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Section 35

EurekaMag Full Text Articles Chapter 34,638



References:

Arlt, W.; Walker, E.A.; Draper, N.; Ivison, H.E.; Ride, J.P.; Hammer, F.; Chalder, S.M.; Borucka Mankiewicz, M.; Hauffa, B.P.; Malunowicz, E.M.; Stewart, P.M.; Shackleton, C.H.L. 2004: Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis analytical study. Lancet (north American Edition). 363(9427): 2128-2135, E 26
Guerra, G.Jr; Nascimento, S.R.D.; Araujo, M.; Condino Neto, A.; Lemos Marini, S.H.V.; Arruk, V.; Kirschfink, M.; Grumach, A.S.; De Mello, M.P. 2002: Congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency Possible association with C4 deficiency. International Immunopharmacology 2(9): 1380-1381
Guerra, G.Jr; Nascimento, S.R.D.; Araujo, M.; Condino Neto, A.; Lemos Marini, S.H.V.; Arruk, V.; Kirschfink, M.; Grumach, A.S.; De Mello, M.P. 2002: Congenital adrenal hyperplasia due to classic 3-hydroxysteroid dehydrogenase deficiency associated with low serum C4 levels and molecular alteration on C4 genes. International Immunopharmacology 2(9): 1383
Kovacs, J.; Heinze, G.; Votava, F.; Lebl, J.; Pribilincova, Z.; Frisch, H.; Battelino, T.; Solyom, J.; Waldhauser, F. 2000: Congenital adrenal hyperplasia in Middle-Europe between 1969-98 Analysis of the sex-ratio and time to diagnosis. Pediatric Research 47(4 Part 2): 133A
Van Der Kamp, H.J.; Noordam, C.; Wit, J.M.; Otten, B.J. 1999: Congenital adrenal hyperplasia in newborns; Screening and case-surveillance in the Netherlands. Hormone Research 51(Suppl 2): 29
Speiser, P.W. 2001: Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Endocrinology and Metabolism Clinics of North America 30(1): 31-59 Vi
Migeon, C.J.; Wisniewski, A.B. 2001: Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Growth, development, and therapeutic considerations. Endocrinology and Metabolism Clinics of North America 30(1): 193-206
Lemos Marini, S.H.V.; Castro, M.; Assumpco, J.G.; Belangero, V.M.S.; Guerra, G.Jr; Baptista, M.T.M.; De Mello, M.P. 2000: Congenital adrenal hypoplasia A case report in a Brazilian child. Hormone Research 53(Suppl 2): 73
Vlietman, J.é J.; Verhage, J.; Vos, H.L.; van Wijk, R.; Remijn, J.A.; van Solinge, W.W.; Brus, F. 2002: Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene. British Journal of Haematology 119(1): 282-283
Becker, S.; Martinez Saguer, I.; Heller, C.; Escuriola Ettingshausen, C.; Funk, M.; Klarmann, D.; Kreuz, W. 2001: Congenital afibrinogenemia Longterm experiences with a pasteurized fibrinogen concentrate in four patients. Annals of Hematology 80(Suppl 1): A6
Favier, R.; Aoki, N.; de Moerloose, P. 2001: Congenital alpha(2)-plasmin inhibitor deficiencies: a review. British Journal of Haematology 114(1): 4-10
Galambos, C.; Vargas, S.O.; Arnold, J.; Reid, L.; Perez Atayde, A.R.; Kozakewich, H. 2003: Congenital alveolar dysplasia. Modern Pathology 16(1): 3P
Stewart, L.; Walsh, V. 2002: Congenital amusia: all the songs sound the same. Current Biology: Cb 12(12): R420-R421
Bella, S.D.; Peretz, I. 2003: Congenital amusia interferes with the ability to synchronize with music. Annals of the new York Academy of Sciences 999: 166-169
Brezin, A.P.; Cisneros, B. 1999: Congenital and acquired infection in ocular toxoplasmosis. IOVS Investigative Ophthalmology and Visual Science 40(4): S383
Mira, Y.; Aznar, J.; Estelles, A.; Vaya, A.; Villa, P.; Ferrando, F. 2000: Congenital and acquired risk factors of thrombosis in women users of oral contraceptives Clinical aspects. Haemostasis 30(Suppl 1): 39
Appel, I.M.; Van Kessel Bakvis, C.L. 2000: Congenital and acquired thrombophilia as a risk factor for thrombosis in patients with AL or NHL. Haemostasis 30(1-2): 50
Merbs, C.F. 1999: Congenital and early developmental defects of the skeleton Their identification and significance in native North Americans. American Journal of Physical Anthropology (Suppl 28): 200-201
Kralovics, R.; Prchal, J.T. 2000: Congenital and inherited polycythemia. Current Opinion in Pediatrics 12(1): 29-34
Greco, D.S. 2001: Congenital and inherited renal disease of small animals. Veterinary Clinics of North America. Small Animal Practice 31(2): 393-399 Viii
Miró, O.; Laguno, M.; Masanés, F.; Perea, M.; Urbano-Márquez, A.; Grau, J.M. 2000: Congenital and metabolic myopathies of childhood or adult onset. Seminars in Arthritis and Rheumatism 29(6): 335-347
Sande, J.E.; Arceci, R.J.; Lampkin, B.C. 1999: Congenital and neonatal leukemia. Seminars in Perinatology 23(4): 274-285
Lilje, C.; Wilhelm, C.; Gildein, H.P. 1999: Congenital aneurysm of the descending aorta in a neonate. American Journal of Cardiology 84(4): 491
Piram, A.; Peres, L.C.; Pina Neto, J.M. 2000: Congenital anomalies A review of 279 consecutive autopsies in Ribeirao Preto, Brazil. American Journal of Human Genetics 67(4 Suppl 2): 130
Synnes, A.; Koravangattu, S.; Berry, M.; Jones, H.; Chien, L.Y.; Lee, S.K. 2000: Congenital anomalies affect neonatal intensive care unit mortality rates independently of illness severity and population risk factors. Pediatric Research 47(4 Part 2): 326A
Hasanhodzic, M.; Garne, E.; Clement, M.; Stoll, C. 2000: Congenital anomalies associated with fetal congenital heart diseases. American Journal of Human Genetics 67(4 Suppl 2): 115
Crombez, E.A.; Fox, M.; Gregersen, N.; Vilain, E. 2003: Congenital anomalies associated with short-chain acyl-coenzyme A dehydrogenase deficiency. Genetics in Medicine 5(3): 208
Siebner, R.; Merlob, P.; Kaiserman, I.; Sack, J. 1992: Congenital anomalies concomitant with persistent primary congenital hypothyroidism. American Journal of Medical Genetics 44(1): 57-60
Greene, R.; Jenkins, T.; Kaufmann, M.; Wapner, R. 2001: Congenital anomalies diagnosed by ultrasound prior to 24 weeks How future risk of handicap affects parental decision. American Journal of Obstetrics and Gynecology 184(1): S139
Edison, R.; Muenke, M. 2003: Congenital anomalies following gestational statin exposure. American Journal of Human Genetics 73(5): 212
Watanabe, M.; Kohge, N.; Akagi, S.; Uchida, Y.; Sato, S.; Kinoshita, Y. 2001: Congenital anomalies in a child born from a mother with interferon-treated chronic hepatitis B. American Journal of Gastroenterology 96(5): 1668-1669
Ozmen, O. 2003: Congenital anomalies in goats. Indian Veterinary Journal 80(5): 467-469
E.Desouki, M. 1999: Congenital anomalies in infants with congenital hypothyroidism Is it a coincidental or an associated finding?. Journal of Nuclear Medicine 40(5 Suppl): 207P
Shah, L.; Choi, Y. 1999: Congenital anomalies in liveborn infants of adolescent mothers. American Journal of Obstetrics and Gynecology 180(1 Part 2): S171
Vats, K.R.; Chandra, I.; Ferrell, R.E.; Sinha, S.; Mortiz, M.L.; Ellis, D.; Surti, U.; Daood, M.; Jayakar, P.; Vats, A.N. 2003: Congenital anomalies of kidneys and urinary tract in association with chromosome 13q Delineation of a critical region. Pediatric Research 53(4 Part 2): 58A
Johnson, A.M.; Hubbard, A.M. 2004: Congenital anomalies of the fetal/neonatal chest. Seminars in Roentgenology 39(2): 197-214
Sampaolesi, R.; Sampaolesi, J.R.; Ucha, R.A. 2001: Congenital anomalies of the optic nerve head Review. International Ophthalmology 23(4-6): 263-265
Tang, Y.; Yamashita, Y.; Abe, Y.; Namimoto, T.; Tsuchigame, T.; Takahashi, M. 2001: Congenital anomalies of the pancreaticobiliary tract Findings on MR cholangiopancreatography using half-Fourier-acquisition single-shot turbo spin-echo sequence. Computerized Medical Imaging and Graphics 25(5): 423-431
Shental, J.; Katz, Z.; Yudkevitch, B.; Rozenman, J. 2000: Congenital anomalies of the upper urinary tract diagnosed in children with blunt renal trauma. European Urology 37(Suppl 2): 38
Pina Neto, J.M.; Piram, A.; Peres, L.C. 2001: Congenital anomalies on 279 necropsies of children; a prospective study at Ribeirao Preto, Brazil. European Journal of Human Genetics 9(Suppl 1): P0342
Chalam, K.V.; Gupta, S.K.; Vinjamaram, S.; Shah, V.A. 2003: Congenital anomalous retinal artery associated with a leaking macroaneurysm. Archives of Ophthalmology 121(3): 409-410
Nina, M.; Rotaru, L. 1999: Congenital anomaly in Moldova. Cytogenetics and Cell Genetics 85(1-2): 156-157
Wyatt, J.; Frias, J.; Hoyme, H.E.; Kerr, L.; Tan, M.; Ions Study Group 2003: Congenital anomaly rate in offspring of women with diabetes treated with Humalog. Diabetologia 46(Suppl 2): A 259
Corona Rivera, J.R.; Corona Rivera, A.; Bobadilla Morales, L.; Gonzalez Abarca, S.; Hernadez Rocha, J.; Garcia Cruz, D. 2003: Congenital anterior cervical hypertrichosis and mental retardation A new association?. American Journal of Human Genetics 73(5): 283
O'Donovan, M.; Byrne, P. 2000: Congenital antithrombin III deficiency in pregnancy treated with low-molecular-weight heparin. Journal of Obstetrics and Gynaecology: the Journal of the Institute of Obstetrics and Gynaecology 20(1): 85
Lamberti, J.J. 2002: Congenital aortic stenosis: is repair an option?. Advances in Cardiology 39: 70-73
Wu, S.; Buccafusca, R.; Golden, J.; Mallee, J.J.; Lucente, A.D.; Mcveigh, K.E.; Berry, G.T. 1999: Congenital apnea in newborn mice lacking the Na+/myo-Inositol cotransporter gene. American Journal of Human Genetics 65(4): A373
Wu, S.; Buccafusca, R.; Golden, J.; Mallee, J.J.; Lucente, A.D.; Mcveigh, K.E.; Berry, G.T. 2000: Congenital apnea in newborn mice with myo-inositol deficiency. Pediatric Research 47(4 Part 2): 79A
Stolina, M.L.; Polikutin, A.V.; Shapkin, V.V.; Britsin, V.D.; Burma, V.N. 1999: Congenital atrioventricular block Early detection and treatment. Rossiiskii Vestnik Perinatologii i Pediatrii 44(4): 55
Aderinboye, O.; Syed, S.S. 2010: Congenital babesiosis in a four-week-old female infant. Pediatric Infectious Disease Journal 29(2): 188
Mieusset, R.; Daudin, M.; Bieth, E.; Bujan, L.; Pontonnier, F. 2001: Congenital bilateral absence of the vas deferens Clinical and seminal parameters, and CFTR gene mutations. Journal of Andrology (Suppl): 193
Grézard, P.; Berard, F.; Balme, B.; Perrot, H. 1999: Congenital bilateral dermal melanocytosis with a dermatomal pattern. Dermatology 198(1): 105-106
Sharda, R.; Ingole, S.P. 2002: Congenital bilateral hydrocephalus in a Jersey cow calf A case report. Indian Veterinary Journal 79(9): 965-966
Valerio, R.M.F.; Dubeau, F.; Kuzniecky, R.; Garcia, J.; Richardson, J.; Andermann, F. 1999: Congenital bilateral perisylvian polymicrogyria Clinicopathological correlations in three patients. Neurology 52(6 Suppl 2): A51
Kishi, T.; Moriya, M.; Kimoto, Y.; Nishio, Y.; Tanaka, T. 1999: Congenital bilateral perisylvian syndrome and eating epilepsy. European Neurology 42(4): 241-243
Sakura, N.; Mizoguchi, N.; Ono, H.; Yamaoka, H.; Hamakawa, M. 2000: Congenital biliary atresia detected as a result of galactosemia screening by the Beutler method. Clinica Chimica Acta; International Journal of Clinical Chemistry 298(1-2): 175-179
Zia-Ul-Miraj, M. 1999: Congenital bladder diverticulum: a rare cause of bladder outlet obstruction in children. Journal of Urology 162(6): 2112-2113
Hall, E.C.; Semmlow, J.L.; Priyadarshini, K.; Gordon, J.; Hainline, L.; Abramov, I.; Wyatt, H.J. 2000: Congenital blindness affects human ocular motor neural activity. IOVS Investigative Ophthalmology and Visual Science 41(4): S883
Sieff, C.A.; Nisbet-Brown, E.; Nathan, D.G. 2000: Congenital bone marrow failure syndromes. British Journal of Haematology 111(1): 30-42
Slayton, W.B.; Schibler, K.R. 2000: Congenital bone marrow failure syndromes associated with protean developmental defects and leukemia. Clinics in Perinatology 27(3): 543-558
Tiraboschi, I.C.N.; Niveyro, C.; Mandarano, A.M.; Messer, S.A.; Bogdanowicz, E.; Kurlat, I.; Lasala, M.ía.B. 2010: Congenital candidiasis: confirmation of mother-neonate transmission using molecular analysis techniques. Medical Mycology 48(1): 177-181
Moon, A.M.; Capecchi, M.R. 2001: Congenital cardiac defects in Fibroblast Growth Factor 8 hypomorphic mice. Journal of Investigative Medicine 49(1): 7A
Hall, T.L.; Magdesian, K.G.; Kittleson, M.D. 2010: Congenital cardiac defects in neonatal foals: 18 cases (1992-2007). Journal of Veterinary Internal Medicine 24(1): 206-212
Bembea, D.; Spineanu, L.; Bembea, M.; Vancsik, O.; Jurca, C.; Spineanu, R. 2001: Congenital cataract Autosomal recessive form In an ethnic isolate, intensely inbred. European Journal of Human Genetics 9(Suppl 1): P0904
Tornqvist, K. 2002: Congenital cataract -- results of treatment. Acta Ophthalmologica Scandinavica 80(6): 569
Lewis, T.L. 2001: Congenital cataract Seeing beyond acuity. IOVS Investigative Ophthalmology and Visual Science 42(4): S312
Knopf, C.; Mezer, E.; Idin, A.; Jakobs, C.; Mandel, H. 2003: Congenital cataract associated with D-glyceric aciduria. Journal of Inherited Metabolic Disease 26(Suppl 2): 50
Magnusson, G.; Abrahamsson, M.; Sjostrand, J. 2000: Congenital cataracts in western Sweden A 14-year longitudinal follow-up of visual acuity. IOVS Investigative Ophthalmology and Visual Science 41(4): S480
Kanter, K.R.; Berg, A.M.; Vincent, R.N.; Mahle, W.T.; Forbess, J.M.; Kirshbom, P.M. 2004: Congenital category is not a risk factor for pediatric heart transplantation. Journal of Heart and Lung Transplantation 23(2S): S59
Vaughan, J.L.; Lonsdale, R.A.; Jackson, G.; Ryan, D.P. 2000: Congenital caudal vertebral malformations in the alpaca (Lama pacos). Australian Veterinary Journal 78(6): 412-415
Heinrichs, C.; Parma, J.; Scherberg, N.H.; Delange, F.; Duprez, L.; Bergmann, P.; Vassart, G.; Refetoff, S. 1999: Congenital central hypothyroidism caused by abnormal TSH due to a homozygous mutation in the TSH-beta subunit gene. Hormone Research 51(Suppl 2): 106
Okuhara, K.; Tajima, T.; Shinohara, N.; Fukushi, M.; Mikami, A.; Fujita, K.; Murashita, M.; Nakae, J.; Fujieda, K. 2000: Congenital central hypothyroidism detected by neonatal mass screening in Sapporo City of Japan. Endocrine Journal 47(Suppl August): 254
Gaultier, C.; Trang Pham, H.; Dauger, S.; Simonneau, M.; Gallego, J. 1999: Congenital central hypoventilation syndrome A window on the genes involved in respiratory control. M-S (Medecine Sciences) 15(6-7): 851-856
Shabib, S.M.; Omran, S.; Al Abbad, A.; El Bushra, H.; Al Mehaidib, A.; Al Sabban, E.; Nazer, H. 2000: Congenital chloride diarrhea A single centre experience with 43 children. JPGN 31(Suppl 2): S125
Yang, H.; Yang, W.; He, T. 1999: Congenital choledochal cyst The experience of re-operation. Hepatology 30(4 Part 2): 562A
Shaoul, R.; Papsin, B.; Cutz, E.; Durie, P. 1999: Congenital cholesteatoma in a child carrying a gene mutation for adenomatous polyposis coli. Journal of Pediatric Gastroenterology and Nutrition 28(1): 100-103
Chia, S.; Litman, D.; Handler, S. 1999: Congenital cholesteatoma presenting as facial nerve paralysis. Pediatrics 104(3 Part 3): 730-731
Boccardo, F.; Bellini, C.; Arioni, C.; Baldi, M.; Sacchi, R.; Ciotti, S.; Bonioli, E.; Campisi, C.; Serra, G. 2003: Congenital chylothorax in newborns. American Journal of Human Genetics 73(5): 330
Urakami, S.; Igawa, M.; Shiina, H.; Shigeno, K.; Yoneda, T.; Yagi, H. 1999: Congenital collateral urethral duplication in the frontal plane. Journal of Urology 162(6): 2097-2098
Yamade, S. 1999: Congenital color anomalies-What we can do for them. Rinsho Ganka 53(1): 9-12
Anic, B.; Dasovic Buljevic, A. 2001: Congenital complete AV block in children of SSA/SSB negative mothers with SLE. Lupus 10(Suppl 1): S28
Prasad, V.; Fishman, S.; Powell, J.; Pearse, J.; Mulliken, J.; Fox, V.; Liang, M.; Burrows, P.; Perez Atayde, A.R.; Kozakewich, H. 2003: Congenital cutaneo-visceral angiomatosis with thrombocytopenia. Modern Pathology 16(1): 6P
Trevett, T., J.; Kelly, T.; Budorick, N.; Pretorius, D.; Scioscia, A.; Hull, A. 2001: Congenital cystic adenomatoid malformation An outcome study. American Journal of Obstetrics and Gynecology 185(6 Suppl): S235
Oepkes, D.; Windrim, R.; Seaward, P.G.R.; Barrett, J.F.R.; Davies, G.A.L.; Hornberger, L.; Flake, A.W.; Kelly, E.N.; Ryan, G. 2000: Congenital cystic adenomatoid malformation of the lung with fetal hydrops A spectrum of in-utero management. American Journal of Obstetrics and Gynecology 182(1 Part 2): S173
Hayashi, N.; Repka, M.X.; Ueno, H.; Iliff, N.T.; Green, W.R. 1999: Congenital cystic eye: report of two cases and review of the literature. Survey of Ophthalmology 44(2): 173-179
Yamamoto, A.Y.; Mussi Pinhata, M.M.; Pinto, P.C.G.; Jorge, S.M.; Figueiredo, L.T.M. 2000: Congenital cytomegalovirus infection among preterm infants. Pediatric Research 47(4 Part 2): 349A
Demmler, G.J. 2003: Congenital cytomegalovirus infection treatment. Pediatric Infectious Disease Journal 22(11): 1005-1006
Go, Cindy; De Jong, Andrew L.; Paysse, Evelyn; Coats, David; Friedman, Ellen M.; Sulek, Marcelle; Bernstein, Joseph 1999: Congenital dacryocele with intranasal cyst. Pediatrics 104(3 Part 3): 728
Strain, G.M. 1999: Congenital deafness and its recognition. Veterinary Clinics of North America. Small Animal Practice 29(4): 895-907 Vi
Rosenzweig, S.D.; Holland, S.M. 2004: Congenital defects in the interferon-gamma/interleukin-12 pathway. Current Opinion in Pediatrics 16(1): 3-8
Voropaev, E.V.; Matveev, V.A.; Chernovitsky, M.A.; Zavoronok, S.V. 1999: Congenital defects of development, herpesviral infection and rubella. Rossiiskii Vestnik Perinatologii i Pediatrii 44(3): 55
Burlina, A.B.; Bonafe, L.; Van Schaftingen, E.; Jaeken, J. 2000: Congenital defects of glycosylation with retardation-dysmorphy syndrome and myopathic changes. Journal of Inherited Metabolic Disease 23(Suppl 1): 180
Pischalnikov, A.Yu 2000: Congenital defects of humoral immunity according to regional register of primary immunodeficiencies. Immunologiya 4: 58-60
Titov, V.N. 2003: Congenital defects of post-heparin lipoprotein lipase Diagnosis of familial combined hyperlipoproteinemia. Klinicheskaya Laboratornaya Diagnostika 6: 10-17
Ehrenforth, S.; Scharrer, I.; Kreuz, W. 1999: Congenital deficiency of vitamin K dependent hemostatic factors along with decreased FXI and FXII. Annals of Hematology 78(Suppl 1): A41
Puetz, J.; Knutsen, A.; Bouhasin, J. 2004: Congenital deficiency of vitamin K-dependent coagulation factors associated with central nervous system anomalies. Thrombosis and Haemostasis 91(4): 819-821
Hatzidaki, E.G.; Relakis, K.J.; Giannakopoulos, K.C.; Papanikolaou, N.C.; Kokori, H.G.; Giannakopoulou, C.C. 1999: Congenital depression of the skull. Report of two cases. Clinical and Experimental Obstetrics and Gynecology 26(1): 10-11
Breen, C.M.; Butnor, K.J.; Mcdonald, M.T.; Bradford, W.D. 2001: Congenital diaphragmatic defects An autopsy case series. Laboratory Investigation 81(1): 5A
Sydorak, R.M.; Harrison, M.R. 2003: Congenital diaphragmatic hernia: advances in prenatal therapy. Clinics in Perinatology 30(3): 465-479
Dott, M.M.; Rasmussen, S.A.; Wong, L.Y. 2002: Congenital diaphragmatic hernia Associated anomalies and mortality Metropolitan Atlanta, 1968-1999. Teratology 65(6): 310
Dott, M.M.; Wong, L.Y.; Rasmussen, S.A. 2002: Congenital diaphragmatic hernia Associated defects and syndromes and their impact on mortality. American Journal of Human Genetics 71(4 Suppl): 197
Gonda, P.; Szabo, M.; Illyes, G.; Kovacs, M. 2001: Congenital diaphragmatic hernia and associated malformations. Virchows Archiv 439(3): 426
Van Dooren, M.F.; Torfs, C.P.; Brooks, A.; Tibboel, D. 1999: Congenital diaphragmatic hernia and limb defects in a Dutch tertiary hospital and in a California registry. Teratology 59(6): 397
Bedoyan, J.K.; Blackwell, S.C.; Treadwell, M.C.; Johnson, A.; Klein, M.D. 2003: Congenital diaphragmatic hernia at two Detroit hospitals Which factors impact the outcome of infants with CDH?. Pediatric Research 53(4 Part 2): 468A
Cusmano, K.P.; Kousseff, B.G. 1999: Congenital diaphragmatic hernia in genetics. American Journal of Human Genetics 65(4): A146
Chapin, C.J.; Yoshizawa, J.; Sbragia, L.; Albanese, C.T.; Kitterman, J.A. 2001: Congenital diaphragmatic hernia reduces and tracheal occlusion increases lung growth and type I cell marker, RTI40, without affecting type II cell function in fetal rats. Pediatric Research 49(4 Part 2): 31A
Dilber, E.; Gocmen, A.; Kiper, N.; Ozcelik, U.; Dogru, D.; Buyukpamukcu, N.; Tanyel, F.C.hit 2003: Congenital diaphragmatic hernia; clinical presentation and long term pulmonary function. Cocuk Sagligi ve Hastaliklari Dergisi 46(3): 177-181
Cerda-Gonzalez, S.; Dewey, C.W. 2010: Congenital diseases of the craniocervical junction in the dog. Veterinary Clinics of North America. Small Animal Practice 40(1): 121-141
Girona Comas, Josep 2001: Congenital diseases of the heart Clinical-physiological considerations. Rudolph, Abraham M. Congenital Diseases Of The Heart: Clinical-Physiological Considerations. I-Viii, 1-808
Singh, S.; Garg, M. 2002: Congenital dislocation of radial head. Journal of Bone and Mineral Research 17(Suppl 1): S294
Cser, B.; Morava, E.; Karteszi, J.; Huyben, K.; Szonyi, L.; Wevers, R.; Kosztolanyi, G. 2002: Congenital disorder of glycosilation type Ia in a patient with Jouber syndrome and arachnodactyly. European Journal of Human Genetics 10(Suppl 1): 204-205
Dupre, T.; Cuer, M.; Barrot, S.; Barnier, A.; Cormier-Daire, V.; Munnich, A.; Durand, G.; Seta, N. 2001: Congenital disorder of glycosylation Ia with deficient phosphomannomutase activity but normal plasma glycoprotein pattern. Clinical Chemistry 47(1): 132-134
Barone, R.; Pavone, V.; Pennisi, P.; Fiore, C.E.; Fiumara, A. 2000: Congenital disorder of glycosylation due to phosphomannomutase deficiency Skeletal status assessment by bone densitometry, ultrasonography and biochemical markers of bone turnover. Journal of Inherited Metabolic Disease 23(Suppl 1): 181
Enns, G.M.; Gallagher, R.; Conrad, S.; O'brien, J.F.; Freeze, H.H. 2003: Congenital disorder of glycosylation type Ib The second North American patient. American Journal of Human Genetics 73(5): 457
Garcia Silva, M.T.; Briones, P.; Schollen, E.; Cabrera, J.L.; Sanchez Del Pozo, J.; Marti Herreros, M.; Simon, R.; Maties, M.; Hennet, T.; Matthijs, G. 2002: Congenital disorder of glycosylation type Ie A new patient. Journal of Inherited Metabolic Disease 25(Suppl 1): 133
Goker Alpan, O.; Lavine, J.; Krasnewich, D. 2000: Congenital disorders of glycosylation A group of metabolic disorders presenting with gastrointestinal and hepatic involvement. JPGN 31(Suppl 2): S58
Schenk, B.; Imbach, T.; Frank, C.; Grubenmann, C.; Helenius, J.; Jaeken, J.; Matthijs, G.; Hennet, T.; Aebi, M. 2001: Congenital disorders of glycosylation Deficiencies in the ER pathway. Glycobiology 11(10): 863
Freeze, H. 2001: Congenital disorders of glycosylation More disorders, more patients, more puzzles. Glycobiology 11(10): 871-872
Jaeken, J.; Carchon, H. 2001: Congenital disorders of glycosylation: the rapidly growing tip of the iceberg. Current Opinion in Neurology 14(6): 811-815
Jaeken, J.; Carchon, H. 2004: Congenital disorders of glycosylation: a booming chapter of pediatrics. Current Opinion in Pediatrics 16(4): 434-439
Freeze, H.H.; Westphal, V.; Winchester, B.; Murch, S. 2000: Congenital disorders of glycosylation cause protein-losing enteropathy and loss of enterocyte heparan sulfate proteoglycans. JPGN 31(Suppl 2): S155
Briones, P.; Vilaseca, M.A.; Schollen, E.; Maties, M.; Ferrer, I.; Gomez, O.; Dalfo, E.; Colome, C.; Artuch, R.; Chabas, A.; Marco, M.; Van Schaftingen, E.; Matthijs, G.; Jaeken, J. 2001: Congenital disorders of glycosylation in 31 Spanish patients. Journal of Inherited Metabolic Disease 24(Suppl 1): 110
Briones, P.; Vilaseca, M.A.; Garcia Silva, M.T.; Pineda, M.; Colomer, J.; Ferrer, I.; Artigas, J.; Matthijs, G.; Jaeken, J.; Chabas, A. 2000: Congenital disorders of glycosylation may be underdiagnosed when mimicking mitochondrial disease. Journal of Inherited Metabolic Disease 23(Suppl 1): 180
Pascual-Castroviejo, I. 2002: Congenital disorders of glycosylation syndromes. Developmental Medicine and Child Neurology 44(5): 357-358
Quelhas, D.; Vilarinho, L.; Teles, E.L.; Rodrigues, E.; Diogo, L.; Garcia, P.; Jaeken, J. 2001: Congenital disorders of glycosylation type-x with type 2 pattern of transferrin isoelectric focusing. Journal of Inherited Metabolic Disease 24(Suppl 1): 112
Inoue, K.; Tsuda, M.; Shigemoto Mogami, Y.; Koizumi, S. 2002: Congenital down-regulation of sensory P2X3 in A/J inbred mouse strain. Japanese Journal of Pharmacology 88(Suppl 1): 84P
Mouriaux, F.éd.ér.; Leroy-Rattier, M.-P.; Maurage, C.-A.; Guilbert, F.ço.; Cree, I.; Rouland, J.F.ço. 2002: Congenital duplication of the anterior segment with central hamartomatous plaque. Archives of Ophthalmology 120(10): 1377-1379
McLeod, R.S.; Cohen, Z. 2001: Congenital duplication of the rectum: endoscopic and radiologic appearance of an unusual condition. Surgery 130(5): 895-896
Denecke, J.; Kranz, C.; Conradt, H.; Heimpel, H.; Feldmann, R.; Marquardt, T. 2001: Congenital dyserythropoetic anemia type II , new biochemical insights in a disorder of glycosylation. Journal of Inherited Metabolic Disease 24(Suppl 1): 111
Cattan, D.; Pariente, E.A.; Borot, N.; Tulliez, M. 1999: Congenital dyserythropoiesis without anemia can mimic hereditary hemochromatosis. Gastroenterology 116(4 Part 2): A50
Koduri, P.R.; Gowrishankar, S. 2002: Congenital dyserythropoietic anemia type Ii with a positive sucrose hemolysis test. American Journal of Hematology 71(1): 64-66
Iolascon, A. 2000: Congenital dyserythropoietic anemias: a still unsolved puzzle. Haematologica 85(7): 673-674
Brigitte, B.M.; Guy, L.; Olivier, S.; Gil, T.; Andre, B.; Claire, B.; Francoise, B.; Christian, B.; Yves, B.; Jean Pierre, L.; Thierry, L.; Emmanuel, P.; Laurent, R.; Herve, R.; Christine, S.; Isabelle, T.; Marianne, B.; Jean, D. 2003: Congenital dyserythropoietic anemias in children Report on patients from a French multicentre Study. Blood 102(11): 14b
Ohno, K.; Brengman, J.M.; Nakano, S.; Walsh, P.; Heidenreich, F.; Vincent, A.; Nagwaney, S.; Engel, A.G. 1999: Congenital endplate acetylcholinesterase deficiency caused by nonsense, splice-site, and missense mutations in the collagenic tail subunit of asymmetric AChE. Neurology 52(6 Suppl 2): A184
Kasthuri, S.; Mathievathaniy, M.; Jayawardane, D. 2001: Congenital epulis in a neonate. Ceylon Medical Journal 46(3): 104-105
Chang, S.E.; Choi, J.H.; Koh, J.K. 1999: Congenital erythrodermic psoriasis. British Journal of Dermatology 140(3): 538-539
Depetris Boldini, C.; Civallero, G.; Videla, M.P.; Antonozzi, S.; De Kremer Dodelson, R. 2000: Congenital erythropoeitic porphyria Decreased essential fatty acids in erythrocytes. Journal of Inherited Metabolic Disease 23(Suppl 1): 279
Rogounovitch, T.; Takamura, N.; Hombrados, I.; Morel, C.; Tanaka, T.; Kameyoshi, Y.; Shimizu-Yoshida, Y.; de Verneuil, H.; Yamashita, S. 2000: Congenital erythropoietic porphyria: a novel homozygous mutation in a Japanese patient. Journal of Investigative Dermatology 115(6): 1156
Desnick, R.J.; Astrin, K.H. 2002: Congenital erythropoietic porphyria: advances in pathogenesis and treatment. British Journal of Haematology 117(4): 779-795
Cunha, L.; Shady, A.; Astrin, K.; Colby, B.; Desnick, R. 2001: Congenital erythropoietic porphyria Characterization of novel mutations in uroporphyrinogen III synthase. Journal of Inherited Metabolic Disease 24(Suppl 1): 146
Solis, C.; Aizencang, G.I.; Cunha, L.; Bishop, D.F.; Astrin, K.H.; Desnick, R.J. 2000: Congenital erythropoietic porphyria Identification and characterization of housekeeping and erythroid-specific promoters in the uroporphyrinogen III synthase gene and erythroid promoter mutations causing this porphyria. Pediatric Research 47(4 Part 2): 245A
Shady, A.A.; Colby, B.; Astrin, K.H.; Desnick, R.J. 2001: Congenital erythropoietic porphyria Identification, characterization and genotype/phenotype correlations of novel gene mutations. American Journal of Human Genetics 69(4 Suppl): 492
Lehrer, J.K.; Katz, P.O. 2003: Congenital esophageal stenosis may present in adulthood. American Journal of Gastroenterology 98(9 Suppl): S129
Korge, B.P.; Berg, D.; Casper, C.; Hausser, I. 2000: Congenital exfoliative dermatitis, thrichorrhexis invaginata, and recurrent septicemia A case of Netherton-Syndrome?. Journal of Investigative Dermatology 115(5): 926
Othman, A.A.; Shoheib, Z.S.; Saied, E.M.; Soliman, R.H. 2010: Congenital exposure to Schistosoma mansoni infection: impact on the future immune response and the disease outcome. Immunobiology 215(2): 101-112
Pellerin, J.; Carioto, L.; Plante, J. 2002: Congenital extrahepatic portosystemic shunts in the dog. Medecin Veterinaire du Quebec 32(1): 28-29
Shivaram, S.M.; Engle, E.C.; Petersen, R.A.; Robb, R.M. 2001: Congenital fibrosis syndromes. International Ophthalmology Clinics 41(4): 105-113
Max,A. 2010: Congenital fissure of the abdominal wall in puppies. Medycyna Weterynaryjna 66(2): 131-133
Maruyama, K.; Suzuki, T.; Koizumi, T.; Sugie, H.; Fukuda, T.; Ito, M.; Hirato, J. 2004: Congenital form of glycogen storage disease type IV: a case report and a review of the literature. Pediatrics International: Official Journal of the Japan Pediatric Society 46(4): 474-477
Bates, A.W.; Feakins, R.M.; Scheimberg, I. 1999: Congenital gastro-intestinal stromal tumour A comparison with similar tumours in adult subjects. Journal of Pathology 187(Suppl): 19A
Bottani, A.; Desmangles, V.; Egger, J.F.; Brundler, M.A.; Calza, A.M.; Pfister, R. 2001: Congenital generalized fibromatosis associated with birth defects; a third patient. European Journal of Human Genetics 9(Suppl 1): P0478
Van Maldergem, L.; Magre, J.; Khallouf, E.; Gedde Dahl, T.Jr.; The Berardinelli Seip Study Group 2001: Congenital generalized lipodystrophy of Berardinelli-Seip A study of 47 patients belonging to 9q34 and non-9q34 subgroups. American Journal of Human Genetics 69(4 Suppl): 301
Crow, Y.; Massey, R.F.; Pairaudeau, P.W.; Innes, J.R.; Nischall, K.; Winter, R. 2003: Congenital glaucoma as a feature of Aicardi-Goutieres syndrome. Journal of Medical Genetics 40(Suppl 1): S38
Wickramasinghe, P.; Lamabadusuriya, S.P.; Lalani, H.A. 2001: Congenital glucose galactose malabsorption. Ceylon Medical Journal 46(1): 26-27
Watson, P.J.; Scholes, S.F.E. 2010: Congenital goitre and alopecia in pedigree Saler cattle. Veterinary Record 166(1): 29-30
Clayton, P.E.; Freeth, J.S.; Norman, M.R. 1999: Congenital growth hormone insensitivity syndromes and their relevance to idiopathic short stature. Clinical Endocrinology 50(3): 275-283
Sebire, N.J.; Malone, M.; Risdon, R.A.; Ramsay, A. 2003: Congenital hairy polyp of the nasopharynx A series of seven cases from a paediatric histopathology department. Journal of Pathology 201(Suppl): 41A
Buyon, J.P.; Rupel, A.; Clancy, R.M. 2003: Congenital heart block: do fetal factors fuel the fire from inflammation to fibrosis?. Lupus 12(10): 731-734
Ayed, K.; Gorgi, Y.; Sfar, I.; Khrouf, M. 2004: Congenital heart block associated with maternal anti SSA/SSB antibodies :a report of four cases. Pathologie-Biologie 52(3): 138-147
Bulun, A.; Ozkutlu, S.; Caglar, M. 2004: Congenital heart block in the newborn associated with maternal antibodies in connective tissue disorders. Cocuk Sagligi ve Hastaliklari Dergisi 47(2): 152-157
Li, F.X.; Fick, G.H.; Love, E.J. 1999: Congenital heart defects among offspring of firemen. Teratology 59(6): 397
Marino, B.; Digilio, M.C.; Toscano, A.; Giannotti, A.; Dallapiccola, B. 1999: Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11. Genetic Counseling 10(1): 25-33
Marelli, A.J.; Rhame, E.; Pilote, L. 2003: Congenital heart disease Prevalence rates in a population of 5,363,695 adults. Journal of the American College of Cardiology 41(6 Suppl A): 490A
Horstkotte, D.; Fassbender, D.; Piper, C. 2003: Congenital heart disease and acquired valvular lesions in pregnancy. Herz 28(3): 227-239
Wray, J.C.; Sensky, T.; Banner, N.R. 1999: Congenital heart disease and cardiac surgery Impact on cognitive function and academic ability. Circulation 100(18): 1; 735
Gnanalingham, M.G.; Gnanalingham, K.K.; Singh, A. 1999: Congenital heart disease and parental consanguinity in South India. Acta Paediatrica 88(4): 473-474
Bialer, M.G.; Ritz, S.B.; Olson, M.E. 1999: Congenital heart disease in Goldberg-Shprintzen syndrome. American Journal of Human Genetics 65(4): A142
Hunter, S. 2000: Congenital heart disease in adolescence. Journal of the Royal College of Physicians of London 34(2): 150-152
Murakami,T.; Yasuda,M.; Hagio,M.; Moritomo,Y. 2010: Congenital heart disease in adult cattle. Bulletin of the Faculty of Agriculture, Miyazaki University 57: 137-144
Brickner, M.E.; Hillis, L.D.; Lange, R.A. 2000: Congenital heart disease in adults. First of two parts. New England Journal of Medicine 342(4): 256-263
Meijboom, E.; Lisowski, L.A.; Verheijen, P.M.; Kleinman, C.S.; Copel, J. 2001: Congenital heart disease in diabetic pregnancies. European Heart Journal 22(Abstract Suppl): 425
Levy, H.L.; Guldberg, P.; Güttler, F.; Hanley, W.B.; Matalon, R.; Rouse, B.M.; Trefz, F.; Azen, C.; Allred, E.N.; de la Cruz, F.; Koch, R. 2001: Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study. Pediatric Research 49(5): 636-642
Barlow, G.M.; Chen, X.N.; Calabrese, G.; Palka, G.; Caldwell, P.; Booth, C.; Linck, L.; Korenberg, J.R. 1999: Congenital heart disease in monosomy 21 Definition of two distinct loci. American Journal of Human Genetics 65(4): A67
Korenberg, J.R. 2000: Congenital heart disease proteins and products related thereto. Official Gazette of the United States Patent and Trademark Office Patents 1232(3)
Pyles, L.A.; Einzig, S.; Neal, W.A.; Moller, J.H. 1999: Congenital heart disease regional variability from a multicenter consortium. Circulation 100(18): 1; 736
Wilson, D.; Cox, H.; Fiegler, H.; Wilkinson, K.; Fowler, D.; Moore, K.; Carter, N.P.; Wellesley, D.; Barber, J. 2003: Congenital heart disease, deafness and duplications of 3q; refining a new critical region. Journal of Medical Genetics 40(Suppl 1): S60
Sperling, S.; Seelow, D.; Mebus, S.; Lange, P.E.; Lehrach, H. 2001: Congenital heart diseases; gene expression database. European Journal of Human Genetics 9(Suppl 1): P1126
Lin, L.; Lavery, C.E.; Kooken, A.R.; Mccarron, K.F.; Tuthill, R.J.; Goldblum, J.R.; Bergfeld, W.F.; Kahn, T. 2001: Congenital hemangiomas with hobnail features and diffuse involvement of the gastrointestinal tract. Journal of Cutaneous Pathology 28(10): 574
Caldarelli, M.; Tamburrini, G.; Di Rocco, C. 2002: Congenital hemiparesis and seizures secondary to perinatal occlusion of the middle cerebral artery. Pediatric Neurosurgery 37(4): 220
Eyre, J.A.; Smith, M.; Villagra, F.; Dabydeen, L.; Cowan, F.; Rutherford, M.; Mercuri, E. 2004: Congenital hemiplegia A potentially treatable disorder?. Journal of Neurology Neurosurgery and Psychiatry 75(5): 801
D'Agostino, D.; Orsi, M. 1999: Congenital hepatic arterioportal fistula. Journal of Pediatric Gastroenterology and Nutrition 29(4): 487
Murray, K.L.; Gilmour, H.M. 2000: Congenital hepatic fibrosis and malignancy A case report and review of the literature. Journal of Pathology 192(Suppl): 18A
Wichrzycka Lancaster, E.; Targonski, J.A.; Gaire, K.M.; Targonska, I.B.J. 2003: Congenital hepatic fibrosis with liver failure in an infant. Virchows Archiv 443(3): 246-247
Ammann, R.A.; Plaschkes, J.; Leibundgut, K. 1999: Congenital hepatoblastoma: a distinct entity?. Medical and Pediatric Oncology 32(6): 466-468
Gilbert, S.F.; Zevit, Z. 2001: Congenital human baculum deficiency: the generative bone of Genesis 2:21-23. American Journal of Medical Genetics 101(3): 284-285
Aolad, H.M.; Inouye, M.; Hayasaka, S.; Darmanto, W.; Murata, Y. 2000: Congenital hydrocephalus following exposure to X-radiation at early gestational stage in mice. Teratology 62(3): 16A-17A
Basel Vanagaite, L.; Klinger, G.; Shohat, M.; Udler, Y.; Levit, O.; Linder, N.; Sirota, L. 2001: Congenital hydrocephalus, ambiguous genitalia in males and early lethality A new syndrome?. American Journal of Human Genetics 69(4 Suppl): 278
Seseke, F.; Thelen, P.; Hemmerlein, B.; Kliese, D.; Zoeller, G.; Ringert, R.H.rmann 2000: Congenital hydronephrosis in rats A representative model of congenital renal obstruction?. European Urology 37(Suppl 2): 17
Fournet, J.C.; Gross Morand, M.S.; De Lonlay, P.; Robert, J.J.; Brunelle, F.; Rahier, J.; Fekete, C.; Saudubray, J.M.; Junien, C. 2002: Congenital hyperinsulinism Clinicopathological correlations with molecular data. Modern Pathology 15(1): 3P
Suchi, M.; Thornton, P.S.; Adzick, N.S.; Macmullen, C.; Ganguly, A.; Stanley, C.A.; Ruchelli, E.D. 2003: Congenital hyperinsulinism Intraoperative biopsy interpretation can direct the extent of pancreatectomy. Modern Pathology 16(1): 110A
Magge, S.; Macmullen, C.; Shyng, S.L.; Katz, L.; Ganguly, A.; Digeorge, A.; Stanley, C. 2003: Congenital hyperinsulinism due to a dominant SUR1 mutation in familial Leucine-sensitive hypoglycemia of infancy. Diabetes 52(Suppl 1): A337
Tiker, F.; Gurakan, B.; Tarcan, A.; Ozon, A. 2002: Congenital hyperinsulinism treated with long-acting somatostatin analogue octreotide A case report. Cocuk Sagligi ve Hastaliklari Dergisi 45(3): 242-245
Garcia Cazorla, A.; Delonlay, P.; Nassogne, M.C.; Touati, G.; Saudubray, J.M. 2000: Congenital hyperlactacidaemias Clinical presentation and diagnostic procedure of 273 cases. Journal of Inherited Metabolic Disease 23(Suppl 1): 138
Koch, K.; Peter, M.; Viemann, M.; Sippell, W. 1999: Congenital hypoaldosteronism Report on 10 new mutations of the CYP11B2 gene in 13 patients. Hormone Research 51(Suppl 2): 80
Crowley, W.F.; Pitteloud, N. 2004: Congenital hypogonadotropic hypogonadism Clinical features and pathophysiology. Winters, Stephen J , Reprint Author Male hypogonadism: Basic, clinical and therapeutic principles: 81-100
Zehnder Schlapbach, S.A.; Printzen, G.; von Vigier, R.O.; Bianchetti, M.G. 2000: Congenital hypohaptoglobinemia in childhood hemolytic uremic syndrome?. Nephron 85(3): 285-286
Pouget, J.Y.; Levy, N.; Bernard, R.; Pellissier, J.F.ancois 2002: Congenital hypomyelination neuropathy related to a new MPZ mutation and with long-term outcome. Neurology 58(7 Suppl 3): A376
Reif, C.; Ullrich, K.P.; Franke Beckmann, E.; Kuehn, T.; Von Bueren, E.; Gerlach, K. 1999: Congenital hypothyroidism - 58 outcomes. Hormone Research 51(Suppl 2): 133
Tassi, V.; Calaciura, F.; Miscio, G.; Majorana, A.; Parrinello, G.; Ranieri, A.; Regalbuto, C.; Sava, L.; Trischitta, V. 2000: Congenital hypothyroidism A population based study. American Journal of Human Genetics 67(4 Suppl 2): 347
Polak, M. 2003: Congenital hypothyroidism. Molecular defects in familial disease. Annales d'Endocrinologie 64(1): 54-57
Weber, G.; Vigone, M.C.; Rovelli, R.; Boldrighini, B.; Corbetta, C.; Chiumello, G. 1999: Congenital hypothyroidism Revision of the etiology. Hormone Research 51(Suppl 2): 107
Marziani, E.; Marziani, G. 2000: Congenital hypothyroidism Role of ultrasonography and serum thyroglobulin for detection of etiologic cause and therapys monitoring. Hormone Research 53(Suppl 2): 172
Sertedaki, A.; Papadimitriou, A.; Voutetakis, A.; Dracopoulou, M.; Dacou Voutetakis, C. 2000: Congenital hypothyroidism caused by a new genetic defect of the thyrotropin beta subunit gene associated with different hormonal derangement in the same sibship. Hormone Research 53(Suppl 2): 11
MacNabb, C.; O'Hare, E.; Cleary, J.; Georgopoulos, A.P. 1999: Congenital hypothyroidism impairs response alternation discrimination behavior. Brain Research 847(2): 231-239
Persani, L.; Bonomi, M.; Proverbio, M.C.; Weber, G.; Alberti, L. 2000: Congenital hypothyroidism with normal TSH serum levels in a female carrying a novel homozygous mutation in TSHbeta gene. Endocrine Journal 47(Suppl August): 177
Yoon, J.H.; Kim, J.; Park, C. 2002: Congenital immature teratoma of the tongue: an autopsy case. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontics 94(6): 741-745
Boudjemaa, S.; Josset, P.; Boccon Gibod, L. 2000: Congenital infantile fibrosarcoma Report of four cases. Pathology International 50(Suppl): A193
Abdel Salam, G.; Timar, L.; Halasz, A.A.; Czeizel, A.E. 1999: Congenital infection-like syndrome Different clinical and genetic features. European Journal of Human Genetics 7(Suppl 1): 48
Nagasako, E.M.; Oaklander, A.Louise.; Dworkin, R.H. 2003: Congenital insensitivity to pain: an update. Pain 101(3): 213-219
Misery, L.; Hermier, M.; Staniek, V.; Kanitakis, J.; Gaudillere, A.; Lachaux, A.; Schmitt, D.; Claudy, A. 1999: Congenital insensitivity to pain with anhidrosis: absence of substance P receptors in the skin. British Journal of Dermatology 140(1): 190-191
Toscano, E.; Andria, G. 2001: Congenital insensitivity to pain with anhidrosis: an NGF/TrkA-related disorder. American Journal of Medical Genetics 99(2): 164-165
Mardy, S.; Miura, Y.; Endo, F.; Matsuda, I.; Indo, Y. 2001: Congenital insensitivity to pain with anhidrosis Effect of TRKA missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor. Human Molecular Genetics 10(3): 179-188, 1 February
Jordan, J.A.; Lewis, M.; Rollins, N.; Roland, P.S. 2000: Congenital internal carotid artery aneurysm with absence of the petrous portion of the contralateral internal carotid artery. Annals of Otology Rhinology and Laryngology 109(12 Part 1): 1167-1169
Stormon, M.O.; Mitchell, J.D.; Smoleniec, J.S.; Tobias, V.; Day, A.S. 2002: Congenital intestinal lymphatic hypoplasia presenting as non-immune hydrops in utero, and subsequent neonatal protein-losing enteropathy. Journal of Pediatric Gastroenterology and Nutrition 35(5): 691-694
Mezzano, P.; Bellini, C.; Massocco, D.; Zullino, E.; Campone, F.; Mazzella, M.; Bonacci, W.; Serra, G. 1999: Congenital intracranial lipoma. American Journal of Human Genetics 65(4): A335
Im, S-Hyang.; Wang, K-Chang.; Kim, S-Ki.; Lee, Y-Ho.; Chi, J.G.; Cho, B-Kyu. 2003: Congenital intracranial teratoma: prenatal diagnosis and postnatal successful resection. Medical and Pediatric Oncology 40(1): 57-61
Chan, C.-C.; Datiles, M.; Kaiser-Kupfer, M.I.; Kupfer, C. 2003: Congenital iridocorneal malformation in Rieger syndrome. Archives of Ophthalmology 121(4): 582-583
Dubin, A.M.; Van Hare, G.F.; Druzin, M.; Sandborg, C.; Shirai, L.K.; Bernstein, D.; Rosenthal, D.N. 2000: Congenital junctional ectopic tachycardia A proposed etiology. Circulation 102(18): 2; 698
Nishizawa, S.; Peters, J.; Cuckow, P.M.; Winyard, P.J. 2000: Congenital kidney and bladder malformations in the T 30H mouse. Journal of the American Society of Nephrology 11(Program and Abstract Issue): 380A
Zimbler, S.; Hresko, T.; Karlin, L. 1999: Congenital kyphosis in myelodysplasia Long term review. Pediatrics 104(3 Part 3): 724
Larsen Haidle, J.; Keppler Noreuil, K.; Kanis, A.B.; Muilenburg, A.; Welch, J.; Qian, Q.; Yang, L.; Patil, S. 2001: Congenital laryngotracheal webs and early onset colorectal carcinoma in a family with three-generation transmission of del. American Journal of Human Genetics 69(4 Suppl): 290
Miller, M.T.; Stromland, K. 2000: Congenital lateral rectus deficits and associated malformations and syndromes. Teratology 61(6): 448
Tullu, M.S.; Vaideeswar, P.; Deshmukh, C.T. 2000: Congenital left ventricular diverticula. International Journal of Cardiology 73(3): 293-295
Belbis,G.; Gartioux,J.P.; Lagalisse,Y.; Maillard,R.; Breard,E.; Zientara,S.; Millemann,Y. 2010: Congenital lesions associated with FCO virus in calves from vaccinated dams. Summa, Animali Da Reddito: 1, 61-67
Walczak, C.; Mueller Hansen, I.; Lang, P.; Schlegel, P.; Kendziorra, H.; Enders, H.; Dufke, A. 2001: Congenital leukaemia or transient myeloproliferative disease in a neonate with mosaicism for trisomy 21; a case report. European Journal of Human Genetics 9(Suppl 1): P0586
Kolker, S.E.; Zane, L.; Frieden, I.; Mccalmont, T.H. 2001: Congenital leukemia initially presenting as leukemia cutis without systemic involvement. Journal of Cutaneous Pathology 28(10): 572
Moss, A.J.; Zareba, W.; Robinson, J.L. 2001: Congenital long QT syndrome Genotype and phenotype correlations and treatment. Oto, Ali , Breithardt, Guenter Myocardial repolarization: From gene to bedside 261-268
Nadroo, A.M.; Lieber, E.; Zak, M.; Bialik, I.; Menos, D. 1999: Congenital lymphedema, unilateral choanal atresia, pericardial effusion, high arched palate and preauricular pits A possible new autosomal recessive syndrome. American Journal of Human Genetics 65(4): A336
Enders, G.; Varho-Göbel, M.; Löhler, J.; Terletskaia-Ladwig, E.; Eggers, M. 1999: Congenital lymphocytic choriomeningitis virus infection: an underdiagnosed disease. Pediatric Infectious Disease Journal 18(7): 652-655
Murray, S.C.; Dawber, R.P.; Khumalo, N. 2001: Congenital malalignment of the left index fingernail. British Journal of Dermatology 144(4): 911-912
Tiwari,A.K.; DevinderSingh; Chopra,M.; ShashiRekha 2010: Congenital malaria in preterm neonate - a case report of atypical presentation. Indian Journal Of Practical Pediatrics: 1, 97-98
Bever, B.J.; Conoscenti, G.; Kalache, K.D.; Qureshi, F.; Jacques, S.M.; Jones, T.B.; Joshi, A.; Romero, R.; Johnson, A. 2002: Congenital malformation of the lung coexisting with a small mar chromosome presenting as fetal hydrops. Genetics in Medicine 4(3): 214
Aboujaoude, I.; Hachem, G.; Aboujaoude, M.; Karam, H.; Aboujaoude, F. 1999: Congenital malformations and genetic birth defects in Lebanon War and seasonal variations The role of folic acid. Human Reproduction 14(ABSTR BOOK 1): 223
Marinho, A.S.N.; Coser Filho, O.A.; Llerena, J.C.J. 2002: Congenital malformations and genetic disorders as a source of investigation of the psychosocial repercussions in pregnant women in a state hospital prenatal clinical care from Rio de Janeiro, Brazil. European Journal of Human Genetics 10(Suppl 1): 317
Szumilo, J.; Skomra, D.; Burdan, F.; Korobowicz, E. 2002: Congenital malformations in children aged up to one-year deceased in the years 1981-2000 in east central Poland. Teratology 65(6): 326
Wennerholm, U.B.; Bergh, C.; Hamberger, L.; Lundin, K.; Nilsson, L.; Wikland, M.; Kallen, B. 2000: Congenital malformations in children born after intracytoplasmic sperm injection. American Journal of Obstetrics and Gynecology 182(1 Part 2): S182
Valdes, L.; Marquez, A.; Santana, O.; Santurio, A.; Robaina, M.; Rodriguez, B.R.; Lang, J.; Zaldivar, O.; Herrera, B.E. 2000: Congenital malformations in children born to diabetic mothers. Diabetes Research and Clinical Practice 50(Suppl 1): S424-S425
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Kos, M. 2001: Congenital malformations of genitourinary system in the 10 years period An autopsy study. Laboratory Investigation 81(1): 214A
Vézina, G. 2004: Congenital malformations of the brain: prenatal and postnatal imaging. Seminars in Roentgenology 39(2): 165-181
Dimofte, I.; Poalelungi, T.; Popa, A.; Balaban, D.; Enache, L.; Broasca, V.; Nedelcovici, S. 2001: Congenital malformations of the central nervous system in spontaneous abortion. European Journal of Human Genetics 9(Suppl 1): P0547
Karnsakul, W.; Swallow, D.; Hahn, D.; Sterchi, E.E.; Lifschitz, C.; Nichols, B.L. 2000: Congenital maltase-glucoamylase deficiency associated with lactase and sucrase deficiencies is regulated by trans-acting factors. JPGN 31(Suppl 2): S101
Kawahara, H.; Kamata, S.; Nose, K.; Oue, T.; Okada, A.; Wasada, K.; Murata, Y. 2001: Congenital mediastinal cystic abnormalities detected in utero: report of two cases. Journal of Pediatric Gastroenterology and Nutrition 33(2): 202-205
Ranells, J.D.; Kousseff, B.G. 1999: Congenital melanocytic hairy nevi in the genetic clinic. American Journal of Human Genetics 65(4): A340
Makkar, H.S.; Frieden, I.J. 2002: Congenital melanocytic nevi: an update for the pediatrician. Current Opinion in Pediatrics 14(4): 397-403
Willert, J.R.; Feusner, J.; Beckwith, J.B. 1999: Congenital mesoblastic nephroma: a rare cause of perinatal anemia. Journal of Pediatrics 134(2): 248
Jackson, D.N.; Haag, M.; Brown, L.; Keel Thompson, K.; Phillips, S.M.; Tunby, M.; Beischel, L.S.; Bennett, T.L. 2000: Congenital mesoblastic nephroma Perinatal, surgical and genetic features and associated 2D and 3D imaging. Genetics in Medicine 2(1): 110
Fitchev, P.; Beckwith, J.B.; Perlman, E.J.; Nwtsg 2003: Congenital mesoblastic nephroma Prognostic factors. Modern Pathology 16(1): 2P
Heinz-Erian, P.; Schmidt, H.; Le Merrer, M.; Phillips, A.D.; Kiess, W.; Hadorn, H.B. 1999: Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia. Journal of Pediatric Gastroenterology and Nutrition 28(2): 203-205
Gitlin, J.; Kaefer, M. 2002: Congenital mid ureteral stricture presenting as prenatal hydronephrosis. Journal of Urology 168(3): 1154-1155
Kapadia, L.A.; McClay, J.E. 2000: Congenital midline submandibular sinus tract. International Journal of Pediatric Otorhinolaryngology 53(3): 221-224
Turdean, M.T.; Tatulescu, T.D.; Carstina, D.C.; Goroiu, G.G. 2001: Congenital miliary tuberculosis? Case report. International Journal of Antimicrobial Agents 17(Suppl 1): S45
Serraf, A.; Zoghby, J.G.; Lacour Gayet, F.; Belli, E.; Aznag, H.; Planche, C. 1999: Congenital mitral stenosis and associated defects When should it be addressed?. Circulation 100(18): 1; 211
Oztürk, A.; Gunes, T.; Cetin, N.; Kurtoglu, S.; Oztürk, F. 2004: Congenital multiple myofibromatosis: is it really due to under estrogenic stimulation?. Pediatrics International: Official Journal of the Japan Pediatric Society 46(1): 91-93
Voit, T.; Staub, V.; Herrmann, R. 2000: Congenital muscular dystrophies Disorders of the basement membrane and extracellular matrix?. Brain Pathology 10(4): 498
Pascale, G. 2000: Congenital muscular dystrophies Primary and secondary laminin alpha2 chain deficiency. European Journal of Human Genetics 8(Suppl 1): 29-30
Eeg-Olofsson, K.E. 1999: Congenital muscular dystrophy. Care of children and families. Scandinavian Journal of Rehabilitation Medicine. Supplement 39: 53-57
Taratuto, A.; Lubieniecki, F.; Pirra, L.; Dubrovsky, A. 2000: Congenital muscular dystrophy with merosin deficiency, white matter abnormalities, and late onset epilepsy. Brain Pathology 10(4): 534
Maertens, C.; Tsujino, A.; Ohno, K.; Shen, X.M.; Harper, C.M.; Engel, A.G.; Cannon, S.C. 2003: Congenital myasthenia associated with skeletal muscle Na channel SCN4A mutations. Biophysical Journal 84(2 Part 2): 216a-217a
Gruber Sedlmayr, U.; Brunner Krainz, M.; Plecko, B.; Loescher, W.; Sieb, J.P. 2004: Congenital myasthenia with homozygotic mutation N88K of the rapsyn gene with infect associated respiratory insufficiency. Neuropediatrics 35(1): 83
Shen, X.M.; Ohno, K.; Brengman, J.M.; Fukuda, T.; Illa, I.; Engel, A.G. 2003: Congenital myasthenic syndrome associated with three missense mutations in the extracellular domain of the AChR delta subunit. Neurology 60(5 Suppl 1): A420
Neocleous, V.; Papadimitriou, A.; Divari, R.; Zamba, E.; Kyriakides, T.; Christodoulou, K. 2001: Congenital myasthenic syndrome due to a novel mutation in the acetylcholine receptor epsilon subunit gene. American Journal of Human Genetics 69(4 Suppl): 643
Schrader, K.; Broxtermann, W.; Sieb, J.; Steinlein, O.; Ebinger, F.; Rating, D. 2004: Congenital myasthenic syndrome in a girl from Albania. Neuropediatrics 35(1): 83
Sieb, J.P.; Kraner, S.; Thompson, P.N.; Steinlein, O.K. 2003: Congenital myasthenic syndrome in cattle due to homozygosity for a truncating mutation in the acetylcholine receptor epsilon-subunit gene. Agius, Mark A , Reprint Author, Richman, David P , Reprint Author, Fairclough, Robert H , Reprint Author, Maselli, Ricardo A , Reprint Author Myasthenia gravis and related disorders: Biochemical basis for disease of the neuromuscular junction: 125-127
Karcagi, V.; Tourrnev, I.; Schmidt, C.; Herczegfalvi, A.; Guergueltcheva, V.; Litvinenko, I.; Song, I.; Abicht, A.; Lochmueller, H. 2002: Congenital myasthenic syndrome in southeastern European Roma. European Journal of Human Genetics 10(Suppl 1): 182
Barisic, N.; Lochmuller, H.; Song, I.H.; Schmidt, C. 2001: Congenital myasthenic syndrome in two siblings due to a homozygous splice mutation of the epsilon-acetylcholine receptor subunit gene. Neurology 56(8 Suppl 3): A43-A44
Engel, A.G.; Ohno, K.; Shen, X.-M.; Sine, S.M. 2003: Congenital myasthenic syndromes: multiple molecular targets at the neuromuscular junction. Annals of the new York Academy of Sciences 998: 138-160
Eymard, B.; Ioos, C.; Barois, A.; Estournet, B.; Mayer, M.; Fournier, E.; Yasaki, E.; Prioleau, C.; Bauché, S.; Gaudon, K.; Leroy, J.P.; Koenig, J.; Richard, P.; Hantaï, D. 2004: Congenital myasthenic syndromes due to mutations in the rapsyn gene. Revue Neurologique (Paris) 160(5 Part 2): S78-S84
Sieb, J.P.; Kraner, S.; Rauch, M.; Harzheim, M.; Steinlein, O.K. 2000: Congenital myasthenic syndromes with paucity of secondary synaptic clefts caused by mutations in the epsilon-AChR subunit. Neurology 54(7 Supp 3): A183
Tubridy, N.; Fontaine, B.; Eymard, B. 2001: Congenital myopathies and congenital muscular dystrophies. Current Opinion in Neurology 14(5): 575-582
Taratuto, A.L. 2002: Congenital myopathies and related disorders. Current Opinion in Neurology 15(5): 553-561
Maurage, C.A.; Stojkovic, T.; Moerman, A.; Hurtevent, J.F.; Krivosic Horber, R.; Pellissier, J.F.; Ruchoux, M.M. 2000: Congenital myopathy of fingerprint body type with malignant hyperthermia susceptibility Report on a family. Brain Pathology 10(4): 537
Schnur, R.E.; Kurnik, R.A.; Reed, L.A.; Mockridge, K.A.; Imaizumi, S.O.; Evans, B.J.; Courtney, S.E.; Razi, N.M.; Pandit, P.B.; Saslow, J.G.; Stahl, G.E. 1999: Congenital myotonic dystrophy Novel phenotypic features. American Journal of Human Genetics 65(4): A343
Fornelli, R.A.; Ramadan, H.H. 2000: Congenital nasal pyriform aperture stenosis: clinical review. Otolaryngology--Head and Neck Surgery: Official Journal of American Academy of Otolaryngology-Head and Neck Surgery 122(1): 113-114
Gurnani, A.; Nenov, V.; Taal, M.W.; Troy, J.L.; Mackenzie, H.S.; Brenner, B.M. 2000: Congenital nephron deficit predicts increased renal injury in uninephrectomized rats. Journal of the American Society of Nephrology 11(Program and Abstract Issue): 619A-620A
Vats, A.N.; Chandra, I.; Moritz, M.; Ellis, D.; Baweja, P.; Sharma, M.; Surti, U.; Ferrell, R. 2001: Congenital nephropathy and uropathy in association with chromosome 13q Delineation of two critical regions. Journal of the American Society of Nephrology 12(Program and Abstract Issue): 562A
DeMarco, R.T.; Casale, A.J.; Davis, M.M.; Yerkes, E.B. 2001: Congenital neuroblastoma: a cystic retroperitoneal mass in a 34-week fetus. Journal of Urology 166(6): 2375
Ohyama, M.; Kobayashi, S.; Aida, N.; Toyoda, Y.; Ijiri, R.; Tanaka, Y. 1999: Congenital neuroblastoma diagnosed by placental examination. Medical and Pediatric Oncology 33(4): 430-431
North, P.E.; Waner, M.; James, C.A.; Mizeracki, A.; Mihm, M.C.Jr 2002: Congenital nonprogressive hemangioma A distinct clinicopathological entity unlike infantile hemangioma. Laboratory Investigation 82(1): 104A
Ogawa, Y.; Kobayashi, H.; Ebihara, K.; Hayashi, T.; Hosoda, K.; Inoue, H.; Ishihara, T.; Kurahachi, H.; Nakao, K. 2003: Congenital obesity caused by a novel mutation of human melanocortin receptor 4. Journal of the Japan Diabetes Society 46(1): 29-33
Sutherland, R.W.; Hicks, M.J.; Roth, D.R.; Gonzales, E.T.Jr; Lamb, D.J. 2000: Congenital obstructed megaureter Possible role for apoptosis. Journal of Urology 163(4 Suppl): 137
Moore, C.P.; Shaner, J.B.; Halenda, R.M.; Rosenfeld, C.S.; Suedmeyer, W.K. 1999: Congenital ocular anomalies and ventricular septal defect in a dromedary camel (Camelus dromedarius). Journal of Zoo and Wildlife Medicine: Official Publication of the American Association of Zoo Veterinarians 30(3): 423-430
Dunker, S.; Bous, M.; Roggenkaemper, P. 1999: Congenital ocular motor apraxia associated with ERG abnormalities in two sisters. IOVS Investigative Ophthalmology and Visual Science 40(4): S651
Van Son, J.A.; Autschbach, R.; Hambsch, J. 1999: Congenital ostial membrane of left coronary artery in truncus arteriosus. Journal of Thoracic and Cardiovascular Surgery 118(6): 1132-1134
Khan, K.; Mitton, S.G. 1999: Congenital pancreatic insufficiency and coeliac disease. Journal of Pediatric Gastroenterology and Nutrition 28(1): 97-99
Kim, S.H.; Koh, K.J.; Choi, J.H.; Sung, K.J.; Moon, K.C.; Koh, J.K. 2000: Congenital papular xanthoma. British Journal of Dermatology 142(3): 569-571
Solomon, D.; Shepard, N.; Mishra, A. 2002: Congenital periodic alternating nystagmus: response to baclofen. Annals of the new York Academy of Sciences 956: 611-615
Dell'osso, L.F.; Shallo Hoffmann, J.; Moore, A.T. 2000: Congenital periodic alternating nystagmus with unusual slow-phase waveforms. IOVS Investigative Ophthalmology and Visual Science 41(4): S702
Ittner, K.; Ding, X.; Hagel, C.; Neuen Jacob, E.; Herkenrath, P.; Kohlschuetter, A. 2004: Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions. Neuropediatrics 35(1): 81-82
Okamoto, A.; Sakata, T.; Katayama, Y.; Mannami, T.; Baba, T.; Ogata, J.; Matsuo, H.; Miyata, T.; Kato, H. 2000: Congenital plasminogen deficiency in Japanese Prevalence and relevance to cardiovascular diseases. Fibrinolysis and Proteolysis 14(Suppl 1): 78
Kumar, R.; Kumar, P.; Luthra, R.A. 2002: Congenital polycystic kidney and liver lesions in an ascitic buffalo foetus. Indian Journal of Animal Sciences 72(12): 1110-1111
Sapojnikov, V.G.; Trenina, M.S.; Tolstikova, E.E.; Kulikov, V.A. 1999: Congenital polycystosis of common hepatic duct diagnosed in the age of 8 years old. Pediatriya (Moscow) (6): 93-94
Pastore, Y.D.; Guan, Y.; Liu, E.; Ang, S.O.; Jelinek, J.; Prchal, J.T. 2002: Congenital polycythemia A new disease due to VHL mutation. Pediatric Research 51(4 Part 2): 224A
Redman, J.F.; Lightfoot, M.L. 2003: Congenital posterior urethral polyp in a boy. Urology 61(2): 460-461
Anticevic, D.; Stanec, Z.; Jelic, M.; Vukicevic, S. 2002: Congenital pseudarthrosis of the tibia Treatment with a bone morphogenetic protein. Calcified Tissue International 70(4): 256
Yamaguchi, M.; Rothwell, D.G.; Slater, N.J.; Chopra, R. 2003: Congenital pulmonary alveolar proteinosis is associated with disruption of GMCSF beta subunit signalling by a secreted receptor. British Journal of Haematology 121(Suppl 1): 51
Bellini, C.; Boccardo, F.; Campisi, C.; Taddei, G.; Bonioli, E.; Baldi, M.; Arioni, C.; Sacchi, R.; Ciotti, S.; Serra, G. 2003: Congenital pulmonary lymphangiectasia and congenital chylothorax are closely related entities. American Journal of Human Genetics 73(5): 330
Tuladhar, J.T.; Storgion, S.A.; Bugnitz, M.C.; Stidham, G.; Lasater, O. 2000: Congenital pulmonary lymphangiectasia associated with congenital heart disease. Chest 118(4 Suppl): 296S-297S
Bachiri, A.; Djebara, A.; Klosowski, S.; Haouari, N.; Thelliez, P.; Voisin, O.; Devisme, L.; Morisot, C. 2003: Congenital pulmonary lymphangiectasia revealed by cardiac arrest. Archives de Pediatrie: Organe Officiel de la Societe Francaise de Pediatrie 10(7): 615-618
Morrell, D.S.; Rubenstein, D.S.; Briggaman, R.A.; Fine, J.D.; Pulkkinen, L.; Uitto, J. 2000: Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex. British Journal of Dermatology 143(6): 1342-1343
Guirgis, M.F.; Wong, A.M.F.; Tychsen, L. 2002: Congenital restrictive external ophthalmoplegia and gustatory epiphora associated with fetal isotretinoin toxicity. Archives of Ophthalmology 120(8): 1094-1095
Metze, D.; Raghunath, M.; Traupe, H. 2000: Congenital reticular ichthyosiform erythroderma a histologic, immunohistochemical and ultra-structural study of a rare keratinization disorder. Journal of Investigative Dermatology 115(5): 923
Dalgiç, N.; Ergenekon, E.; Bideci, A.; Erbaş, G.; Koç, E.; Tali, T.; Atalay, Y. 2001: Congenital retropharyngeal goiter in a newborn as a magnetic resonance imaging finding. Pediatrics International: Official Journal of the Japan Pediatric Society 43(4): 431-433
Acharya, G.; Thambapillai, E.; Hartwell, R. 1999: Congenital rhabdomyosarcoma of maxillo-facial region associated with polyhydramnios. Journal of Obstetrics and Gynaecology: the Journal of the Institute of Obstetrics and Gynaecology 19(2): 204-205
Miller, K.; Giuffre, R.M.; Kellner, B.; Disler, D. 2002: Congenital right ventricular diverticulum accompanying disseminated neonatal hemangiomatosis. Journal of Investigative Medicine 50(1): 69A
Lee, A.C.; Wong, Y.C.; Fung, S.H.; Kwong, N.S.; Tsui, K.Y.; Ramsay, A.D. 2000: Congenital sacrococcygeal primitive neuroectodermal tumor. Medical and Pediatric Oncology 34(6): 448-450
Hicks, J.; Levy, M.; Barrish, J.; Metry, D.W. 2003: Congenital self-healing Langerhans cell histiocytosis Role of ultrastructure in diagnosis. Modern Pathology 16(1): 330A
Adeyoju, A.B.; Taylor, P.; Payne, S.R. 2001: Congenital seminal vesicle cysts: an unusual but treatable cause of lower urinary tract/genital symptoms. Bju International 87(9): 901-902
Ohama, K.; Ishida, Y.; Morishita, M.; Horita, S.; Matsumoto, H. 1999: Congenital short bowel syndrome Report of a case and review of the literature. Journal of Parenteral and Enteral Nutrition 23(5 Suppl): S158
Geaghan, S.M.; Glader, B. 2001: Congenital sideroblastic anemia in two East Indian siblings. Leukemia Research 25(Suppl 1): S42-S43
Vermeulen, S.; Messiaen, L.; Delanote, S.; Speleman, F.; De Paepe, A. 1999: Congenital spherocytosis, infertility, mild dysmorphism and normal intelligence in a patient with a subtle interstitial deletion 8p112. Cytogenetics and Cell Genetics 85(1-2): 170
Lonstein, J.E. 1999: Congenital spine deformities: scoliosis, kyphosis, and lordosis. Orthopedic Clinics of North America 30(3): 387-405 Viii
Holder, G.E.; Kabanarou, S.A.; Fitzke, F.W.; Bird, A.C.; Willis, C.E.; Zito, I.; Hardcastle, A.J.; Webster, A.R. 2001: Congenital stationary night blindness and a Schubert-Bornshein type electrophysiology in a family with dominant inheritance. IOVS Investigative Ophthalmology and Visual Science 42(4): S78
Grimm, V.; Mempel, M.; Ring, J.; Abeck, D. 2000: Congenital symptomatic dermographism as the first symptom of mastocytosis. British Journal of Dermatology 143(5): 1109
Sheffield, J.S.; Wendel, G.D.Jr.; Zeray, F.; Leos, N.K.; Sanchez, P.J. 1999: Congenital syphilis The influence of maternal stage of syphilis on vertical transmission. American Journal of Obstetrics and Gynecology 180(1 Part 2): S85
Dencheva, R.; Nyagolova, D.; Petrova, E.; Stoimenov, A.; Tsankov, N. 2001: Congenital syphilis in Bulgaria, 1990-1999. International Journal of STD and AIDS 12(Suppl 2): 143
Lopes, V.L.G.S.L.; Luquetti, D.V.L. 2003: Congenital temporomandibular joint ankylosis Clinical characterization of 3 unrelated affected. American Journal of Human Genetics 73(5): 294
Franck, J.; Lanza Silhol, F.; Vuillemot, L.; Pelissier, V.; Dumon, H. 2000: Congenital toxoplasmosis diagnosis by immunoblot; a prospective study using a new commercial immunobloting kit. Acta Parasitologica 45(3): 133
Brady-McCreery, K.M.; Hussein, M.A.W.; Paysse, E.A. 2003: Congenital toxoplasmosis with unusual retinal findings. Archives of Ophthalmology 121(8): 1200-1201
Peragallo, R.A.; Swenson, J.D. 2000: Congenital tracheal bronchus: the inability to isolate the right lung with a univent bronchial blocker tube. Anesthesia and Analgesia 91(2): 300-301
Koshy, O.; Ion, L.; Waterhouse, N. 2000: Congenital transmandibular dermoid: case report. British Journal of Oral and Maxillofacial Surgery 38(2): 107-109
Wicher, V.; Wicher, K.; Abbruscato, F.; Baughn, R.E. 1999: Congenital transmission of Treponema pallidum through several litters of guinea pigs is associated with a booster in the maternal humoral responses. FASEB Journal 13(4 Part 1): A641
Smith, K.C. 2002: Congenital tuberculosis: a rare manifestation of a common infection. Current Opinion in Infectious Diseases 15(3): 269-274
Sood, M.; Trehan, A.; Arora, S.; Jayashanker, K.; Marwaha, R.K. 2000: Congenital tuberculosis manifesting as cutaneous disease. Pediatric Infectious Disease Journal 19(11): 1109-1111
Pejham, S.; Altman, R.; Li, K.I.; Munoz, J.L. 2002: Congenital tuberculosis with facial nerve palsy. Pediatric Infectious Disease Journal 21(11): 1085-1086
Kos, M.; Hlupic, L.; Babic, D.; Jukic, S. 2003: Congenital tumours at foetal and neonatal autopsies during 17-years period. Virchows Archiv 443(3): 246
Saradamma, T.; Anoop, S.; Sooryadas, S.; Jose, S.; Nayar, K.N.M. 2000: Congenital umbilical defect with visceral eventration in a kid. Indian Journal of Veterinary Surgery 21(2): 112
Jay, P.Y.; Maguire, C.T.; Buerger, A.; Wakimoto, H.; Kupershmidt, S.; Roden, D.M.; Schultheiss, T.M.; Berul, C.I.; Izumo, S. 2002: Congenital underdevelopment of the central conduction system in Nkx2-5 knockout mice. Circulation 106(19): II286
Miller, J.A.; Hesse, M.; Haenze, J.; Weidner, W.; Knerr, I.; Rascher, W. 2001: Congenital unilateral ureteropelvic junction obstruction of the rat A useful animal model for human UPJO?. Journal of Urology 165(5 Suppl): 85-86
Ingelfinger, J.R. 2003: Congenital ureteral obstruction: new technology, new targets. Kidney International 64(1): 361-362
Miller, J.; Knerr, I.; Doetsch, J.; Kummer, W.; Rascher, W.; Weidner, W. 2000: Congenital ureteropelvic junction obstruction -increased endothelin-1 expression and decreased adrenomedullin expression. Journal of Urology 163(4 Suppl): 66
Fazili, M.R.; Buchoo, B.A.; Makhdoomi, D.M.; Darzi, M.M.; Hussain, S.S. 2000: Congenital urethral diverticulum in two kids. Indian Journal of Veterinary Surgery 21(2): 104-105
Lendvay, T.S.; Smith, E.A.; Kirsch, A.J.; Boddy, M.; Dewan, P. 2002: Congenital urethral stricture. Journal of Urology 168(3): 1156-1157
Camlibel, T.; Cankat, D. 1999: Congenital urogenital malformations in infants concieved by intracytoplasmic sperm injection. Pediatric Nephrology 13(7): C31
Dure-Smith, P.; Lau, L.; Khan, B.; David, A. 2002: Congenital variations in mucomuscular development of the ureter. Bju International 90(1): 130-134
Ernest, J.M. 2000: Congenital varicella syndromes is rare in a prospective cohort of 347 pregnant women. American Journal of Obstetrics and Gynecology 182(1 Part 2): S97
Chee, Y.L.; Culligan, D.J.; Greaves, M.; Watson, H.G. 2001: Congenital venous anomalies as a risk factor for deep venous thrombosis. British Journal of Haematology 113(Suppl 1): 8
Chessa, M.; Butera, G.; Bini, R.M.; Pome, G.; Giamberti, A.; Drago, M.; Rosti, L.; Carminati, M. 2001: Congenital ventricular septal defect closure with Amplatzer septal occluder. European Heart Journal 22(Abstract Suppl): 417
Anonymous 1999: Congenital vesicoureteral reflux in sheep is associated with reduced expression levels of aquaporin-1 and aquaporin-2 in kidney inner medulla. Pediatrics 104(3 Part 3): 831
Huff, D.S.; Zhang, P.J.; Golden, J.A.; Mcginn Mcdonald, D.M.; Zackai, E.H. 2002: Congenital visceral and neurocutaneous glomangiomatosis, an aneurysm of the subhepatic inferior vena cava and diffuse arterial dysplasia. American Journal of Human Genetics 71(4 Suppl): 261
Gerein, V.; Schmitt Graeff, A.; Malycheva, L.; Coerdt, W.; Muentefering, H. 2003: Congenital visceral fibrosis in two cases with trisomy 21 and TAM A contribution to the pathogenesis. Pathology Research and Practice 199(4): 284
Stirling, D.; Ludlam, C.A.; Thomas, A. 1999: Congenital vitamin K dependent coagulation factor deficiency associated with a 14 base deletion within intron 1 of the gamma carboxylase gene. British Journal of Haematology 105(Suppl 1): 27
van Winden, S.C.L.; Kuiper, R. 2002: Congenital white muscle disease in a Belgian blue calf. Tijdschrift Voor Diergeneeskunde 127(3): 74-77
Dimitrov, D.F.; Bronec, P.R.; Friedman, A.H. 2003: Congenitally absent C-7 pedicle presenting as a jumped locked facet. Case illustration. Journal of Neurosurgery 99(2 Suppl): 239
Carlson, B.C.; Jacobsson, L.; Luthman, H.; Lorentzen, J.C. 2000: Congenization of DA rat chromosome 10 terminus Oia3 confers arthritis susceptibility. Immunology Letters 73(2-3): 107
Woolf, A.S. 2003: Congential obstructive nephropathy gets complicated. Kidney International 63(2): 761-763
Bergman, P.; Grjibovski, A.M.; Hagströmer, M.; Patterson, E.; Sjöström, M. 2010: Congestion road tax and physical activity. American Journal of Preventive Medicine 38(2): 171-177
Rafii, Bijan; Engelberts, Doreen; Kavanagh, Brian; O.&&amp&n39.; Brodovich, Hugh 2004: Congestive Heart Failure Edema Fluid Increases in Vivo Alveolar Liquid Clearance. FASEB Journal 18(4-5): Abstract 469
Wang, A.Y.M.; Sea, M.M.M.; Sanderson, J.E.; Ip, R.; Lui, S.F.; Li, P.K.T.; Woo, J. 2001: Congestive cardiac failure, an important, yet unrecognized cause of inadequate dietary nutrient intake in continuous ambulatory peritoneal dialysis patients. Journal of the American Society of Nephrology 12(Program and Abstract Issue): 443A
Belz, G.G. 1999: Congestive heart failure - Is there still a need for cardiac glycosides?. European Journal of Clinical Investigation 29(Suppl 1): 62
Baessler, A.; Fischer, M.; Schunkert, H. 2003: Congestive heart failure - often a preventable condition. Deutsche Medizinische Wochenschrift 128(27): 1489-1493; 4 Juli
Basso, C.A.A.gelini; Thiene, G.; Nava, A.; Livi, U.; Dalla Volta, S. 1999: Congestive heart failure A not so rare event in the natural history of arrhythmogenic right ventricular cardiomyopathy. Modern Pathology 12(1): 35A
Thivierge, C.; Feldman, D.; Dery, V.; Guerard, L.; Kapetanakis, C.; Lavoie, G. 2000: Congestive heart failure Hospitalization and mortality in those over 65 years in Montreal, 1990-97. Canadian Journal of Cardiology 16(Suppl F): 128F
Oduwole, A.M. 2002: Congestive heart failure: improving outcomes for at-risk populations. Ethnicity and Disease 12(1): S2
Mckinnon, J.E.; Khandelwal, A.K.; Shenkman, H.J.; Pampati, V.; Nori, D.M.; Mccullough, P.A. 2000: Congestive heart failure and QRS duration Utilization in establishing prognosis in systolic and diastolic dysfunction Results of the conquest study. Chest 118(4 Suppl): 221S
Jung, J.H.; Min, P.-K.; Moon, Y.-W.; Shim, W.H. 2004: Congestive heart failure and a swollen breast. Lancet 363(9404): 210
Williams, D.M.; Sreedhar, S.S.; Mickell, J.J.; Chan, J.C.M. 2001: Congestive heart failure and acute renal failure A pediatric experience over 20 years. Journal of the American Society of Nephrology 12(Program and Abstract Issue): 186A
Valencia, R.; Theroux, P.; Granger, C.B.; Mahaffey, K.W.; Gudaye, T.; Malloy, K.; Weaver, W.D.; Todaro, T.G.; Mojcik, C.F.; Armstrong, P.W.; Hochman, J.S. 2004: Congestive heart failure and cardiogenic shock complicating acute myocardial infarction have high mortality and are associated with intense inflammatory response Results from the CARDINAL Trials. Journal of the American College of Cardiology 43(5 Suppl A): 291A
Skotzko, C.; Krichten, C.; Zietowski, G.; Alves, L.; Fisher, M.; Gottlieb, S.S. 1999: Congestive heart failure and depression Frequency and impact of depression on functional status. Journal of the American College of Cardiology 33(2 Suppl A): 210A
Schamberger, M.S.; Farrell, A.G.; Olson, I.L.; Layton, L.L.; Ensing, G.J.; Denne, S.C.; Leitch, C.A. 1999: Congestive heart failure and large left to right shunts increase total energy expenditure in infants with ventricular septal defects. Pediatric Research 45(4 Part 2): 30A
Leitch, C.A.; Olson, I.L.; Schamberger, M.S.; Farrell, A.G. 2000: Congestive heart failure and left to right shunting increase total energy expenditure in infants with ventricular septal defects. FASEB Journal 14(4): A791
Zuppiroli, A.; Mori, F.; Castelli, G.; Olivotto, J.; Favilli, S.; Dolara, A. 2001: Congestive heart failure associated with previously unrecognized severe aortic stenosis The role of dobutamine echocardiography in clinical decision making. European Heart Journal 22(Abstract Suppl): 314
Zhang, D.; Mott, J.L.; Chang, S.W.; Zassenhaus, P.H. 2001: Congestive heart failure caused by chronic apoptotic cell death in a transgenic mouse model with elevated mitochondrial DNA mutations. Circulation 104(17): 2; 248
Spencer, F.A.; Goldberg, R.J.; Gore, J.M. 1999: Congestive heart failure complicating acute myocardial infarction NRMI-2 registry. Circulation 100(18): 1; 396
Lagrasta, C.; Maestri, R.; Corradi, D.; Bertani, N.; Graiani, G.; Cigola, E.; Quaini, F.; Olivetti, G. 1999: Congestive heart failure does not affect nuclear DNA content in human cardiac myocytes. European Heart Journal 20(ABSTR Suppl ): 197
Gami, A.S.; Grande, J.P.; Garovic, V.D. 2002: Congestive heart failure in hemolytic uremic syndrome and thrombotic thrombocytopenic purpura. Journal of the American Society of Nephrology 13(Program and Abstracts Issue): 453A
Bertault, V.; Fatemi, M.; Etienne, Y.; Gilard, M.; Pennec, P.Y.; Blanc, J.J. 2003: Congestive heart failure in patients with right-ventricular pacing after atrioventricular node ablation Is upgrading to biventricular pacing an effective treatment?. European Heart Journal 24(Abstract Suppl): 521
Kay, J.D.; Colan, S.D.; Graham, T.P. 2001: Congestive heart failure in pediatric patients. American Heart Journal 142(5): 923-928
Wolfe, F.; Michaud, K.; Mendelsohn, A. 2004: Congestive heart failure in rheumatoid arthritis patients Rates, predictors, and the effect of antitumor necrosis factor therapy. Journal of the American College of Cardiology 43(5 Suppl A): 220A
Akosah, K.O.; Moncher, K.; Schaper, A.; Havlik, P.; Sundaram, R.; Devine, S. 2001: Congestive heart failure in the community Missed diagnosis and missed opportunities. Journal of the American College of Cardiology 37(2 Suppl A): 511A
Tayara, L.; Douglas, S.; Ao, Z.; Ohlstein, E.; Giaid, A. 2001: Congestive heart failure is associated with increased expression of myocardial urotensin II. Circulation 104(17): 2; 240
D.S.usa, E.; Veksler, V.; Mateo, P.; Bigard, X.; Ventura Clapier, R. 2000: Congestive heart failure profoundly alters mitochondrial function of rat skeletal muscles. FASEB Journal 14(4): A51
Blair, J.; Holper, E.M.; Faxon, D.P.; Jolly, N.; Jacobs, A.K.; Shaw, R.; Coady, P.; Selzer, F.; Vlachos, H.; Williams, D.O. 2003: Congestive heart failure remains a strong independent predictor of adverse outcomes after percutaneous coronary intervention Current results from the NHLBI Dynamic Registry. Circulation 108(17): IV458-IV459
Jackson, J.; Farrelly, E.; Ziska, D.; Frech, F.; Hibler, S. 2002: Congestive heart failure therapies within managed care. Pharmacotherapy 22(10): 1331
Czerny, M.; Kilo, J.; Baumer, H.; Kramer, L.; Madl, C.; Taghavi, S.; Zuckermann, A.; Ankersmit, J.; Laufer, G.; Grimm, M. 2000: Congitive brain function dramatically decreases in long term survivors after successful cardiac transplantation. Journal of Heart and Lung Transplantation 19(1): 52
Rosario, C.; Sheffield, C.; Eslava, C.; Anderson, R.; Tellez, G.; Nisbet, D. 2002: Congo red binding of Escherichia coli strains isolated from yolk sac infections. Poultry Science 81(Suppl 1): 85-86
Sen, S.; Basdemir, G. 2001: Congo red fluorescence on the frozen sections of renal biopsies. Journal of the American Society of Nephrology 12(Program and Abstract Issue): 737A
Jouve, S.; Schwarz, D. 2004: Congosaurus bequaerti, a Paleocene Dyrosaurid from Landana. Bulletin de l'Institut Royal des Sciences Naturelles de Belgique Sciences de la Terre 74: 129-146
Godany, A.; Turna, J. 2003: Congratulations on 60th birthday of Assoc Professor Jozef Timko, DSc. Biologia (Bratislava) 58(3): 413
Hausmann, A.; Sommerer, M.; Stuening, D. 2002: Congratulations to Prof Dr Hiroshi Inoue on his 85th birthday. Spixiana 25(2): 162
Hartig, J.H. 2003: Congressional briefing on Detroit River and Lake St Clair issues. IAGLR Conference Program and Abstracts 46: 39
Carmona, J.A.; Domínguez, J.; Doadrio, I. 2000: Congruence between allozyme and cytochrome b gene sequence data in assessing genetic differentiation within the Iberian endemic Chondrostoma lemmingii (Pisces: cyprinidae). Heredity 84: 721-732
Brochu, C.A. 2001: Congruence between hysiology, phylogenetics and the fossil record on crocodylian historical biogeography. Grigg, Gordon C, Seebacher, Frank, Franklin, Craig E Crocodilian biology and evolution 9-28
Alarcon,R. 2010: Congruence between visitation and pollen-transport networks in a California plant-pollinator community. Oikos 9(1): 35-44
Clemmons, J.P. 2001: Conical blood pressure cuff with rectangular bladder. Official Gazette of the United States Patent and Trademark Office Patents 1247(2)
Hankh, S.; Gianotti, M.; Hofmann, E. 1999: Conical stent. Official Gazette of the United States Patent and Trademark Office Patents 1224(2)
Siwy, Z.; Heins, E.; Harrell, C.C.; Kohli, P.; Martin, C.R. 2004: Conical-nanotube ion-current rectifiers: the role of surface charge. Journal of the American Chemical Society 126(35): 10850-10851
Leclercq, M. 1999: Conicera tibialis Schmitz, 1925 Diptera Phoridae new for Belgian fauna. Bulletin de la Societe Royale Belge d'Entomologie 135(1-6): 66
Ludemann,V.; Greco,M.; PazRodriguez,M.; Basilico,J.C.; Pardo,A.G. 2010: Conidial production by Penicillium nalgiovense for use as starter cultures in dry fermented sausages by solid state fermentation. Lwt: 2, 315-318
Stewart, J.E.; Halik, S.; Bergdahl, D.R. 2003: Conidiospores of the butternut canker fungus carried on the exoskeletons of three different potential beetle vectors. Phytopathology 93(6 Suppl): S135-S136
Kaye, M.W.; Binkley, D.; Stohlgren, T.J. 2002: Conifer invasion of quaking aspen stands in Rocky Mountain National Park, Colorado. Ecological Society of America Annual Meeting Abstracts 87: 175
Pisaric, M.F. 2001: Conifer stomates as indicators of the subarctic and subalpine treeline. Ecological Society of America Annual Meeting Abstracts 86: 179
Carlson, J.E.; Dharmawardhana, D.P.; Douglas, C.J.; Ellis, B.E. 1999: Coniferin beta-glucosidase cDNA for modifying lignin content in plants. Official Gazette of the United States Patent and Trademark Office Patents 1227(4)
Ceulemans, R.; Kowalski, A.S.; Berbigier, P.; Dolman, A.J.; Grelle, A.; Janssens, I.A.; Lindroth, A.; Moors, E.; Rannik, U.; Vesala, T. 2003: Coniferous forests Carbon and water fluxes, balances, ecological and ecophysiological determinants. Valentini, Riccardo , Reprint Author Fluxes of carbon water and energy of European forests: 71-97
Vertesy, L.; Knauf, M.; Markus Erb, A.; Toti, L.; Raynal Wetzel, M.C.; Fassy, F. 2003: Coniosetin and derivatives thereof, process for the preparation and the use thereof. Official Gazette of the United States Patent and Trademark Office Patents 1272(5)
Laroche, A.J.; Huang, T.Y.; Frick, M.M.; Lu, Z.X.; Huang, H.C.; Cheng, K.J. 2004: Coniothyrium minitans beta- exoglucanase gene cbeg 1. Official Gazette of the United States Patent and Trademark Office Patents 1282(2)
Stoneman, W.F. 2002: Coniothyrium minitans for practical control of sclerotinia diseases. Phytopathology 92(6 Suppl): S105
Smith, W.B.; Russell, S.; Ghali, J.K.; Painchaud, C.A.; Ghazzi, M.M.; Konstam, M.A.; Udelson, J.E.; Selaru, P. 2001: Conivaptan , a combined vasopressin V1A/V2 antagonist, reduces pulmonary capillary wedge pressure independent of baseline serum Na or vasopressin levels in heart failure. European Heart Journal 22(Abstract Suppl): 541
Smith, W.B.; Russell, S.; Ghali, J.K.; Painchaud, C.A.; Selaru, P.; Ghazzi, M.M.; Konstam, M.A.; Udelson, J.E. 2001: Conivaptan , a combined vasopressin V1A/V2 receptor antagonist, reduces pulmonary capillary wedge pressure independent of baseline serum sodium or vasopressin levels in heart failure patients. Journal of the American College of Cardiology 37(2 Suppl A): 172A-173A
Norman, P.; Leeson, P.A.; Rabasseda, X.; Castaner, J.; Castaner, R.M. 2000: Conivaptan hydrochloride Treatment of heart failure, treatment of hyponatremia, vasopressin V1a/V2 antagonist CI-1025, YM-087. Drugs of the Future 25(11): 1121-1130
Fieggen, G.; Peter, J.; Millar, A.; Rode, H. 2002: Conjoined spinal cords in pygopagus twins. Lancet 360(9349): 1934
Topcuoglu, M.Ata 2003: Conjoined twins A case report. Cerrahpasa Tip Dergisi 34(1): 39-41
Metneki, J. 1999: Conjoined twins in Hungary, 1970-95. European Journal of Human Genetics 7(Suppl 1): 62
Molina, B.S.G.; Bukstein, O.G.; Lynch, K.G. 2000: Conjoint ADHD and CD in adolescents with alcohol use disorders. Alcoholism Clinical and Experimental Research 24(5 Suppl): 72A
Boxall, A.R. 1999: Conjoint activation of Src-protein tyrosine kinase by mGluR1, and TrkB by BDNF, modulates synaptic GABAA receptors. Society for Neuroscience Abstracts 25(1-2): 1247
Ritter, J.H.; Krigman, H.R.; Swanson, P.E.; Wick, M.R. 2000: Conjoint expression of the melanoma markers HMB-45 and Melan-A by the proliferating cells of pulmonary lymphangiomyomatosis An immunohistochemical study. Laboratory Investigation 80(1): 216A
Traynor, B.J.; Brennan, D.; Kelly, A.; Shah, I.; Hardiman, O. 1999: Conjugal amyotrophic lateral sclerosis Simultaneous onset in an elderly couple. Neurology 52(6 Suppl 2): A528-A529
Piotte, S.; Gower Rousseau, C.; Peeters, M.; Van Gossum, A.; Belaiche, J.; Fiasse, R.; Dupas, J.L.; Lerebours, E.; Cortot, A.; Grandbastien, B.; Colombel, J.F. 1999: Conjugal forms of inflammatory bowel diseases in Northwestern France and Belgium More than expected by chance. Gastroenterology 116(4 Part 2): A688
Sato, M.; Watanabe, K.; Sato, Y. 1999: Conjugal transfer of multi-drugs resistance genes between epiphytic Enterobacter cloacae and Erwinia herbicola. Abstracts of the General Meeting of the American Society for Microbiology 99: 454
Farias, M.E.; Espinosa, M. 2001: Conjugal transfer of plasmid pMV158 Features of the plasmid-encoded MobM protein and its oriT target DNA. Plasmid 45(2): 150
Marquez, C.; Xia, M.; Borthagaray, G.; Roberts, M.C. 1999: Conjugal transfer of the 3.05 beta-lactamase plasmid by the 25.2 Mda plasmid in Neisseria gonorrhoeae. Sexually Transmitted Diseases 26(3): 157-159
Graser, M.; Manaouil, C.; Ledoux, B.; Jarde, O. 2003: Conjugal violence A prospective study. Forensic Science International 136(Suppl 1): 256-257
Brown, T.; Caplan, T.; Werk, A.; Seraganian, P. 2001: Conjugal violence in couples of men attending alcoholism treatment. Alcoholism Clinical and Experimental Research 25(5 Suppl A): 46A
Steinhoff, M.; Goldblatt, D. 2003: Conjugate Hib vaccines. Lancet 361(9355): 360-361
Sinn, H.; Schrenk, H.H.; Maier Borst, W.; Frei, E.; Stehle, G. 2004: Conjugate comprising a folic acid antagonist and a carrier. Official Gazette of the United States Patent and Trademark Office Patents 1281(2)
Sinn, H.; Maier Borst, W.; Schrenk, H.H.; Stehle, G.; Fiebig, H.H. 2002: Conjugate comprising an active agent, a polypeptide and a polyether. Official Gazette of the United States Patent and Trademark Office Patents 1258(4)
Ezrin, A.M.; Bridon, D.P.; Holmes, D.L.; Milner, P.G. 2002: Conjugate comprising an antinociceptive agent covalently bonded to a blood component. Official Gazette of the United States Patent and Trademark Office Patents 1265(5)
Sinn, H.; Schrenk, H.H.; Maier Borst, W.; Stehle, G.; Wunder, A.; Hoff Biederbeck, D.; Heene, D.L. 2004: Conjugate consisting of an active substance and a non-exogenous native protein. Official Gazette of the United States Patent and Trademark Office Patents 1288(1)
Haigh, T.; Mead, G.P.; Drayson, M.T.; Mangham, D.C.; Bradwell, A.R. 1999: Conjugate delivery system offers a more rapid protocol for immunofluorescence. Clinical Chemistry 45(6 Part 2): A154
Keppler, D.; Koenig, J.; Cui, Y.; Nies, A.T. 2002: Conjugate export pumps of the MRP - family Their relevance for detoxification and pharmacokinetics. Naunyn-Schmiedeberg's Archives of Pharmacology 365(Suppl 1): R1
Keppler, D. 2000: Conjugate export pumps of the MRP family in detoxification. Drug Metabolism Reviews 32(Suppl 1): 8
Keppler, D.; Cui, Y.; Leier, I.; Rost, D.; Nies, A.; Koenig, J. 1999: Conjugate export pumps of the multidrug resistance protein family in liver, intestine and kidney. Journal of Physiology (Cambridge) 520P: 8S-9S
Sinn, H.; Schrenk, H.H.; Maier Borst, W.; Stehle, G. 2004: Conjugate for treating inflammatory infectious and/or skin diseases. Official Gazette of the United States Patent and Trademark Office Patents 1280(3)
Zalipsky, S.; Gabizon, A.A. 2002: Conjugate having a cleavable linkage for use in a liposome. Official Gazette of the United States Patent and Trademark Office Patents 1257(1)
Mintzer, R.A.; Aarsvold, J.N.; Batth, D.; Valentine, J.D. 2000: Conjugate imaging for regional-uptake estimation Some analytic considerations. Journal of Nuclear Medicine 41(5 Suppl): 190P
Sinn, H.; Schrenk, H.H.; Maier Borst, W.; Stehle, G. 2000: Conjugate of an active agent, a polyether and possibly a native protein regarded as acceptable by the body. Official Gazette of the United States Patent and Trademark Office Patents 1240(3)
Yatvin, M.B.; Stowell, M.H.B.; Gallicchio, V.S.; Meredith, M.J. 2000: Conjugate of biologically active compound and polar lipid conjugated to a microparticle for biological targeting. Official Gazette of the United States Patent and Trademark Office Patents 1234(3)
Kilburn, D.G.; Miller, R.C.; Gilkes, N.; Warren, A.J.R. 1999: Conjugate of non-protein chemical moiety and polypeptide having cellulose binding region. Official Gazette of the United States Patent and Trademark Office Patents 1224(4)
Davis, S.S.; Lin, W.; Bignotti, F.; Ferruti, P. 2004: Conjugate of polyethylene glycol and chitosan. Official Gazette of the United States Patent and Trademark Office Patents 1282(1)
Dagan, R.; Fraser, D. 2000: Conjugate pneumococcal vaccine and antibiotic-resistant Streptococcus pneumoniae: herd immunity and reduction of otitis morbidity. Pediatric Infectious Disease Journal 19(5 Suppl): S79
Gu, X.X.; Tsai, C.M. 2003: Conjugate vaccine for Neisseria meningitidis. Official Gazette of the United States Patent and Trademark Office Patents 1268(2)
Michel, J.L.; Kasper, D.L.; Ausubel, F.M.; Madoff, L.C. 1999: Conjugate vaccine for group B Streptococcus. Official Gazette of the United States Patent and Trademark Office Patents 1227(3)
Gu, X.X.; Tsai, C.M.; Lim, D.J.; Robbins, J.B. 2003: Conjugate vaccine for nontypeable Haemophilus influenzae. Official Gazette of the United States Patent and Trademark Office Patents 1273(3)
Buchholz, H.; Poetsch, E.; Rosskopf, R.; Anselmann, R.; Kirschbaum, M.; Pflucker, F. 2004: Conjugate, its preparation and use. Official Gazette of the United States Patent and Trademark Office Patents 1278(1)
Delany, J.; West, D. 2004: Conjugated Linoleic Acid Reduces Body Fat in Overweight Mice. FASEB Journal 18(4-5): Abstract 583
Butz, D.E.; Cook, M.E. 2004: Conjugated Linoleic Acid Reduces Inflammation in Anti-Type II Collagen Monoclonal Antibody-Induced Arthritis in Mice. FASEB Journal 18(4-5): Abstract 133
Porter, S.F.; Dhiman, T.R.; Cornforth, D.P.; Wiedmeier, R.D.; Olson, K.C.; Bowman, B.R.; Luchini, N.D. 2003: Conjugated Linoleic Acid in tissues from beef cattle fed different lipid supplements. Journal of Dairy Science 86(Suppl 1): 110-111
Mohede, I.C. Maria; Taran, V.D.; Albers, R.; Van Der Wielen, R.; Brink, L. 2003: Conjugated Linoleic Acid stimulates antigen specific antibody production in humans. FASEB Journal 17(7): C31
Emmett, M.; Hofmann, A.F.; Santa Ana, C.; Porter, J.; Neimark, S.; Kapral, C.; Fordtran, J.S. 2001: Conjugated bile acid replacement therapy decreases hyperoxaluria in short bowel syndrome. Journal of the American Society of Nephrology 12(Program and Abstract Issue): 752A
Moser, S.A.; Savage, D.C. 1999: Conjugated bile salt hydrolase of Lactobacillus and toxicity of conjugated bile salts. Abstracts of the General Meeting of the American Society for Microbiology 99: 458
Crosignani, A.; Muraca, M.; Longo, M.; Battezzati, P.M.; Invernizzi, P.; Zermiani, P.; Vilei, M.T.; Mingardi, M.; Perego, F.; Meda, F.; Podda, M. 2000: Conjugated bilirubin is an accurate marker of cholestasis in primary biliary cirrhosis. Gastroenterology 118(4 Suppl 2 Pt 1): AASLD A900