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Section 44

EurekaMag Full Text Articles Chapter 43,112



References:

Cendrowski, W.S. 1966: Familial multiple sclerosis in Poland. 1. Geographical distribution of the disease. Journal of the Neurological Sciences 4(1): 95-99
Escalar, G.; Majeron, M.A. 1969: Familial multiple sclerosis. Case report. Minerva Medica 60(50): 2497-2499
Viparelli, U.; Di Lorenzo, R.; Crispi, G.; Abbate, G. 1965: Familial multiple sclerosis. Clinico-cytogenetic contribution. Considerations on the endogeno-constitutional factor. L'Ospedale Psichiatrico 33(1): 1-40
Kitamoto, T.; Neshige, R.; Kuroda, Y.; Noda, K.; Shibasaki, H. 1984: Familial multiple sclerosis: report of two cases with immunogenetic studies. Rinsho Shinkeigaku 24(2): 159-164
Mishalany, H.G.; Der Kaloustian, V.M. 1971: Familial multiple-level intestinal atresias: report of two siblings. Journal of Pediatrics 79(1): 124-125
Baillet, J.; Gentit, F.; Quiret, J.C.; Lienart, J.; Descombes, P. 1970: Familial mushroom poisoning. 3 cases. Lille Medical: Journal de la Faculte de Medecine et de Pharmacie de l'Universite de Lille 15(4): 676-680
Warrier, C.B.; Pillai, T.D. 1967: Familial myasthenia gravis. British Medical Journal 3(5569): 839-840
Yoshida, T.; Takino, Y.; Yarita, H.; Asato, H.; Ishibashi, H. 1982: Familial myasthenia gravis occurring in a mother and her daughter. Rinsho Shinkeigaku 22(11): 969-971
Rao, B.S.; Sateesh, S.; Baburaj, S.; Mohan Das, P.; Sarkar, N.K.; Arjun Das, G. 1985: Familial myasthenia gravis--a case report. Indian Journal of Pediatrics 52(416): 315-317
Sieff, C.A.; Malleson, P. 1980: Familial myelofibrosis. Archives of Disease in Childhood 55(11): 888-893
Kolarz, G.; Pietschmann, H. 1972: Familial myeloid leukaemias. Wiener Klinische Wochenschrift 84(49): 790-792
Boga, M.; Jákó, J.; Domán, J.; Magyar, E.; Konyár, E. 1973: Familial myeloma. Folia Haematologica 100(3): 201-212
Maldonado, J.E.; Kyle, R.A. 1974: Familial myeloma. Report of eight families and a study of serum proteins in their relatives. American Journal of Medicine 57(6): 875-884
Slee, P.H.; van Everdingen, J.J.; Geraedts, J.P.; te Velde, J.; den Ottolander, G.J. 1981: Familial myeloproliferative disease. Hematological and cytogenetic studies. Acta Medica Scandinavica 210(4): 321-327
Tatti, V.; Marfurt, P.; Sirchia, G.; Pescia, G.; Luscieti, P.; Losa, G. 1984: Familial myeloproliferative syndrome. Schweizerische Medizinische Wochenschrift 114(6): 196-204
Kelemen, J.; Rice, D.R.; Bradley, W.G.; Munsat, T.L.; DiMauro, S.; Hogan, E.L. 1982: Familial myoadenylate deaminase deficiency and exertional myalgia. Neurology 32(8): 857-863
Cristodorescu, R.; Ardeleanu, R.; Drăgulescu, I.; Coreanu, G. 1971: Familial myocardial disease. on 2 clinical cases. Medicina Interna 23(10): 1229-1238
Barriales Ardura, R. 1967: Familial myocardial diseases. Revista Espanola de Cardiologia 20(3): 358-365
Zamora, C.; Eizaguirre, A.J.; Ruipérez, J.A.; Avecillas, E. 1970: Familial myocardial diseases. Study of 14 members of a family. Archivos del Instituto de Cardiologia de Mexico 40(3): 241-250
Takatsu, T.; Kitaura, Y.; Kurimoto, K.; Hori, K. 1974: Familial myocardial diseases: clinical features and postpericardiotomy. Nihon Rinsho. Japanese Journal of Clinical Medicine 32(11): 3364-3375
Nieveen, J.; Huber, J. 1970: Familial myocardial fibrosis. Acta Medica Scandinavica 188(5): 439-445
Noya Del Rio, A.; De Oya, J.C. 1972: Familial myocardiopathy with Wolff-Parkinson-White syndrome. Revista Clinica Espanola 124(3): 299-302
Lucier, K.J.; Movilla, R.V.; Parvizian, M.K.; Siddiqui, R.; Gabriele, E.H.; Bourque, M.; MacIsaac, J.; Moorehead, P.C.; Chan, A.K.; Heddle, N.M.; Lane, S.J. 2018: A brief survey of clinicians' perceptions of parent preferences for involvement in obstetrical and perinatal management decisions in haemophilia. Haemophilia: the Official Journal of the World Federation of Hemophilia 24(2): E80-E83
Hall, J.G.; Preziosi, T.J. 1971: Familial myoclonic epilepsy. Birth Defects Original Article Series 7(1): 227
Stuart, W.H.; Schwartz, J.F.; Mayer, W.B.; Karp, H.E. 1968: Familial myoclonus. Neurology 18(3): 302
May, D.L.; White, H.H. 1968: Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease. Archives of Neurology 19(3): 331-338
Christensen, T.E.; Saxtrup, O.; Hansen, T.I.; Kristensen, B.H.; Beck, B.L.; Plesner, T.; Krogh, I.M.; Andersen, V.; Strandgaard, S. 1983: Familial myoglobinuria. a study of muscle and kidney pathophysiology in three brothers. Danish Medical Bulletin 30(2): 112-115
Genge, A.; Karpati, G.; Arnold, D.; Shoubridge, E.A.; Carpenter, S. 1995: Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease. Neuromuscular Disorders: Nmd 5(2): 139-144
Cancilla, P.A.; Kalyanaraman, K.; Verity, M.A.; Munsat, T.; Pearson, C.M. 1971: Familial myopathy with probable lysis of myofibrils in type i fibers. Neurology 21(6): 579-585
Saunders, M.; Ashworth, B.; Emery, A.E.; Benedikz, J.E. 1968: Familial myotonic periodic paralysis with muscle wasting. Brain: a Journal of Neurology 91(2): 295-304
Sher, J.H.; Rimalovski, A.B.; Athanassiades, T.J.; Aronson, S.M. 1967: Familial myotubular myopathy: a clinical, pathological, histochemical, and ultrastructural study. Journal of Neuropathology and Experimental Neurology 26(1): 132-133
Monk, B.E.; Vollum, D.I. 1982: Familial naevus sebaceus. Journal of the Royal Society of Medicine 75(8): 660-661
Herrera Pombo, J.L.; Lozano, I.; Ruíz-Valdepeñas, P.; Arrieta, F.; Rodríguez-Miñon, J.L. 1973: Familial nanism with high levels of immunoreactive STH. Revista Clinica Espanola 131(2): 149-152
Igarashi, S.; Koyama, T.; Shimosaka, S.; Uchibori, M. 1982: Familial narrow spinal canal (lumbar canal stenosis with narrow cervical canal): case reports of three brothers. No Shinkei Geka. Neurological Surgery 10(9): 961-966
Fischer, A.; Fischer, G.O.; Cooper, E. 1984: Familial nasopharyngeal carcinoma. Pathology 16(1): 23-24
Reisberg, B.; deLeon, M.J.; Ferris, S.H. 1984: Familial nature of Alzheimer's disease?. New England Journal of Medicine 311(20): 1318-1319
Dimitrov, T. 1983: Familial nature of Balkan endemic nephropathy. Vutreshni Bolesti 22(5): 63-65
Cazzato, G.; Zorzon, M. 1983: Familial nature of acute cerebral vasculopathies of the ischemic type. Rivista di Neurologia 53(6): 359-368
Nora, J.J.; Meyer, T.C. 1966: Familial nature of congenital heart diseases. Pediatrics 37(2): 329-334
Vaudour, G.; Leballe, J.C.; Beauvais, P.; Costil, J.; Brissaud, H.E. 1974: Familial neo-natal thrombopenic purpura with cerebro-meningeal hemorrhage by feto-maternal allo-immunization. Archives Francaises de Pediatrie 31(1): 37-57
Zonana, J.; Silvey, K.; Strimling, B. 1984: Familial neonatal and infantile seizures: an autosomal-dominant disorder. American Journal of Medical Genetics 18(3): 455-459
Suton, R.A. 1968: Familial neonatal hypoproteinaemia. Proceedings of the Royal Society of Medicine 61(3): 288-289
Matsuura, N.; Yamada, Y.; Nohara, Y.; Konishi, J.; Kasagi, K.; Endo, K.; Kojima, H.; Wataya, K. 1980: Familial neonatal transient hypothyroidism due to maternal TSH-binding inhibitor immunoglobulins. New England Journal of Medicine 303(13): 738-741
Caroti Ghelli, C.; Presciuttini, S.; Scarcello, E.; Vannucci, L.; Mosca, F. 1994: Familial neoplasms: investigation of genealogic trees of patients surgically treated for colonic adenocarcinoma. Annali Italiani di Chirurgia 65(5): 517-526
Di Vagno, G.; Nacci, G.; Cormio, G.; Loverro, G. 1994: Familial neoplastic syndromes of the ovary. a family study. Minerva Ginecologica 46(10): 571-574
Kusunoki, N.; Tamaki, S. 1966: Familial nephritis. Nihon Rinsho. Japanese Journal of Clinical Medicine 24(4): 668-673
Oknińska, A.; Szotowa, W.; Szczypiorski, K.; Wróblewska, E. 1970: Familial nephro-uropathies. Wiadomosci Lekarskie 23(8): 617-625
Dyszy-Laube, B.; Glyda, J.; Sekowska-Zmuda, J.; Wojnarowski, M. 1971: Familial nephronophthisis (medullary cystic disease). Pediatria Polska 46(12): 1537-1540
Afanasenko, P.P. 1971: Familial nephropathies. Pediatriia 50(4): 30-33
Ignatova, M.S.; Briskina, M.M.; Fokeeva, V.V.; Artemkina, L.N. 1970: Familial nephropathies in children. Pediatriia 49(2): 8-13
Acecka, H.; Dowbor, B. 1972: Familial nephropathy. Wiadomosci Lekarskie 25(2): 133-136
Dubach, U.C.; Minder, F.C.; Antener, I. 1966: Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland. Helvetica Medica Acta 33(1): 36-43
Gekle, D.; Essler, H.; Brunner, H. 1969: Familial nephropathy and impaired sound perception (Alport syndrome). Archiv für Kinderheilkunde 178(3): 290-302
Kobierska-Szczepańska, A.; Jończyk, K.; Dziuba, P. 1974: Familial nephropathy in the light of cases at the Department of Pediatrics at Zabrze. Polski Tygodnik Lekarski 29(6): 233-234
Pohorecka-Zagroba, L.; Twardowski, Z. 1974: Familial nephropathy in the light of observed cases. Polski Tygodnik Lekarski 29(33): 1433-1435
Leumann, E.P.; Wegmann, W. 1983: Familial nephropathy with hyperuricemia and gout. Nephron 34(1): 51-57
Hanicki, Z.; Hanicka, M.; Miezyński, W. 1970: Familial nephropathy with neurogenic hypoacusia (Alport's syndrome). Polskie Archiwum Medycyny Wewnetrznej 45(5): 635-639
Chandra, M.; Mouradian, J.; Hoyer, J.R.; Lewy, J.E. 1981: Familial nephrotic syndrome and focal segmental glomerulosclerosis. Journal of Pediatrics 98(4): 556-560
Burke, E.C.; Holley, K.E.; Stickler, G.B. 1973: Familial nephrotic syndrome with nephrocalcinosis and tubular dysfunction. Journal of Pediatrics 82(2): 202-206
Trefz, F.K.; Schmidt, H.; Hammersen, G.; Helmstädter, V.; Bolkenius, M. 1980: Familial nesidioblastosis. Monatsschrift für Kinderheilkunde 128(5): 337-338
Vance, J.E.; Stoll, R.W.; Kitabchi, A.E.; Buchanan, K.D.; Hollander, D.; Williams, R.H. 1972: Familial nesidioblastosis as the predominant manifestation of multiple endocrine adenomatosis. American Journal of Medicine 52(2): 211-227
Konigsmark, B.W.; Hollander, M.B.; Berlin, C.I. 1968: Familial neural hearing loss and atopic dermatitis. JAMA 204(11): 953-957
Geiger, L.R.; Mancall, E.L.; Penn, A.S.; Tucker, S.H. 1974: Familial neuralgic amyotrophy. Report of three families with review of the literature. Brain: a Journal of Neurology 97(1): 87-102
Nakamura, Y. 1982: Familial neuroaxonal dystrophy with principal lesions of nigro-pallido-subthalamic degeneration. Folia Psychiatrica et Neurologica Japonica 36(2): 151-162
Feingold, M.; Gheradi, G.J.; Simons, C. 1971: Familial neuroblastoma and trisomy 13. American Journal of Diseases of Children 121(5): 451
Klein, H.; Plöchl, E. 1974: Familial neuroblastoma of the suprarenal glands in the newborn. Münchener Medizinische Wochenschrift 116(23): 1163-1168
Griffin, M.E.; Bolande, R.P. 1969: Familial neuroblastoma with regression and maturation to ganglioneurofibroma. Pediatrics 43(3): 377-382
Chatten, J.; Voorhess, M.L. 1967: Familial neuroblastoma. Report of a kindred with multiple disorders, including neuroblastomas in four siblings. New England Journal of Medicine 277(23): 1230-1236
Hardy, P.C.; Nesbit, M.E. 1972: Familial neuroblastoma: report of a kindred with a high incidence of infantile tumors. Journal of Pediatrics 80(1): 74-77
Willshaw, M.E.; Pérez, M.; Lacassie, Y. 1982: Familial neurocutaneous melanosis. Revista Chilena de Pediatria 53(5): 443-446
Iampol'skaia, G.I. 1972: Familial neurofibromatosis with unusual clinical manifestations. Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 72(6): 841-846
Vital, C.; Julien, J.; Vallat, J.M.; Le Blanc, M. 1970: Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study. Revue Neurologique (Paris) 122(1): 15-28
Bank, W.J.; Morrow, G. 1971: Familial neuromuscular disease with nonketotic hyperglycinemia. Transactions of the American Neurological Association 96: 21-23
Meyers, K.R.; Golomb, H.M.; Hansen, J.L.; McKusick, V.A. 1974: Familial neuromuscular disease with "myotubes". Clinical Genetics 5(4): 327-337
Di Piazza, P.; Rasi, F.; Neri, W.; Govoni, E.; Martinelli, P. 1982: Familial neuropathy with a tendency toward compression paralysis: problems in differential diagnosis from occupational neuropathies. Rivista di Neurobiologia: Organo Ufficiale Della Societa Dei Neurologi Neuroradiologi e Neurochirurghi Ospedalieri 28(3-4): 535-543
Jedrzejowska, H.; Hausmanowa-Petrusewicz, I. 1981: Familial neuropathy with liability to pressure palsies. Report of a case. Italian Journal of Neurological Sciences 2(3): 229-236
Serrate, A. 1966: Familial neuroses. Archivos de Neurobiologia 29(2): 119-124
Feroli, E.J. 1967: Familial neutropenia. Report of six cases in one family. Medical Annals of the District of Columbia 36(12): 742
Chadfield, H.W. 1969: Familial non-allergic angioneurotic oedema. Proceedings of the Royal Society of Medicine 62(6): 588-590
Van Baars, F.; van den Broek, P.; Cremers, C.; Veldman, J. 1981: Familial non-chromaffinic paragangliomas (glomus tumors) : clinical aspects. Laryngoscope 91(6): 988-996
Hooft, C.; De Hauwere, R.; Van Acker, K.J. 1968: Familial non-congenital microcephaly, peculiar appearance, mental and motor retardation, progressive evolution to spasticity and choreo-athetosis. Helvetica Paediatrica Acta 23(1): 1-12
Martoni, L.; Paolucci, G. 1968: Familial non-hemolytic hyperbilirubinemia. Minerva Medica 59(36): 2127-2128
Lucey, J.F. 1969: Familial non-hemolytic jaundice: light therapy. Pediatrics 43(5): 909-910
Fielding, J.F. 1969: Familial non-polypotic carcinoma of colon. British Medical Journal 1(5642): 512-513
Bethlem, J.; van Gool, J.; Hülsmann, W.C.; Meijer, A.E. 1966: Familial non-progressive myopathy with muscle cramps after exercise. a new disease associated with cores in the muscle fibres. Brain: a Journal of Neurology 89(3): 569-588
Austen, K.F. 1965: Familial nonallergic angioneurotic edema (C'1 esterase inhibitor deficiency). Archives of Dermatology 92(4): 471-472
Blumenschein, S.D.; Kallen, R.J.; Storey, B.; Natzschka, J.C.; Odell, G.B.; Childs, B. 1968: Familial nonhemolytic jaundice with late onset of neurological damage. Pediatrics 42(5): 786-792
Gardner, W.A.; Konigsmark, B.W. 1969: Familial nonhemolytic jaundice: bilirubinosis and encephalopathy. Pediatrics 43(3): 365-376
Perona, G.; Frezza, M.; Leonardi, P.; De Sandre, G. 1967: Familial nonhemolytic jaundice: clinical and morpho-functional observations on 20 patients. Archivio Italiano Delle Malattie Dell'apparato Digerente 34(5): 508-512
Gupta, K.; Chintu, C. 1982: Familial nonhemolytic unconjugated hyperbilirubinemia (Crigler Najjar syndrome) with kernicterus - report of a case in Zambian child. East African Medical Journal 59(3): 225-229
Ito, T.; Suzuki, H.; Yamada, M.; Metoki, K.; Iinuma, K.; Ito, H. 1982: Familial nonprogressive chorea: report of four cases in a family. No to Shinkei 34(8): 775-780
Drets, M.E.; Cardoso, J.H.; Delfino, A.H.; Carrau, J. 1970: Familial normal-partial trisomy 16 with selective endoreduplication in malformed proband. Cytogenetics 9(5): 333-350
Bicanová, J.; Kelbich, J.; Scheihauer, E. 1981: Familial normolipidemic dyslipoproteinemia. Vnitrni Lekarstvi 27(2): 115-121
Laskarzewski, P.M.; Khoury, P.; Morrison, J.A.; Kelly, K.; Mellies, M.J.; Glueck, C.J. 1983: Familial obesity and leanness. International Journal of Obesity 7(6): 505-527
D'Emma, C.; Crippa, L.; Delozier, C.; Michail, E.; Graber, P. 1982: Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation. Journal de Genetique Humaine 30(1): 39-50
Michel, M. 1970: Familial obstructive myocardiopathy. Pediatrie 25(1): 105-107
Wośko, I.; Warda, E.; Borzecka, I.; Pietroń, K. 1968: Familial occurence of Engelmann's disease. Chirurgia Narzadow Ruchu i Ortopedia Polska 33(4): 497-501
Oliva, H.; Rapado, A.; Apado, A.; De La Barreda, P.; Casado Pérez, S.; Plaza Pérez, J.J.; Sabando Suárez, P.; Thol; Lymph Nodes/Pathol; Spleen/Pathol; Spain 1974: Familial occurence of Hodgkin's disease. Revista Clinica Espanola 135(5): 417-423
Wale, R.J.; Williams, J.A.; Beeley, A.H.; Hughes, E.S. 1983: Familial occurrence in carcinoid tumours. Australian and New Zealand Journal of Surgery 53(4): 325-328
Nowak, J.; Lastowska, M.; Jankowska, A. 1984: Familial occurrence of Albers-Schoenberg disease. Polski Tygodnik Lekarski 39(32): 1075-1077
Miyazaki, T.; Shiomi, K.; Hachiya, T.; Yoshimura, M.; Ochi, Y. 1973: Familial occurrence of Basedow's disease. Nihon Naibunpi Gakkai Zasshi 49(7): 995-1000
Strik, W.O.; Strik, W. 1972: Familial occurrence of Crohn's regional enteritis in binovular twins and 2 other siblings. Münchener Medizinische Wochenschrift 114(43): 1852-1856
Pecoldowa, K.; Warchalewska-Pykalowa, U. 1970: Familial occurrence of Ekman-Lebstein-van der Hoeve syndrome. Klinika Oczna 40(2): 227-232
Pernhaupt, G.; Tschabitscher, H.; Wessely, P. 1974: Familial occurrence of Fahr's syndrome. Der Nervenarzt 45(12): 647-653
Riku, S.; Kumagai, T.; Sobue, I. 1983: Familial occurrence of Fukuyama type congenital muscular dystrophy and limb-girdle syndrome. Rinsho Shinkeigaku 23(8): 711-716
Friedman-Birnbaum, R.; Abraham, Z. 1983: Familial occurrence of Kaposi's sarcoma. Report of two brothers. Tumori 69(4): 365-367
Berlin, S.O.; Odeberg, H.; Weingart, L. 1968: Familial occurrence of M-components. Acta Medica Scandinavica 183(4): 347-350
Posselt, H.G.; Kohls, C.; Ball, F.; Bender, S.W. 1985: Familial occurrence of Peutz-Jeghers syndrome and Crohn disease with manifestation of both diseases in the same patient. Zeitschrift für Gastroenterologie 23(12): 670-675
Czarnowski, J.; Gasiorek, J. 1984: Familial occurrence of Quincke's edema. Otolaryngologia Polska 38(6): 507-509
Netto, C.F.; Castro, R.M.; Gonçalves, A.P.; Dillon, N.L. 1965: Familial occurrence of South American blastomycosis. Apropos of 14 cases. Revista do Instituto de Medicina Tropical de Sao Paulo 7(6): 332-336
Fischer, P.R.; Shigeoka, A.O. 1983: Familial occurrence of Stevens-Johnson syndrome. American Journal of Diseases of Children 137(9): 914-916
Schneider, R.G. 1969: Familial occurrence of Wolff-Parkinson-White syndrome. American Heart Journal 78(1): 34-37
Zoethout, H.E.; Ubbink, G.J. 1966: Familial occurrence of a deficiency of immune globulins. Maandschrift Voor Kindergeneeskunde 34(11): 353-359
Yoshida, M.C.; Honda, T. 1969: Familial occurrence of a short arm deletion of a G-group chromosome. Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 14(2): 140-144
Passarge, E. 1983: Familial occurrence of a short rib syndrome with hydrops fetalis but without polydactyly. American Journal of Medical Genetics 14(2): 403-405
Teja, K.; Cooper, P.H. 1981: Familial occurrence of accessory tragus. Journal of Pediatric Surgery 16(5): 725-726
Von Studnitz, W.; Ljungberg, O. 1970: Familial occurrence of adrenaline-producing pheochromocytoma associated with medullar thyroid carcinoma. Klinische Wochenschrift 48(3): 144-148
Tobo, M.; Mitsuyama, Y.; Ikari, K.; Itoi, K. 1984: Familial occurrence of adult-type neuronal ceroid lipofuscinosis. Archives of Neurology 41(10): 1091-1094
Breit, S.M.; Clark, P.; Robinson, J.P.; Luckhurst, E.; Dawkins, R.L.; Penny, R. 1983: Familial occurrence of alpha 1-antitrypsin deficiency and Weber-Christian disease. Archives of Dermatology 119(3): 198-202
Berlińska, A. 1982: Familial occurrence of amyotrophic lateral sclerosis with a peculiar clinical picture. Neurologia i Neurochirurgia Polska 16(1-3): 107-110
Goldschmidt, H.; Glöbl, H. 1972: Familial occurrence of anorectal abnormalities associated with vertebral abnormalities. Helvetica Paediatrica Acta 27(4): 361-370
Fukamizu, H.; Matsumoto, K.; Inoue, K.; Moriguchi, T. 1982: Familial occurrence of aplasia cutis congenita. Journal of Dermatologic Surgery and Oncology 8(12): 1068-1070
Cihula, J.; Vortel, V.; Steiner, I.; Zizka, J.; Hametová, M. 1969: Familial occurrence of aplasia of intrahepatic bile ducts with partial giant cell transformation of liver parenchyma in 2 siblings. Ceskoslovenska Pediatrie 24(9): 792-796
Lockey, R.F.; Rucknagel, D.L.; Vanselow, N.A. 1973: Familial occurrence of asthma, nasal polyps and aspirin intolerance. Annals of Internal Medicine 78(1): 57-63
Navrátil, M.; Hanák, S. 1970: Familial occurrence of benign jaundice in a 14-year-old boy. Ceskoslovenska Pediatrie 25(7): 341-342
Gollop, T.R.; Lucchesi, E.; Martins, R.M.; Nione, A.S. 1980: Familial occurrence of bifid femur and monodactylous ectrodactyly. American Journal of Medical Genetics 7(3): 319-322
Sakkonen, J.; Sääf, J. 1973: Familial occurrence of breast cancer. Lancet 2(7829): 626
Nakanishi, M. 1972: Familial occurrence of bronchiectasis. Bulletin of the Chest Disease Research Institute Kyoto University 6(1): 37-45
Sroczyńska, F.; Dudkowski, L. 1970: Familial occurrence of calcinosis of the pulmonary alveoli. Gruzlica i Choroby Pluc; Tuberculosis et Pneumonologia 38(1): 92-93
Kesztele, V. 1974: Familial occurrence of cancer. Wiener Medizinische Wochenschrift 124(25): 412-413
Burkland, C.E.; Juzek, R.H. 1966: Familial occurrence of carcinoma of the ureter. Journal of Urology 96(5): 697-701
Yamashita, J.; Handa, H.; Kim, C.; Kim, S. 1982: Familial occurrence of cerebellar hemangioblastomas--analysis of five families. Neurosurgery 11(6): 761-763
Marckwort, H.J.; Stapper, G. 1972: Familial occurrence of cerebral palsy and changes in the eye with coloboma of the choroid. Monatsschrift für Kinderheilkunde 120(7): 292-293
Prochorow, M.; Gidlecki, Z. 1972: Familial occurrence of childhood diabetes. Polski Tygodnik Lekarski 27(45): 1752-1755
Kiszely, K. 1982: Familial occurrence of childhood epilepsy and related clinical data. Orvosi Hetilap 123(7): 407-410
Perry, E.L.; Overholt, E.L.; Newcomer, K.L. 1969: Familial occurrence of chondrocalcinosis (pseudogout syndrome). Wisconsin Medical Journal 68(11): 321-324
Ming, P.M.; Parker, R.; Goodner, D.M. 1980: Familial occurrence of chromosome 7/12 translocation. Clinical Genetics 18(6): 445-449
Philip, J. 1970: Familial occurrence of chromosome abnormalities. Nordisk Medicin 83(18): 568-569
Nekula, J.; Meduna, J.; Bruner, V. 1972: Familial occurrence of cleidocranial dysostosis. Ceskoslovenska Radiologie 26(2): 92-96
Delaney, J.F. 1982: Familial occurrence of coexistent periodic paralysis and spinal muscular atrophy: case reports. Military Medicine 147(3): 229-231
Schieche, M. 1970: Familial occurrence of congenital angiocardiopathies. Zeitschrift für die Gesamte Innere Medizin und ihre Grenzgebiete 25(24): 1103-1108
Gencík, A.; Moser, H.; Gencíkova, A.; Kehrer, B. 1982: Familial occurrence of congenital diaphragmatic defect in three families. Helvetica Paediatrica Acta 37(3): 289-293
Ide, C.H.; Holt, R.; Holt, J.E. 1974: Familial occurrence of congenital diffuse hemangiomatosis. Klinische Monatsblatter für Augenheilkunde 165(4): 644-646
Matsuki, H.; Iuchi, K.; Nishimura, M.; Chikamori, J.; Minami, S. 1970: Familial occurrence of congenital heart diseases. Kyobu Geka. Japanese Journal of Thoracic Surgery 23(10): 741-746
Rybak, K.; Zwierzchowska, D.; Zwierzchowski, H. 1984: Familial occurrence of congenital hip dislocation. Chirurgia Narzadow Ruchu i Ortopedia Polska 49(6): 545-547
Jankowicz, E.; Banach, S.; Pikiel, L. 1971: Familial occurrence of congenital intracranial aneurysf associated with cystic degeneration of the kidneys. Neurologia i Neurochirurgia Polska 5(2): 263-265
Phelan, P.D.; Stocks, J.G.; Williams, H.E.; Danks, D.M. 1973: Familial occurrence of congenital laryngeal clefts. Archives of Disease in Childhood 48(4): 275-278
Gacs, G.; Schuler, D.; Sellyei, M. 1970: Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr). Journal of Medical Genetics 7(2): 177-179
Scott-Emuakpor, A.B.; Warren, S.T.; Kapur, S.; Quiachon, E.B.; Higgins, J.V. 1981: Familial occurrence of congenital pulmonary lymphangiectasis. Genetic implications. American Journal of Diseases of Children 135(6): 532-534
Birõ, I.; Brittig, F.; Gottwald, G. 1971: Familial occurrence of cryoglobulinemia. Orvosi Hetilap 112(37): 2245-2246
Pfitzer, P.; Splitt, M.; Müntefering, H.; Friesenecker, J.E. 1982: Familial occurrence of cyclops over several generations. Verhandlungen der Deutschen Gesellschaft für Pathologie 66: 169-172
Chmielewski, J.; Stasikiewicz-Chmielewska 1968: Familial occurrence of cystic kidney. Zeitschrift für Urologie und Nephrologie 61(12): 865-867
Bandura, A. 1971: Familial occurrence of defective development of permanent teeth. Ceskoslovenska Stomatologie 71(5): 316-319
Bruszt, P. 1971: Familial occurrence of denticle. Fogorvosi Szemle 64(4): 112-114
Nitscheff, W.; Stereff, S. 1966: Familial occurrence of diffuse endoalveolar pulmolithiasis. Description of 3 cases in 1 family. Radiologia Diagnostica 7(2): 159-166
Driessen, A.P.; Scherpenisse, L.A. 1970: Familial occurrence of diffuse interstitial pulmonary fibrosis complicated by alveolar cell carcinoma. Nederlands Tijdschrift Voor Geneeskunde 114(49): 2041-2045
Danbara, T.; Matsuoka, R.; Nukiwa, T.; Natori, H.; Arai, T.; Kira, S. 1982: Familial occurrence of diffuse panbronchiolitis accompanied with elevation of cold agglutinin titer in a father and his two daughters. Nihon Kyobu Shikkan Gakkai Zasshi 20(5): 597-603
Rosenkranz, W.; Holzer, S.; Scholz, H. 1971: Familial occurrence of double satellites in group D chromosomes. Deutsche Medizinische Wochenschrift 96(13): 554 Passim
Johnsonbaugh, R.E.; Drexler, H.G.; Light, I.J.; Sutherland, J.M. 1974: Familial occurrence of drug-induced hearing loss. American Journal of Diseases of Children 127(2): 245-247
Vizkelety, T.; Szijj, E. 1964: Familial occurrence of dysostosis enchondralis. Zeitschrift für Orthopadie und ihre Grenzgebiete 99(2): 133-146
Urbanová, O. 1973: Familial occurrence of dysphonia. Ceskoslovenska Otolaryngologie 22(3): 180-183
Lee, M.H.; Liebman, J.; Steinberg, A.G.; Perrin, E.V.; Whitman, V. 1973: Familial occurrence of endocardial fibroelastosis in three siblings, including identical twins. Pediatrics 52(3): 402-411
Schwarz, E.; Meze, G. 1969: Familial occurrence of endocardial fibrosis in 3 siblings. Padiatrie und Grenzgebiete 8(1): 67-72
Beck, E. 1968: Familial occurrence of epiphysiolysis capitis femoris. Zeitschrift für Orthopadie und ihre Grenzgebiete 105(3): 112-118
Arakawa, T.; Tamura, T.; Ohara, K.; Narisawa, K.; Tanno, K. 1968: Familial occurrence of formiminotransferase deficiency of syndrome. Tohoku Journal of Experimental Medicine 96(3): 211-217
Van der Linden, W.; Simonson, N. 1973: Familial occurrence of gallstone disease. Incidence in parents of young patients. Human Heredity 23(2): 123-127
Bergstrom, J.F.; Long, J.M. 1974: Familial occurrence of ganglioneuromas. Texas Medicine 70(7): 62-65
Veselinović, A.; Hofer, Z. 1973: Familial occurrence of glaucoma. Medizinische Monatsschrift 27(2): 65-68
Van Baars, F.M.; Cremers, C.W.; van den Broek, P.; Veldman, J.E. 1981: Familial occurrence of glomus tumors; clinical and genetic aspects. Nederlands Tijdschrift Voor Geneeskunde 125(23): 909-914
Gasparová, D.; Szedélyová, L. 1980: Familial occurrence of grouped pigmentation of the ocular fundus. Ceskoslovenska Oftalmologie 36(6): 406-408
Moeschler, J.; Clarren, S.K. 1982: Familial occurrence of hemifacial microsomia with radial limb defects. American Journal of Medical Genetics 12(4): 371-375
Splino, M.; Peychl, L.; Kotrlík, J.; Kyntera, F. 1969: Familial occurrence of human pseudotuberculosis caused by Pasteurella pseudotuberculosis. Casopis Lekaru Ceskych 108(44): 1316-1320
Hara, M.; Sato, Y.; Sato, T.; Izumi, M. 1970: Familial occurrence of hyperthyroidism. Horumon to Rinsho. Clinical Endocrinology 18(2): 127-129
Portenoy, R.K.; Berger, A.; Gross, E. 1984: Familial occurrence of idiopathic normal-pressure hydrocephalus. Archives of Neurology 41(3): 335-337
Ottensooser, F.; de Araujo, J.T.; Rosales, T. 1970: Familial occurrence of increased activity of blood-group a in serum. Transfusion 10(1): 6-9
Pelikán, L.; Doubravský, J.; Mikes, K.; Cerný, M. 1967: Familial occurrence of infantile cortical hyperostosis. (Caffey-de Toni-Silvermann syndrome). Acta Chirurgiae Orthopaedicae et Traumatologiae Cechoslovaca 34(5): 430-434
Masár, I.; Puceková, G.; Stukovský, R. 1968: Familial occurrence of infectious hepatitis under conditions of gamma globulin prophylaxis. Ceskoslovenska Epidemiologie Mikrobiologie Imunologie 17(5): 257-269
Sakai, N.; Miwa, M.; Takada, M.; Yamada, H.; Sakata, K. 1974: Familial occurrence of intracranial aneurysm. Report of 3 sibling cases and review of literature. No Shinkei Geka. Neurological Surgery 2(2): 161-167
Erickson, R.P.; Woolliscroft, J.; Allen, R.J. 1980: Familial occurrence of intracranial arterial occlusive disease (Moyamoya) in neurofibromatosis. Clinical Genetics 18(3): 191-196
Grunert, V.; Horcajada, J.; Sunder-Plassmann, M. 1970: Familial occurrence of intracranial meningiomas. Wiener Medizinische Wochenschrift 120(46): 807-808
Breebaart-de Miranda, J.G.; Velzeboer, C.M.; Delleman, J.W. 1970: Familial occurrence of iris atrophy and cataract. Ophthalmologica. Journal International d'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift für Augenheilkunde 160(5): 291
Van Loghem, E. 1974: Familial occurrence of isolated IgA deficiency associated with antibodies to IgA. Evidence against a structural gene defect. European Journal of Immunology 4(1): 57-60
Richards, B.W.; Sylvester, P.E.; Hodgson, S.J. 1965: Familial occurrence of juvenile amaurotic family idiocy and phenylketonuria in the same subjects. Journal of Mental Deficiency Research 9(3): 210-218
Vogel, R.I.; Deasy, M.J. 1980: Familial occurrence of juvenile periodontitis. Annals of Dentistry 39(2): 31-36
Hoffman, I.D. 1983: Familial occurrence of juvenile periodontitis with varied treatment of one of the siblings with five-year follow-up. Case report. Journal of Periodontology 54(1): 44-49
Hellgren, L. 1983: Familial occurrence of lichen ruber planus. Dermatologische Monatschrift 169(1): 6-8
Dziuba, P.; Jończyk, K.; Dziekanowska, D.; Bulsiewicz, H. 1972: Familial occurrence of long arm deletion in chromosome 18 (46,18q-). Pediatria Polska 47(8): 1037-1042
Boczkowski, K.; Wawryk, R.; Krupa, B.; Mickiewicz, E. 1972: Familial occurrence of male pseudohermaphrodites with ambiguous external genitals. American Journal of Obstetrics and Gynecology 112(2): 192-198
Vilcek, E. 1973: Familial occurrence of malignant testicular tumors. Bratislavske Lekarske Listy 59(2): 199-202
Pamphlett, R.; Mackenzie, R.A. 1981: Familial occurrence of meningioma: a case report. Clinical and Experimental Neurology 18: 169-173
Sahar, A. 1965: Familial occurrence of meningiomas. Case report. Journal of Neurosurgery 23(4): 444-445
Neuhäuser, G. 1973: Familial occurrence of meningomyeloceles. Acta Universitatis Carolinae. Medica. Monographia 56: 127-129
Miettinen, T.A.; Penttilä, I.M.; Lampainen, E. 1972: Familial occurrence of mild hyperlipoproteinaemias. Clinical Genetics 3(4): 271-280
Nagae, K.; Goto, I.; Ueda, K.; Morotomi, Y. 1972: Familial occurrence of multiple intracranial aneurysms. Case report. Journal of Neurosurgery 37(3): 364-367
Ambrosetto, P.; Galassi, E. 1981: Familial occurrence of multiple intracranial aneurysms. Case reports and review of the literature. Acta Neurochirurgica 56(3-4): 233-238
Finke, J.; Schott, R. 1968: Familial occurrence of multiple sclerosis. Der Nervenarzt 39(11): 513-515
Johnson, E.R.; Gardner, D.M. 1981: Familial occurrence of nonmedullary thyroid carcinoma. Experience at the University of Missouri Health Sciences Center. Missouri Medicine 78(10): 647-649
Svobodová, L.; Svoboda, J. 1973: Familial occurrence of osteochondropathy of the child hip joint. Acta Chirurgiae Orthopaedicae et Traumatologiae Cechoslovaca 40(4): 324-327
Doktorczyk, H.; Knapikowa, D.; Mielecki, T.; Woźniak, J. 1970: Familial occurrence of osteopoikilosis. Polski Tygodnik Lekarski 25(42): 1585-1586
Sarosi, G.; Doe, R.P. 1968: Familial occurrence of parathyroid adenomas, pheochromocytoma, and medullary carcinoma of the thyroid with amyloid stroma (Sipple's syndrome). Annals of Internal Medicine 68(6): 1305-1309
Gencik, A.; Gencikova, A.; Pálova, A. 1982: Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation. Acta Paediatrica Academiae Scientiarum Hungaricae 23(3): 291-298
Niznikowska-Marks, M.J.; Wróblewska-Cieliszak, K. 1970: Familial occurrence of patent ductus arteriosus. Pediatria Polska 45(3): 339-341
Rosner, J.; Peisert, E. 1974: Familial occurrence of pemphigus vulgaris chronicus. Przeglad Dermatologiczny 61(5): 675-680
Koziol, H.; Wlodarz, A. 1974: Familial occurrence of peptic ulcer. Pediatria Polska 49(1): 71-74
Brook, C.G.; Wagner, H.; Zachmann, M.; Prader, A.; Armendares, S.; Frenk, S.; Alemán, P.; Najjar, S.S.; Slim, M.S.; Genton, N.; Bozic, C. 1973: Familial occurrence of persistent Mullerian structures in otherwise normal males. British Medical Journal 1(5856): 771-773
Feltynowski, T.; Wieteska, A.; Januszewicz, A.; Wocial, B.; Szostek, M.; Januszewicz, W. 1995: Familial occurrence of pheochromocytoma. Polskie Archiwum Medycyny Wewnetrznej 93(5): 427-432
Zák, M.; Mirejovský, P. 1969: Familial occurrence of pneumocystis pneumonia due to congenital immunological deficiency. Ceskoslovenska Pediatrie 24(11): 974-979
Schminda, R. 1973: Familial occurrence of pneumoencephalographic changes in the course of chronic alcoholism. Psychiatria Polska 7(5): 583-586
Chmielewski, J.; Jackowski, T.; Stasikiewicz-Chmielewska 1966: Familial occurrence of polycystic kidneys in association with other developmental abnormalities. (Report of a family). Polskie Archiwum Medycyny Wewnetrznej 36(5): 587-589
Gram, B.R. 1983: Familial occurrence of porphyria cutaneous tarda. the biochemical background and own clinical studies. Ugeskrift for Laeger 145(48): 3736-3739
Jaup, B.H.; Zettergren, L.S. 1980: Familial occurrence of primary biliary cirrhosis associated with hypergammaglobulinemia in descendants: a family study. Gastroenterology 78(3): 549-555
Sander, J. 1966: Familial occurrence of primary pulmonary fibrosis. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 86(11): 851-854
Ventruto, V.; Catani, L.; Celona, A.; Fioretti, G.; Stabile, M.; Gallo, G. 1980: Familial occurrence of protrusio acetabuli (Otto's disease). Ten members affected in four generations. Italian Journal of Orthopaedics and Traumatology 6(3): 423-426
Szymczak, G.; Zawilska, K. 1970: Familial occurrence of pseudohypoparathyroidism. Endokrynologia Polska 21(4): 393-400
Florczak-Mikicińska, E.; Winnicki, S. 1982: Familial occurrence of pseudohypoparathyroidism and pseudopseudohypoparathyroidism. Polski Przeglad Radiologii i Medycyny Nuklearnej 46(4): 149-152
Moll, J.M.; Wright, V. 1973: Familial occurrence of psoriatic arthritis. Annals of the Rheumatic Diseases 32(3): 181-201
Lisch, K. 1969: Familial occurrence of relapsing facial paralysis with paralysis of the oculomotor muscles. Klinische Monatsblatter für Augenheilkunde 155(3): 400-404
Ellis, D.; Fisher, S.E.; Smith, W.I.; Jaffe, R. 1982: Familial occurrence of renal and intestinal disease associated with tissue autoantibodies. American Journal of Diseases of Children 136(4): 323-326
De Die-Smulders, C.; Schrander-Stumpel, C.; Fryns, J.P. 1993: Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay: a 4p deletion?. American Journal of Medical Genetics 47(6): 936
Azimi, F.; Bryan, P.J. 1974: Familial occurrence of renal pseudotumour due to enlarged Column of Bertin in two brothers and their first cousin. Clinical Radiology 25(4): 467-470
Gumowska, M.; Czarnecka, D.; Czekalski, S.; Kosowicz, J. 1968: Familial occurrence of renal tubular acidosis. Pediatria Polska 43(8): 1017-1021
Bartkowska-Orlowska, M.; Przybyl-Ereńska, K. 1970: Familial occurrence of retinal detachment. Klinika Oczna 40(1): 51-55
Wiman, L.G. 1972: Familial occurrence of sarcoidosis. Scandinavian Journal of Respiratory Diseases. Supplementum 80: 115-119
Grönhagen-Riska, C.; Fyhrquist, F.; Hortling, L.; Koskimies, S. 1983: Familial occurrence of sarcoidosis and Crohn's disease. Lancet 1(8336): 1287-1288
Augustín, J.; Losonský, S.; Korcok, F. 1983: Familial occurrence of sarcoma. Ceskoslovenska Gynekologie 48(7): 492-493
Szczepanski, A.; Jakubowicz, K. 1972: Familial occurrence of scleroderma. Przeglad Dermatologiczny 59(3): 361-364
Stephenson, C.; Franken, E.A.; Ha-Upala, S.; Christian, J.C. 1971: Familial occurrence of single ventricle. Archives of Disease in Childhood 46(249): 730-731
Fornatto, L.; Portaleone, P.; Schiffer, D. 1972: Familial occurrence of solitary angioblastoma of the cerebellum and its relationship with von Hippel-Lindau disease. Acta Neurologica 27(3): 286-290
Witzel, L. 1967: Familial occurrence of stomach carcinoma. Medizinische Klinik 62(28): 1088-1089
Michałowicz, R.; Ignatowicz, R.; Kostrzewska, M. 1983: Familial occurrence of subacute sclerosing panencephalitis (SSPE) in children. Neurologia i Neurochirurgia Polska 17(6): 651-654
Biehl, G. 1971: Familial occurrence of subperiostal bone fibroma. Zeitschrift für Orthopadie und ihre Grenzgebiete 109(1): 124-129
Novák, J. 1973: Familial occurrence of supernumerary teeth. Ceskoslovenska Stomatologie 73(1): 50-56
Weinhold, P.; Wegner, J.T.; Kane, J.M. 1981: Familial occurrence of tardive dyskinesia. Journal of Clinical Psychiatry 42(4): 165-166
Gulley, R.M.; Kowalski, R.; Neuhoff, C.F. 1974: Familial occurrence of testicular neoplasms: a case report. Journal of Urology 112(5): 620-622
Bárta, M. 1970: Familial occurrence of the Albers-Schönberg disease. Ceskoslovenska Radiologie 24(4): 175-179
Gross-Kieselstein, E.; Abrahamov, A.; Ben-Hur, N. 1971: Familial occurrence of the Freeman-Sheldon syndrome: cranio-carpotarsal dysplasia. Pediatrics 47(6): 1064-1067
Homola, D.; Srnová, V. 1968: Familial occurrence of the Wolff-Parkinson-White (WPW) syndrome. Vnitrni Lekarstvi 14(9): 850-856
Rapant, V.; Dvorácek, C.; Turek, K.; Valach, V. 1965: Familial occurrence of the Zollin ger-Ellison syndrome associated with diabetes. Gastroenterologia 104(5): 289-301
Yunis, J.J.; Ramsay, N.K. 1980: Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1. Journal of Pediatrics 96(6): 1027-1030
Fixler, D.E.; Cole, R.B.; Paul, M.H.; Lev, M.; Girod, D.A. 1970: Familial occurrence of the contracted form of endocardial fibroelastosis. American Journal of Cardiology 26(2): 208-213
Hogewind, B.L.; de la Rivière, G.B.; van Es, L.A.; Veltkamp, J.J. 1980: Familial occurrence of the haemolytic uraemic syndrome. Acta Medica Scandinavica 207(1-2): 73-77
Walker, N. 1972: Familial occurrence of the high scapula syndrome. Zeitschrift für Orthopadie und ihre Grenzgebiete 110(2): 203-211
Jørgensen, H.R.; Kristensen, B.; Mortensen, P.B. 1984: Familial occurrence of the reduced activity of the pancreas correlated with amylase isoenzyme in the serum. Ugeskrift for Laeger 146(9): 657-659
McFadzean, A.J.; Yeung, R. 1969: Familial occurrence of thyrotoxic periodic paralysis. British Medical Journal 1(5646): 760
Ziobrowski, S. 1985: Familial occurrence of toxoplasmosis. Klinika Oczna 87(5): 210-211
Uchida, I.A.; Ray, M.; McRae, K.N.; Besant, D.F. 1968: Familial occurrence of trisomy 22. American Journal of Human Genetics 20(2): 107-118
Ambani, L.M.; Vaidya, R.A.; Rao, C.S.; Daftary, S.D.; Motashaw, N.D. 1980: Familial occurrence of trophoblastic disease - report of recurrent molar pregnancies in sisters in three families. Clinical Genetics 18(1): 27-29
Horvat, Z.; Radosević, Z.; Ahmetović, S. 1970: Familial occurrence of visceral erythematosus. Acta Medica Iugoslavica 24(2): 143-150
Pelikán, L.; Hanák, S. 1970: Familial occurrence of vitamin D resistant rickets (mother and 2 sons). Ceskoslovenska Pediatrie 25(3): 122-125
Ichihashi, T.; Harano, H.; Mizuno, J.; Kasahara, R.; Hoshino, D.; Nakagawa, H. 1995: Familial occurrence of von Hippel-Lindau disease--a case report. No to Shinkei 47(7): 692-697
Corder, M.P.; Culp, N.W.; Barrett, O. 1973: Familial occurrence of von Willebrand's disease, thrombocytopenia, and severe gastrointestinal bleeding. American Journal of the Medical Sciences 265(3): 219-223
Stokke, D.B.; Andresen, P. 1970: Familial occurrence of "cryptothyroidism" with functioning ectopic thyroid tissue in solitary subhyoid localization. Danish Medical Bulletin 17(6): 189-192
Krarup, N.B. 1969: Familial occurrence of "palindromic rheumatism". Ugeskrift for Laeger 131(42): 1794-1796
Lynch, H.T.; Krush, A.J.; Mulcahy, G.M.; Reed, W.B. 1974: Familial occurrences of a variety of premalignant diseases and uncommon malignant neoplasms. Cancer 33(5): 1474-1479
Godel, V.; Iaina, A.; Goldman, B. 1980: Familial ocular anomalies in juvenile nephronophthisis. Metabolic and Pediatric Ophthalmology 4(1): 25-29
Alberca, R.; Coca, M.C.; Gil Peralta, A.; Gómez Bosque, P.; Navarro, A. 1971: Familial ocular myopathy. (Immunoelectrophoretic and electron microscopy studies). Revista Clinica Espanola 123(1): 45-52
Tamura, K.; Santa, T.; Kuroiwa, Y. 1974: Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria. Brain: a Journal of Neurology 97(4): 665-672
Tamura, K.; Santa, T.; Kuroiwa, Y. 1974: Familial oculocraniosomatic neuromuscular disease with ragged red fibers. Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 19(1): 109-110
Goren, H.; Steinberg, M.C.; Farboody, G.H. 1980: Familial oculoleptomeningeal amyloidosis. Brain: a Journal of Neurology 103(3): 473-495
Currie, S. 1970: Familial oculomotor palsy with Bell's palsy. Brain: a Journal of Neurology 93(1): 193-198
Vita, G.; Dattola, R.; Santoro, M.; Messina, C. 1983: Familial oculopharyngeal muscular dystrophy with distal spread. Journal of Neurology 230(1): 57-64
Roosen, N.; De La Porte, C.; Van Vyve, M.; Solheid, C.; Selosse, P. 1984: Familial oligodendroglioma. Case report. Journal of Neurosurgery 60(4): 848-849
Tong, K.Q. 1983: Familial oligodontia with ectodermal dysplasia: a sex-linked recessive hereditary disease. Zhonghua Kou Qiang Ke Za Zhi 18(3): 151-153
Berciano, J.; Ricoy, J.R.; Rebollo, M.; Combarros, O.; Coria, F.; Val, F. 1983: Familial olivopontocerebellar atrophy (Menzel type). Apropos of a family followed for 46 years. Archivos de Neurobiologia 46(1): 51-58
Steele, K.; Nevin, N.C. 1985: Familial omphalocele. Ulster Medical Journal 54(2): 214-215
Iwashita, H.; Inoue, N.; Kuroiwa, Y. 1969: Familial optic and acoustic nerve degeneration with distal amyotrophy. Lancet 2(7613): 219-220
Cordier, J.; Reny, A.; Raspiller, A. 1970: Familial optic atrophy and juvenile diabetes. Revue d'Oto-Neuro-Ophtalmologie 42(5): 269-280
Wolf, M. 1995: Familial oral Streptococcus mutans infections--a contribution to oral prophylaxis by pediatric nurses. Kinderkrankenschwester: Organ der Sektion Kinderkrankenpflege 14(8): 312-316
Miranda-Nieves, G. 1967: Familial orthochromatic leukodystrophy associated with complex abiotrophies, some classifiable as neuroaxonal degeneration. Resumption of the study of the Huys family published by van Bogaert, Edgar and Karcher, 1961. Acta Neurologica et Psychiatrica Belgica 67(12): 1116-1137
Andrew, T.A.; Spivey, J.; Lindebaum, R.H. 1981: Familial osteochondritis dissecans and dwarfism. Acta Orthopaedica Scandinavica 52(5): 519-523
Anderson, L.G.; Cook, A.J.; Coccaro, P.J.; Coro, C.J.; Bosma, J.F. 1972: Familial osteodysplasia. JAMA 220(13): 1687-1693
Niijima, K.H.; Kondo, A.; Ishikawa, J.; Kim, C.; Itoh, H. 1984: Familial osteodysplasia associated with trigeminal neuralgia: case report. Neurosurgery 15(4): 562-565
Swaney, J.J. 1973: Familial osteogenic sarcoma. Clinical Orthopaedics and Related Research 1973(97): 64-68
Chu, X.Y. 1984: Familial osteomalacia. Zhonghua Nei Ke Za Zhi 23(6): 355-358; 398
Cortina, H.; Vallcanera, A.; Vidal, J. 1981: Familial osteopathia striata with cranial condensation. Pediatric Radiology 11(2): 87-90
King, R.E.; Lovejoy, J.F. 1973: Familial osteopetrosis with coxa vara. A case report. Journal of Bone and Joint Surgery. American Volume 55(2): 381-385
Forgács, S. 1970: Familial osteopoikilosis. Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 112(2): 254-259
Serre, H.; Simon, L.; Barjon, M.C.; Sany, J.; Privat, J.M. 1968: Familial osteopoikilosis (3 cases). Rhumatologie 20(6): 233-239
Stelmasiak, Z.; Rozynkowa, D. 1973: Familial osteosclerosis associated with facial hemispasm in 3 generations. Polski Tygodnik Lekarski 28(21): 774-776
Fára, M.; Chlupácková, V.; Hrivnákova, J. 1967: Familial oto-facio-cervical dysmorphia. Acta Chirurgiae Orthopaedicae et Traumatologiae Cechoslovaca 34(6): 511-520
Koga, K.; Suzuki, Y.; Sakai, M.; Mukai, M. 1974: Familial otosclerosis with chromosomal aberration. Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 19(1): 85-86
Matheson, J.A.; Matheson, H.; Anderson, S.A. 1981: Familial ovarian cancer. how rare is it?. Journal of the Royal College of General Practitioners 31(233): 743-745
Franceschi, S.; La Vecchia, C.; Mangioni, C. 1982: Familial ovarian cancer: eight more families. Gynecologic Oncology 13(1): 31-36
Vesely, D.L.; Bower, R.H.; Kohler, P.O.; Char, F. 1980: Familial ovarian dysgenesis in 46,XX females. American Journal of the Medical Sciences 280(3): 157-166
Fienberg, R. 1972: Familial ovarian hyperthecosis. American Journal of Obstetrics and Gynecology 112(2): 309-311
Takahashi, A.; Saito, K.; Kondo, Y.; Kurosawa, T. 1973: Familial oxalosis. Report of three cases and review of the literature. Acta Pathologica Japonica 23(3): 559-575
Mathieu, H.; Gagnadoux, M.F.; Mongour, P.; Czernichow, P.; Volter, F.; Kaplan, M. 1968: Familial oxalosis. Study of 2 cases. Attempted treatment. Bulletins et Memoires de la Societe Medicale des Hopitaux de Paris 119(9): 719-730
Harbison, J.B.; Nice, C.M. 1971: Familial pachydermoperiostosis presenting as an acromegaly-like syndrome. American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine 112(3): 532-536
Tramier, G. 1969: Familial palmo-plantar keratoderma of the Thost-Unna type. Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 76(2): 176
Grajower, M.M. 1983: Familial pancreatic cancer. Annals of Internal Medicine 98(1): 111
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Mann, T.P.; Rubin, J. 1969: Familial pancreatic exocrine dysfunction with pancreatic calcification. Proceedings of the Royal Society of Medicine 62(4): 326
Bergström, K.; Hellström, K.; Kallner, M.; Lundh, G. 1973: Familial pancreatitis associated with hyperglycinuria. Scandinavian Journal of Gastroenterology 8(3): 217-223
Mian, T.A.; Zuberi, S.J. 1980: Familial pancreatitis with lithiasis. Jpma. Journal of the Pakistan Medical Association 30(12): 275-278
Choudhry, V.P.; Srivastava, R.N.; Ghai, O.P. 1971: Familial pancreatitis. (A case report). Indian Pediatrics 8(9): 466-468
Phade, V.R.; Lawrence, W.R.; Max, M.H. 1981: Familial papillary carcinoma of the thyroid. Archives of Surgery 116(6): 836-837
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Berliner, S.; Weinberger, A.; Zamir, R.; Salomon, F.; Joshua, H.; Pinkhas, J. 1981: Familial systemic lupus erythematosus and C4 deficiency. Scandinavian Journal of Rheumatology 10(4): 280-282
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