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Section 44

EurekaMag Full Text Articles Chapter 43,111



References:

Chen, R.D.; Liu, X.D.; Liu, L.X. 1994: Familial cervical lung hernia: a report of 4 cases in a family. Zhonghua Jie he He Hu Xi Za Zhi 17(4): 230
Boucher, M.; Normand, J.; Tommasi, M.; Kopp, N.; Carrier, H.; Boulliat, G. 1973: Familial changes in L.D.H. isoenzymes associated with a myopathic syndrome in one case and with angina and normal coronary arteries in another. Revue Neurologique (Paris) 129(4): 173-184
Rakhal'skiĭ, I.E.; Sirovskiĭ, A.A. 1970: Familial character of Shereshevskiĭ-Turner syndrome with karyotype 45, XO-46, XX. Problemy Endokrinologii 16(3): 44-45
Strumeliev, S. 1970: Familial character of pulmolithiasis endoalveolaris diffusa. (Microlithiasis alveolaris pulmonum). Zeitschrift für Erkrankungen der Atmungsorgane Mit Folia Bronchologica 132(1): 31-38
Tual-Pierre, Y. 1974: Familial characteristics of Class II, division 2. Clinical study. Revue d'Orthopedie Dento-Faciale 8(1): 59-66
Scott, D.L.; Delamere, J.P.; Mackintosh, L.P.; Jobson, S. 1982: Familial cheiroarthropathy without juvenile onset diabetes mellitus. Rheumatology International 2(3): 141-143
Rai, M.; Agrawal, J.K.; Sasikumar, V.; Singh, S.K.; Saraf, S.K.; Kumar, M.; Shukla, H.S. 1994: Familial childhood parathyroid adenoma. Journal of Pediatric Surgery 29(12): 1530-1531
Launiala, K.; Perheentupa, J.; Pasternack, A.; Hallman, N. 1968: Familial chloride diarrhea-chloride malabsorption. Bibliotheca Paediatrica 87: 137-149
Davidson, A.G.; Insley, J.; Capps, F.P.; Anderson, C.M. 1972: Familial chloride diarrhoea (congenital alkalosis with diarrhoea). Australian Paediatric Journal 8(4): 187-190
Parkes, M.L.; Brennan, H.G. 1973: Familial choanal atresia in a rhinoplasty candidate--a case report. Eye Ear Nose and Throat Monthly 52(6): 222-226
Texier, G. 1972: Familial choices and procreative behavior of the clientele of familial planning centers. Gynecologie Pratique 23(2): 77-87
Tazawa, Y.; Konno, T. 1982: Familial cholestasis with gallstone, ataxia and visual disturbance. Tohoku Journal of Experimental Medicine 137(2): 137-144
Nunez-Roldan, A.; Sanchez-Burson, J.; Prieto, J.; Pujol, E. 1981: Familial chondrocalcinosis and HLA system. Arthritis and Rheumatism 24(12): 1590-1591
Rodriguez-Valverde, V.; Tinture, T.; Zuñiga, M.; Peña, J.; Gonzalez, A. 1980: Familial chondrocalcinosis. Prevalence in Northern Spain and clinical features in five pedigrees. Arthritis and Rheumatism 23(4): 471-478
Awan, K.J. 1980: Familial chorioretinal vascular anastomoses and congenital cataracts. Journal of Pediatric Ophthalmology and Strabismus 17(6): 384-388
Déodati, F.; Bec, P.; Camezind, M.; Labro, J.B. 1972: Familial choroideremia. Bulletins et Memoires de la Societe Francaise d'Ophtalmologie 85: 321-334
Zellweger, H. 1966: Familial chromosomal aberrations. I. Annales Paediatrici. International Review of Pediatrics 206(5): 317-332
Zellweger, H. 1966: Familial chromosomal aberrations. II. Annales Paediatrici. International Review of Pediatrics 206(6): 381-395
Kostant, G.H. 1972: Familial chronic biologic false-positive seroreactions for syphilis. Report of two families, one with three generations affected. JAMA 219(1): 45-48
Bruk, M.I. 1968: A comparison of the articular and vascular manifestations of polymyalgia rheumatica and giant-cell arteritis. South African Medical Journal 42(45): 1235-1236
Matsuoka, T.; Miyoshi, K.; Saka, K.; Hayashi, S. 1966: Familial chronic encephalopathy with convulsive seizures, disturbance in gait, postural changes and dementia--a contribution to the study of atypical brain atrophy. Seishin Shinkeigaku Zasshi 68(9): 1043-1059
Fillastre, J.P.; Marx, P.; Laumonier, R.; Métayer, J.; Dubois, D.; Mallet, E. 1974: Familial chronic interstitial nephropathy and retinal dystrophy (Senior-Loken syndrome). La Nouvelle Presse Medicale 3(6): 309-312
Rodrigo, M.; Garrido, G.; Carrasquer, J.; Berenguer, J.; Marty, M.; Prieto, F.; Badía, L. 1971: Familial chronic jaundice caused by nonspherocytic hemolytic anemia, with increase of erythrocyte pyruvate kinase. Revista Clinica Espanola 123(2): 167-172
Magaraggia, L.; Vettori, G. 1968: Familial chronic lymphatic leukemia associated with cutaneous epithelioma. Il Fracastoro 61(3): 269-273
Fraumeni, J.F.; Vogel, C.L.; DeVita, V.T. 1969: Familial chronic lymphocytic leukemia. Annals of Internal Medicine 71(2): 279-284
Morrison, J.G.; Anderson, R. 1981: Familial chronic mucocutaneous candidiasis successfully treated with oral ketoconazole. South African Medical Journal 59(7): 237-239
García-Pérez, A.; Gómez de la Concha, E.; Guerra Rodríguez, P. 1984: Familial chronic mucocutaneous candidiasis. Study of 2 families. Medicina Cutanea Ibero-Latino-Americana 12(1): 33-40
Avilés, A.; Sinco, A.; Zapata, N.; Ambriz, R.; Pizzuto, J. 1982: Familial chronic myelogenous leukemia. Report of 3 cases in a family. Sangre 27(5): 953-958
Lillicrap, D.A.; Sterndale, H. 1984: Familial chronic myeloid leukaemia. Lancet 2(8404): 699
Moseley, J.H. 1967: Familial chronic nephritis. Proceedings of the Royal Society of Medicine 60(3): 246-247
Klajman, A.; Steiner, Z.; Rosenszajn, A. 1970: Familial chronic neutropenia with bone marrow maturation arrest. Harefuah 78(3): 103-106
Centa, A. 1967: Familial chronic non-hemolytic jaundice (Dubin-Johnson syndrome). Clinical and histological study in a premature twin. Pathologica 59(869): 35-41
Sato, T.; Saito, Y. 1974: Familial chronic pancreatitis associated with pancreatic lithiasis. American Journal of Surgery 127(5): 511-517
Hoshiyama, M.; Nakazima, H.; Arai, O.; Yuasa, T.; Shirakawa, K. 1980: Familial chronic thyroiditis and its similarity to myotonic dystrophy. Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 69(1): 27-32
Freycon, M.T.; Gilly, J.; Bouvier, R.; Braye, A. 1982: Familial chronic tubulointerstitial nephritis with antibodies to the tubular basement membrane. Pediatrie 37(5): 371-381
Brunzell, J.D.; Miller, N.E.; Alaupovic, P.; St Hilaire, R.J.; Wang, C.S.; Sarson, D.L.; Bloom, S.R.; Lewis, B. 1983: Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity. Journal of Lipid Research 24(1): 12-19
Joske, R.A.; Laurence, B.H. 1970: Familial cirrhosis with autoimmune features and raised immunoglobulin levels. Gastroenterology 59(4): 546-552
Khodadad, G. 1971: Familial cirsoid aneurysm of the scalp. Journal of Neurology Neurosurgery and Psychiatry 34(6): 664-667
Cheraskin, E.; Ringsdorf, W.M. 1970: Familial clinical patterns. I. Reported symptoms and signs in the dentist and his wife. Geriatrics 25(2): 123-126
Minohara, Y.; Kato, T.; Kanki, K.; Goshima, T.; Nakajima, N.; Kaku, H.; Arimoto, Y.; Goshima, F.; Doi, K.; Saitoh, K. 1995: Familial clustering case of hepatitis delta. Kansenshogaku Zasshi. Journal of the Japanese Association for Infectious Diseases 69(6): 747-751
Rico Lenza, H. 1983: Familial clustering in Paget's disease. Medicina Clinica 81(16): 736-737
Sans Valeta, J. 1983: Familial clustering in Paget's disease of bone: an epidemiological perspective of interest. Medicina Clinica 81(2): 60-63
Morales Piga, A.; González Lanza, M.; Arnaiz Villena, A.; Martínez Escribano, B.; Alonso Ruiz, A.; Zea Mendoza, A. 1983: Familial clustering in Paget's disease: etiopathogenic implications. Presentation of a family with 12 affected members. Medicina Clinica 81(2): 43-46
Chironna, M.; Quarto, M.; Specchia, G.; Liso, V.; Barbuti, S. 1995: Familial clustering of HTLV-i infection in southeastern Italy. Lancet 346(8968): 179-180
Tennant, S.N.; Hammon, J.W.; Bender, H.W.; Graham, T.P.; Primm, R.K. 1984: Familial clustering of atrioventricular canal defects. American Heart Journal 108(1): 175-177
Bruguera, M.; Bosch, J.; Rodés, J.; Pedreira, J. 1974: Familial clustering of hepatitis B antigen: a study in relatives of patients with liver diseases and hepatitis B antigenaemia. British Medical Journal 3(5929): 495-497
Barreyro, D.A.; Baras, M.; Squires, P.; Walerstein, M.; Yodfat, Y.; Levy, L. 1982: Familial clustering of leprosy patients in an Israeli village. Leprosy Review 53(4): 277-283
Gajwani, B.W.; Devereaux, J.M.; Beg, J.A. 1980: Familial clustering of nasopharyngeal carcinoma. Cancer 46(10): 2325-2327
Niikawa, N.; Kohsaka, S.; Mizumoto, M.; Hamada, I.; Kajii, T. 1983: Familial clustering of situs inversus totalis, and asplenia and polysplenia syndromes. American Journal of Medical Genetics 16(1): 43-47
Katznelson, D.; Gross, S. 1980: Familial clustering of tonsillectomies and adenoidectomies. Clinical Pediatrics 19(4): 276-283
Trimarchi, F.; Carella, G.; Asperti, G. 1968: Familial coexistence of Stargardt's disease and pigmented retinal degeneration. Annali di Ottalmologia E Clinica Oculistica 94(7): 787-792
Fallet, G.H.; Meyer, E.; Ott, H.; Radi, I. 1970: Familial coexistence of chronic inflammatory polyarthropathy with sacro-iliac joint involvement. Revue du Rhumatisme et des Maladies Osteo-Articulaires 37(3): 213-224
Malbrel, C.; Jouhaud, F. 1982: Familial coexistence of dyschromatopsia and tapetoretinal degeneration. Bulletin des Societes d'Ophtalmologie de France 82(5): 645-647
Tindall, J.P.; Beeker, S.K.; Rosse, W.F. 1969: Familial cold urticaria. a generalized reaction involving leukocytosis. Archives of Internal Medicine 124(2): 129-134
Roux, H.; Gaborit, P.; Chabrier, P.; Sayag, J.; Weiller, M. 1982: Familial cold urticaria. Apropos of a case. Revue du Rhumatisme et des Maladies Osteo-Articulaires 49(2): 131-135
Kalogeromitros, D.; Katsarou, A.; Armenaka, M.; Polizou, E.; Zografakis, I.; Stratigos, I. 1995: Familial cold urticaria: a father and daughter with typical clinical and laboratory features. Annals of Allergy Asthma and Immunology: Official Publication of the American College of Allergy Asthma and Immunology 74(4): 295-298
Nagengast, F.M.; Speth, P.A.; van Tongeren, J.H. 1984: Familial colon carcinoma. Nederlands Tijdschrift Voor Geneeskunde 128(17): 796-800
Johansen, J.K.; Nielsen, R. 1971: Familial colon polyposis. Nordisk Medicin 86(38): 1111
Dhawan, V.K.; Thadepalli, H.; Ulmer, D.D.; Akhtar, A. 1983: Polymicrobial septicemia after liver biopsy. Western Journal of Medicine 139(3): 376-378
Burg, L.; Golubović, G.; Malbaŝić, V.; Boromisa, D.; Teodorović, J. 1980: Familial colonic polyposis. 2 case reports. Srpski Arhiv Za Celokupno Lekarstvo 108(9): 943-948
Macrae, F.A.; Roberts-Thomson, I.C.; Russell, D.M.; St John, D.J. 1981: Familial colorectal cancer and hereditary brachydactyly. British Medical Journal 282(6274): 1431-1432
Cortner, J.A.; Coates, P.M.; Liacouras, C.A.; Jarvik, G.P. 1994: Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and management. Current Problems in Pediatrics 24(9): 295-305
Merimee, T.J. 1980: Familial combined hyperlipoproteinemia. Evidence for a role of growth hormone deficiency in effecting its manifestation. Journal of Clinical Investigation 65(4): 829-835
Glueck, C.J.; Fallat, R.; Buncher, C.R.; Tsang, R.; Steiner, P. 1973: Familial combined hyperlipoproteinemia: studies in 91 adults and 95 children from 33 kindreds. Metabolism, Clinical and Experimental 23(2): 1403-1428
Bedi, T.R.; Bhutani, L.K. 1974: Familial comedones (a case report). Indian Journal of Dermatology 20(1): 6-7
Bradnan, W.A.; Talmage, J.B.; Van Sickle, G.R. 1972: Familial communicational patterns of a patient with Gilles-De-La-Tourette syndrome. Journal of Nervous and Mental Disease 154(1): 60-68
Anonymous 1967: Familial concentration of ischaemic heart disease. British Medical Journal 2(5543): 4-5
Philpot, J.; Topaloglu, H.; Pennock, J.; Dubowitz, V. 1995: Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy. Neuromuscular Disorders: Nmd 5(3): 227-231
Namba, T.; Grob, D. 1970: Familial concurrence of myasthenia gravis and rheumatoid arthritis. Archives of Internal Medicine 125(6): 1056-1058
Bernard, R.; Giraud, F.; Mattéi, J.F. 1972: Familial condensing osteopathy with leontiasis ossium. Archives Francaises de Pediatrie 29(4): 447
Marill, F.G.; Mérioua, M.A.; Sayag, J.; Ysmaïl-Dahlouk, M. 1970: Familial conditions of xeroderma pigmentosum in Algeria. Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 77(6): 837-841
Klint, R.; Hernandez, A.; Bloom, M. 1972: Familial conduction disturbance. American Journal of Cardiology 30(4): 450-451
Donaldson, M.D.; Grant, D.B.; O'Hare, M.J.; Shackleton, C.H. 1981: Familial congenital Cushing's syndrome due to bilateral nodular adrenal hyperplasia. Clinical Endocrinology 14(5): 519-526
Brook, C.G.; Bambach, M.; Zachmann, M.; Prader, A. 1973: Familial congenital adrenal hypoplasia. Helvetica Paediatrica Acta 28(4): 277-282
Seeliger, H.; Koch, H.R. 1968: Familial congenital adrenal hypoplasia with failure of the adrenal cortex. Verhandlungen der Deutschen Gesellschaft für Pathologie 52: 481-485
Rezza, E.; Iannaccone, G.; Lendvai, D. 1984: Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings. Pediatric Radiology 14(5): 323-327
Polse, K.A.; Harris, M.G.; Rosen, N.J. 1974: Familial congenital coralliform cataract. American Journal of Optometry and Physiological Optics 51(10): 770-773
Norio, R.; Kääriäinen, H.; Rapola, J.; Herva, R.; Kekomäki, M. 1984: Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment. American Journal of Medical Genetics 17(2): 471-483
Klein, R.; Haddow, J.E.; DeLuca, C. 1972: Familial congenital disorder resembling stiff-man syndrome. American Journal of Diseases of Children 124(5): 730-731
Mishalany, H.G.; Der Kaloustian, V.M.; Ghandour, M. 1970: Familial congenital duodenal atresia. Pediatrics 46(4): 629-632
Cedrato, A.E.; Traversaro, N.R.; Hojman, D. 1965: Familial congenital dysproteinemia. Pediatria Panamericana 10(3): 92-94
Goette, D.K. 1974: Familial congenital epidermolytic hyperkeratosis confined to the palms and soles. Southern Medical Journal 67(9): 1126-1128
Van Staey, M.; De Bie, S.; Matton, M.T.; De Roose, J. 1984: Familial congenital esophageal atresia. Personal case report and review of the literature. Human Genetics 66(2-3): 260-266
Tango, M.; Ujiie, A.; Ishikawa, N.; Yasukouchi, T. 1965: Familial congenital factor V deficiency (parahemophilia). Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 54(7): 816-820
Hower, J.; Göbel, F.J.; Rüttner, J.R.; Wurster, K. 1971: Familial congenital generalized fibromatosis in two half-sisters. Schweizerische Medizinische Wochenschrift 101(38): 1381-1385
Jerndal, T. 1968: Familial congenital glaucoma with dominant heredity. Acta Ophthalmologica 46(3): 459-462
Cooke, R.W.; Mettau, J.W.; Van Cappelle, A.W.; de Villeneuve, V.H. 1980: Familial congenital heart block and hydrops fetalis. Archives of Disease in Childhood 55(6): 479-480
Akhunbaeva, N.I.; Dzhumadilov, S.D. 1972: Familial congenital heart defects. Sovetskoe Zdravookhranenie Kirgizii 3: 58-59
German, J.; Ehlers, K.H.; Engle, M.A. 1966: Familial congenital heart disease. II. Chromosomal studies. Circulation 34(3): 517-523
Rappaport, R.; Dray, F.; Legrand, J.C.; Royer, P. 1968: Familial congenital hypoaldosteronism caused by 18-OH-dehydrogenase deficiency. Pediatric Research 2(6): 456-463
Nakamura, J.; Kanahara, K.; Endo, Y. 1984: Familial congenital hypoplasia of the thumb--report on a family. Journal of Hand Surgery 9(2): 145-148
Velázquez-Ferrari, M.; González-Jiménez, Y.; Lisker, R. 1971: Familial congenital hypothyroidism without goiter. Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 23(3): 199-205
Schmidseder, R.; Hausamen, J.E. 1973: Familial congenital occurrence of multiple odontomas. Deutsche Zahnarztliche Zeitschrift 28(5): 628-632
Redding, F.K. 1970: Familial congenital ocular motor apraxia. Neurology 20(4): 405
Narbona, J.; Crisci, C.D.; Villa, I. 1980: Familial congenital ocular motor apraxia and immune deficiency. Archives of Neurology 37(5): 325
Craigen, M.A.; Clarke, N.M. 1995: Familial congenital pseudarthrosis of the ulna. Journal of Hand Surgery 20(3): 331-332
Sansaricq, C.; Chen, W.J.; Manka, M.; Davis, D.; Snyderman, S. 1984: Familial congenital short small bowel with associated defects. a long-term survival. Clinical Pediatrics 23(8): 453-455
Figueroa, R.; Rivera, M.; Tamburrino, E.; Moroso, M. 1983: Familial congenital spherocytosis. Revista Chilena de Pediatria 54(5): 340-344
Kotoulas, K.; Salaminios, F. 1970: Familial congestion of a Zenker diverticulum. Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 112(3): 411-412
Shul'ga, I.D.; Baru, I.M.; Brynzevich, A.K. 1983: Familial congestive cardiomyopathy. Terapevticheskii Arkhiv 55(10): 75-76
Kishimoto, C.; Fujiwara, H.; Kaburagi, T.; Yokoyama, S.; Takayama, S.; Tomimoto, K.; Taneichi, Y.; Matsumoto, S.; Murakami, T. 1982: Familial congestive cardiomyopathy with positive rheumatoid factor. Report of one family. Japanese Circulation Journal 46(3): 303-309
Ni, S.Z. 1980: Familial congestive-dilatative type of cardiomyopathy. Zhonghua Nei Ke Za Zhi 19(1): 42-44
Fanconi, G. 1967: Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects. Seminars in Hematology 4(3): 233-240
Schmid, W. 1967: Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia. Seminars in Hematology 4(3): 241-249
Heid, E.; Ben Harbit, R.; Lazrak, B. 1983: Familial continual desquamation. Annales de Dermatologie et de Venereologie 110(2): 141-143
Kurban, A.K.; Azar, H.A. 1969: Familial continual skin peeling. British Journal of Dermatology 81(3): 191-195
Petrovicz, E.; Busa, M.; Méhes, K. 1982: Familial copper deficiency. Orvosi Hetilap 123(30): 1855-1857
Dałkowska, A.; Pecoldowa, K. 1981: Familial corneal degeneration--type Reis-Bücklers. Klinika Oczna 83(10-12): 515-518
Hirst, L.W.; Farmer, E.R.; Green, W.R.; Silver, A.; Walsh, F.B. 1984: Familial corneal scarring: a new dystrophy?. Ophthalmology 91(2): 174-178
Greenberg, I.M.; Rosenberg, G. 1966: Familial correlates of the 14 and 6 cps EEG positive spike pattern. Psychiatric Research Reports 20: 121-131
Thomas, H. 1983: Familial correlational analyses, sex differences, and the X-linked gene hypothesis. Psychological Bulletin 93(3): 427-440
Fernández Piqueras, J.; Santos, J.; Visedo, G.; Pérez de Castro, I.; Puertollano, R.; Montejo, J.; Ramo Tello, C.; Valle, J. 1995: Familial cosegregation of manic-depressive illness and a form of hereditary cerebellar ataxia. American Journal of Medical Genetics 60(3): 206-209
Lejeune, E.; Anjou, A.; Bouvier, M.; Robert, J.; Vauzelle, J.L.; Jeanneret, J. 1966: Familial cranio-metaphyseal dysplasia. Revue du Rhumatisme et des Maladies Osteo-Articulaires 33(12): 714-726
Kernohan, D.C.; Nevin, N.C.; Dodge, J.A. 1970: Familial craniosynostosis with oral anomalies. Developmental Medicine and Child Neurology 12(3): 315-320
Blehová, B. 1968: Familial cretinism with goiter--an inborn metabolic error. Ceskoslovenska Pediatrie 23(2): 134-137
Berliner, S.; Weinberger, A.; Zamir, R.; Hazaz, B.; Pinkhas, J. 1984: Familial cryoglobulinemia and C4 deficiency. Scandinavian Journal of Rheumatology 13(2): 151-154
Partington, M.W.; Marriott, P.J.; Prentice, R.S.; Cavaglia, A.; Simpson, N.E. 1981: Familial cutaneous amyloidosis with systemic manifestations in males. American Journal of Medical Genetics 10(1): 65-75
Nair, B.K. 1973: Familial cutaneous leiomyoma. Indian Journal of Pathology and Bacteriology 16(3): 75-77
Valdivia, L.; Temiño, M.A.; Tuñon, M.; Sandoval, C.; Quintanilla, E. 1983: Familial cutaneous leiomyomas and their association with uterine myoma. Study of a 3-generation pedigree. Medicina Cutanea Ibero-Latino-Americana 11(2): 133-138
Thyresson, H.N.; Su, W.P. 1981: Familial cutaneous leiomyomatosis. Journal of the American Academy of Dermatology 4(4): 430-434
Greene, M.H.; Goldin, L.R.; Clark, W.H.; Lovrien, E.; Kraemer, K.H.; Tucker, M.A.; Elder, D.E.; Fraser, M.C.; Rowe, S. 1983: Familial cutaneous malignant melanoma: autosomal dominant trait possibly linked to the Rh locus. Proceedings of the National Academy of Sciences of the United States of America 80(19): 6071-6075
Rocha, G.L.; Lobato, R.M. 1970: Familial cutaneous mastocytosis. Anais Brasileiros de Dermatologia 45(4): 317-324
Baden, H.P. 1965: Familial cutaneous papillomatosis. Archives of Dermatology 92(4): 394-395
Kallistratos, G.; Dimopoulos, C.; Kalfakakou-Vadalouka, V.; Evangelou, A.; Stockidis, D.; Vezyraki, P.; Charalambopoulos, C.; Mita, I. 1983: Familial cystinuria in Ioannina District (Greece). Diagnosis and treatment. Urological Research 11(6): 291-296
Hay, I.D.; Smail, P.J.; Forsyth, C.C. 1981: Familial cytomegalic adrenocortical hypoplasia: an X-linked syndrome of pubertal failure. Archives of Disease in Childhood 56(9): 715-721
Falek, A.; Schmidt, R.; Jervis, G.A. 1966: Familial de Lange syndrome with chromosome abnormalities. Pediatrics 37(1): 92-101
Beratis, N.G.; Hsu, L.Y.; Hirschhorn, K. 1971: Familial de Lange syndrome. Report of three cases in a sibship. Clinical Genetics 2(3): 170-176
Walbaum, R.; Fontaine, G.; Lienhardt, J.; Piquet, J.J. 1970: Familial deafness with osteo-onycho-dysplasia. Journal de Genetique Humaine 18(1): 101-108
Micheels, K.H.; Weirich, J. 1967: Familial defect dysproteinemia with antibody deficiency syndrome. Das Deutsche Gesundheitswesen 22(47): 2212-2220
Sack, E.; Doglio, G.; Buraschi, J. 1970: Familial defect of platelet adhesion and aggregation. Medicina 30(4): 330-348
McLean, R.H.; Peter, G.; Gold, R.; Guerra, L.; Yunis, E.J.; Kreutzer, D.L. 1981: Familial deficiency of C5 in humans: intact but deficient alternative complement pathway activity. Clinical Immunology and Immunopathology 21(1): 62-76
Kübler, W.; Kuhn, H.; Mertens, H.M.; Seipel, L. 1971: Familial deficiency of NADH-dependent methemoglobin-reductase associated with glycerin-1-phosphate-dehydrogenase activity in the erythrocytes. Klinische Wochenschrift 49(23): 1294-1298
Norum, R.A.; Lakier, J.B.; Goldstein, S.; Angel, A.; Goldberg, R.B.; Block, W.D.; Noffze, D.K.; Dolphin, P.J.; Edelglass, J.; Bogorad, D.D.; Alaupovic, P. 1982: Familial deficiency of apolipoproteins A-I and C-III and precocious coronary-artery disease. New England Journal of Medicine 306(25): 1513-1519
Gonzalo, G.B.; Lucia, R.O.; Alejandro, V.G.; Pablo, L.V. 1973: Familial deficiency of factor X. Sangre 18(2): 178-189
Jørgensen, K.A.; Pedersen, R.S. 1981: Familial deficiency of prostacyclin production stimulating factor in the hemolytic uremic syndrome of childhood. Thrombosis Research 21(3): 311-315
Wehinger, H.; Karitzky, D.; Witt, I. 1971: Familial deficiency on alpha-1-antitrypsin. Zeitschrift für Kinderheilkunde 110(2): 115-127
Pigrau, C.; Galve, E.; Ocaña, I.; Capdevila, J.A.; Ribera, E.; Martínez-Vázquez, J.M. 1984: Familial deficit of antithrombin IIi and mitral valve prolapse. Medicina Clinica 83(1): 43
Kozlowski, B. 1974: Familial degeneration of the anterior cornea. Klinika Oczna 44(7): 707-710
Antonioli, G.; Zanardi, F.; D'Agostino, F.; Masoni, A. 1973: Familial degeneration of the conduction system. Giornale Italiano di Cardiologia 3(4): 519-529
Zaleski, T. 1966: Familial delayed development of speech. Otolaryngologia Polska 20(2): 367-371
Parker, C.E.; Koch, R.; Mavalwala, J.; Derencsenyi, A.; Hatashita, A. 1969: Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity. Clinical Pediatrics 8(8): 453-458
Kim, R.C.; Collins, G.H.; Parisi, J.E.; Wright, A.W.; Chu, Y.B. 1981: Familial dementia of adult onset with pathological findings of a 'non-specific' nature. Brain: a Journal of Neurology 104(Part 1): 61-78
Winokur, G.; Coryell, W.; Endicott, J.; Akiskal, H.; Keller, M.; Maser, J.D.; Warshaw, M. 1995: Familial depression versus depression identified in a control group: are they the same?. Psychological Medicine 25(4): 797-806
Alawi, M.H.; Hobby, J.A.; Lesna, M. 1982: Familial dermal cylindroma with involvement of the parotid gland. British Journal of Plastic Surgery 35(2): 167-170
Matton, M.; De Bie, S.; Anseeuw, A. 1981: Familial dermatoglyphic analysis in syndactyly type i. Journal of Hand Surgery 6(6): 537-542
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Esparza, A.; Thompson, W.R. 1966: Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome)--report of three cases. Cases presented are of two sisters and a female cousin with complete clinical and post mortem findings. Rhode Island Medical Journal 49(2): 103-110
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Caraceni, T.; Broggi, G.; Avanzini, G. 1974: Familial idiopathic basal ganglia calcification exhibiting "dystonia musculorum deformans" features. European Neurology 12(5-6): 351-359
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Wenzel, A.; Hørsted, P. 1984: Familial idiopathic generalized root resorption. Tandlaegebladet 88(14): 475-479
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Toledo, S.P.; Luthold, W.; Mattar, E. 1983: Familial idiopathic gonadotropin deficiency: a hypothalamic form of hypogonadism. American Journal of Medical Genetics 15(3): 405-416
Mărgineanu, O.; Miu, N.; Szantay, V.; Acalovschi, R. 1974: Familial idiopathic hyperlipemis: diagnostic and therapeutic considerations. Pediatria 23(1): 73-78
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Nagler, H.M.; deVere White, R.; Roberts, M. 1984: Familial idiopathic priapism: a case report. Journal of Urology 131(3): 542-543
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Melli, G.; Mazzei, D.; Invernizzi, F. 1972: Familial immunoglobulin anomalies in paraproteinemic diseases. Minerva Medica 63(22): 1257-1273
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Vandalem, J.L.; Pirens, G.; Hennen, G. 1981: Familial inappropriate TSH secretion: evidence suggesting a dissociated pituitary resistance to T3 and T4. Journal of Endocrinological Investigation 4(4): 413-422
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Vicenzi, G. 1981: Familial incidence in two cases of aneurysmal bone cyst. Italian Journal of Orthopaedics and Traumatology 7(2): 251-253
Constantinidis, J.; Garrone, G.; Tissot, R.; De Ajuriaguerra, J. 1965: Familial incidence of Alzheimer's cortical neurofibrillar changes. Psychiatria et Neurologia 150(4): 235-247
Bürger, L.; Karoff, C.; Wagner, H. 1981: Familial incidence of Crohn disease. Fortschritte der Medizin 99(10): 340-341
Goetz, P.; Svagrová, E.; Seemanová, E.; Macek, M. 1973: Familial incidence of Down's disease. Ceskoslovenska Pediatrie 28(2): 81-83
Friel, P.B. 1973: Familial incidence of Gilles de la Tourette's disease, with observations on aetiology and treatment. British Journal of Psychiatry: the Journal of Mental Science 122(571): 655-658
Vettori, G.; Erle, G. 1967: Familial incidence of Hodgkin's disease. Archivio "e. Maragliano" di Patologia E Clinica 23(3): 391-394
Kossakiewicz, B. 1967: Familial incidence of Leptospira canicola infections and Weil's disease and diagnostic difficulties in differentiation from Heine-Medina disease. Wiadomosci Lekarskie 20(8): 737-739
Ruzsonyi, Z.; Balogh, J. 1973: Familial incidence of Pasteurella pseudotuberculosis infection. Orvosi Hetilap 114(21): 1248-1250
Libshitz, H.I.; Barth, K.H. 1974: Familial incidence of atrial septal defect. A report of four siblings and review of the literature. Chest 65(1): 56-58
Simon, L.; Bajtai, A.; Szabó, E.; Figus, I.A. 1980: Familial incidence of benign recurrent intrahepatic cholestasis. Orvosi Hetilap 121(45): 2771-2774
Atwell, J.D.; Cook, P.L.; Howell, C.J.; Hyde, I.; Parker, B.C. 1974: Familial incidence of bifid and double ureters. Archives of Disease in Childhood 49(5): 390-393
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Morell, F.; Morera, J.; Orriols, R.; Mercader, J.; Aranda, A. 1981: Familial incidence of bird-breeder's lung and HLA. Medicina Clinica 76(5): 221-222
Winzeler, M.; Braun, P.; Grob, P.J. 1974: Familial incidence of bronchiectasis and alpha-1 antitrypsin deficiency. Schweizerische Medizinische Wochenschrift 104(48): 1705-1711
Péc, J.; Lányi, A.; Kliment, J. 1984: Familial incidence of carcinoma of the kidney in patients with von Hippel-Lindau disease. Bratislavske Lekarske Listy 81(4): 465-471
Chakravorty, B.; Gleadhill, C.A. 1966: Familial incidence of cerebral aneurysms. British Medical Journal 1(5480): 147-148
Cooper, W. 1968: Familial incidence of cerebral palsy. Developmental Medicine and Child Neurology 10(2): 250
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Troconis Rodríguez, O. 1965: Familial incidence of certain congenital urinary anomalies. Revista Venezolana de Urologia 17(3): 321-326
Koblík, J.; Dvorák, J. 1980: Familial incidence of congenital alopecia and hypotrichosis. Ceskoslovenska Dermatologie 55(3): 196-201
Schwoebel, M.G.; Hirsig, J.; Schinzel, A.; Stauffer, U.G. 1984: Familial incidence of congenital anorectal anomalies. Journal of Pediatric Surgery 19(2): 179-182
Fendel, K. 1966: Familial incidence of congenital choanal atresia. Zeitschrift für Laryngologie Rhinologie Otologie und ihre Grenzgebiete 45(2): 67-73
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Brodanová, M.; Balas, V.; Bednr, B.; Blazek, O. 1981: Familial incidence of congenital hepatic fibrosis. Casopis Lekaru Ceskych 120(41): 1258-1261
Kartagener, M.; Wyler, J. 1966: Familial incidence of double malignancies. Schweizerische Medizinische Wochenschrift 96(7): 218-219
Blazovský, J.; Buchvald, J. 1973: Familial incidence of favus in 3 generations. Ceskoslovenska Dermatologie 48(2): 103-107
Frank, K.; Solymoss, B. 1966: Familial incidence of fructose intolerance. Orvosi Hetilap 107(40): 1893-1895
Chynoranský, M.; Gerinec, A. 1983: Familial incidence of granular corneal dystrophy. Ceskoslovenska Oftalmologie 39(4): 240-243
Cekovský, L.; Böör, A.; Veréb, J.; Liba, J.; Kasprisin, V. 1983: Familial incidence of infantile arterial calcification. Ceskoslovenska Pediatrie 38(11): 658-661
Feinstein, R.; Fahrländer, H. 1972: Familial incidence of intestinal carcinoma. Schweizerische Medizinische Wochenschrift 102(46): 1687-1692
Novaes, V.; Campos, J.S.; Pereira, G.A. 1973: Familial incidence of intracranial aneurysms. Arquivos de Neuro-Psiquiatria 31(3): 171-179
Miyai, K.; Azukizawa, M.; Kumahara, Y. 1974: Familial incidence of isolated TSH deficiency. Nihon Rinsho. Japanese Journal of Clinical Medicine 32(7): 2411-2413
Stevens, P.R.; Macfadyen, W.A. 1972: Familial incidence of juvenile diabets mellitus, progressive optic atrophy, and neurogenic deafness. British Journal of Ophthalmology 56(6): 496-500
Gathright, J.B.; Cofer, T.W. 1974: Familial incidence of juvenile polyposis coli. Surgery Gynecology and Obstetrics 138(2): 185-188
Sakal, V.; Sakalová, A.; Izakovic, V. 1972: Familial incidence of kidney cysts with liver cirrhosis, portal hypertension and hypersplenism (including chromosome analysis). Zeitschrift für Urologie und Nephrologie 65(9): 679-682
Grimstvedt, M. 1969: Familial incidence of malignant melanoma. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 89(24): 1900-1902
Agarwal, R.P.; Goel, M.K. 1980: Familial incidence of osseous lesions in neurofibromatosis. Journal of the Indian Medical Association 74(5): 93-94
Shrivastava, D.K.; Yesikar, S.S. 1965: Familial incidence of osteogenesis imperfecta: seven cases in two families. Indian Pediatrics 2(12): 442-445
Plattner, G.; Oxorn, H. 1973: Familial incidence of ovarian dermoid cysts. Canadian Medical Association Journal 108(7): 892-893
Knapik, Z.; Paczyńska, D.; Zarski, J. 1965: Familial incidence of peptic ulcer. Polski Tygodnik Lekarski 20(21): 769-770
Niebuhr, E.; Seemanová, E.; Losan, F. 1974: Familial incidence of pericentric inversion of X chromosome. Ceskoslovenska Pediatrie 29(5): 245-247
Martínez, J.; Piedrahita, V.; Restrepo, C.; Builes, M.; San Martín, J.E.; Aguilar, L.; de Sánchez, L.M. 1981: Familial incidence of post-streptococcal glomerulonephritis. Boletin Medico del Hospital Infantil de Mexico 38(1): 119-129
Marcheselli, W.; De Panfilis, G. 1971: Familial incidence of psoriasis. Giornale Italiano di Dermatolotia. Minerva Dermatologica 46(12): 543-544
Chmielewski, J.; Janusz, L.; Stasikiewicz-Chmielewska; Gazdowska-Nawrocka, D. 1971: Familial incidence of renal malformations. Wiadomosci Lekarskie 24(22): 2087-2090
Gerinec, A.; Chynoranský, M. 1983: Familial incidence of reticular corneal dystrophy. Ceskoslovenska Oftalmologie 39(4): 235-239
Petersen, B.N. 1969: Familial incidence of sarcoidosis. Ugeskrift for Laeger 131(10): 413-416
Benedikt, O.; Ehalt, H. 1970: Familial incidence of the Bloch-Sulzberger syndrome (Incontinentia pigmenti) with ocular involvement. Klinische Monatsblatter für Augenheilkunde 157(5): 652-663
Zanoio, L. 1969: Familial incidence of the Morris syndrome. Attualita di Ostetricia E Ginecologia 15(2): 109-119
Ionescu, A.; Rugină, V.; Baran, T.; Mărgineanu, L.; Ungureanu, L. 1971: Familial incidence of thyroid functional changes in patients with gonadal dysgenesis. Studii Si Cercetari de Endocrinologie 22(3): 203-214
Buffoni, L.; Centa, A.; Lavia, G. 1965: Familial incidence of "ecto-mesodermal dysplasia" (Ellis-van Creveld syndrome). Study of the syndrome in 3 brothers. Minerva Pediatrica 17(25): 1322-1330
Kamihira, S.; Ichimaru, M.; Kinosita, K.; Yamada, Y. 1982: Familial incidences of adult T-cell leukemia-lymphoma--with special reference to recent observations on 2 families. Japanese Journal of Clinical Hematology 23(4): 464-471
Yokoyama, S.; Matsuda, K.; Hirahara, K.; Asakura, T.; Ichitsubo, H. 1983: Familial incidences of hemangioblastoma of the cerebellum. No Shinkei Geka. Neurological Surgery 11(5): 549-555
Walsh, P.C.; Madden, J.D.; Harrod, M.J.; Goldstein, J.L.; MacDonald, P.C.; Wilson, J.D. 1974: Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias. New England Journal of Medicine 291(18): 944-949
Strasberg, B.; Welch, W.; Palileo, E.; Swiryn, S.; Bauernfeind, R.; Rosen, K.M. 1983: Familial inducible torsade de pointes with normal QT interval. European Heart Journal 4(6): 383-390
Attal, C.; Farkas-Bargeton, E.; Edgar, G.W.; Pham-Huu-Trung; Girard, F.; Mozziconacci, P. 1967: Familial infantile amaurotic idiocy with visceral involvement. Annales de Pediatrie 14(6): 457-465
Schärer, K.; Szabó, J. 1966: Familial infantile cortical hyperostosis with prenatal beginning. Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 105(2): 154-163
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Sevastikoglou, J.A.; Eriksson, I. 1967: Familial infantile osteochondrosis deformans tibiae. Idiopathic tibia vara. A case report. Acta Orthopaedica Scandinavica 38(1): 81-87
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Garagnani, A.; Suriani, L.; Lancellotti, A.; Brillante, C. 1966: Familial infantile splenomegalic hepatic cirrhosis. Study of 2 cases. Archivio Italiano Delle Malattie Dell'apparato Digerente 33(1): 73-104
Graux, C.; Wauters, G. 1966: Familial infection by Yersinia enterocolitica. Acta Clinica Belgica 21(3): 206-215
Yamada, H. 1971: Familial infection routes of fungi in the fields of obstetrics and gynecology. Nihon Sanka Fujinka Gakkai Zasshi 23(6): 501-508
Kurnatowska, A.; Komorowska, A. 1973: Familial infection with T. vaginalis. Wiadomosci Parazytologiczne 19(3): 335-336
Kurnatowska, A. 1973: Familial infections with candida. Dermatologische Monatschrift 159(4): 410-411
Beardslee, W.R. 1984: Familial influences in childhood depression. Pediatric Annals 13(1): 32-36
Le-Tan-Vinh; Tran-Van-Duc; Alcardi, J.; Thieffry, S. 1968: Familial infra-diaphragmatic total abnormal pulmonary venous return. Archives Francaises de Pediatrie 25(10): 1141-1149
Blanc, J.F.; Bouvier, R.; Plauchu, H.; Salle, B. 1981: Familial infradiaphragmatic total anomalous pulmonary venous return. Pediatrie 36(6): 463-468
Linde, R.; Alexander, N.; Island, D.P.; Rabin, D. 1982: Familial insensitivity of the pituitary and periphery to thyroid hormone: a case report in two generations and a review of the literature. Metabolism, Clinical and Experimental 31(5): 510-513
Grace, E.; Sutherland, G.R.; Bain, A.D. 1972: Familial insertional translocation. Lancet 2(7770): 231
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Rüdiger, H.W.; Dreyer, M.; Kühnau, J.; Bartelheimer, H. 1983: Familial insulin-resistant diabetes secondary to an affinity defect of the insulin receptor. Human Genetics 64(4): 407-411
Feldman, R.G.; Iseri, O.A.; Gottlieb, L.S.; Greenberg, J.P. 1969: Familial intention tremor, ataxia, and lipofuscinosis. Liver biopsy studies. Neurology 19(5): 503-509
Miller, M.H.; Kling, A.; Dicks, D. 1973: Familial interactions of male rhesus monkeys in a semi-free-ranging troop. American Journal of Physical Anthropology 38(2): 605-611
Fuster Siebert, M.; Rubio Alvarez, J.; García-Bengochea, J.B. 1983: Familial interatrial communication and long PR. Medicina Clinica 80(19): 862-863
Livingstone, I.R.; Gardner-Medwin, D.; Pennington, R.J. 1984: Familial intermittent ataxia with possible X-linked recessive inheritance. two patients with abnormal pyruvate metabolism and a response to acetazolamide. Journal of the Neurological Sciences 64(1): 89-97
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Perry, K.M.; Benson, M.K.; Hughes, D.T. 1971: Familial interstitial pulmonary fibrosis. Prensa Medica Argentina 58(10): 495-500
Rintala, A.; Norio, R. 1982: Familial intra-areolar polythelia with mammary hypoplasia. Scandinavian Journal of Plastic and Reconstructive Surgery 16(3): 287-291
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Zorrilla Dendarieta, J.M. 1970: Familial intrinsic hypothyroidism (2 brothers) and induced gout crisis caused by opotherapy. Revista Clinica Espanola 119(5): 451-454
Rivera, H.; Alvarez-Arratia, M.C.; Moller, M.; Díaz, M.; Cantú, J.M. 1984: Familial inv(1) (p3500q21.3) associated with azoospermia. Human Genetics 66(2-3): 165-167
Pilgaard, B.; Jørgensen, E.; Knudsen, V.S.; Mortensen, E.; Mikkelsen, M. 1983: Familial inversion translocation (8;13) with partial trisomy 13 in several family members. European Journal of Pediatrics 140(2): 105-108
Kuhlo, W.; Heintel, H.; Reichenmiller, H.E.; Vogel, F. 1969: Familial investigation of the 4-5 c-sec variation of the basic rhythm. Electroencephalography and Clinical Neurophysiology 26(4): 445
Kartaleva, M.; Tzonev, K. 1982: Familial investigations in persons with obesity. Folia Medica 24(3): 36-39
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Comings, D.E.; Skubi, K.B.; Van Eyes, J.; Motulsky, A.G. 1967: Familial multifocal fibrosclerosis. Findings suggesting that retroperitoneal fibrosis, mediastinal fibrosis, sclerosing cholangitis, Riedel's thyroiditis, and pseudotumor of the orbit may be different manifestations of a single disease. Annals of Internal Medicine 66(5): 884-892
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White, I.R.; MacDonald, D.M. 1981: Familial multiple melanocytic naevi--the B-K mole syndrome. Clinical and Experimental Dermatology 6(5): 549-553
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Karpati, G.; Carpenter, S.; Eisen, A.A.; Feindel, W. 1973: Familial multiple peripheral nerve entrapments--an unusual manifestation of a peripheral neuropathy. Transactions of the American Neurological Association 98: 267-269
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