.de.Brito.Macedo.; Rios, A.Sales.do.Nascimento., 2008:
Rare nasosinusal tumors: case series and literature review

Khan, M.; Komanduri, S., 2010:
Rare natural killer cell lymphoma found during surveillance endoscopy

Rivas-Crespo, M.Francisco.; Miñones-Suárez, L.; G-Gallarza, S.Serrano., 2012:
Rare neonatal diabetes insipidus and associated late risks: case report

Strom, T.; Kleinschmidt-Demasters, B.K.; Donson, A.; Foreman, N.K.; Lillehei, K.O., 2009:
Rare nerve lesions of non-nerve sheath origin: a 17-year retrospective series

Soltoggio, A.; Lemme, A.; Reinhart, F.; Steil, J.J., 2013:
Rare neural correlations implement robotic conditioning with delayed rewards and disturbances

Cheng, S-Ping.; Doherty, G.M., 2010:
Rare neuroendocrine tumors of the pancreas

Landais, A.F., 2015:
Rare neurologic complication of bariatric surgery: acute motor axonal neuropathy (AMAN), a severe motor axonal form of the Guillain Barré syndrome

Kuehn, B.M., 2009:
Rare neurological condition linked to newer monoclonal antibody biologics

The Lancet Neurology, 2011 :
Rare neurological diseases: a united approach is needed

Vanicek, J.; Stastnik, M.; Kianicka, B.; Bares, M.; Bulik, M., 2013:
Rare neurological presentation of human granulocytic anaplasmosis

Chan, L.Gwen.; Lee, J.; Ng, B.Tat.; Chua, H.Choon.; Sim, K.; Lee, E.Lian., 2008:
Rare neuropsychiatric sequelae following neuroleptic malignant syndrome: a case report and review of the literature

Kourti, M.; Hatzipantelis, E.; Zaramboukas, T.; Tragiannidis, A.; Petrakis, G.; Athanassiadou-Piperopoulou, F., 2012:
Rare non-Wilms' tumors in children

Kondi-Pafiti, A.; Dellaportas, D.; Myoteri, D.; Tsagkas, A.; Ntakomyti, E.; Kairi-Vasilatou, E., 2013:
Rare non-epithelial primary breast neoplasms: a ten-year experience at a Greek University Hospital

Vrieze, S.I.; Feng, S.; Miller, M.B.; Hicks, B.M.; Pankratz, N.; Abecasis, Gçalo.R.; Iacono, W.G.; McGue, M., 2014:
Rare nonsynonymous exonic variants in addiction and behavioral disinhibition

Xu, C.; Chou, G-Xin.; Wang, C-Hong.; Wang, Z-Tao., 2013:
Rare noriridoids from the roots of Andrographis paniculata

Tsentilo, V.G.; Chiganenko, G.F.; Kraĭnikova, E.V.; Pavlenko, M.Iu., 2009:
Rare observation of coexistant medial cervical split with papilloma and atypical medial fistula

Konik, I.M.; Kozlenko, I.I.; Kniazeva, V.G., 2008:
Rare observation of destructive diverticulum of colon ascendens

Shevchuk, A.N.; Sidorenko, I.S.; Galenko, V.S., 2011:
Rare observation of gastric diverticulum

Kulaga, V.V.; Reshetniak, V.V.; Butenko, I.V., 2008:
Rare observation of gastric wound

Tropinskaia, O.F.; Shishkina, L.V.; Shkarubo, A.N.; Astaf'eva, L.I.; Shimanskiĭ, V.N., 2010:
Rare observation of giant pituitary adenoma spreading into posterior cranial fossa

Davidov, M.I.; Gerner, A.O.; P'iankova, O.B., 2014:
Rare observation of giant trichobezoar of the stomach, duodenum and jejunum

Kadasheva, A.B.; Cherekaev, V.A.; Arutiunov, N.V.; Galkin, M.V., 2010:
Rare observation of hyperostotic cranial lesions in osteogenesis imperfecta

Odem, J.E., 2011:
Rare obstetrical cases in our ancient literature

Uysal, A.Cagri.; Orbay, H.; Uraloglu, M.; Sensoz, O.; Hyakusoku, H., 2007:
Rare occupational disease of hair dressers: interdigital pilonidal sinus

Thol, F.; Winschel, C.; Lüdeking, A.; Yun, H.; Friesen, I.; Damm, F.; Wagner, K.; Krauter, Jürgen.; Heuser, M.; Ganser, A., 2012:
Rare occurrence of DNMT3A mutations in myelodysplastic syndromes

Khattri, A.; Zuo, Z.; Brägelmann, J.; Keck, M.K.; E.D.nali, M.; Brown, C.D.; Stricker, T.; Munagala, A.; Cohen, E.E.W.; Lingen, M.W.; White, K.P.; Vokes, E.E.; Seiwert, T.Y., 2015:
Rare occurrence of EGFRvIII deletion in head and neck squamous cell carcinoma

McKeown, S.M.; Carmichael, H.; Markowitz, R-Beth.; Kutlar, A.; Holley, L.; Kutlar, F., 2008:
Rare occurrence of Hb Lepore-Baltimore in African Americans: molecular characteristics and variations of Hb Lepores

Adam, P.; Haralambieva, E.; Hartmann, M.; Mao, Z.; Ott, G.; Rosenwald, A., 2008:
Rare occurrence of IgVH gene translocations and restricted IgVH gene repertoire in ocular MALT-type lymphoma

Kimura, H.; Karube, K.; Ito, Y.; Hirano, K.; Suzuki, M.; Iwata, S.; Seto, M., 2015:
Rare occurrence of JAK3 mutations in natural killer cell neoplasms in Japan

Prokofyeva, D.; Bogdanova, N.; Bermisheva, M.; Zinnatullina, G.; Hillemanns, P.; Khusnutdinova, E.; Dörk, T., 2013:
Rare occurrence of PALB2 mutations in ovarian cancer patients from the Volga-Ural region

Serra, A.; Häberle, B.; König, I.R.; Kappler, R.; Suttorp, M.; Schackert, H.K.; Roesner, D.; Fitze, G., 2008:
Rare occurrence of PHOX2b mutations in sporadic neuroblastomas

Chen, M.; Yao, H.; Chen, S.; Wang, Q.; Wang, Q.; Wen, L.; Xie, J.; Qin, L.; Wu, L.; Qiu, H.; Cen, J., 2015:
Rare occurrence of SET binding protein 1 mutation in patients with acute lymphoblastic leukemia, mixed phenotype acute leukemia and chronic myeloid leukemia in blast crisis

Powell, A.; Parry, G.S.; Houghton, J.D.R.; Herdson, D.M., 2010:
Rare occurrence of a bigeye tuna Thunnus obesus in British waters, with notes on other occurrences of sub-tropical tunas

Vasavada, A.; Parekh, P.; Agrawal, N.; Vinchurkar, M., 2014:
Rare occurrence of a transient isolated unilateral partial third nerve palsy after angioplasty

Schmidt, A.; Schmitz, R.; Giefing, M.; Martin-Subero, J.Ignacio.; Gesk, S.; Vater, I.; Massow, A.; Maggio, E.; Schneider, M.; Hansmann, M-Leo.; Siebert, R.; Küppers, R., 2010:
Rare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma

Chan, R.Shyuan.; Kumar, G.; Vijayananthan, A.A.P., 2013:
Rare occurrence of bilateral breast and peritoneal metastases from osteogenic sarcoma

Ray, A.; Bhattacharya, S.; Kumar, A.; Bhattacharya, K., 2009:
Rare occurrence of carcinoma esophagus in a case of epidermolysis bullosa

Ucima, N.; Tuka, D.Debola.; Kimbongila, M.Matondo.; Lumbala, P.Kasuyi.; Biselele, Térèse.; Tady, B.Muyala.; Nkidiaka, E.Dimbu.; Aloni, M.Ntetani., 2016:
Rare occurrence of ectopia cordis in a Congolese neonate

Yuvaraj, A.; Rohit, A.; Koshy, P.Joseph.; Nagarajan, P.; Nair, S.; Abraham, G., 2015:
Rare occurrence of fatal Candida haemulonii peritonitis in a diabetic CAPD patient

Knebel, C.; Bumm, R.; Becker, K.; Burian, M.; Siewert, J.R., 2007:
Rare occurrence of fulminant acid burn of the esophagus

Antaki, F.; Irwin, B.C.; Levi, E., 2009:
Rare occurrence of gastric pseudomelanosis

Bansal, A.Kumar.; Bindal, R.; Shetty, D.Charan.; Dua, M., 2012:
Rare occurrence of intraosseous schwannoma in a young child, its review and its pathogenesis

Togoo, R.Ahmad., 2013:
Rare occurrence of inverted maxillary third molar impaction: a case report

Cuny, C.; Layer, F.; Strommenger, B.; Witte, W., 2012:
Rare occurrence of methicillin-resistant Staphylococcus aureus CC130 with a novel mecA homologue in humans in Germany

Ahmadu, B.Usman.; Nnanubumom, A.Angela.; Ibrahim, R.Adamu., 2014:
Rare occurrence of mix stromal tumours: a case report of gastrointestinal and extra-intestinal stromal tumour on the jejunum and omentum of a nine year old girl from Adamawa State, Nigeria

Utumi, E.Rubens.; Pedron, I.G.; Zambon, C.E.; Neto, N.P.Castro.; Rocha, Aé.C., 2010:
Rare occurrence of myositis ossificans traumatica in a patient with Rubinstein-Taybi syndrome

Malhotra, G., 2015:
Rare occurrence of renal metastasis from thyroid carcinoma: lessons not to forget in evaluation

Bian, S-Yan.; Duan, L-Fa., 2013:
Rare occurrence of simultaneous coronary artery perforation and intracoronary thrombus formation following angioplasty

Nozary, Y.; Hashemi Fard, O., 2010:
Rare occurrence of simultaneous dissection, perforation and thrombosis of external iliac artery following diagnostic coronary angiography: a case report

Boraiah, S.; Krishna, S.A.V.; Rangappa, S.S., 2014:
Rare occurrence of symphysis pubis diastasis following normal vaginal delivery

Yin, J.; Xu, Y.; Pan, J.; Wu, C.; Wang, Q.; Yao, H.; Wen, L.; Tian, X.; Wu, D.; Sun, A.; Chen, S., 2014:
Rare occurrence of the JAK1 mutation in acute promyelocytic leukemia patients

Ho, P-Leung.; Lai, E.; Chan, P-Ying.; Lo, W-U.; Chow, K-Hung., 2014:
Rare occurrence of vancomycin-resistant Enterococcus faecium among livestock animals in China

Chadha, V.; Barr, A., 2007:
Rare ocular and systemic associations in a case of neurofibromatosis 2

Chen, Y-Hsing.; Sun, M-Hui.; Hsia, S-Hsuan.; Lai, C-Chun.; Wu, W-Chi., 2015:
Rare ocular features in a case of Kabuki syndrome (Niikawa-Kuroki syndrome)

Malhotra, K.; Ramanathan, R.Santosh.; Synowiec, A.; Rana, S., 2014:
Rare ocular manifestation in a case of West Nile virus meningoencephalitis

Krejčířová, I.; Varadyová, B.; Doležel, Z.; Autrata, R.; Matúšová, J.; Gregorová, E., 2015:
Rare ocular manifestation with suspect alport syndrome

Jones, M.D.; May, I.C.; Sweet, K.J., 2015:
Rare open hallux interphalangeal joint dislocations sustained in combatives training: a case series

Chitasombat, M.N.; Kofteridis, D.P.; Jiang, Y.; Tarrand, J.; Lewis, R.E.; Kontoyiannis, D.P., 2012:
Rare opportunistic (non-Candida, non-Cryptococcus) yeast bloodstream infections in patients with cancer

Lloret, A.; Hartmann, K.; Pennisi, M.Grazia.; Ferrer, L.; Addie, D.; Belák, Sándor.; Boucraut-Baralon, C.; Egberink, H.; Frymus, T.; Gruffydd-Jones, T.; Hosie, M.J.; Lutz, H.; Marsilio, F.; Möstl, K.; Radford, A.D.; Thiry, E.; Truyen, U.; Horzinek, M.C., 2014:
Rare opportunistic mycoses in cats: phaeohyphomycosis and hyalohyphomycosis: ABCD guidelines on prevention and management

Baxter, P., 2012:
Rare or orphan diseases -- a useful political concept

Mandeel, Q.A.; Blackwell, M., 2008:
Rare or rarely collected? Comatricha mirabilis from the desert of Bahrain

Ale-Agha, N.; Jensen, M.; Brassmann, M.; Kautz, S.; Eilmus, S.; Ballhorn, D.J., 2009:
Rare or remarkable microfungi from Oaxaca (south Mexico)--Part II

Cribier, B., 2012:
Rare or unusual forms of psoriasis

Mehta, A.; Chandra, M., 2010:
Rare orbitocranial tumour in an adult

Ramasamy, S.; Paramasivam, J.; Janardhanam, K., 2008:
Rare ovarian lesion in an adolescent girl

Fernández-Prada, S.; Tobías-González, P.; de Santiago-García, J.; Zapardiel, I., 2013:
Rare ovarian tumor

Gungor, T.; Altinkaya, S.O.; Baser, E.; Guler, I.; Uzunlar, O., 2014:
Rare ovarian tumors: a single center experience of 15 years

Ray-Coquard, I.; Pautier, P.; Pujade-Lauraine, E.; Méeus, P.; Morice, P.; Treilleux, I.; Duvillard, P.; Alexandre, J.; Lhommé, C.; Selle, F.; Guastalla, J., 2010:
Rare ovarian tumours: therapeutic strategies in 2010, national website observatory for rare ovarian cancers and delineation of referent centers in France

Lerebours, F.; Callens, Céline.; Vacher, S.; Hatem, R.; Guinebretière, J-Marc.; Bièche, I., 2013:
Rare overexpression of anaplastic lymphoma kinase gene in inflammatory and non-inflammatory breast cancer

Stoumpos, C.C.; Inglis, R.; Roubeau, O.; Sartzi, H.; Kitos, A.A.; Milios, C.J.; Aromí, G.; Tasiopoulos, A.J.; Nastopoulos, V.; Brechin, E.K.; Perlepes, S.P., 2010:
Rare oxidation-state combinations and unusual structural motifs in hexanuclear Mn complexes using 2-pyridyloximate ligands

Akyuz, F.; Sahin, D.; Akyuz, U.; Vatansever, S., 2014:
Rare pancreas tumor mimicking adenocarcinoma: Extramedullary plasmacytoma

Krysiak, R.; Okopień, Bław.; Herman, Z.Stanisław., 2008:
Rare pancreatic endocrine tumors

Palmucci, S.; Uccello, A.; Leone, G.; Failla, G.; Ettorre, G.Carlo., 2012:
Rare pancreatic neoplasm: MDCT and MRI features of a typical solid pseudopapillary tumor

Imaoka, H.; Yamao, K.; Bhatia, V.; Shimizu, Y.; Yatabe, Y.; Koshikawa, T.; Kinoshita, Y., 2009:
Rare pancreatic neoplasms: the utility of endoscopic ultrasound-guided fine-needle aspiration-a large single center study

Vissers, L.E.L.M.; Bhatt, S.S.; Janssen, I.M.; Xia, Z.; Lalani, S.R.; Pfundt, R.; Derwinska, K.; de Vries, B.B.A.; Gilissen, C.; Hoischen, A.; Nesteruk, M.; Wisniowiecka-Kowalnik, B.; Smyk, M.; Brunner, H.G.; Cheung, S.Wai.; van Kessel, A.Geurts.; Veltman, J.A.; Stankiewicz, P., 2009:
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture

Hauer, B.; Loddenkemper, R., 2010:
Rare pathologies

Geiger, J.; Arnold, R.; Baumann, T.; Uhl, M.; Jung, B.A.; Langer, M.; Markl, M., 2009:
Rare pattern of aortic arch branching in a patient with operated congenital heart disease

Agarwal, S.; Agarwal, K., 2011:
Rare pediatric adrenocortical carcinoma with oncocytic change: a cytologic dilemma

Penk, J.; Koenig, P.; Mavroudis, C., 2010:
Rare pediatric cardiac tumor presentation

Setty, B.A.; Termuhlen, A.M., 2010:
Rare pediatric non-hodgkin lymphoma

Urs, A.B.; Augustine, J.; Arora, S.; Kumar, P., 2013:
Rare pediatric presentation of aneurysmal bone cyst with trabecular juvenile ossifying fibroma and ossifying fibroma

Bakhshaee, M.; Khazaeni, K.; Khadivi, E., 2008:
Rare penetrating orbital trauma

Trost, B.; Kanduc, D.; Kusalik, A., 2008:
Rare peptide segments are found significantly more often in proto-oncoproteins than control proteins: implications for immunology and oncology

Ide, F.; Mishima, K.; Saito, I.; Kusama, K., 2008:
Rare peripheral odontogenic tumors: report of 5 cases and comprehensive review of the literature

Gupta, A.; Purkait, S.; Das, K.Shankar.; Sarkar, S.; Maity, P.; Sasmal, N.Kumar.; Mandal, R.; Roy, S.; Ghanta, A.Kumar.; Biswas, M.Chandra., 2012:
Rare persistent kerato-acanthoma of left lower eyelid: a case report

Fonkem, E.; Lun, M.; Wong, E.T., 2012:
Rare phenomenon of extracranial metastasis of glioblastoma

Schönsteiner, S.S.; Bommer, M.; Haenle, M.M.; Klaus, B.; Scheuerle, A.; Schmid, M.; Mayer-Steinacker, R., 2011:
Rare phenomenon: liver metastases from glioblastoma multiforme

Süsskind, D.; Rohrbach, J.M.; Aisenbrey, S.; Coupland, S.E.; Bartz-Schmidt, K.U., 2015:
Rare pigmented fundus tumor

Zlobin, I.A., 2012:
Rare plant species: floristic, phytocoenotic and population approach

Nisar, S.P.; Jones, M.L.; Cunningham, M.R.; Mumford, A.D.; Mundell, S.J., 2016:
Rare platelet GPCR variants: what can we learn?

Townshend, A.P.; Lakshminarayanan, B.; Ucar, A.E.Martin.; Chaudry, Z.R.; Duffy, J.P., 2007:
Rare pleural recurrence of typical pulmonary carcinoid tumor 30 years after lobectomy

Seligová, J.; Belyová, A.; Culmanová, A.; Oleár, Vír.; Cisláková, Lýdia., 2012:
Rare positive laboratory tests for the presence of influenza virus A/H1N1--2009 in May, June, July, 2011, in the districts of Kosice I-IV and surroundings of Kosice in the Slovak Republic

Singh, P.K.; Masood, A.; Chawla, O.P., 2008:
Rare post-tonsillectomy complication in human immunodeficiency virus positive patient: ulcero-necrotic lesion of tonsillar fossa

Ribeiro, S.; Monteiro, M.; Moreira, B.; França, M., 2014:
Rare posterior reversible encephalopathy syndrome in a patient with HIV

Tan, Y.L.; Naidu, A., 2015:
Rare postpartum ruptured degenerated fibroid: a case report

Akpinar, I.; Guray, Y.; Demirkan, B.; Boyaci, A.Ayca.; Basar, N.; Cagli, K.; Kisacik, H.Lutfu., 2012:
Rare postsurgical complication of atrial septal defect closure: right inflow obstruction due to inadvertent suturing of eustachian valve to interatrial septum

Polyzos, S.A.; Anastasilakis, A.D., 2011:
Rare potential complications of thyroid fine needle biopsy

Wang, B.; Hunter, W.J.; Bin-Sagheer, S.; Bewtra, C., 2009:
Rare potential pitfall in endoscopic ultrasound-guided fine needle aspiration biopsy in gastric duplication cyst: a case report

Hegazy, M-Elamir.F.; Abd el-Razek, M.H.; Nagashima, F.; Asakawa, Y.; Paré, P.W., 2010:
Rare prenylated flavonoids from Tephrosia purpurea

Ganapaty, S.; Nair, V.; Devi, D.Rama.; Pannakal, S.Thomas.; Laatsch, H.; Dittrich, B., 2014:
Rare prenylated isoflavones from Tephrosia calophylla

Ge, P.; Wang, H.; Zhong, Y.; Chen, B.; Ling, F.; Luo, Y., 2011:
Rare presentation in an adult patient with neurocutaneous melanosis

Green, J.; Saigal, G.; Rojas, C.P.; Post, M.Judith.Donovan., 2013:
Rare presentation of BK encephalitis in a child: imaging and pathological findings

Vyas, S.; Skipworth, J.R.A.; Lytras, D.; Smyth, C.; Mee, A.; Hatfield, A.; Imber, C.; Webster, G., 2012:
Rare presentation of Brunner's gland adenoma: another differentiation in patients with recurrent "idiopathic" pancreatitis

A.B.gami, M.Mohammed.; A.A.hgar, H.Ibrahim.; A.S.haibani, H.Saleh.; Khuroo, M.Sultan., 2003:
Rare presentation of Budd-Chiari syndrome

Jerome, J.Terrence.Jose.; Sankaran, B.; Varghese, M.; Thomas, S.; Thirumagal, S.K., 2009:
Rare presentation of Ewing's sarcoma: a case report and literature review

Viswanathan, S.; Narurkar, S.D.; Rajpal, A.; Nagpur, N.G.; Avasare, S.S., 2008:
Rare presentation of Kyrle's disease in siblings

E.M.lla, M.; Mahasneh, T.; Holmes, S-Ellen.; Al-Khawaja, D., 2014:
Rare presentation of Rosai-Dorfman disease mimicking a cervical intramedullary spinal cord tumor

Gangahanumaiah, S.; Raju, V.; Jayavelan, R.Kumar.; Kavunkal, A.Mathew.; Cherian, V.Koshy.; Danda, D.; Bashi, V.V., 2008:
Rare presentation of Takayasu's aortoarteritis after double valve replacement

Ayakannu, T.; Wordsworth, S.; Parveen, S.; Shehadeh, Z.; Moselhi, M., 2008:
Rare presentation of Trisomy 8 syndrome

Khaira, A.; Gupta, V.; Gupta, A.; Mahajan, S.; Bhowmik, D.; Tiwari, S.C., 2009:
Rare presentation of a common disease of tropics

Ghosh, K.; Sengupta, N.; Sau, T.Jyoti.; Chatterjee, A., 2012:
Rare presentation of a common disease: Idiopathic hypoparathyroidism presenting with extrapyramidal symptoms and status epilepticus

D'souza, I.Edwin.; Patidar, R.Chandra.; Mani, R.; Shamseldeen, M.; Jose, J., 2010:
Rare presentation of a congenital neuroblastoma

Sjogren, P.P.; Banerji, N.; Batts, K.P.; Graczyk, M.J.; Dunn, D.H., 2013:
Rare presentation of a gastrointestinal stromal tumor with spontaneous esophageal perforation: A case report

Combalía, Aés.; Marco, V.; Seijas, R.; Domínguez, R., 2015:
Rare presentation of a soft-tissue myoepithelial carcinoma

Shah, K.; Molmenti, E.P.; Coppa, G.F.; Procaccino, J.A.; Angel, L.P., 2011:
Rare presentation of an intrauterine device migration into the rectum

Salerni, S.; Barison, A.; Andrea, B.; Masci, P.Giorgio.; Aquaro, G.Donato., 2014:
Rare presentation of asymptomatic pericardial effusion: hemangioma of the atrioventricular groove in cardiac magnetic resonance imaging

Kohli, A.; Singh, G.; Sharma, S., 2008:
Rare presentation of bilateral femoral arteriovenous fistula

Rather, A.; Salati, S.Ahmad., 2010:
Rare presentation of biliary ascariasis

Arora, A.; Sharma, C.Mohan.; Kumawat, B.; Khandelwal, D., 2014:
Rare presentation of botulism with generalized fasciculations

Nguyen, T.T.; Warnke, R.A.; Seo, K.; Rosenberg, S.A.; Arber, D.A., 2010 :
Rare presentation of classical Hodgkin lymphoma with a clonal T-cell receptor gene rearrangement in the tissue

Caltik, A.; Akyüz, S.Gülfem.; Erdogan, O.; Bülbül, M.; Demircin, Gülay., 2010:
Rare presentation of cystinosis mimicking Bartter's syndrome: reports of two patients and review of the literature

Al-Fraikh, H.; Al-Dahmash, S., 2010:
Rare presentation of definitive ocular tuberculosis in an immunocompetent young patient

Atabekoğlu, C.Somer.; Gözükuçük, M.; Ozkavukçu, S.; Sönmezer, M., 2009:
Rare presentation of ectopic pregnancy following IVF-ET: live twin gestation in the same fallopian tube

Artioli, G.; Cassaro, M.; Pedrini, L.; Borgato, L.; Corti, L.; Cappetta, A.; Lombardi, G.; Nicoletto, M.O., 2011:
Rare presentation of endometrial carcinoma with singular bone metastasis

Persu, A.; Amyere, M.; Gutierrez-Roelens, I.; Rustin, P.; Sempoux, C.; Lecouvet, Fédéric.E.; Van Beers, B.E.; Horsmans, Y.; D.P.aen, J-François.; MarcHamoir; Vikkula, M., 2009:
Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity

Rafique, A.; Arshad, A.; Abu-Zaid, A., 2014:
Rare presentation of foot postaxial polydactyly

Kumar, S.; Shankaregowda, S.Ajjoor.; Choudhary, G.Ram.; Singla, K., 2014:
Rare presentation of genitourinary tuberculosis masquerading as renal cell carcinoma: a histopathological surprise

Otaigbe, B.E.; Orubide, D., 2013:
Rare presentation of gerbode defect in a 4-month-old nigerian and a review of the literature

Bajpai, J.; Saini, S.; Bajpai, A.; Khera, R., 2013 :
Rare presentation of giant cell tumor of bone in the lateral end of the clavicle

Sasmaz, S.; Uzel, M.; Sener, S.; Ucmak, H., 2011:
Rare presentation of human orf as multiple lesions

Alaraj, A.; Behbahani, M.; Valyi-Nagy, T.; Aardsma, N.; Aletich, V.A., 2016:
Rare presentation of intracranial vascular blowout after tumor resection and radiation therapy

Jain, A.; Mathur, K.; Khatri, S.; Kasana, S.; Jain, S.K., 2012:
Rare presentation of juvenile xanthogranuloma in the thoracic spine of an adult patient: case report and literature review

Ghosh, S.; Joy, R.; Hickey, S., 2007:
Rare presentation of laryngeal neuroma in a patient with multiple endocrine neoplasia type two B

Gupta, S.; Misra, S., 2013:
Rare presentation of malignant porcelain gallbladder with intrahepatic ductal calcification and surgical obstructive jaundice

Choong, C.; Chan, H.; Azuhairy, A.; Hau, M.Anwar.; Zulkiflee, O., 2014:
Rare presentation of metachronous multicentric pelvic and extracranial chondrosarcoma : a case report

Daraki, V.; Koukouraki, S.; Velegrakis, G.; Mamalaki, E.; Haniotis, V.T.; Kalikakis, G.; Stathaki, M.I.; Karkavitsas, N.; Papavasiliou, S.S., 2013:
Rare presentation of occult medullary carcinoma of the thyroid as a mediastinal mass

Tofigh, A.Mohammadi.; Hashemi, M.; Honar, B.Nemati.; Solhjoo, F., 2008:
Rare presentation of pancreatic schwannoma: a case report

Erdem, E.; Kayıran, P.; Ozcelik, G.; Ozel, A.; Yildiz Yildirmak, Z., 2012:
Rare presentation of pediatric acute lymphoblastic leukemia: nephromegaly at time of diagnosis

Nair, M.; Kusumakumary, P.; Nair, P.Sindhu., 2015:
Rare presentation of pediatric acute promyelocytic leukemia as multiple lytic bone lesions: case report and review of literature

Etkin, Y.; Chao, E., 2013:
Rare presentation of perforated diverticulitis

Wang, C.; Qiu, T-Tian.; Yu, X-Feng.; Xuan, M.; Gu, Q-Quan.; Qian, W.; Zhang, M-Ming., 2014:
Rare presentation of peripheral primitive neuroectodermal tumor in the maxilla and mandible: A report of two cases

Saligoudar, P.; Seshadri, R.; Pandey, P., 2013:
Rare presentation of pial arteriovenous malformations as proptosis: case report and review of literature

Khan, M.; Thyagiarajan, M.; Laugharne, M.; Clinch, J., 2014:
Rare presentation of polyarticular juvenile idiopathic arthritis and the role of the radiograph in initial diagnosis

Gupta, S.; Jauhari, R.Kumar., 2013:
Rare presentation of porcelain gall bladder: carcinoma gall bladder with a large intra-abdominal cystic swelling

Haverkos, B.M.; Oza, V.M.; Johnson, A.; Walker, J.; Shana'ah, A., 2013:
Rare presentation of post-transplant lymphoproliferative disorder isolated to gastroesophageal junction

Ali, M.F.; Patel, A.; Muller, S.; Friedel, D., 2014:
Rare presentation of primary (AL) amyloidosis as gastrointestinal hemorrhage without systemic involvement

Pronisceva, V.; Bagla, N.; Lakshmaiah, S.; Sharp, E., 2012:
Rare presentation of primary coloduodenal fistula

Chen, S-Chueh.; Liu, J-Cherng.; Tseng, G-Chin.; Chen, C-Yi., 2011:
Rare presentation of pulmonary cryptococcosis as a calcified nodule

Mozafar, M.; Lotfollahzadeh, S.; Atqiaee, K.; Adhamy, F., 2014:
Rare presentation of retroperitoneal schwannoma: a case report

Mohebbi, A.; Jahandideh, H.; Harandi, A.Amini., 2011:
Rare presentation of rhino-orbital-cerebral zygomycosis: bilateral facial nerve palsy

Lester, R.A.; Torgerson, R.R.; Sandhu, N.P., 2014:
Rare presentation of sebaceous hyperplasia

Cohen, J.M.; Nazarian, R.M.; Ferry, J.A.; Takvorian, R.W.; Carter, J.B., 2015:
Rare presentation of secondary cutaneous involvement by splenic marginal zone lymphoma: report of a case and review of the literature

Puri, Y.; Lytras, D.; Luong, T.Vihn.; Fusai, G.Kito., 2014:
Rare presentation of self-resolving multifocal inflammatory pseudo-tumour of liver

Roldan-Martin, M.B.; Rodriguez-Ogando, A.; Sanchez-Galindo, A.C.; Parente-Hernandez, A.; Luengo-Herrero, V.; Sanchez-Sanchez, C., 2013:
Rare presentation of shock and acute mesenteric ischaemia secondary to acute adrenal insufficiency in an 11-year-old male

Gupta, S.; Bali, R.Kaur.; Das, K.; Sisodia, A.; Dewan, R.K.; Singla, R., 2011:
Rare presentation of spontaneous acquired diaphragmatic hernia

Ashrafian, H.; Tsang, V.; Kostolny, M., 2007:
Rare presentation of subclavian artery isolation in a neonate with a family history of aortic arch anomalies

Srinivasan, A.; Hayes, M.; Chepeha, D.; Mukherji, S.K., 2007:
Rare presentation of thyroglossal duct cyst after radiation therapy to the neck

Reece, B.; Ord, R.; Papadimitriou, J., 2012:
Rare presentation of unicentric Castleman's disease in the parotid gland

Indiran, V.; Maduraimuthu, P., 2012:
Rare presentation of unilateral weakness, involuntary movements and ataxia with subcortical t2 hypointensity in a diabetic patient: a case report

Ravindranath, K.Shankarappa.; Bhat, S.; Setty, K.; Subramanyam, S.; Dhanalakshmi, C., 2009:
Rare presentation of unruptured sinus of valsalva aneurysm involving all three sinuses

Smolkin, T.; Ulanovsky, I.; Blazer, S.; Makhoul, I.R., 2012:
Rare presentations of congenital hypothyroidism

Ardalan, M., 2013:
Rare presentations of cytomegalovirus infection in renal allograft recipients

Chen, Y-Hsien.; Lin, H-Jung.; Chen, K-Tai., 2009:
Rare presentations of hyperthyroidism--Basedow's paraplegia and pancytopenia

Kottschade, L.A.; Grotz, T.E.; Dronca, R.S.; Salomao, D.R.; Pulido, J.S.; Wasif, N.; Jakub, J.W.; Bagaria, S.P.; Kumar, R.; Kaur, J.S.; Morita, S.Y.; Moran, S.L.; Nguyen, J.T.; Nguyen, E.C.; Hand, J.L.; Erickson, L.A.; Brewer, J.D.; Baum, C.L.; Miller, R.C.; Swanson, D.L.; Lowe, V.; Markovic, S.N., 2015:
Rare presentations of primary melanoma and special populations: a systematic review

Rhea, J.M.; Molinaro, R., 2014:
Rare presumptive Hb variant misidentification prevents appropriate Hb A1c result

Kubicky, C.Dai.; Sahgal, A.; Chang, E.L.; Lo, S.S., 2014:
Rare primary central nervous system tumors

Fekih, L.; Boussoffara, L.; Fenniche, S.; Abdelghaffar, H.; Akrout, I.; Ayadi, A.; Megdiche, M-L., 2011:
Rare primary chest wall sarcoma: the synovialosarcoma

Ikebe, T.; Amemiya, Y.; Saburi, M.; Ando, T.; Kohno, K.; Ogata, M.; Hiramatsu, K.; Kadota, J., 2010:
Rare primary effusion lymphoma associated with HHV-8 in Japan

De, U., 2009:
Rare primary extrahepatic intra-abdominal hydatid cysts

Rajnics, Péter.; Demeter, J.; Csomor, J.; Krenács, László.; Pajor, László.; Kollár, Bázs.; Kertész, Z.; Egyed, Mós., 2009:
Rare primary extranodal lymphomas: diffuse large B-cell lymphomas of the genital tract

Oztürk, V., 2007:
Rare primary headache syndromes

Holle, D.; Obermann, M., 2015:
Rare primary headaches

Venara, Aélien.; Mehinto, D.K.; Lermite, E.; Chabasse, D.; Hamy, A.; Arnaud, J-Pierre., 2011:
Rare primary localization of hydatidosis

Achilli, A.; Iommarini, L.; Olivieri, A.; Pala, M.; Hooshiar Kashani, B.; Reynier, P.; L.M.rgia, C.; Valentino, M.Lucia.; Liguori, R.; Pizza, F.; Barboni, P.; Sadun, F.; D.N.gri, A.Maria.; Zeviani, M.; Dollfus, H.; Moulignier, A.; Ducos, G.; Orssaud, C.; Bonneau, D.; Procaccio, V.; Leo-Kottler, B.; Fauser, S.; Wissinger, B.; Amati-Bonneau, P.; Torroni, A.; Carelli, V., 2013:
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy

Majchrzak, K.; Bierzyńska-Macyszyn, Gżyna.; Bobek-Billewicz, B.; Majchrzak, H.; Ładziński, P., 2011:
Rare primary tumours of the hypothalamus in adults: clinical course and surgical treatment

Anonymous, 2013:
Rare problem with the insertion of a Supreme™ laryngeal mask airway device. Case of the trimester

Goldberg, D.J.; Dodds, K.; Rychik, J., 2011:
Rare problems associated with the Fontan circulation

Hughes, G., 2013:
Rare procedures

Fu, W.; Peng, H.; Chen, Z.; Wang, S.; Li, Y.; Xie, M.; Yang, S., 2014:
Rare prostate metastasis of lung adenocarcinoma: a case report and literature review

Giordano, V.; Hermens, J.A.J.M.; Wajon, E.M.C.J.; Grandjean, J.G., 2011:
Rare prosthesis failure after aortic valve replacement with a Freedom Solo

Plenge, R.M., 2009:
Rare protection against type 1 diabetes

Dibbens, L.M.; Hodgson, B.L.; Helbig, K.L.; Oliver, K.L.; Mulley, J.C.; Berkovic, S.F.; Scheffer, I.E., 2013:
Rare protein sequence variation in SV2A gene does not affect response to levetiracetam

Fuckar, K.; Lakusić, N.; Cerovec, D., 2010:
Rare psychotropic adverse event of moxonidine

Zhao, H.; Wang, H-Qin.; Fan, Q-Qiu.; Chen, X-Xian.; Lou, J-Ying., 2008:
Rare pulmonary and cerebral complications after transarterial chemoembolisation for hepatocellular carcinoma: a case report

Harari, S.; Agostini, C., 2010:
Rare pulmonary diseases: a path to the future

Mao, L.; Wang, H.; Xie, G.; Zhang, N.; Liao, G., 2013:
Rare pulmonary primitive neuroectodermal tumor metastasizing to the right atrium: a case report

Chien, S-Chin.; Li, Y-Chun.; Ho, M.; Hsu, P-Ching.; Teng, R-Hsiou.; Lin, W-De.; Tsai, F-Jen.; Lin, C-Chyang., 2010:
Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX male

Yuan, Z.; Maihesuti, M.; Wenya, L.; Cheng, Z.; Biyemu, N.; Haitao, W., 2016:
Rare reason for pulmonary embolism: one case of pulmonary hydatid cyst and review of the literature

van Meel, E.; Wegner, D.J.; Cliften, P.; Willing, M.C.; White, F.V.; Kornfeld, S.; Cole, F.Sessions., 2014:
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype

Brady, B., 2013:
Rare recovery for acid attack victim in Cambodia

Hsu, K-Feng.; Hsieh, C-Bao.; Yu, J-Cherng.; Chan, D-Chuan.; Wu, C-Chieh.; Jin, J-Shiaw.; Jao, S-Wen.; Chao, P-Chieh., 2011:
Rare rectal mucocele mimic tumor following hemorrhoidectomy in an adult patient

E.M.hdi, T.; Essadi, I.; M'rabti, H.; Errihani, H., 2011:
Rare recurrence of a rare ovarian stromal tumor with luteinized cells: a case report

Hashmi, S.; Heidari, A.; Jeng, A., 2008:
Rare red rash

Šileikienė, R.; Kudzytė, J.; Jankauskas, A.; Labanauskas, L.; Rakauskienė, V.; Jurkienė, N.; Kėvalas, R., 2014:
Rare refractory Kawasaki disease in an adolescent boy with cardiac and diffuse coronary artery involvement

Vojta, T.; Igo, J.; Hoyos, Jé.A., 2015:
Rare regions and Griffiths singularities at a clean critical point: the five-dimensional disordered contact process

Ódor, Géza., 2014:
Rare regions of the susceptible-infected-susceptible model on Barabási-Albert networks

Fatimi, S.H.; Schuuring, M.J.; Sheikh, S., 2007:
Rare relapsed extrapulmonary hydatid disease

Ranieri, E., 2009:
Rare renal diseases: diagnosis and nephrological mangement of Anderson-Fabry disease

Qiu, Z-Ling.; Xue, Y-Li.; Luo, Q-Yong., 2015:
Rare renal metastases from differentiated thyroid carcinoma: early clinical detection and treatment based on radioiodine

Duckworth, D.A., 1949:
Rare renal ruptures

Grigore, A.; Toma, L.; Stoicea, M.; Dinu, M.; Ardeleanu, C., 2012:
Rare renal tumor--mucinous tubular and spindle cell carcinoma

Compérat, E., 2014:
Rare renal tumors. Case No 8. Collision tumors and multiple tumors

Rioux-Leclercq, N., 2014:
Rare renal tumors. Case no 6. Renal metastases

Compérat, E., 2014:
Rare renal tumors. Case no 7. "Atypical" oncocytoma: how many atypia can we accept?

Leroy, X., 2014:
Rare renal tumors. Case no. 3. Renal carcinoid tumor

Leroy, X., 2014:
Rare renal tumors. Case no. 4. Atypical epithelioid angiomyolipoma

Lindner, Véronique., 2014:
Rare renal tumors. Case n° 1. Collecting duct renal cell carcinoma

Lindner, Véronique., 2014:
Rare renal tumors. Case n° 2. Clear cell (tubulo) papillary renal cell carcinoma

Rioux-Leclercq, N., 2014:
Rare renal tumors. Case n° 5. Translocation renal carcinomas

Rioux-Leclercq, N., 2014:
Rare renal tumors. Introduction

Rioux-Leclercq, N., 2014:
Rare renal tumors. Pretest

Molinié, V., 2014:
Rare renal tumors: a frequent pathology!

Peter, J.; David, S.; Joseph, G.; Horo, S.; Danda, D.; Peter, J.Victor., 2014:
Rare retinal manifestations in Takayasu arteritis

Hemalatha, A.L.; D.V.; M.G.; M.B.; S.G., 2014:
Rare retro-orbital intraconal occurrence of benign schwannoma - a case report

Beckmann, R.; Homberg, R.; Niemann, P.; Reiter-Owona, I., 2012:
Rare retrovesical tumor manifestation of cystic echinococcosis (Echinococcus granulosus)

Myrianthefs, P.; Markou, N.; Gregorakos, L., 2012:
Rare roentgenologic manifestations of pulmonary edema

Ch'ng, L-Sing.; Lee, W.S.; Kirkwood, C.D., 2011:
Rare rotavirus strains in children with severe diarrhea, Malaysia

Li, S.; Zhao, J.; Ma, P.; Du, J.; Niu, J.; Wang, J., 2009:
Rare sandwich-type polyoxomolybdates constructed from Di-/tetra-nuclear transition-metal clusters and trivacant keggin germanomolybdate fragments

Taghi, A.S.; Ali, A.; Kuchai, R.; Saleh, H., 2013:
Rare sarcoma presented as sinusitis

Puntambekar, P.; Basha, M.M.; Zak, I.T.; Madhavan, R., 2010:
Rare sensory and autonomic disturbances associated with vitamin B12 deficiency

Goel, S.K.; Kuruvila, M., 2007:
Rare sequelae of herpes zoster in HIV positive patient

Zech, M.; Gross, N.; Jochim, A.; Castrop, F.; Kaffe, M.; Dresel, C.; Lichtner, P.; Peters, A.; Gieger, C.; Meitinger, T.; Haslinger, B.; Winkelmann, J., 2014:
Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

Deucher, A.; Chiang, T.; Schrijver, I., 2010:
Rare sequence variation in the genome flanking a short tandem repeat locus can lead to a question of "nonmaternity"

Kapoor, S., 2013:
Rare serious complications of erlotinib therapy

Michael, N.L., 2012:
Rare serotype adenoviral vectors for HIV vaccine development

Li, L.; Wang, R.; Liang, W.; Gan, X.; Huang, T.; Huang, Y.; Li, J.; Shi, Y.; Chen, M.; Luo, H., 2014:
Rare serotype occurrence and PFGE genotypic diversity of Streptococcus agalactiae isolated from tilapia in China

Simşek, P.Ozlem.; Utine, Gülen.Eda.; Alikaşifoğlu, A.; Alanay, Y.; Boduroğlu, K.; Kandemir, Nün., 2009:
Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes

Martinelli-Filho, J.E.; Melo-Júnior, M.; Cunha, D.R.; Lopes, R.M., 2010:
Rare sexual anomalies in Temora stylifera (Dana, 1849) (Copepoda: Calanoida)

Kapoor, S., 2013:
Rare side effects of subcutaneous methotrexate therapy

Couto, M.; Miranda, Mário., 2014:
Rare simultaneous occurrence of two supposedly antagonistic diseases: Vogt-Koyanagi-Harada disease and allergic conjunctivitis

Kovač, J.; Macedoni Lukšič, M.; Trebušak Podkrajšek, K.; Klančar, Gšper.; Battelino, T., 2014:
Rare single nucleotide polymorphisms in the regulatory regions of the superoxide dismutase genes in autism spectrum disorder

García-Lliberós, A.; Gómez, Mía-José.; Armengot-Carceller, M., 2013:
Rare sinonasal and laryngeal manifestations of Cowden's disease

Treglia, G.; Bongiovanni, M.; Giovanella, L., 2015 :
Rare sinonasal small cell neuroendocrine carcinoma evaluated by F-18-FDG PET/MRI

Saikia, K.C.; Bhuyan, S.K.; Goswami, S.; Bora, A., 2010:
Rare site giant cell tumors: report of two cases on phalanges of the finger and review of literature

Stathopoulos, G.P.; Rigatos, S.K., 2010:
Rare site of metastasis of non-small-cell lung cancer

Li, Z-Ming.; Zhang, F-Jun., 2010:
Rare site osteochondroma: a report of 2 cases

Chawla, A.; Mishra, D.; Bansal, R.; Chundru, M., 2014:
Rare sites of delayed metastasis in renal cell carcinoma

Pasagadugula, K.V.; Chennamsetty, T.; Avvaru, K.; Chennamsetty, K., 2014:
Rare skeletal abnormalities in Rothmund-Thomson syndrome: a case report

Togral, G.; Arıkan, M.; Gungor, S., 2014:
Rare skeletal muscle metastasis after radical nephrectomy for renal cell carcinoma: evaluation of two cases

Riou-Gotta, M.Odile.; Fournier, E.; Danzon, A.; Pelletier, F.; Levang, J.; Mermet, I.; Blanc, D.; Humbert, P.; Aubin, Fçois., 2009:
Rare skin cancer: a population-based cancer registry descriptive study of 151 consecutive cases diagnosed between 1980 and 2004

Kanitakis, J., 2010:
Rare skin cancers

Manfredelli, S.; Andrea, Z.; Stefano, P.; Giovanni, L.; Maria, M.; Angelo, F.; Alberto, A.; Renato, M., 2013:
Rare small bowel obstruction: Right paraduodenal hernia. Case report

Dabkowski, K.; Kojder, K.; Smereczyński, A.; Lubikowski, J.; Patalan, M.; Starzyńska, T., 2013:
Rare solid pancreatic tumors

Kersting, S.; Janot, M.S.; Munding, J.; Suelberg, D.; Tannapfel, A.; Chromik, A.M.; Uhl, W.; Bergmann, U., 2012:
Rare solid tumors of the pancreas as differential diagnosis of pancreatic adenocarcinoma

Cheng, Y.; Zhang, C.; Gao, Y.; Dong, S., 2012:
Rare solitary fibrous tumor of diaphragmatic pleura: a case report

Shen, C.; Liang, Y.; Xu, H.; Che, G., 2015:
Rare solitary neoplasm of the costa in an adult: a case report

Chen, H-Yang.; Wu, J-Lin.; Chen, C-Ti.; Chen, C-Tsen., 2011:
Rare solvent annealing effective benzo(1,2-b:4,5-b')dithiophene-based low band-gap polymer for bulk heterojunction organic photovoltaics

Roy, S.; Gascard, P.; Dumont, N.; Zhao, J.; Pan, D.; Petrie, S.; Margeta, M.; Tlsty, T.D., 2013:
Rare somatic cells from human breast tissue exhibit extensive lineage plasticity

Kim, M.Sung.; An, C.Hyeok.; Yoo, N.Jin.; Lee, S.Hyung., 2011:
Rare somatic mutation and loss of expression of EMX2 gene in common solid cancers

Kim, M.Sung.; Kim, S.Soo.; Yoo, N.Jin.; Lee, S.Hyung., 2013:
Rare somatic mutation of pro-apoptotic BAX and BAK genes in common human cancers

Attar, K.Hama.; Waghorn, D.; Lyons, M.; Cunnick, G., 2007:
Rare species of actinomyces as causative pathogens in breast abscess

Mouillot, D.; Bellwood, D.R.; Baraloto, C.; Chave, J.; Galzin, R.; Harmelin-Vivien, M.; Kulbicki, M.; Lavergne, S.; Lavorel, S.; Mouquet, N.; Paine, C.E.Timothy.; Renaud, J.; Thuiller, W., 2014:
Rare species support vulnerable functions in high-diversity ecosystems

Agrawal, A.; Jatale, P.; Purandare, N.; Shah, S.; Rangarajan, V., 2014:
Rare splenic metastasis of renal cell carcinoma detected on (99m)Tc-MDP bone scan

Ushigome, H.; Koshino, K.; Sakai, K.; Suzuki, T.; Nobori, S.; Matsuyama, M.; Okajima, H.; Okamoto, M.; Yoshimura, N., 2012:
Rare spontaneous remission of hepatic artery aneurysm following ABO incompatible living donor liver transplantation: a case report

Teschke, R.; Frenzel, C.; Wolff, A.; Eickhoff, A., 2013:
Rare statin hepatotoxicity: convincing evidence based on breakthrough case study

Yakut, S.; Çetin, Z.; Şİmşek, M.; Mendilcioğlu, I.Inanç.; Toru, H.Serap.; Berker Karaüzüm, S.; Lüleci, Güven., 2015:
Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases

Sebat, J.; Levy, D.L.; McCarthy, S.E., 2009:
Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

Tremolada, S.; Akan, S.; Otte, J.; Khalili, K.; Ferrante, P.; Chaudhury, P.Roy.; Woodle, E.Steve.; Trofe-Clark, J.; White, M.K.; Gordon, J., 2010:
Rare subtypes of BK virus are viable and frequently detected in renal transplant recipients with BK virus-associated nephropathy

Ou, S-Hong.Ignatius.; Kawaguchi, T.; Soo, R.A.; Kitaichi, M., 2012:
Rare subtypes of adenocarcinoma of the lung

Yamaguchi, F.; Kamitori, K.; Sanada, K.; Horii, M.; Dong, Y.; Sui, L.; Tokuda, M., 2008:
Rare sugar D-allose enhances anti-tumor effect of 5-fluorouracil on the human hepatocellular carcinoma cell line HuH-7

Naha, N.; Lee, H.Young.; Jo, M.Ja.; Chung, B.Chul.; Kim, S.Hoon.; Kim, M.Ok., 2008:
Rare sugar D-allose induces programmed cell death in hormone refractory prostate cancer cells

Yamada, K.; Noguchi, C.; Kamitori, K.; Dong, Y.; Hirata, Y.; Hossain, M.A.; Tsukamoto, I.; Tokuda, M.; Yamaguchi, F., 2012:
Rare sugar D-allose strongly induces thioredoxin-interacting protein and inhibits osteoclast differentiation in Raw264 cells

Hossain, M.A.; Kitagaki, S.; Nakano, D.; Nishiyama, A.; Funamoto, Y.; Matsunaga, T.; Tsukamoto, I.; Yamaguchi, F.; Kamitori, K.; Dong, Y.; Hirata, Y.; Murao, K.; Toyoda, Y.; Tokuda, M., 2011:
Rare sugar D-psicose improves insulin sensitivity and glucose tolerance in type 2 diabetes Otsuka Long-Evans Tokushima Fatty (OLETF) rats

Lemm, D.; de Oliveira, F.Hehn.; Bernays, Ré-Ludwig.; Kockro, R.Alfons.; Kollias, S.; Fischer, I.; Rushing, E.J., 2013:
Rare suprasellar glioblastoma: report of two cases and review of the literature

Takama, N.; Hoshizaki, H.; Naito, S.; Oshima, S.; Taniguchi, K.; Kurabayashi, M., 2007:
Rare survival in a patient with severe complications of acute myocardial infarction: a case report

Mahajan, R.; Bang, D.; Nagar, A.; Bilimoria, F., 2012:
Rare sweat gland tumors of vulva: Report of two cases

Becker, N.B.; ten Wolde, P.Rein., 2012:
Rare switching events in non-stationary systems

Iacoangeli, M.; D.R.enzo, A.; Colasanti, R.; Alvaro, L.; Nocchi, Nò.; Polonara, G.; D.S.mma, L.Giovanna.Maria.; Zizzi, A.; Scarpelli, M.; Scerrati, M., 2012:
Rare synchronous association of vestibular schwannoma and indolent insular oligodendroglioma in a patient without neurofibromatosis: controversial issue of timing for surgical treatment of asymptomatic low-grade gliomas

Rajarubendra, N.; Pook, D.; Frydenberg, M.; Appu, S. , 2014:
Rare synchronous metastases of renal cell carcinoma

Ghimire, P.; Wu, G.Y.; Zhu, L., 2011:
Rare synchronous primary large B-cell gastric lymphoma and huge retroperitoneal liposarcoma with inguinal hernia in chronic hepatitis B patient

Breuning, M., 2013:
Rare syndromes are not hard to recognize

Tan, T.Yang.; Farlie, P.G., 2014:
Rare syndromes of the head and face-Pierre Robin sequence

Zhang, Y.; Deng, S.; Qu, L.; An, Y-Ting.; Wu, C-Hua.; Han, L-Feng.; Gao, X-Mei.; Wang, T., 2013:
Rare syringyl acylated flavonol glycosides from the aerial parts of Leonurus japonicus Houtt

Lloret, A.; Hartmann, K.; Pennisi, M.Grazia.; Ferrer, L.; Addie, D.; Belák, Sándor.; Boucraut-Baralon, C.; Egberink, H.; Frymus, T.; Gruffydd-Jones, T.; Hosie, M.J.; Lutz, H.; Marsilio, F.; Möstl, K.; Radford, A.D.; Thiry, E.; Truyen, U.; Horzinek, M.C., 2014:
Rare systemic mycoses in cats: blastomycosis, histoplasmosis and coccidioidomycosis: ABCD guidelines on prevention and management

Kikuchi, K., 2014:
Rare systemic mycosis. (1) Systemic mycosis caused by rare yeast-like fungi

Fleck, M.S.; Mitroff, S.R., 2007:
Rare targets are rarely missed in correctable search

Akerman, Måns.; Domanski, H.A.; Jonsson, K., 2010:
Rare targets for FNAC and diagnostic problems with benign tumours/lesions with variable numbers of osteoclast-like giant cells

van der Wijst, T.; Fonseca Guerra, Célia.; Swart, M.; Bickelhaupt, F.Matthias.; Lippert, B., 2008:
Rare tautomers of 1-methyluracil and 1-methylthymine: tuning relative stabilities through coordination to PtII complexes

Kawaguchi, N.; Yamada, T.; Hattori, T., 2008:
Rare tendency of catching cold in Parkinson's disease

Epperson, J.R.; Pope, N.M.; Abuzeid, M.J., 2013:
Rare testicular tumor discovered by assault: an unusual presentation of a primary testicular neuroendocrine tumor grade 2

Karotsis, G.; Jones, L.F.; Papaefstathiou, G.S.; Collins, A.; Parsons, S.; Nguyen, T.D.; Evangelisti, M.; Brechin, E.K., 2008:
Rare tetranuclear mixed-valent [Mn(II)2Mn(IV)2] clusters as building blocks for extended networks

Jarosova, M.; Nedomova, R.; Hubacek, J.; Holzerova, M.; Mickova, P.; Katrincsakova, B.; Pikalova, Z.; Papajik, T.; Indrak, K., 2012:
Rare tetraploidy with large 5q deletion in acute myeloid leukemia with myelodysplasia-related changes (AML-MRC)

Siesling, S.; van der Zwan, J.Maarten.; Izarzugaza, I.; Jaal, J.; Treasure, T.; Foschi, R.; Ricardi, U.; Groen, H.; Tavilla, A.; Ardanaz, E.; Zielonk, N.; Van Eycken, E.; Schrijvers, D.; Sundseth, H.; Hedelin, G.; Bouvier, A.M.; Woronoff, A.S.; Buemi, A.; Tretarre, B.; Colonna, M.; Bara, S.; Ganry, O.; Grosclaude, P.; Holleczek, B.; Tryggvadottir, L.; Deady, S.; Bellù, F.; Ferretti, S.; Serraino, D.; Vercelli, M.; Vitarell, S.; Federico, M.; Fusco, M.; Michiara, M.; Giacomin, A.; Tumino, R.; Ma, 2012:
Rare thoracic cancers, including peritoneum mesothelioma

Emmerich, J., 2008:
Rare thrombophilic states

Martinelli, I.; D.S.efano, V., 2010:
Rare thromboses of cerebral, splanchnic and upper-extremity veins. A narrative review

Abrosimov, A.Iu.; Dvinskikh, N.Iu.; Rotin, D.L., 2008:
Rare thyroid tumors: spindle-cell epithelial tumor and thyroid carcinoma with thymus-like differentiation

Becerro de Bengoa, R.; Gates, J.R.; Losa Iglesias, M.Elena.; Alija Martinez, B., 2011:
Rare toenail onychomatricoma: surgical resolution of five cases

Scherl, S.; Alon, E.E.; Karle, W.E.; Clain, J.B.; Khorsandi, A.; Urken, M.L., 2013:
Rare tracheal tumors and lesions initially diagnosed as isolated differentiated thyroid cancers

Tesar, V., 2014:
Rare transformation in repeat renal biopsies suggests a different pathogenesis of segmental and global lesions in proliferative lupus nephritis

Casci, T., 2011:
Rare treasures

Chandra, S.R.; Shenoy, R.K.; Karthikeyan; Suresh, K.; Chithr, P.; Annapoorni, C.S.Vidhya., 2013:
Rare treatable limb girdle muscle disease

Patel, S.N.; Sauvageau, E.; Padhya, T.A., 2013:
Rare treatment of radiation induced carotid pseudoaneurysm and ensuing carotid blowout syndrome with placement of multiple contiguous endovascular stents: a case report

Rieseberg, L.H., 1996:
Rare trees

Gosk, J.; Rutowski, R.; Urban, M.; Koszewicz, M.; Moroń, K., 2011:
Rare triphalangeal thumb polydactyly: a case report

Tomé-Bermejo, Félix.; Garrido, E.; Glasby, M.; Thinn, S., 2014:
Rare true-positive isolated SSEP loss with preservation of MEPs response during scoliosis correction

Tsanava, M.; Abuladze, T.; Zenaishvili, B.; Kvaratskhelia, E.; Pagava, K., 2011:
Rare tubulopathy - primary hypophosphatemic rickets (case report)

Hirche, Z.; Kapellmann, R.; Klippel, S.; Jakobs, R.; Willis, S., 2014:
Rare tumor masses of the pancreas

Kumar, A.; Shah, R.M.; Gupta, N., 2012:
Rare tumor of conus medullaris in an adult with a favorable outcome

Braun, K-P.; Gastinger, I.; Theissig, F.; May, M.; Ernst, H., 2009:
Rare tumor of the epididymis

Rodríguez-Velasco, A.; Fermán-Cano, F.; Cerecedo-Díaz, F., 2008:
Rare tumor of the tongue in a child: alveolar soft part sarcoma

Schweyer, S., 2015:
Rare tumors and tumor-like lesions of the testis and paratesticular structures

Andrén-Sandberg, A., 2012:
Rare tumors in the pancreatic region

Doshi, D.V.; Tripathi, U.; Dave, R.I.; Pandya, S.J.; Shukla, H.K.; Parikh, B.C., 2010:
Rare tumors of sinonasal track

Kalac, J.; Veverková, L.; Wechsler, J.; Piskac, P.; Zambo, I., 2010:
Rare tumors of the gallbladder and bile ducts. A case review

Baujat, B.; Thariat, J.; Baglin, A.Catherine.; Costes, Vérie.; Testelin, S.; Reyt, E.; Janot, Fçois., 2014:
Rare tumors of the head and neck; on behalf of the REFCOR, the French Network of rare head and neck tumors

Stoian, I.; Piser, I.Tepes.; Kulcsar, I.; Chioncel, O.; Carp, A.; Macarie, C., 2010:
Rare tumors of the heart--angiosarcoma, pericardial lipoma, leiomyosarcoma. Three case reports

Peltier, J.; Capel, C.; Nicot, B.; Baroncini, M.; Fichten, A.; Toussaint, P.; Desenclos, C.; Lefranc, M.; L.G.rs, D.; Lejeune, J-P., 2012:
Rare tumors of the lateral ventricle. Review of the literature

Wang, R-Guang.; Wang, G., 2011:
Rare tumors of the nasopharynx: a systematic review

Palade, O.D.; Cobzeanu, M.D.; Axinte, S.; Costinescu, V., 2011:
Rare tumors of the neck--report of two cases

Errasti Alustiza, Jé.; Espín Basany, E.; Reina Duarte, A., 2016:
Rare tumors of the rectum. Narrative review

Colecchia, M.; Mikuz, G.; Algaba, F., 2012:
Rare tumors of the testis and mesothelial proliferation in the tunica vaginalis

Mano, M.S.; Arai, R.J.; Hoff, P.M.G., 2010:
Rare tumors research in emerging countries

Martinez, S.R.; Barr, K.L.; Canter, R.J., 2011:
Rare tumors through the looking glass: an examination of malignant cutaneous adnexal tumors

Glehen, O.; Gilly, Fçois-Noêl., 2014:
Rare tumors: limits of expertise and external consultation

Arel, F., 1949:
Rare tumors; etiology and localization; report of three cases

Eren, F.; Candan, T.; Eren, Bülent.; Aydin, O.; Comunoglu, N.; Comunoglus, C., 2008:
Rare tumour of the thoracic wall: elastofibroma

Tomsová, M.; Pohnĕtalová, D.; Spacek, J., 2007:
Rare tumours of myometrium--intravenous leiomyomatosis and benign metastatic leiomyoma

Muñoz, E.; Cedrés, S.; Felip, E., 2010:
Rare tumours of the chest

Mohapatra, D.Prasad.; Badhe, B.A.; Chittoria, R.Kumar.; Vijayaraghavan; Ashokan, A., 2013:
Rare tumours of the hard palate

Massard, C.; Droz, J-P., 2010:
Rare tumours: a new heading in Bulletin du cancer

Sturma, J., 1949:
Rare twin pregnancy and acromegalia

Celik, O.; Turk, H.; Budak, S.; Ilbey, Y.Ozlem., 2014:
Rare type of bladder cancer: malign fibrous histiocytoma

Jarmoszewicz, K.; Rogowski, J.; Łepska, L., 2014:
Rare type of cardiac tumor in a healthy young woman

Watanabe, M.; Aoki, M.; Fujiwara, T., 2009:
Rare type of congenital aneurysm of the right sinus of Valsalva protruding superiorly into the pericardial space

Avazashvili, D.; Nonikashvili, Z.; Gugulashvili, Z.; Huhunaishvili, L., 2012:
Rare types of aneurysms-aneurysms of the hand and fingers: case reports

Mihai, B.; Mihai, Cătălina.; Cijevschi-Prelipcean, C.; Lăcătuşu, C., 2013:
Rare types of diabetes mellitus

Viste, A., 2008:
Rare types of gastrointestinal hemorrhage

Camaschella, C.; Poggiali, E., 2009:
Rare types of genetic hemochromatosis

Kokkinos, P.A.; Ziros, P.G.; Monini, M.; Lampropoulou, P.; Karampini, A.; Papachatzi, E.; Mantagos, S.; Ruggeri, F.M.; Vantarakis, A., 2013:
Rare types of rotaviruses isolated from children with acute gastroenteritis in Patras, Greece

Kysucan, J.; Malý, T.; Neoral, C., 2011:
Rare umbilical anomalies

Socea, B.; Constantin, V.; Carâp, A.; Moculescu, C.; Pãdeanu, N.; Popa, F., 2013:
Rare urogenital malformation associated with complex vascular malformation -- case report

Crawford, D.C.; Dumitrescu, L.; Goodloe, R.; Brown-Gentry, K.; Boston, J.; McClellan, B.; Sutcliffe, C.; Wiseman, R.; Baker, P.; Pericak-Vance, M.A.; Scott, W.K.; Allen, M.; Mayo, P.; Schnetz-Boutaud, N.; Dilks, H.H.; Haines, J.L.; Pollin, T.I., 2015:
Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study

De, G.; Yip, W-Ki.; Ionita-Laza, I.; Laird, N., 2013:
Rare variant analysis for family-based design

Asimit, J.; Zeggini, E., 2011:
Rare variant association analysis methods for complex traits

Lin, W-Yu.; Lou, X-Yang.; Gao, G.; Liu, N., 2014:
Rare variant association testing by adaptive combination of P-values

Tachmazidou, I.; Morris, A.; Zeggini, E., 2013:
Rare variant association testing for next-generation sequencing data via hierarchical clustering

Navon, O.; Sul, J.Hoon.; Han, B.; Conde, L.; Bracci, P.M.; Riby, J.; Skibola, C.F.; Eskin, E.; Halperin, E., 2014:
Rare variant association testing under low-coverage sequencing

Cherkas, Y.; Raghavan, N.; Francke, S.; Defalco, F.; Wilcox, M.A., 2012:
Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data

Peng, G.; Fan, Y.; Palculict, T.B.; Shen, P.; Ruteshouser, E.Cristy.; Chi, A-Kyaw.; Davis, R.W.; Huff, V.; Scharfe, C.; Wang, W., 2013:
Rare variant detection using family-based sequencing analysis

Rampersaud, E.; Siegfried, J.D.; Norton, N.; Li, D.; Martin, E.; Hershberger, R.E., 2011:
Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

Morales, A.; Painter, T.; Li, R.; Siegfried, J.D.; Li, D.; Norton, N.; Hershberger, R.E., 2010:
Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy

Ghosh, P.; Chauhan, A., 2012:
Rare variant of an anomalous left coronary artery: arising from the distal continuation of a single right coronary artery

Nepple, K.G.; Cooper, C.S.; Austin, J.Christopher., 2008:
Rare variant of bladder exstrophy associated with urethral, bladder, and colonic duplication

Lee, J-Young.; Choi, J-Yeob.; Lee, K-Mu.; Park, S.Kyung.; Han, S-Hee.; Noh, D-Young.; Ahn, S-Hyun.; Kim, D-Hyun.; Hong, Y-Chul.; Ha, E.; Yoo, K-Young.; Ambrosone, C.B.; Kang, D., 2007:
Rare variant of hypoxia-inducible factor-1alpha (HIF-1A) and breast cancer risk in Korean women

Hirabayashi, T.; Ueno, S., 2014:
Rare variant of inguinal hernia, interparietal hernia and ipsilateral abdominal ectopic testis, mimicking a spiegelian hernia. Case report

Nasirian, M.; Banazadeh, N.; Kheradmand, A., 2009:
Rare variant of lycanthropy and ecstasy

Singh, J.; Mohite, P.N.; Rana, S.Singh., 2012:
Rare variant of mixed total anomalous pulmonary venous connection

Kong, D.; Pan, C.; Dong, L.; Jin, H.; Shu, X., 2015:
Rare variant of mixed total anomalous pulmonary venous drainage (TAPVD) in a 55-year-old patient

Lee, E.Joo.; Chang, H.Won.; Cho, C.Hyun.; Kim, E.; Lee, S.Kwon.; Kwon, J.Hyuk., 2011:
Rare variant of persistent primitive hypoglossal artery in magnetic resonance angiography

Nanto, M.; Takado, M.; Ohbuchi, H.; Mandai, A.; Osaka, Y.; Nakahara, Y.; Tenjin, H., 2013:
Rare variant of persistent primitive hypoglossal artery, arising from the external carotid artery

Sarkar, A.; Chandra G S.N.; Majhi, B.; Mandal, S.; Pande, A.; Ahmed, I., 2013:
Rare variant of pulmonary arteriovenous fistula: direct communication between right pulmonary artery and left atrium associated with aortopulmonary collaterals

Prasun, P., 2015:
Rare variant of unknown significance in POLG1 and diagnostic dilemma

Fang, H.; Hou, B.; Wang, Q.; Yang, Y., 2014:
Rare variants analysis by risk-based variable-threshold method

Camacho-Garcia, R.J.; Hervás, A.; Toma, C.; Balmaña, Ní.; Cormand, B.; Martinez-Mir, A.; Scholl, F.G., 2014:
Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses

Massey, J.; Eyre, S., 2015:
Rare variants and autoimmune disease

Wain, L.V., 2015:
Rare variants and cardiovascular disease

Jordan, B., 2014:
Rare variants and demographic explosion

Barrett, J.H., 2015:
Rare variants and disease

Rapoport, J.; Ahn, K., 2012:
Rare variants and risk for schizophrenia: more support

Nawy, T., 2012:
Rare variants and the power of association

Dickson, S.P.; Wang, K.; Krantz, I.; Hakonarson, H.; Goldstein, D.B., 2010:
Rare variants create synthetic genome-wide associations

Zeng, P.; Zhao, Y.; Zhang, L.; Huang, S.; Chen, F., 2015:
Rare variants detection with kernel machine learning based on likelihood ratio test

Hopfner, F.; Bungeroth, M.; Pendziwiat, M.; Tittmann, L.; Deuschl, Günther.; Schneider, S.A.; Kuhlenbäumer, G., 2014:
Rare variants in ANO3 are not a susceptibility factor in essential tremor

Cruchaga, C.; Haller, G.; Chakraverty, S.; Mayo, K.; Vallania, F.L.M.; Mitra, R.D.; Faber, K.; Williamson, J.; Bird, T.; Diaz-Arrastia, R.; Foroud, T.M.; Boeve, B.F.; Graff-Radford, N.R.; St Jean, P.; Lawson, M.; Ehm, M.G.; Mayeux, R.; Goate, A.M.; Green, R.; Kowall, N.; Farrer, L.; Williamson, J.; Santana, V.; Schmechel, D.; Gaskell, P.; Welsh-Bohmer, K.; Pericak-Vance, M.; Ghetti, B.; Farlow, M.R.; Horner, K.; Growdon, J.H.; Blacker, D.; Tanzi, R.E.; Hyman, B.T.; Boeve, B.; Kuntz, K.; Norgaard, 2012:
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

Ealy, M.; Meyer, N.C.; Corchado, J.Cruz.; Schrauwen, I.; Bress, A.; Pfister, M.; Van Camp, G.; Smith, R.J.H., 2014:
Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling

Buchan, J.G.; Alvarado, D.M.; Haller, G.E.; Cruchaga, C.; Harms, M.B.; Zhang, T.; Willing, M.C.; Grange, D.K.; Braverman, A.C.; Miller, N.H.; Morcuende, J.A.; Tang, N.Leung-Sang.; Lam, T-Ping.; Ng, B.Kin-Wah.; Cheng, J.Chun-Yiu.; Dobbs, M.B.; Gurnett, C.A., 2015:
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis

Schulte, E.C.; Ellwanger, D.C.; Dihanich, S.; Manzoni, C.; Stangl, K.; Schormair, B.; Graf, E.; Eck, S.; Mollenhauer, B.; Haubenberger, D.; Pirker, W.; Zimprich, A.; Brücke, T.; Lichtner, P.; Peters, A.; Gieger, C.; Trenkwalder, C.; Mewes, H-Werner.; Meitinger, T.; Lewis, P.A.; Klünemann, H.H.; Winkelmann, J., 2014:
Rare variants in LRRK1 and Parkinson's disease

Al Turki, S.; Manickaraj, A.K.; Mercer, C.L.; Gerety, S.S.; Hitz, M-Phillip.; Lindsay, S.; D'Alessandro, L.C.A.; Swaminathan, G.Jawahar.; Bentham, J.; Arndt, A-Karin.; Louw, J.; Low, J.; Breckpot, J.; Gewillig, M.; Thienpont, B.; Abdul-Khaliq, H.; Harnack, C.; Hoff, K.; Kramer, H-Heiner.; Schubert, S.; Siebert, R.; Toka, O.; Cosgrove, C.; Watkins, H.; Lucassen, A.M.; O'Kelly, I.M.; Salmon, A.P.; Bu'lock, F.A.; Granados-Riveron, J.; Setchfield, K.; Thornborough, C.; Brook, J.David., 2014:
Rare variants in NR2F2 cause congenital heart defects in humans

Schulte, E.C.; Stahl, I.; Czamara, D.; Ellwanger, D.C.; Eck, S.; Graf, E.; Mollenhauer, B.; Zimprich, A.; Lichtner, P.; Haubenberger, D.; Pirker, W.; Brücke, T.; Bereznai, B.; Molnar, M.J.; Peters, A.; Gieger, C.; Müller-Myhsok, B.; Trenkwalder, C.; Winkelmann, J., 2014:
Rare variants in PLXNA4 and Parkinson's disease

Majithia, A.R.; Flannick, J.; Shahinian, P.; Guo, M.; Bray, M-Anthony.; Fontanillas, P.; Gabriel, S.B.; Rosen, E.D.; Altshuler, D.; Flannick, J.; Manning, A.K.; Hartl, C.; Agarwala, V.; Fontanillas, P.; Green, T.; Banks, E.; DePristo, M.; Poplin, R.; Shakir, K.; Fennell, T.; Njølstad, Pål.R.; Altshuler, D.; Burtt, Nël.; Gabriel, S.; Fuchsberger, C.; Kang, H.Min.; Sim, X.; Ma, C.; Locke, A.; Blackwell, T.; Jackson, A.; Teslovich, T.M.; Stringham, H.; Chines, P.; Kwan, P.; Huyghe, J.; Tan, A.;, 2015:
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

Quast, C.; Altmann, A.; Weber, P.; Arloth, J.; Bader, D.; Heck, A.; Pfister, H.; Müller-Myhsok, B.; Erhardt, A.; Binder, E.B., 2013:
Rare variants in TMEM132D in a case-control sample for panic disorder

Diskin, S.J.; Capasso, M.; Diamond, M.; Oldridge, D.A.; Conkrite, K.; Bosse, K.R.; Russell, M.R.; Iolascon, A.; Hakonarson, H.; Devoto, M.; Maris, J.M., 2014:
Rare variants in TP53 and susceptibility to neuroblastoma

Hilbers, F.S.; Wijnen, J.T.; Hoogerbrugge, N.; Oosterwijk, J.C.; Collee, M.J.; Peterlongo, P.; Radice, P.; Manoukian, S.; Feroce, I.; Capra, F.; Couch, F.J.; Wang, X.; Guidugli, L.; Offit, K.; Shah, S.; Campbell, I.G.; Thompson, E.R.; James, P.A.; Trainer, A.H.; Gracia, J.; Benitez, J.; van Asperen, C.J.; Devilee, P., 2013:
Rare variants in XRCC2 as breast cancer susceptibility alleles

Rubio-Moscardo, F.; Setó-Salvia, Núria.; Pera, M.; Bosch-Morató, Mònica.; Plata, C.; Belbin, O.; Gené, G.; Dols-Icardo, O.; Ingelsson, M.; Helisalmi, S.; Soininen, H.; Hiltunen, M.; Giedraitis, V.; Lannfelt, L.; Frank, A.; Bullido, M.Jesús.; Combarros, O.; Sánchez-Juan, P.; Boada, Mè.; Tárraga, Lís.; Pastor, P.; Pérez-Tur, J.; Baquero, M.; Molinuevo, Jé.L.; Sánchez-Valle, R.; Fuentes-Prior, P.; Fortea, J.; Blesa, R.; Muñoz, F.J.; Lleó, A.; Valverde, M.A.; Clarimón, J., 2014:
Rare variants in calcium homeostasis modulator 1 (CALHM1) found in early onset Alzheimer's disease patients alter calcium homeostasis

Jouan, L.; Gauthier, J.; Dion, P.A.; Rouleau, G.A., 2013:
Rare variants in complex traits: novel identification strategies and the role of de novo mutations

Su, M.; Wang, J.; Kang, L.; Wang, Y.; Zou, Y.; Feng, X.; Wang, D.; Ahmad, F.; Zhou, X.; Hui, R.; Song, L., 2015:
Rare variants in genes encoding MuRF1 and MuRF2 are modifiers of hypertrophic cardiomyopathy

Roop, J.I.; Brem, R.B., 2014:
Rare variants in hypermutable genes underlie common morphology and growth traits in wild Saccharomyces paradoxus

Cole, J.W.; Stine, O.Colin.; Liu, X.; Pratap, A.; Cheng, Y.; Tallon, L.J.; Sadzewicz, L.K.; Dueker, N.; Wozniak, M.A.; Stern, B.J.; Meschia, J.F.; Mitchell, B.D.; Kittner, S.J.; O'Connell, J.R., 2012:
Rare variants in ischemic stroke: an exome pilot study

Hyun, Y.S.; Park, H.J.; Heo, S-H.; Yoon, B.R.; Nam, S.H.; Kim, S-B.; Park, C.I.; Choi, B-O.; Chung, K.W., 2015:
Rare variants in methionyl- and tyrosyl-tRNA synthetase genes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy

Ramachandrappa, S.; Raimondo, A.; Cali, A.M.G.; Keogh, J.M.; Henning, E.; Saeed, S.; Thompson, A.; Garg, S.; Bochukova, E.G.; Brage, S.; Trowse, V.; Wheeler, E.; Sullivan, A.E.; Dattani, M.; Clayton, P.E.; Datta, V.; Datta, V.; Bruning, J.B.; Wareham, N.J.; O'Rahilly, S.; Peet, D.J.; Barroso, I.; Whitelaw, M.L.; Farooqi, I.Sadaf., 2013:
Rare variants in single-minded 1 (SIM1) are associated with severe obesity

Ramagopalan, S.V.; Dyment, D.A.; Cader, M.Zameel.; Morrison, K.M.; Disanto, G.; Morahan, J.M.; Berlanga-Taylor, A.J.; Handel, A.; D.L.ca, G.C.; Sadovnick, A.Dessa.; Lepage, P.; Montpetit, A.; Ebers, G.C., 2012:
Rare variants in the CYP27B1 gene are associated with multiple sclerosis

Barizzone, N.; Monti, S.; Mellone, S.; Godi, M.; Marchini, M.; Scorza, R.; Danieli, M.G.; D'Alfonso, S., 2014:
Rare variants in the TREX1 gene and susceptibility to autoimmune diseases

Evans, D.; Arzer, J.; Aberle, J.; Beil, F.U., 2011:
Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia

Nejentsev, S.; Walker, N.; Riches, D.; Egholm, M.; Todd, J.A., 2009:
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

Ayatollahi, J.; Fattahi Bafghi, A.; Shahcheraghi, S.Hossein., 2014:
Rare variants of cutaneous leishmaniasis presenting as eczematous lesions

Tomar, M.; Radhakrishnan, S.; Iyer, K.S.; Shrivastava, S., 2009:
Rare variants of total anomalous pulmonary venous connection to coronary sinus-echocardiographic recognition and surgical correction

Kent, J.W., 2012:
Rare variants, common markers: synthetic association and beyond

Bowes, J.; Lawrence, R.; Eyre, S.; Panoutsopoulou, K.; Orozco, G.; Elliott, K.S.; Ke, X.; Morris, A.P.; Thomson, W.; Worthington, J.; Barton, A.; Zeggini, E.; Wilson, A.G.; Morgan, A.W.; Emery, P.; Steer, S.; Hocking, L.J.; Reid, D.M.; Harrison, P.; Wordsworth, P., 2011:
Rare variation at the TNFAIP3 locus and susceptibility to rheumatoid arthritis

O'Connor, T.D.; Fu, W.; Mychaleckyj, J.C.; Logsdon, B.; Auer, P.; Carlson, C.S.; Leal, S.M.; Smith, J.D.; Rieder, M.J.; Bamshad, M.J.; Nickerson, D.A.; Akey, J.M., 2016:
Rare variation facilitates inferences of fine-scale population structure in humans

Yildiz, C.Eray.; Babaoglu, K.; Korkmaz, A.; Dursun, M.; Altun, I.; Mert, M.; Guden, M.; Cetin, G., 2011:
Rare variation in partial anomalous venous drainage in 2 cases: diagnosis, assessment methods, and surgical approach

Zhou, Y-Qi.; Shan, P-Jia.; Xu, J., 2008:
Rare variation of abdominal aorta breaking in two

Satyanarayana, N.; Vishwakarma, N.; Kumar, G.P.; Guha, R.; Dattal, A.K.; Sunitha, P., 2010:
Rare variations in the formation of median nerve--embryological basis and clinical significance

Pednekar, S.; Morge, V.; Rawal, S.; Korivi, D.; Ramteke, V.; Naik, K., 2012:
Rare variety of T-cell lymphoma

Verma, S.Kumar.; Mahajan, V., 2011:
Rare vascular anomaly mimicking bronchogenic carcinoma

Menjot de Champfleur, N.; Pierredon Foulongne, M.A.; Salaheddine, T.; Garibaldi, F.; Bruel, J.M.; Gallix, B., 2007:
Rare vascular complication from acute pancreatitis: intra-hepatic false aneurysm of the hepatic artery: a report of 2 cases

Niu, T.; Kalia, J.S.; Zaidat, O.O., 2012:
Rare vascular complication of percutaneous balloon compression of trigeminal neuralgia treated endovascularly

Calanca, L.; Depairon, Mèle.; Tribout, B.; Aebischer, N.; Burnier, M.; Fellmann, F.; Lazor, R.; Mazzolai, L., 2014:
Rare vascular diseases

Farooqi, F.; Alexander, J.; Sarma, A., 2014:
Rare vascular perforation complicating radial approach to percutaneous coronary angioplasty

Hayabuchi, Y.; Inoue, M.; Kagami, S., 2008:
Rare venous connection causing severe hypoxia after Fontan operation

Smith, T.M., 2010:
Rare view of thebesian venous system

Glück, T., 2012:
Rare viral infections during immunosuppressive therapy: a "normal" side effect?

Millischer, D.; Logeart, D.; Cohen-Solal, A.; Tournoux, Fçois., 2011:
Rare visualization of entrapped left ventricular thrombi in noncompacted myocardium

Forbes, M.L., 2007:
Rare window: functional magnetic resonance imaging and mild traumatic brain injury

Hayward, P., 2013:
Rare zoonoses in the USA

Bosnic, D.; Baresic, M.; Anic, B.; Sentic, M.; Cerovec, M.; Mayer, M.; Cikes, N., 2010:
Rare zoonosis (hemotrophic mycoplasma infection) in a newly diagnosed systemic lupus erythematosus patient followed by a Nocardia asteroides pneumonia

Malling, T.H.; Carlsen, L.Sloth.; Ferrarotti, I.; Omland, O., 2015:
Rare α₁-antitrypsin genotype in a grass seed worker

Alekhin, D.I.; Koudrina, A.V.; Goloshchapova, J.A.; Kokorishvili, M.A.; Vlasko, A.A., 2011:
Rare, but clinically significant cases of abnormalities of coronary arteries: "pathological valves"

Reincke, M., 2014:
Rare, but important: Endocrine diseases that every internist needs to know

Biggs, A.T.; Adamo, S.H.; Mitroff, S.R., 2014:
Rare, but obviously there: effects of target frequency and salience on visual search accuracy

Tavtigian, S.V.; Oefner, P.J.; Babikyan, D.; Hartmann, A.; Healey, S.; L.C.lvez-Kelm, F.; Lesueur, F.; Byrnes, G.B.; Chuang, S-Chun.; Forey, N.; Feuchtinger, C.; Gioia, L.; Hall, J.; Hashibe, M.; Herte, B.; McKay-Chopin, S.; Thomas, A.; Vallée, M.P.; Voegele, C.; Webb, P.M.; Whiteman, D.C.; Sangrajrang, S.; Hopper, J.L.; Southey, M.C.; Andrulis, I.L.; John, E.M.; Chenevix-Trench, G., 2009:
Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

L.C.lvez-Kelm, F.; Lesueur, F.; Damiola, F.; Vallée, M.; Voegele, C.; Babikyan, D.; Durand, G.; Forey, N.; McKay-Chopin, S.; Robinot, N.; Nguyen-Dumont, Tù.; Thomas, A.; Byrnes, G.B.; Hopper, J.L.; Southey, M.C.; Andrulis, I.L.; John, E.M.; Tavtigian, S.V., 2014:
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

Speight, R.A.; Nicolle, A.; Needham, S.J.; Verrill, M.W.; Bryon, J.; Panter, S., 2013:
Rare, germline mutation of KIT with imatinib-resistant multiple GI stromal tumors and mastocytosis

Diogo, Dée.; Kurreeman, F.; Stahl, E.A.; Liao, K.P.; Gupta, N.; Greenberg, J.D.; Rivas, M.A.; Hickey, B.; Flannick, J.; Thomson, B.; Guiducci, C.; Ripke, S.; Adzhubey, I.; Barton, A.; Kremer, J.M.; Alfredsson, L.; Sunyaev, S.; Martin, J.; Zhernakova, A.; Bowes, J.; Eyre, S.; Siminovitch, K.A.; Gregersen, P.K.; Worthington, J.; Klareskog, L.; Padyukov, L.; Raychaudhuri, S.; Plenge, R.M., 2013:
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis

Nowak-Wegrzyn, A.; Fiocchi, A., 2009:
Rare, medium, or well done? The effect of heating and food matrix on food protein allergenicity

Kuang, S-Qing.; Kwartler, C.S.; Byanova, K.L.; Pham, J.; Gong, L.; Prakash, S.K.; Huang, J.; Kamm, K.E.; Stull, J.T.; Sweeney, H.Lee.; Milewicz, D.M., 2012:
Rare, nonsynonymous variant in the smooth muscle-specific isoform of myosin heavy chain, MYH11, R247C, alters force generation in the aorta and phenotype of smooth muscle cells

Annen, E.; Girard, T.; Urwyler, A., 2012:
Rare, potentially fatal, poorly understood propofol infusion syndrome

Simpson, B.S.; Claudie, D.J.; Smith, N.M.; McKinnon, R.A.; Semple, S.J., 2013:
Rare, seven-membered cyclic ether labdane diterpenoid from Dodonaea polyandra

Korsholm, A.Sofie.; Ebbehøj, E.; Richelsen, Børn., 2016:
Rare, severe hypersensitivity reaction to potassium iodide

Mupparapu, M.; Milles, M.; Singer, S.R.; Rinaggio, J., 2009:
Rare, simultaneous, multiple, and recurrent mandibular bone cysts

Philips, C.Abby.; Anand, L.; Kumar, K.N.Chandan.; Kasana, V.; Arora, A., 2014:
Rare, spontaneous trans-splenic shunt and intra-splenic collaterals with attendant splenic artery aneurysms in an adult patient with compensated cirrhosis and portal hypertension

Razonable, R.R., 2012:
Rare, unusual, and less common virus infections after organ transplantation

Olson, J.C.; Shawe, D.R.; Pray, L.C.; Sharp, W.N., 1954:
Rare-Earth Mineral Deposits of the Mountain Pass District, San Bernardino County, California

Yuan, Y-Feng.; Cardinaels, T.; Lunstroot, K.; Hecke, K.Van.; Meervelt, L.Van.; Görller-Walrand, C.; Binnemans, K.; Nockemann, P., 2007:
Rare-Earth complexes of ferrocene-containing ligands: visible-light excitable luminescent materials

Fisk, Z.; Matthias, B.T., 1969:
Rare-Earth elements and high pressures

Voorhoeve, R.J.; Remeika, J.P.; Johnson, D.W., 1973:
Rare-Earth manganites: catalysts with low ammonia yield in the reduction of nitrogen oxides

Croat, J.J.; Tibbetts, G.G.; Katz, S., 1976:
Rare-Earth manganites: surface-segregated platinum increases catalytic activity

Wang, Y-Fu.; Sun, L-Dong.; Xiao, J-Wen.; Feng, W.; Zhou, J-Cai.; Shen, J.; Yan, C-Hua., 2012:
Rare-Earth nanoparticles with enhanced upconversion emission and suppressed rare-Earth-ion leakage

Kratsch, J.; Roesky, P.W., 2014:
Rare-Earth-metal methylidene complexes

Bourquin, Y.; Syed, A.; Reboud, J.; Ranford-Cartwright, L.C.; Barrett, M.P.; Cooper, J.M., 2016:
Rare-cell enrichment by a rapid, label-free, ultrasonic isopycnic technique for medical diagnostics

Thompson, C.A., 2013:
Rare-disease drugs to receive consideration on par with serious-disease drugs

Guo, L.; Zhu, X.; Zhou, S.; Mu, X.; Wei, Y.; Wang, S.; Feng, Z.; Zhang, G.; Deng, B., 2014:
Rare-earth alkyl complexes supported by formamidinate ligands: synthesis, structure, and catalytic activity for isoprene polymerization

Stanlake, L.J.E.; Beard, J.David.; Schafer, L.L., 2008:
Rare-earth amidate complexes. Easily accessed initiators for epsilon-caprolactone ring-opening polymerization

Gong, H-Yuan.; Rambo, B.M.; Nelson, C.A.; Lynch, V.M.; Zhu, X.; Sessler, J.L., 2013:
Rare-earth cation effects on three-dimensional metal-organic rotaxane framework (MORF) self assembly

Kissel, A.A.; Lyubov, D.M.; Mahrova, T.V.; Fukin, G.K.; Cherkasov, A.V.; Glukhova, T.A.; Cui, D.; Trifonov, A.A., 2013:
Rare-earth dichloro and bis(alkyl) complexes supported by bulky amido-imino ligand. Synthesis, structure, reactivity and catalytic activity in isoprene polymerization

Bedekar, V.; Dutta, D.P.; Mohapatra, M.; Godbole, S.V.; Ghildiyal, R.; Tyagi, A.K., 2009:
Rare-earth doped gadolinia based phosphors for potential multicolor and white light emitting deep UV LEDs

Service, R.F., 2010:
Rare-earth elements. Chinese policies could pinch U.S. efforts to make electric vehicles

Wang, H-Qiao.; Batentschuk, M.; Osvet, A.; Pinna, L.; Brabec, C.J., 2011:
Rare-earth ion doped up-conversion materials for photovoltaic applications

Yang, D.L.; Gong, H.; Pun, E.Y.B.; Zhao, X.; Lin, H., 2011:
Rare-earth ions doped heavy metal germanium tellurite glasses for fiber lighting in minimally invasive surgery

D.R.o, A.C.; Thompson, M.C.; Chounthirath, T.; Xiang, H.; Cowles, N.A.; Shmuylovskaya, L.; Smith, G.A., 2014:
Rare-earth magnet ingestion-related injuries among children, 2000-2012

Agha, B.Shalabi.; Sturm, J.J.; Costello, B.E., 2014:
Rare-earth magnet ingestion: a childhood danger reaches adolescence

Ramachandran, K.K.; Stoyko, S.S.; Mullen, C.Scott.; Mar, A., 2014:
Rare-earth manganese copper phosphides REMnCu4P3 (RE = Gd-Ho): the first quaternary ordered variants of the YCo5P3-type structure

Stoyko, S.S.; Ramachandran, K.K.; Mullen, C.Scott.; Mar, A., 2013:
Rare-earth manganese copper pnictides RE2Mn3Cu9Pn7 (Pn = P, As): quaternary ordered variants of the Zr2Fe12P7-type structure

Ohashi, M.; Konkol, M.; Del Rosal, I.; Poteau, R.; Maron, L.; Okuda, J., 2008:
Rare-earth metal alkyl and hydride complexes stabilized by a cyclen-derived [NNNN] macrocyclic ancillary ligand

Trambitas, A.G.; Panda, T.K.; Jenter, J.; Roesky, P.W.; Daniliuc, C.; Hrib, C.G.; Jones, P.G.; Tamm, M., 2010:
Rare-earth metal alkyl, amido, and cyclopentadienyl complexes supported by imidazolin-2-iminato ligands: synthesis, structural characterization, and catalytic application

Abinet, E.; Martin, D.; Standfuss, S.; Kulinna, H.; Spaniol, T.P.; Okuda, J., 2012:
Rare-earth metal allyl and hydrido complexes supported by an (NNNN)-type macrocyclic ligand: synthesis, structure, and reactivity toward biomass-derived furanics

Jian, Z.; Cui, D., 2012:
Rare-earth metal bis(alkyl)s that bear a 2-pyridinemethanamine ligand: dual catalysis of the polymerizations of both isoprene and ethylene

Litlabø, R.; Lee, H.Sul.; Niemeyer, M.; Törnroos, K.W.; Anwander, R., 2010 :
Rare-earth metal bis(tetramethylaluminate) complexes supported by a sterically crowded triazenido ligand

Zhu, X.; Zhou, S.; Wang, S.; Wei, Y.; Zhang, L.; Wang, F.; Wang, S.; Feng, Z., 2013:
Rare-earth metal complexes having an unusual indolyl-1,2-dianion through C-H activation with a novel η1:(μ2-η1:η1) bonding with metals

Liu, B.; Cui, D., 2009:
Rare-earth metal complexes stabilized by amino-phosphine ligand. Reaction with mesityl azide and catalysis of the cycloaddition of organic azides and aromatic alkynes

Ma, H.; Spaniol, T.P.; Okuda, J., 2008:
Rare-earth metal complexes supported by 1,omega-dithiaalkanediyl-bridged bis(phenolato) ligands: synthesis, structure, and heteroselective ring-opening polymerization of rac-lactide

Venugopal, A.; Hepp, A.; Pape, T.; Mix, A.; Mitzel, N.W., 2008:
Rare-earth metal hydroxylamide complexes

Meermann, C.; Törnroos, K.W.; Nerdal, W.; Anwander, R., 2007:
Rare-earth metal mixed chloro/methyl compounds: heterogeneous-homogeneous borderline catalysts in 1,3-diene polymerization

Lee, S-Joon.; Park, S.Soo.; Lee, S.Hyun.; Hong, S-Hyun.; Ha, C-Sik., 2013:
Rare-earth metal oxide doped transparent mesoporous silica plates under non-aqueous condition as a potential UV sensor

Xu, L.; Wang, Z.; Zhang, W-Xiong.; Xi, Z., 2012:
Rare-earth metal tris(trimethylsilylmethyl) anionic complexes bearing one 1-phenyl-2,3,4,5-tetrapropylcyclopentadienyl ligand: synthesis, structural characterization, and application

Strobel, S.; Choudhury, A.; Dorhout, P.K.; Lipp, C.; Schleid, T., 2008:
Rare-earth metal(III) oxide selenides M4O4Se[Se2] (M=La, Ce, Pr, Nd, Sm) with discrete diselenide units: crystal structures, magnetic frustration, and other properties

Zhang, J.; Han, Y.; Chen, Z.; Zhou, X., 2011:
Rare-earth metal-mediated addition/cyclization of the 2-cyanobenzoamino anion

Solovykh, G.N.; Golinskaia, L.V.; Kanunikova, E.A., 2012:
Rare-earth metals as a factor in mutagenicity

Deng, Z-Peng.; Kang, W.; Huo, L-Hua.; Zhao, H.; Gao, S., 2010:
Rare-earth organic frameworks involving three types of architecture tuned by the lanthanide contraction effect: hydrothermal syntheses, structures and luminescence

Wang, D.; Wang, Z.; Zhao, P.; Zheng, W.; Peng, Q.; Liu, L.; Chen, X.; Li, Y., 2010:
Rare-earth oxide nanostructures: rules of rare-earth nitrate thermolysis in octadecylamine

O'Sullivan, G.; Carroll, P.K.; McLlrath, T.J.; Ginter, M.L., 1981:
Rare-earth plasma light source for VUV applications

Cheng, J.; Shima, T.; Hou, Z., 2011:
Rare-earth polyhydride complexes bearing bis(phosphinophenyl)amido pincer ligands

Barrier, N.; Gall, P.; Gougeon, P., 2007:
Rare-earth site splitting in Sm3MoO7

Corso, M.; Verstraete, M.J.; Schiller, F.; Ormaza, M.; Fernández, L.; Greber, T.; Torrent, M.; Rubio, A.; Ortega, J.E., 2010:
Rare-earth surface alloying: a new phase for GdAu2

Zhang, F.; Haushalter, R.C.; Haushalter, R.W.; Shi, Y.; Zhang, Y.; Ding, K.; Zhao, D.; Stucky, G.D., 2011:
Rare-earth upconverting nanobarcodes for multiplexed biological detection

Tomczak, J.M.; Pourovskii, L.V.; Vaugier, L.; Georges, A.; Biermann, S., 2013 :
Rare-earth vs. heavy metal pigments and their colors from first principles

Guan, B-Tao.; Hou, Z., 2012:
Rare-earth-catalyzed C-H bond addition of pyridines to olefins

Pang, M.; Liu, D.; Lei, Y.; Song, S.; Feng, J.; Fan, W.; Zhang, H., 2011:
Rare-earth-doped bifunctional alkaline-earth metal fluoride nanocrystals via a facile microwave-assisted process

Lallier, E., 1992:
Rare-earth-doped glass and LiNbO(3) waveguide lasers and optical amplifiers

Wang, Q.; Jin, W.; Wu, G.; Zhao, Y.; Jin, X.; Hu, X.; Zhou, J.; Tang, G.; Chu, P.K., 2014:
Rare-earth-incorporated polymeric vector for enhanced gene delivery

Jende, L.N.; Maichle-Mössmer, Cäcilia.; Anwander, R., 2013:
Rare-earth-metal alkylaluminates supported by N-donor-functionalized cyclopentadienyl ligands: C-H bond activation and performance in isoprene polymerization

Nieland, A.; Mix, A.; Neumann, B.; Stammler, H-Georg.; Mitzel, N.W., 2013:
Rare-earth-metal dialkynyl dimethyl aluminates

Schädle, D.; Maichle-Mössmer, Cäcilia.; Schädle, C.; Anwander, R., 2014:
Rare-earth-metal methyl, amide, and imide complexes supported by a superbulky scorpionate ligand

Jian, Z.; Cui, D.; Hou, Z., 2012:
Rare-earth-metal-hydrocarbyl complexes bearing linked cyclopentadienyl or fluorenyl ligands: synthesis, catalyzed styrene polymerization, and structure-reactivity relationship

Zhang, S.; Zhao, J.; Ma, P.; Niu, J.; Wang, J., 2012:
Rare-earth-transition-metal organic-inorganic hybrids based on Keggin-type polyoxometalates and pyrazine-2,3-dicarboxylate

Yan, B.; Qiao, X-Fei., 2007:
Rare-earth/inorganic/organic polymeric hybrid materials: molecular assembly, regular microstructure and photoluminescence

Donnenberg, A.D.; Donnenberg, V.S., 2007:
Rare-event analysis in flow cytometry

Williams, S.R., 2013:
Rare-event sampling for driven inertial systems via the nonequilibrium distribution function

Doll, J.D.; Plattner, N.; Freeman, D.L.; Liu, Y.; Dupuis, P., 2012:
Rare-event sampling: occupation-based performance measures for parallel tempering and infinite swapping Monte Carlo methods

Mey, A.S.J.S.; Geissler, P.L.; Garrahan, J.P., 2015:
Rare-event trajectory ensemble analysis reveals metastable dynamical phases in lattice proteins

Schütte, B.; Arbeiter, M.; Fennel, T.; Vrakking, M.J.J.; Rouzée, A., 2014:
Rare-gas clusters in intense extreme-ultraviolet pulses from a high-order harmonic source

Okada, I.; Shiratori, S., 2013:
Rare-metal-free flexible counter electrodes for dye-sensitized solar-cells produced using wet processes only

Juhász, Róbert.; Ódor, Géza.; Castellano, C.; Muñoz, M.A., 2013:
Rare-region effects in the contact process on networks

Lee, S.; Abecasis, Gçalo.R.; Boehnke, M.; Lin, X., 2014:
Rare-variant association analysis: study designs and statistical tests

He, Z.; O'Roak, B.J.; Smith, J.D.; Wang, G.; Hooker, S.; Santos-Cortez, R.Lyn.P.; Li, B.; Kan, M.; Krumm, N.; Nickerson, D.A.; Shendure, J.; Eichler, E.E.; Leal, S.M., 2014:
Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data

Wagner, M.J., 2013:
Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits

Moen, A.; Smørdal, O., 2012:
RareICT: a web-based resource to augment self-care and independence with a rare medical condition

Nilsson, M.; Svanberg, M.; Schalin, S.; Brautaset, R.L., 2012:
Rarebit fovea test in children: reference data for children aged six to 10 years

Nilsson, M.; Abdiu, O.; Laurell, C-Gustaf.; Martin, L., 2010:
Rarebit perimetry and fovea test before and after cataract surgery

Corallo, G.; Iester, M.; Scotto, R.; Calabria, G.; Traverso, C.E., 2008:
Rarebit perimetry and frequency doubling technology in patients with ocular hypertension

Martin, L.M.; Nilsson, A.Lundvall., 2007:
Rarebit perimetry and optic disk topography in pediatric glaucoma

Steven Houston, S.K.; Weber, E.D.; Koga, S.F.; Newman, S.A., 2010:
Rarebit perimetry for bedside testing: comparison with standard automated perimetry

Celebisoy, N.; Oztürk, T.; Köse, T., 2011:
Rarebit perimetry in the evaluation of visual field defects in idiopathic intracranial hypertension

Chin, C-Fang.; Yip, L.W.; Sim, D.C.; Yeo, A.C., 2012:
Rarebit perimetry: normative values and test-retest variability

Mora, P.; Grismayer, T., 2009:
Rarefaction acceleration and kinetic effects in thin-foil expansion into a vacuum

Olufsen, M.S.; Hill, N.A.; Vaughan, G.D.A.; Sainsbury, C.; Johnson, M., 2012:
Rarefaction and blood pressure in systemic and pulmonary arteries

Doyle, M.; Peeceeyan, S.; Bonar, F.; Horton, M., 2015:
Rarefaction of the aorta under Dacron wrap: a rare complication

Reinisch, C.M.; Traxler, H.; Piringer, S.; Tangl, S.; Nader, A.; Tschachler, E., 2008:
Rarefaction of the peripheral nerve network in diabetic patients is associated with a pronounced reduction of terminal Schwann cells

Diaw, A.; Mora, P., 2011:
Rarefaction shock in plasma with a bi-Maxwellian electron distribution function

Liebig, G.V., 1897:
Rarefied And Condensed Air

Ozhgibesov, M.S.; Leu, T.S.; Cheng, C.H., 2013:
Rarefied gas flow through nanoscale tungsten channels

Zhou, W.D.; Liu, B.; Yu, S.K.; Hua, W., 2010:
Rarefied-gas heat transfer in micro- and nanoscale Couette flows

Lawson, R.S., 1925:
Rarefying Osteitis in the Feet of Unknown Origin

Hardwick, S.W.; Luisi, B.F., 2013:
Rarely at rest: RNA helicases and their busy contributions to RNA degradation, regulation and quality control

Fucik, M., 2014:
Rarely diagnosed form of cholangitis lenta

Kondrat'ev, A.N.; Kondrat'eva, E.A., 2008:
Rarely discussed aspects of pharmacological cerebral protection

Mangham, D.Chas.; Kindblom, L-Gunnar., 2014:
Rarely metastasizing soft tissue tumours

Pimenta, F.C.; Gertz, R.E.; Roundtree, A.; Yu, J.; Nahm, M.H.; McDonald, R.R.; Carvalho, M.da.Gloria.; Beall, B.W., 2009:
Rarely occurring 19A-like cps locus from a serotype 19F pneumococcal isolate indicates continued need of serology-based quality control for PCR-based serotype determinations

Ratbi, I.; Bocciardi, R.; Regragui, A.; Ravazzolo, R.; Sefiani, A., 2010:
Rarely occurring mutation of ACVR1 gene in Moroccan patient with fibrodysplasia ossificans progressiva

Serinken, M.; Karcioglu, O.; Korkmaz, A., 2007:
Rarely seen cardiotoxicity of lithium overdose: complete heart block

Rogausch, A.; Hofer, R.; Krebs, Ré., 2011:
Rarely selected distractors in high stakes medical multiple-choice examinations and their recognition by item authors: a simulation and survey

Taksande, B.; Patil, M.; Banode, P.; Deshpande, R., 2013:
Rarer in a rare

Ronald, A.R., 1980:
Rarer infectious diseases

Aminzadeh, M.; Kim, H-Goo.; Layman, L.C.; Cheetham, T.D., 2010:
Rarer syndromes characterized by hypogonadotropic hypogonadism

A.H.nai, Q.S.; Petrecca, K., 2011:
Rarest of the rare: Chordoid glioma infiltrating the optic chiasm

Robertson, G., 2011:
Raring to go

Wynford-Thomas, R.; Johnston, A.; Halpin, S.; Hamandi, K., 2015:
Rarities in neurology: blue rubber bleb naevus syndrome

Richards, Z.T.; Oppen, M.J.H., 2012:
Rarity and genetic diversity in Indo-Pacific Acropora corals

Bryson, G.L., 2013:
Rarity and review: evidence-based practice for uncommon diseases

Do, H.; Salemi, R.; Murone, C.; Mitchell, P.L.; Dobrovic, A., 2011:
Rarity of AKT1 and AKT3 E17K mutations in squamous cell carcinoma of lung

Kan, T.; Paun, B.C.; Mori, Y.; Sato, F.; Jin, Z.; Hamilton, J.P.; Ito, T.; Cheng, Y.; David, S.; Olaru, A.V.; Yang, J.; Agarwal, R.; Abraham, J.M.; Meltzer, S.J., 2008:
Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing

Mammen, A.L.; Pak, K.; Williams, E.K.; Brisson, D.; Coresh, J.; Selvin, E.; Gaudet, D., 2012:
Rarity of anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies in statin users, including those with self-limited musculoskeletal side effects

Gammie, J.S.; Brown, J.W., 2010:
Rarity of aortic thrombus after aortic valve bypass (apicoaortic conduit) surgery

Marion, J.F.; Lachman, P.; Greenstein, A.J.; Sachar, D.B., 1995 :
Rarity of fistulas in Crohn's disease of the jejunum

Lee, H.Yeon.; Song, I.Sup.; Yoo, S.Min.; Rho, J.Young.; Moon, J.Youn.; Kim, I.Jai.; Lim, S.Wook.; Sung, J.Hoon.; Cha, D.Hun.; White, C.S., 2011:
Rarity of isolated pulmonary embolism and acute aortic syndrome occurring outside of the field of view of dedicated coronary CT angiography

Strauchen, J.A., 2011:
Rarity of malignant mesothelioma prior to the widespread commercial introduction of asbestos: the Mount Sinai autopsy experience 1883-1910

Barnett, W.O., 1976:
Rarity of mediastinal parathyroids

El-Kersh, K.; Rawasia, W.Faraz.; Chaddha, U.; Guardiola, J., 2014:
Rarity revisited: cryptococcal peritonitis

Sizling, A.L.; Sizlingová, E.; Storch, D.; Reif, Jí.; Gaston, K.J., 2009:
Rarity, commonness, and the contribution of individual species to species richness patterns

Knapp, S., 2011:
Rarity, species richness, and the threat of extinction--are plants the same as animals?

Heiberg, A.; Frich, J.; Røttingen, J-Arne., 2014:
Rarity--a separate criterion used in prioritization?

Sot, Bña.; Behrmann, E.; Raunser, S.; Wittinghofer, A., 2013:
Ras GTPase activating (RasGAP) activity of the dual specificity GAP protein Rasal requires colocalization and C2 domain binding to lipid membranes

Harata, K.; Kubo, Y., 2015:
Ras GTPase activating protein CoIra1 is involved in infection-related morphogenesis by regulating cAMP and MAPK signaling pathways through CoRas2 in Colletotrichum orbiculare

Harispe, L.; Portela, C.; Scazzocchio, C.; Peñalva, M.A.; Gorfinkiel, L., 2007:
Ras GTPase-activating protein regulation of actin cytoskeleton and hyphal polarity in Aspergillus nidulans

Milner, D.S.; Till, R.; Cadby, I.; Lovering, A.L.; Basford, S.M.; Saxon, E.B.; Liddell, S.; Williams, L.E.; Sockett, R.Elizabeth., 2014:
Ras GTPase-like protein MglA, a controller of bacterial social-motility in Myxobacteria, has evolved to control bacterial predation by Bdellovibrio

Ferro, E.; Goitre, L.; Baldini, E.; Retta, S.Francesco.; Trabalzini, L., 2014:
Ras GTPases are both regulators and effectors of redox agents

Zhang, J.; Zhang, Y.; Zhong, Y.; Qu, Y.; Wang, T., 2013:
Ras GTPases modulate morphogenesis, sporulation and cellulase gene expression in the cellulolytic fungus Trichoderma reesei

Patel, M.; Côté, J-François., 2013:
Ras GTPases' interaction with effector domains: Breaking the families' barrier

Li, S.; D.S.uza, P., 2011:
Ras Isoprenylation and pAkt Inhibition by Zoledronic Acid and Fluvastatin Enhances Paclitaxel Activity in T24 Bladder Cancer Cells

Sepe, L.; Ferrari, M.Carla.; Cantarella, C.; Fioretti, F.; Paolella, G., 2013:
Ras activated ERK and PI3K pathways differentially affect directional movement of cultured fibroblasts

Kortholt, A.; Keizer-Gunnink, I.; Kataria, R.; Van Haastert, P.J.M., 2014:
Ras activation and symmetry breaking during Dictyostelium chemotaxis

Kim, R-Ju.; Kim, S-Rim.; Roh, K-Jin.; Park, S-Bum.; Park, J-Ran.; Kang, K-Sun.; Kong, G.; Tang, B.; Yang, Y-An.; Kohn, E.A.; Wakefield, L.M.; Nam, J-Seok., 2010:
Ras activation contributes to the maintenance and expansion of Sca-1pos cells in a mouse model of breast cancer

Wu, C-Lin.; Tsai, H-Chi.; Chen, Z-Wei.; Wu, C-Ming.; Li, T-Mao.; Fong, Y-Chin.; Tang, C-Hsin., 2014:
Ras activation mediates WISP-1-induced increases in cell motility and matrix metalloproteinase expression in human osteosarcoma

Rowland, S.L.; DePersis, C.L.; Torres, R.M.; Pelanda, R., 2010:
Ras activation of Erk restores impaired tonic BCR signaling and rescues immature B cell differentiation

Logsdon, C.D.; Ji, B., 2010:
Ras activity in acinar cells links chronic pancreatitis and pancreatic cancer

Ji, B.; Tsou, L.; Wang, H.; Gaiser, S.; Chang, D.Z.; Daniluk, J.; Bi, Y.; Grote, T.; Longnecker, D.S.; Logsdon, C.D., 2009:
Ras activity levels control the development of pancreatic diseases

Henis, Y.I.; Hancock, J.F.; Prior, I.A., 2009:
Ras acylation, compartmentalization and signaling nanoclusters (Review)

Safina, A.F.; Varga, A.E.; Bianchi, A.; Zheng, Q.; Kunnev, D.; Liang, P.; Bakin, A.V., 2009:
Ras alters epithelial-mesenchymal transition in response to TGFbeta by reducing actin fibers and cell-matrix adhesion

Rudack, T.; Xia, F.; Schlitter, Jürgen.; Kötting, C.; Gerwert, K., 2012:
Ras and GTPase-activating protein (GAP) drive GTP into a precatalytic state as revealed by combining FTIR and biomolecular simulations

Wu, R.Feng.; Terada, L.S., 2009:
Ras and Nox: Linked signaling networks?

Molognoni, F.; de Melo, F.Henriques.Machado.; da Silva, C.Tainah.; Jasiulionis, M.Galvonas., 2014:
Ras and Rac1, frequently mutated in melanomas, are activated by superoxide anion, modulate Dnmt1 level and are causally related to melanocyte malignant transformation

Stornetta, R.L.; Zhu, J.Julius., 2011:
Ras and Rap signaling in synaptic plasticity and mental disorders

Crespo, P.; Calvo, F.; Sanz-Moreno, V., 2011:
Ras and Rho GTPases on the move: The RasGRF connection

Raudaskoski, M.; Kothe, E.; Fowler, T.J.; Jung, E-Martina.; Horton, J.Stephen., 2012:
Ras and Rho small G proteins: insights from the Schizophyllum commune genome sequence and comparisons to other fungi

Schmukler, E.; Kloog, Y.; Pinkas-Kramarski, R., 2015:
Ras and autophagy in cancer development and therapy

Yoshiki, S.; Matsunaga-Udagawa, R.; Aoki, K.; Kamioka, Y.; Kiyokawa, E.; Matsuda, M., 2010:
Ras and calcium signaling pathways converge at Raf1 via the Shoc2 scaffold protein

Papadakis, E.; Malliri, A.; Linardopoulos, S.; Karaiossifidi, H.; Field, J.; Spandidos, D., 1992:
Ras and p53 expression in non-small-cell lung-cancer patients - p53 over-expression correlates with a poor prognosis

Antonyak, M.A.; Cerione, R.A., 2009:
Ras and the FAK paradox

Alvarado, Y.; Giles, F.J., 2007:
Ras as a therapeutic target in hematologic malignancies

Kim, J.Sang.; Chae, Y.; Ha, Y-Sok.; Kim, I.Yi.; Byun, S.Soo.; Yun, S-Joong.; Kim, W-Jae., 2012:
Ras association domain family 1A: a promising prognostic marker in recurrent nonmuscle invasive bladder cancer

Kloog, Y.; Elad-Sfadia, G.; Haklai, R.; Mor, A., 2014:
Ras chaperones: new targets for cancer and immunotherapy

Fuentes, G.; Valencia, A., 2010:
Ras classical effectors: new tales from in silico complexes

Grant, B.J.; Gorfe, A.A.; McCammon, J.Andrew., 2009:
Ras conformational switching: simulating nucleotide-dependent conformational transitions with accelerated molecular dynamics

Lee, Y.; Nachtrab, G.; Klinsawat, P.W.; Hami, D.; Poss, K.D., 2010:
Ras controls melanocyte expansion during zebrafish fin stripe regeneration

Li, H.; Liu, Y.; Zhang, Q.; Jing, Y.; Chen, S.; Song, Z.; Yan, J.; Li, Y.; Wu, X.; Zhang, X.; Zhang, Y.; Case, J.; Yu, M.; Ingram, D.A.; Yang, F-Chun., 2009:
Ras dependent paracrine secretion of osteopontin by Nf1+/- osteoblasts promote osteoclast activation in a neurofibromatosis type I murine model

McGrath, M.Forero.; Ogawa, T.; de Bold, A.J., 2012:
Ras dexamethasone-induced protein 1 is a modulator of hormone secretion in the volume overloaded heart

Vandal, G.; Geiling, B.; Dankort, D., 2014:
Ras effector mutant expression suggest a negative regulator inhibits lung tumor formation

Reiner, D.J., 2011:
Ras effector switching as a developmental strategy

Zand, T.P.; Reiner, D.J.; Der, C.J., 2011:
Ras effector switching promotes divergent cell fates in C. elegans vulval patterning

Shi, G-Xian.; Andres, D.A.; Cai, W., 2012 :
Ras family small GTPase-mediated neuroprotective signaling in stroke

Spandidos, D.; Liloglou, T.; Arvanitis, D.; Gourtsoyiannis, N., 1993:
Ras gene activation in human small intestinal tumors

Fracalossi, A.C.C.; Comparini, L.; Funabashi, K.; Godoy, C.; Iwamura, E.S.M.; Nascimento, Fábio.D.; Nader, H.B.; Oshima, C.T.F.; Ribeiro, D.A., 2011:
Ras gene mutation is not related to tumour invasion during rat tongue carcinogenesis induced by 4-nitroquinoline 1-oxide

Eliopoulos, A.; Kiaris, H.; Rees, R.; Sivridis, E.; Parsons, M.; Spandidos, D., 1994:
Ras gene-mutations are a rare event in human uveal and cutaneous melanomas

Kono, M.; Yasuda, S.; Stevens, R.L.; Koide, H.; Kurita, T.; Shimizu, Y.; Kanetsuka, Y.; Oku, K.; Bohgaki, T.; Amengual, O.; Horita, T.; Shimizu, T.; Majima, T.; Koike, T.; Atsumi, T., 2015:
Ras guanine nucleotide-releasing protein 4 is aberrantly expressed in the fibroblast-like synoviocytes of patients with rheumatoid arthritis and controls their proliferation

Adachi, R.; Krilis, S.A.; Nigrovic, P.A.; Hamilton, M.J.; Chung, K.; Thakurdas, S.M.; Boyce, J.A.; Anderson, P.; Stevens, R.L., 2012:
Ras guanine nucleotide-releasing protein-4 (RasGRP4) involvement in experimental arthritis and colitis

Takino, J.; Nagamine, K.; Hori, T., 2014:
Ras guanyl nucleotide releasing protein 2 affects cell viability and cell-matrix adhesion in ECV304 endothelial cells

Cox, A.D.; Der, C.J., 2011:
Ras history: The saga continues

Karassek, S.; Berghaus, C.; Schwarten, M.; Goemans, C.G.; Ohse, N.; Kock, G.; Jockers, K.; Neumann, S.; Gottfried, S.; Herrmann, C.; Heumann, R.; Stoll, R., 2010:
Ras homolog enriched in brain (Rheb) enhances apoptotic signaling

Shu, Q.; Xu, Y.; Zhuang, H.; Fan, J.; Sun, Z.; Zhang, M.; Xu, G., 2015:
Ras homolog enriched in the brain is linked to retinal ganglion cell apoptosis after light injury in rats

Ma, J.; Xue, Y.; Cui, W.; Li, Y.; Zhao, Q.; Ye, W.; Zheng, J.; Cheng, Y.; Ma, Y.; Li, S.; Han, T.; Miao, L.; Yao, L.; Zhang, J.; Liu, W., 2012:
Ras homolog gene family, member A promotes p53 degradation and vascular endothelial growth factor-dependent angiogenesis through an interaction with murine double minute 2 under hypoxic conditions

Zheng, H.; Liu, A.; Liu, B.; Li, M.; Yu, H.; Luo, X., 2010:
Ras homologue enriched in brain is a critical target of farnesyltransferase inhibitors in non-small cell lung cancer cells

Charette, N.; Vandeputte, C.; Stärkel, P., 2015:
Ras in digestive oncology: from molecular biology to clinical implications

Drosten, M.; Lechuga, C.G.; Barbacid, M., 2015:
Ras in epidermal proliferation

Sorscher, S.M.; Lockhart, A.Craig., 2011:
Ras inhibition and the survival benefit favoring zoledronic acid compared with denosumab in patients with multiple myeloma

Pando, R.; Cheporko, Y.; Haklai, R.; Maysel-Auslender, S.; Keren, G.; George, J.; Porat, E.; Sagie, A.; Kloog, Y.; Hochhauser, E., 2009:
Ras inhibition attenuates myocardial ischemia-reperfusion injury

Aizman, E.; Mor, A.; George, J.; Kloog, Y., 2010:
Ras inhibition attenuates pancreatic cell death and experimental type 1 diabetes: possible role of regulatory T cells

Barkan, B.; Cox, A.D.; Kloog, Y., 2014:
Ras inhibition boosts galectin-7 at the expense of galectin-1 to sensitize cells to apoptosis

Aizman, E.; Mor, A.; Levy, A.; George, J.; Kloog, Y., 2012:
Ras inhibition by FTS attenuates brain tumor growth in mice by direct antitumor activity and enhanced reactivity of cytotoxic lymphocytes

Schmukler, E.; Grinboim, E.; Schokoroy, S.; Amir, A.; Wolfson, E.; Kloog, Y.; Pinkas-Kramarski, R., 2013:
Ras inhibition enhances autophagy, which partially protects cells from death

Stärkel, P.; Charette, N.; Borbath, I.; Schneider-Merck, T.; D.S.eger, C.; Abarca, J.; Leclercq, I.; Horsmans, Y., 2012:
Ras inhibition in hepatocarcinoma by S-trans-trans-farnesylthiosalicyclic acid: association of its tumor preventive effect with cell proliferation, cell cycle events, and angiogenesis

Mor, A.; Kloog, Y.; Keren, G.; George, J., 2009:
Ras inhibition increases the frequency and function of regulatory T cells and attenuates type-1 diabetes in non-obese diabetic mice

Mor, A.; Aizman, E.; George, J.; Kloog, Y., 2011:
Ras inhibition induces insulin sensitivity and glucose uptake

Wang, W.; Fang, G.; Rudolph, J., 2013:
Ras inhibition via direct Ras binding--is there a path forward?

Yaari-Stark, S.; Shaked, M.; Nevo-Caspi, Y.; Jacob-Hircsh, J.; Shamir, R.; Rechavi, G.; Kloog, Y., 2010:
Ras inhibits endoplasmic reticulum stress in human cancer cells with amplified Myc

Kurig, B.; Shymanets, A.; Bohnacker, T.; Prajwal; Brock, C.; Ahmadian, M.Reza.; Schaefer, M.; Gohla, A.; Harteneck, C.; Wymann, M.P.; Jeanclos, E.; Nürnberg, B., 2010:
Ras is an indispensable coregulator of the class IB phosphoinositide 3-kinase p87/p110gamma

Liu, C.; Takahashi, M.; Li, Y.; Song, S.; Dillon, T.J.; Shinde, U.; Stork, P.J.S., 2008:
Ras is required for the cyclic AMP-dependent activation of Rap1 via Epac2

Abankwa, D.; Gorfe, A.A.; Inder, K.; Hancock, J.F., 2010:
Ras membrane orientation and nanodomain localization generate isoform diversity

Yoshida, S.; Kajitani, N.; Satsuka, A.; Nakamura, H.; Sakai, H., 2008:
Ras modifies proliferation and invasiveness of cells expressing human papillomavirus oncoproteins

Dempke, W.C.M.; Heinemann, V., 2011:
Ras mutational status is a biomarker for resistance to EGFR inhibitors in colorectal carcinoma

Zhou, Y.; Hancock, J.F., 2015:
Ras nanoclusters: Versatile lipid-based signaling platforms

Cho, K-Jin.; Hancock, J.F., 2013:
Ras nanoclusters: a new drug target?

Murugan, A.Kannan.; Munirajan, A.Kannan.; Tsuchida, N., 2012:
Ras oncogenes in oral cancer: the past 20 years

Salzano, M.; Russo, E.; Salzano, S.; Bifulco, M.; Vitale, M., 2014:
Ras oncoprotein disrupts the TSH/CREB signaling upstream adenylyl cyclase in human thyroid cell

Spandidos, D.; Arvanitis, D.; Field, J., 1992:
Ras p21 expression in neuroblastomas and ganglio-neuroblastomas - correlation with patients prognosis

Hamdy, S.; Aprikian, A.; Begin, L.; Fair, W.; Bazinet, M., 1994:
Ras p21 overexpression is a late event in prostate-cancer

Song, S-Ping.; Hennig, A.; Schubert, K.; Markwart, R.; Schmidt, P.; Prior, I.A.; Böhmer, F-Dietmar.; Rubio, I., 2013 :
Ras palmitoylation is necessary for N-Ras activation and signal propagation in growth factor signalling

da Fonseca, C.Orlando.; Linden, R.; Futuro, Débora.; Gattass, C.Rocha.; Quirico-Santos, T., 2008:
Ras pathway activation in gliomas: a strategic target for intranasal administration of perillyl alcohol

Newell, P.; Toffanin, S.; Villanueva, A.; Chiang, D.Y.; Minguez, B.; Cabellos, L.; Savic, R.; Hoshida, Y.; Lim, K.Hon.; Melgar-Lesmes, P.; Yea, S.; Peix, J.; Deniz, K.; Fiel, M.Isabel.; Thung, S.; Alsinet, C.; Tovar, V.; Mazzaferro, V.; Bruix, J.; Roayaie, S.; Schwartz, M.; Friedman, S.L.; Llovet, J.M., 2009:
Ras pathway activation in hepatocellular carcinoma and anti-tumoral effect of combined sorafenib and rapamycin in vivo

Patel, M.R.; Jacobson, B.A.; De, A.; Frizelle, S.P.; Janne, P.; Thumma, S.C.; Whitson, B.A.; Farassati, F.; Kratzke, R.A., 2007:
Ras pathway activation in malignant mesothelioma

Westenskow, P.D.; Kurihara, T.; Aguilar, E.; Scheppke, E.L.; Moreno, S.K.; Wittgrove, C.; Marchetti, V.; Michael, I.P.; Anand, S.; Nagy, A.; Cheresh, D.; Friedlander, M., 2014:
Ras pathway inhibition prevents neovascularization by repressing endothelial cell sprouting

Irving, J.; Matheson, E.; Minto, L.; Blair, H.; Case, M.; Halsey, C.; Swidenbank, I.; Ponthan, F.; Kirschner-Schwabe, R.; Groeneveld-Krentz, S.; Hof, J.; Allan, J.; Harrison, C.; Vormoor, J.; von Stackelberg, A.; Eckert, C., 2015:
Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition

Wu, Y.; Zhuang, Y.; Han, M.; Xu, T.; Deng, K., 2010:
Ras promotes cell survival by antagonizing both JNK and Hid signals in the Drosophila eye

Kim, H.; Choi, J-A.; Kim, J-Hong., 2015:
Ras promotes transforming growth factor-β (TGF-β)-induced epithelial-mesenchymal transition via a leukotriene B4 receptor-2-linked cascade in mammary epithelial cells

Xifró, X.; Miñano-Molina, A.J.; Saura, C.A.; Rodríguez-Álvarez, Jé., 2014 :
Ras protein activation is a key event in activity-dependent survival of cerebellar granule neurons

Li, Y.; Wang, Y., 2013:
Ras protein/cAMP-dependent protein kinase signaling is negatively regulated by a deubiquitinating enzyme, Ubp3, in yeast

Bolourani, P.; Spiegelman, G.; Weeks, G., 2011:
Ras proteins have multiple functions in vegetative cells of Dictyostelium

Bracco, E.; Pergolizzi, B., 2014:
Ras proteins signaling in the early metazoan Dictyostelium discoideum

Mikeladze, D.; Zhuravliova, E.; Barbakadze, T., 2008:
Ras proteins, nitrosylation and homocysteine metabolism

Anonymous, 2013:
Ras puts the brake on doxorubicin-mediated cell death in p53-expressing cells

Schmidt, M.Lee.; Donninger, H.; Clark, G.J., 2015:
Ras regulates SCF(β-TrCP) protein activity and specificity via its effector protein NORE1A

Zhang, S.; Hwaiz, R.; Rahman, M.; Herwald, H.; Thorlacius, H., 2015:
Ras regulates alveolar macrophage formation of CXC chemokines and neutrophil activation in streptococcal M1 protein-induced lung injury

Sharma, V.; Dixit, D.; Koul, N.; Mehta, V.Singh.; Sen, E., 2011:
Ras regulates interleukin-1β-induced HIF-1α transcriptional activity in glioblastoma

Milon, B.C.; Agyapong, A.; Bautista, R.; Costello, L.C.; Franklin, R.B., 2010:
Ras responsive element binding protein-1 (RREB-1) down-regulates hZIP1 expression in prostate cancer cells

Mora, N.; Santa Bárbara Ruiz, P.; Ferreira, N.; Serras, F., 2014:
Ras signal triggers β-amyloid precursor protein (APP) expression

Young, A.; Lyons, J.; Miller, A.L.; Phan, V.T.; Alarcón, I.Rangel.; McCormick, F., 2009:
Ras signaling and therapies

Stoppa, G.; Rumiato, E.; Saggioro, D., 2012:
Ras signaling contributes to survival of human T-cell leukemia/lymphoma virus type 1 (HTLV-1) Tax-positive T-cells

Inglis, D.O.; Sherlock, G., 2014:
Ras signaling gets fine-tuned: regulation of multiple pathogenic traits of Candida albicans

Farassati, F.; Pan, W.; Yamoutpour, F.; Henke, S.; Piedra, M.; Frahm, S.; Al-Tawil, S.; Mangrum, W.I.; Parada, L.F.; Rabkin, S.D.; Martuza, R.L.; Kurtz, A., 2008:
Ras signaling influences permissiveness of malignant peripheral nerve sheath tumor cells to oncolytic herpes

Duan, J-H.; Wang, Y.; Duarte, D.; Vasko, M.R.; Nicol, G.D.; Hingtgen, C.M., 2011:
Ras signaling pathways mediate NGF-induced enhancement of excitability of small-diameter capsaicin-sensitive sensory neurons from wildtype but not Nf1+/- mice

Nelson, M.L.; Kang, H-Seo.; Lee, G.M.; Blaszczak, A.G.; Lau, D.K.W.; McIntosh, L.P.; Graves, B.J., 2010:
Ras signaling requires dynamic properties of Ets1 for phosphorylation-enhanced binding to coactivator CBP

Murholm, M.; Dixen, K.; Hansen, J.B., 2010:
Ras signalling regulates differentiation and UCP1 expression in models of brown adipogenesis

Jeong, W-Jeong.; Yoon, J.; Park, J-Chan.; Lee, S-Hoon.; Lee, S-Hoon.; Kaduwal, S.; Kim, H.; Yoon, J-Bok.; Choi, K-Yell., 2012:
Ras stabilization through aberrant activation of Wnt/β-catenin signaling promotes intestinal tumorigenesis

Casar, B.; Arozarena, I.; Sanz-Moreno, V.; Pinto, Aán.; Agudo-Ibáñez, L.; Marais, R.; Lewis, R.E.; Berciano, Mía.T.; Crespo, P., 2009:
Ras subcellular localization defines extracellular signal-regulated kinase 1 and 2 substrate specificity through distinct utilization of scaffold proteins

Zaganjor, E.; Weil, L.M.; Gonzales, J.X.; Minna, J.D.; Cobb, M.H., 2014:
Ras transformation uncouples the kinesin-coordinated cellular nutrient response

Kennedy, A.L.; Adams, P.D.; Morton, J.P., 2012:
Ras, PI3K/Akt and senescence: Paradoxes provide clues for pancreatic cancer therapy

Xu, W.; Trepel, J.; Neckers, L., 2011:
Ras, ROS and proteotoxic stress: a delicate balance

Solus, J.F.; Kraft, S., 2013:
Ras, Raf, and MAP kinase in melanoma

Lock, R.; Debnath, J., 2011:
Ras, autophagy and glycolysis

Pylayeva, Y.; Gillen, K.M.; Gerald, W.; Beggs, H.E.; Reichardt, L.F.; Giancotti, F.G., 2009:
Ras- and PI3K-dependent breast tumorigenesis in mice and humans requires focal adhesion kinase signaling

Fasano, S.; Brambilla, R., 2011:
Ras-ERK Signaling in Behavior: Old Questions and New Perspectives

Darcy, M.J.; Trouche, Séphanie.; Jin, S-Xue.; Feig, L.A., 2015:
Ras-GRF2 mediates long-term potentiation, survival, and response to an enriched environment of newborn neurons in the hippocampus

Dangle, P.P.; Zaharieva, B.; Jia, H.; Pohar, K.S., 2009 :
Ras-MAPK pathway as a therapeutic target in cancer--emphasis on bladder cancer

Fortwendel, J.R., 2012:
Ras-Mediated Signal Transduction and Virulence in Human Pathogenic Fungi

Stansfield, B.K.; Bessler, W.K.; Mali, R.; Mund, J.A.; Downing, B.D.; Kapur, R.; Ingram, D.A., 2014:
Ras-Mek-Erk signaling regulates Nf1 heterozygous neointima formation

Gupta, V.K.; Rajala, A.; Rajala, R.V.S., 2012:
Ras-associating domain proteins: a new class of cyclic nucleotide-gated channel modulators

Reeves, M.E.; Baldwin, S.W.; Baldwin, M.L.; Chen, S-Tai.; Moretz, J.M.; Aragon, R.J.; Li, X.; Strong, D.D.; Mohan, S.; Amaar, Y.G., 2011:
Ras-association domain family 1C protein promotes breast cancer cell migration and attenuates apoptosis

Oceandy, D.; Cartwright, E.J.; Neyses, L., 2010:
Ras-association domain family member 1A (RASSF1A)-where the heart and cancer meet

Balana, B.; Bahima, L.; Bodhinathan, K.; Taura, J.J.; Taylor, N.M.; Nettleton, M.Y.; Ciruela, F.; Slesinger, P.A., 2013:
Ras-association domain of sorting Nexin 27 is critical for regulating expression of GIRK potassium channels

Johnson, C.; Chun-Jen Lin, C.; Stern, M., 2013:
Ras-dependent and Ras-independent effects of PI3K in Drosophila motor neurons

Calvisi, D.F.; Pinna, F.; Pellegrino, R.; Sanna, V.; Sini, M.; Daino, L.; Simile, M.M.; D.M.glio, M.R.; Frau, M.; Tomasi, M.L.; Seddaiu, M.A.; Muroni, M.R.; Feo, F.; Pascale, R.M., 2008:
Ras-driven proliferation and apoptosis signaling during rat liver carcinogenesis is under genetic control

Patel, A.V.; Eaves, D.; Jessen, W.J.; Rizvi, T.A.; Ecsedy, J.A.; Qian, M.G.; Aronow, B.J.; Perentesis, J.P.; Serra, E.; Cripe, T.P.; Miller, S.J.; Ratner, N., 2013:
Ras-driven transcriptome analysis identifies aurora kinase A as a potential malignant peripheral nerve sheath tumor therapeutic target

Campbell, P.M.; Lee, K.M.; Ouellette, M.M.; Kim, H.Jin.; Groehler, A.L.; Khazak, V.; Der, C.J., 2008:
Ras-driven transformation of human nestin-positive pancreatic epithelial cells

Tereshina, M.B.; Ermakova, G.V.; Ivanova, A.S.; Zaraisky, A.G., 2014:
Ras-dva1 small GTPase regulates telencephalon development in Xenopus laevis embryos by controlling Fgf8 and Agr signaling at the anterior border of the neural plate

Fasano, S.; D'Antoni, A.; Orban, P.C.; Valjent, E.; Putignano, E.; Vara, H.; Pizzorusso, T.; Giustetto, M.; Yoon, B.; Soloway, P.; Maldonado, R.; Caboche, J.; Brambilla, R., 2010:
Ras-guanine nucleotide-releasing factor 1 (Ras-GRF1) controls activation of extracellular signal-regulated kinase (ERK) signaling in the striatum and long-term behavioral responses to cocaine

Wang, Q.; Siminovitch, K.A.; Downey, G.P.; McCulloch, C.A., 2013:
Ras-guanine-nucleotide-releasing factors 1 and 2 interact with PLCγ at focal adhesions to enable IL-1-induced Ca(2+) signalling, ERK activation and MMP-3 expression

Zamkova, M.; Khromova, N.; Kopnin, B.P.; Kopnin, P., 2013:
Ras-induced ROS upregulation affecting cell proliferation is connected with cell type-specific alterations of HSF1/SESN3/p21Cip1/WAF1 pathways

Hosogane, M.; Funayama, R.; Nishida, Y.; Nagashima, T.; Nakayama, K., 2014:
Ras-induced changes in H3K27me3 occur after those in transcriptional activity

Wang, Y.; Li, G.; Mao, F.; Li, X.; Liu, Q.; Chen, L.; Lv, L.; Wang, X.; Wu, J.; Dai, W.; Wang, G.; Zhao, E.; Tang, K-Fu.; Sun, Z.Sheng., 2014:
Ras-induced epigenetic inactivation of the RRAD (Ras-related associated with diabetes) gene promotes glucose uptake in a human ovarian cancer model

Hole, P.S.; Pearn, L.; Tonks, A.J.; James, P.E.; Burnett, A.K.; Darley, R.L.; Tonks, A., 2010:
Ras-induced reactive oxygen species promote growth factor-independent proliferation in human CD34+ hematopoietic progenitor cells

Zoppoli, G.; Moran, E.; Soncini, D.; Cea, M.; Garuti, A.; Rocco, I.; Cirmena, G.; Grillo, V.; Bagnasco, L.; Icardi, G.; Ansaldi, F.; Parodi, S.; Patrone, F.; Ballestrero, A.; Nencioni, A., 2010:
Ras-induced resistance to lapatinib is overcome by MEK inhibition

Dimauro, T.; David, G., 2011:
Ras-induced senescence and its physiological relevance in cancer

Cai, H.; Das, S.; Kamimura, Y.; Long, Y.; Parent, C.A.; Devreotes, P.N., 2010:
Ras-mediated activation of the TORC2-PKB pathway is critical for chemotaxis

Relógio, A.; Thomas, P.; Medina-Pérez, P.; Reischl, S.; Bervoets, S.; Gloc, E.; Riemer, P.; Mang-Fatehi, S.; Maier, B.; Schäfer, R.; Leser, U.; Herzel, H.; Kramer, A.; Sers, C., 2014:
Ras-mediated deregulation of the circadian clock in cancer

Shinjyo, T.; Kurosawa, H.; Miyagi, J-ichi.; Ohama, K.; Masuda, M.; Nagasaki, A.; Matsui, H.; Inaba, T.; Furukawa, Y.; Takasu, N., 2008:
Ras-mediated up-regulation of survivin expression in cytokine-dependent murine pro-B lymphocytic cells

Li, Y.; Takahashi, M.; Stork, P.J.S., 2013:
Ras-mutant cancer cells display B-Raf binding to Ras that activates extracellular signal-regulated kinase and is inhibited by protein kinase A phosphorylation

Christofi, T.; Apidianakis, Y., 2013:
Ras-oncogenic Drosophila hindgut but not midgut cells use an inflammation-like program to disseminate to distant sites

Shao, X.; Miao, M.; Qi, X.; Chen, Z., 2012:
Ras-proximate-1 GTPase-activating protein and Rac2 may play pivotal roles in the initial development of myelodysplastic syndrome

Asahara, S.; Shibutani, Y.; Teruyama, K.; Inoue, H.Y.; Kawada, Y.; Etoh, H.; Matsuda, T.; Kimura-Koyanagi, M.; Hashimoto, N.; Sakahara, M.; Fujimoto, W.; Takahashi, H.; Ueda, S.; Hosooka, T.; Satoh, T.; Inoue, H.; Matsumoto, M.; Aiba, A.; Kasuga, M.; Kido, Y., 2013:
Ras-related C3 botulinum toxin substrate 1 (RAC1) regulates glucose-stimulated insulin secretion via modulation of F-actin

Kim, J-Gyu.; Moon, M-Young.; Kim, H-Jun.; Li, Y.; Song, D-Keun.; Kim, J-Sub.; Lee, J-Yong.; Kim, J.; Kim, S-Chan.; Park, J-Bong., 2012:
Ras-related GTPases Rap1 and RhoA collectively induce the phagocytosis of serum-opsonized zymosan particles in macrophages

Furstenau, D.K.; Mitra, N.; Wan, F.; Lewis, R.; Feldman, M.D.; Fraker, D.L.; Guvakova, M.A., 2012:
Ras-related protein 1 and the insulin-like growth factor type I receptor are associated with risk of progression in patients diagnosed with carcinoma in situ

Wang, D.; Lou, J.; Ouyang, C.; Chen, W.; Liu, Y.; Liu, X.; Cao, X.; Wang, J.; Lu, L., 2010:
Ras-related protein Rab10 facilitates TLR4 signaling by promoting replenishment of TLR4 onto the plasma membrane

Kidd, A.R.; Snider, J.L.; Martin, T.D.; Graboski, S.F.; Der, C.J.; Cox, A.D., 2010:
Ras-related small GTPases RalA and RalB regulate cellular survival after ionizing radiation

Wu, S-Ying.; Lan, S-Hui.; Cheng, D-En.; Chen, W-Kai.; Shen, C-Huang.; Lee, Y-Ray.; Zuchini, R.; Liu, H-Sheng., 2012:
Ras-related tumorigenesis is suppressed by BNIP3-mediated autophagy through inhibition of cell proliferation

Cheng, K.Wa.; Agarwal, R.; Mills, G.B., 2010:
Ras-superfamily GTP-ases in ovarian cancer

Heo, J.; Hong, I., 2010:
Ras-targeting action of thiopurines in the presence of reactive nitrogen species

Jung, S-Mi.; Park, S-Soo.; Kim, W-Jae.; Moon, S-Kwon., 2012 :
Ras/ERK1 pathway regulation of p27KIP1-mediated G1-phase cell-cycle arrest in cordycepin-induced inhibition of the proliferation of vascular smooth muscle cells

Fehrenbacher, N.; Bar-Sagi, D.; Philips, M., 2009:
Ras/MAPK signaling from endomembranes

Ichise, T.; Yoshida, N.; Ichise, H., 2013:
Ras/MAPK signaling modulates VEGFR-3 expression through Ets-mediated p300 recruitment and histone acetylation on the Vegfr3 gene in lymphatic endothelial cells

Lastauskienė, Eė.; Zinkevičienė, Aė.; Čitavičius, D., 2014:
Ras/PKA signal transduction pathway participates in the regulation of Saccharomyces cerevisiae cell apoptosis in an acidic environment

McGlynn, L.M.; Kirkegaard, T.; Edwards, J.; Tovey, S.; Cameron, D.; Twelves, C.; Bartlett, J.M.S.; Cooke, T.G., 2009:
Ras/Raf-1/MAPK pathway mediates response to tamoxifen but not chemotherapy in breast cancer patients

Knight, T.; Irving, J.Anne.Elizabeth., 2014:
Ras/Raf/MEK/ERK Pathway Activation in Childhood Acute Lymphoblastic Leukemia and Its Therapeutic Targeting

McCubrey, J.A.; Steelman, L.S.; Chappell, W.H.; Abrams, S.L.; Franklin, R.A.; Montalto, G.; Cervello, M.; Libra, M.; Candido, S.; Malaponte, G.; Mazzarino, M.C.; Fagone, P.; Nicoletti, F.; Bäsecke, Jörg.; Mijatovic, S.; Maksimovic-Ivanic, D.; Milella, M.; Tafuri, A.; Chiarini, F.; Evangelisti, C.; Cocco, L.; Martelli, A.M., 2013:
Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR cascade inhibitors: how mutations can result in therapy resistance and how to overcome resistance

Chappell, W.H.; Steelman, L.S.; Long, J.M.; Kempf, R.C.; Abrams, S.L.; Franklin, R.A.; Bäsecke, Jörg.; Stivala, F.; Donia, M.; Fagone, P.; Malaponte, G.; Mazzarino, M.C.; Nicoletti, F.; Libra, M.; Maksimovic-Ivanic, D.; Mijatovic, S.; Montalto, G.; Cervello, M.; Laidler, P.; Milella, M.; Tafuri, A.; Bonati, A.; Evangelisti, C.; Cocco, L.; Martelli, A.M.; McCubrey, J.A., 2011:
Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR inhibitors: rationale and importance to inhibiting these pathways in human health

Sowa, Y.; Sakai, T., 2013:
Ras/Raf/MEK/ERK cascade

Yu, Y.; Luk, F.; Yang, J-Lin.; Walsh, W.R., 2011:
Ras/Raf/MEK/ERK pathway is associated with lung metastasis of osteosarcoma in an orthotopic mouse model

Mizunuma, M.; Tsubakiyama, R.; Ogawa, T.; Shitamukai, A.; Kobayashi, Y.; Inai, T.; Kume, K.; Hirata, D., 2013:
Ras/cAMP-dependent protein kinase (PKA) regulates multiple aspects of cellular events by phosphorylating the Whi3 cell cycle regulator in budding yeast

Wood, P.; Mulay, V.; Darabi, M.; Chan, K.Cecilia.; Heeren, J.; Pol, A.; Lambert, G.; Rye, K-Anne.; Enrich, C.; Grewal, T., 2011:
Ras/mitogen-activated protein kinase (MAPK) signaling modulates protein stability and cell surface expression of scavenger receptor SR-BI

Ballou, E.Ripley.; Kozubowski, L.; Nichols, C.B.; Alspaugh, J.Andrew., 2014:
Ras1 acts through duplicated Cdc42 and Rac proteins to regulate morphogenesis and pathogenesis in the human fungal pathogen Cryptococcus neoformans

Zhu, Y.; Fang, H-Ming.; Wang, Y-Ming.; Zeng, G-Sheng.; Zheng, X-De.; Wang, Y., 2010:
Ras1 and Ras2 play antagonistic roles in regulating cellular cAMP level, stationary-phase entry and stress response in Candida albicans

Ma, L.; Liu, S.; Shi, M.; Chen, X-xin.; Li, S., 2014:
Ras1CA-upregulated BCPI inhibits cathepsin activity to prevent tissue destruction of the Bombyx posterior silk gland

Chattwood, A.; Bolourani, P.; Weeks, G., 2015:
RasG signaling is important for optimal folate chemotaxis in Dictyostelium

Rowshanravan, B.; Woodcock, S.A.; Botella, Jé.A.; Kiermayer, C.; Schneuwly, S.; Hughes, D.A., 2015:
RasGAP mediates neuronal survival in Drosophila through direct regulation of Rab5-dependent endocytosis

Bulat, N.; Jaccard, E.; Peltzer, N.; Khalil, H.; Yang, J-Yan.; Dubuis, G.; Widmann, C., 2011:
RasGAP-derived fragment N increases the resistance of beta cells towards apoptosis in NOD mice and delays the progression from mild to overt diabetes

Yaman, E.; Gasper, R.; Koerner, C.; Wittinghofer, A.; Tazebay, U.H., 2009:
RasGEF1A and RasGEF1B are guanine nucleotide exchange factors that discriminate between Rap GTP-binding proteins and mediate Rap2-specific nucleotide exchange

Fernández-Medarde, A.; Barhoum, R.; Riquelme, R.; Porteros, A.; Núñez, A.; de Luis, A.; de Las Rivas, J.; de la Villa, P.; Varela-Nieto, I.; Santos, E., 2009:
RasGRF1 disruption causes retinal photoreception defects and associated transcriptomic alterations

Tarnowski, M.; Schneider, G.; Amann, G.; Clark, G.; Houghton, P.; Barr, F.G.; Kenner, L.; Ratajczak, M.Z.; Kucia, M., 2013:
RasGRF1 regulates proliferation and metastatic behavior of human alveolar rhabdomyosarcomas

Schwechter, B.; Rosenmund, C.; Tolias, K.F., 2013:
RasGRF2 Rac-GEF activity couples NMDA receptor calcium flux to enhanced synaptic transmission

Ksionda, O.; Limnander, A.; Roose, J.P., 2014:
RasGRP Ras guanine nucleotide exchange factors in cancer

Szamałek, M.; Baer-Dubowska, W., 2007:
RasGRP proteins--Ras-activating factors

Sharma, A.; Luke, C.T.; Dower, N.A.; Stone, J.C.; Lorenzo, P.S., 2010:
RasGRP1 is essential for ras activation by the tumor promoter 12-O-tetradecanoylphorbol-13-acetate in epidermal keratinocytes

Lee, S.Hyung.; Yun, S.; Lee, J.; Kim, M.Jeong.; Piao, Z-Hao.; Jeong, M.; Chung, J.Woong.; Kim, T-Don.; Yoon, S.Ran.; Greenberg, P.D.; Choi, I., 2010:
RasGRP1 is required for human NK cell function

Priatel, J.J.; Chen, X.; Huang, Y-Hsuan.; Chow, M.T.; Zenewicz, L.A.; Coughlin, J.J.; Shen, H.; Stone, J.C.; Tan, R.; Teh, H.Sia., 2010:
RasGRP1 regulates antigen-induced developmental programming by naive CD8 T cells

Ko, B.; Kamsteeg, E-Jan.; Cooke, L.L.; Moddes, L.N.; Deen, P.M.T.; Hoover, R.S., 2010:
RasGRP1 stimulation enhances ubiquitination and endocytosis of the sodium-chloride cotransporter

Diez, F.R.; Garrido, A.A.; Sharma, A.; Luke, C.T.; Stone, J.C.; Dower, N.A.; Cline, J.Mark.; Lorenzo, P.S., 2009:
RasGRP1 transgenic mice develop cutaneous squamous cell carcinomas in response to skin wounding: potential role of granulocyte colony-stimulating factor

Golec, D.P.; Dower, N.A.; Stone, J.C.; Baldwin, T.A., 2013:
RasGRP1, but not RasGRP3, is required for efficient thymic β-selection and ERK activation downstream of CXCR4

Yang, D.; Kedei, N.; Li, L.; Tao, J.; Velasquez, J.F.; Michalowski, A.M.; Tóth, Bázs.I.; Marincsák, R.; Varga, A.; Bíró, Tás.; Yuspa, S.H.; Blumberg, P.M., 2010:
RasGRP3 contributes to formation and maintenance of the prostate cancer phenotype

Song, X.; Lopez-Campistrous, A.; Sun, L.; Dower, N.A.; Kedei, N.; Yang, J.; Kelsey, J.S.; Lewin, N.E.; Esch, T.E.; Blumberg, P.M.; Stone, J.C., 2014:
RasGRPs are targets of the anti-cancer agent ingenol-3-angelate

Davies, K.J.A.; Forman, H.Jay., 2011:
RasGrf1 and aging

Borrás, C.; Monleón, D.; López-Grueso, R.; Gambini, J.; Orlando, L.; Pallardó, F.V.; Santos, E.; Viña, Jé.; Font de Mora, J., 2011:
RasGrf1 deficiency delays aging in mice

Ratajczak, M.Z.; Kucia, M.; Liu, R.; Shin, D-Myung.; Bryndza, E.; Masternak, M.M.; Tarnowski, M.; Ratajczak, J.; Bartke, A., 2011:
RasGrf1: genomic imprinting, VSELs, and aging

Hadj-Slimane, Réda.; Pamonsinlapatham, P.; Herbeuval, J-Philippe.; Garbay, C.; Lepelletier, Y.; Raynaud, Fçoise., 2010:
RasV12 induces Survivin/AuroraB pathway conferring tumor cell apoptosis resistance

Sebastian, T.; Johnson, P.F., 2009:
RasV12-mediated down-regulation of CCAAT/enhancer binding protein beta in immortalized fibroblasts requires loss of p19Arf and facilitates bypass of oncogene-induced senescence

Molina-Ortiz, P.; Polizzi, Séléna.; Ramery, E.; Gayral, Séphanie.; Delierneux, Céline.; Oury, Cécile.; Iwashita, S.; Schurmans, Séphane., 2015:
Rasa3 controls megakaryocyte Rap1 activation, integrin signaling and differentiation into proplatelet

Lecht, S.; Haroutiunian, S.; Hoffman, A.; Lazarovici, P., 2008:
Rasagiline - a novel MAO B inhibitor in Parkinson's disease therapy

Elmer, L.W., 2014:
Rasagiline adjunct therapy in patients with Parkinson's disease: post hoc analyses of the PRESTO and LARGO trials

Petit, Géraldine.H.; Berkovich, E.; Hickery, M.; Kallunki, P.; Fog, K.; Fitzer-Attas, C.; Brundin, P., 2013:
Rasagiline ameliorates olfactory deficits in an alpha-synuclein mouse model of Parkinson's disease

Hermanowicz, N., 2007:
Rasagiline as a therapy for Parkinson's disease (PD)

Brusa, L.; Musco, S.; Bernardi, G.; Iani, C.; Pierantozzi, M.; Stanzione, P.; Stefani, A.; Finazzi Agro', E., 2015:
Rasagiline effect on bladder disturbances in early mild Parkinson's disease patients

Brüning, Jürgen.; Bats, J.W.; Schmidt, M.U., 2008:
Rasagiline ethanedisulfonate: an inhibitor for monoamine oxygenase B (MAO(B))

Coria, F.; Cozar-Santiago, Mía.del.Puig., 2007:
Rasagiline improves freezing in a patient with primary progressive freezing gait

Wong, F-Kuan.; Lee, S.Hung-Wah.; Atcha, Z.; Ong, A.Bee-Leng.; Pemberton, D.John.; Chen, W-Shin., 2010:
Rasagiline improves learning and memory in young healthy rats

Linazasoro, G., 2008:
Rasagiline in Parkinson's disease

Chahine, L.M.; Stern, M.B., 2012:
Rasagiline in Parkinson's disease

Jost, W.H., 2014:
Rasagiline in Parkinson's disease: the show must go on

Pagonabarraga, J.; Rodríguez-Oroz, Mía.Cruz., 2013:
Rasagiline in monotherapy in patients with early stages of Parkinson's disease and in combined and adjunct therapy to levodopa with moderate and advanced stages

Schapira, A.H.V., 2008:
Rasagiline in neurodegeneration

Buchanan, R.W.; Weiner, E.; Kelly, D.L.; Gold, J.M.; Keller, W.R.; Waltz, J.A.; McMahon, R.P.; Gorelick, D.A., 2016:
Rasagiline in the Treatment of the Persistent Negative Symptoms of Schizophrenia

Nayak, L.; Henchcliffe, C., 2008:
Rasagiline in treatment of Parkinson's disease