EurekaMag PDF full texts Chapter 43,112

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. Mmw Munchener 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. Munchener 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

Lumadue, J.A.; Griffin, C.A.; Osman, M.; Hruban, R.H. 1995: Familial pancreatic cancer and the genetics of pancreatic cancer. Surgical Clinics of North America 75(5): 845-855

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

Djalali, M.; Steinbach, P.; Barbi, G. 1984: Familial paracentric inversion inv(3)(q21q25.1). Case report and review of the literature. Annales de Genetique 27(1): 41-44

Romain, D.R.; Columbano-Green, L.M.; Whyte, S.; Smythe, R.H.; Parfitt, R.G.; Gebbie, O.B.; Chapman, C.J. 1983: Familial paracentric inversion of 1p. American Journal of Medical Genetics 14(4): 629-634

Del Porto, G.; D'Alessandro, E.; De Matteis, C.; D'Innocenzo, R.; Baldi, M.; Pachi, A.; Cappa, F. 1984: Familial paracentric inversion of chromosome 15 (q15q24). Journal of Medical Genetics 21(6): 451-453

Delwaide, P.J.; Penders, C.A. 1971: Familial paramyotonia and paretic crises with hypokalemia. Revue Neurologique (Paris) 125(4): 287-297

Grant, J.A.; Blumenschein, G.R.; Buckley, C.E. 1971: Familial paraproteinemia. Archives of Internal Medicine 128(3): 427-431

Delacrétaz, J.; Maillard, G.F.; Emch, M.; Glauser, M.P. 1970: Familial paraproteinemia and lichen myxedematosus. I. Clinical study. Schweizerische Medizinische Wochenschrift 100(14): 626-630

Glauser, M.P.; Maillard, G.F.; Emch, M.; Delacrétaz, J. 1970: Familial paraproteinemia and lichen myxedematosus. II. Immunological study. Schweizerische Medizinische Wochenschrift 100(15): 666-671

Coca Martin, M.C. 1971: Familial parasitologic study. La Medicina Tropical 47(1): 25-36

Anonymous 1968: Familial parocystic rhabdomyolysis in children. Revista Clinica Espanola 109(6): 536-539

Aimard, G.; Vighetto, A.; Trillet, M.; Ventre, J.J.; Devic, M. 1983: Familial paroxysmal ataxia responsive to acetazolamide. Revue Neurologique (Paris) 139(4): 251-258

De la Flor Bru, J.; Artigas Pallares, J.; Argemi Fontanet, J.; Salas Guzmán, S. 1985: Familial paroxysmal choreoathetosis treated with carbamazepine. Anales Espanoles de Pediatria 23(4): 291-294

Zukerman, E.; Vilanova, L.C.; Seráfico, J. 1983: Familial paroxysmal choreoathetosis. Report of 2 cases in one family. Arquivos de Neuro-Psiquiatria 41(4): 373-376

Kurlan, R.; Shoulson, I. 1983: Familial paroxysmal dystonic choreoathetosis and response to alternate-day oxazepam therapy. Annals of Neurology 13(4): 456-457

Walker, E.S. 1981: Familial paroxysmal dystonic choreoathetosis: a neurologic disorder simulating psychiatric illness. Johns Hopkins Medical Journal 148(3): 108-113

Barolin, G.S. 1967: Familial paroxysmal hemilateral decrease of function with and without headache attacks. Schweizer Archiv für Neurologie Neurochirurgie und Psychiatrie 99(1): 15-28

Garello, L.; Ottonello, G.A.; Regesta, G.; Tanganelli, P. 1983: Familial paroxysmal kinesigenic choreoathetosis. Report of a pharmacological trial in 2 cases. European Neurology 22(3): 217-221

Anonymous 1967: Familial paroxysmal polyserositis. Journal of the Louisiana State Medical Society: official organ of the Louisiana State Medical Society 119(7): 292-294

Khachadurian, A.K.; Armenian, H.K. 1974: Familial paroxysmal polyserositis (familial Mediterranean fever); incidence of amyloidosis and mode of inheritance. Birth Defects Original Article Series 10(4): 62-66

Mancini, J.L. 1973: Familial paroxysmal polyserositis, phenotype I (familial Mediterranean fever). A rare cause of pleurisy. Case report and review of the literature. American Review of Respiratory Disease 107(3): 461-463

Armenian, H.K.; Khachadurian, A.K. 1973: Familial paroxysmal polyserositis. Clinical and laboratory findings in 120 cases. Le Journal Medical Libanais. Lebanese Medical Journal 26(6): 605-614

Mignon, F.; Méry, J.P.; Cuvelier, R.; Delons, S.; Meyrier, A.; Rottembourg, J. 1981: Familial paroxysmal polyserositis: modern therapeutic possibilities. Annales de Medecine Interne 132(7): 501-506

Favara, B.E.; Vawter, G.F.; Wagner, R.; Kevy, S.; Porter, E.G. 1967: Familial paroxysmal rhabdomyolysis in children. a myoglobinuric syndrome. American Journal of Medicine 42(2): 196-207

Sacks, H.S.; Matisonn, R.; Kennelly, B.M. 1974: Familial paroxysmal ventricular tachycardia in two sisters. American Heart Journal 87(2): 217-222

Culbertson, W.W.; Giles, C.L.; West, C.; Stafford, T. 1983: Familial pars planitis. Retina 3(3): 179-181

Travi, V.H.; Ferreti, E. 1966: Familial partial anodontia. Revista de la Asociacion Odontologica Argentina 54(9): 354-357

Arya, B.S.; Savara, B.S. 1974: Familial partial anodontia: report of a case. Asdc Journal of Dentistry for Children 41(1): 47-54

McLean, R.H.; Weinstein, A.; Chapitis, J.; Lowenstein, M.; Rothfield, N.F. 1980: Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndrome. American Journal of Medicine 68(4): 549-558

De Muelenaere, A.; Fryns, J.P.; Van den Berghe, H. 1981: Familial partial distal 18q (18q22-18q23) trisomy. Annales de Genetique 24(3): 184-186

Beemer, F.A.; de France, H.F.; Rosina-Angelista, I.J.; Gerards, L.J.; Cats, B.P.; Guyt, R. 1984: Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333). Clinical Genetics 26(3): 209-215

Krzentowski, G.; Vandalem, J.L. 1981: Familial partial resistance to thyroid hormones. A report on one case. Annales d'Endocrinologie 42(6): 541-542

de Nayer, P.; Oei, L.S.; Broeckx, J.; de Visscher, M. 1971: Familial partial thyroxine-binding globulin deficiency. Annales D'endocrinologie 52(4): 617-620

Orye, E.; van Caster, A. 1972: Familial partial trisomy 18. Acta Paediatrica Belgica 26(1): 41-52

Duca, D.; Bene, M.; Ioan, D.; Maximilian, C. 1980: Familial partial trisomy: 6q25 leads to 6qter. Journal de Genetique Humaine 28(1): 31-37

Fischer, F. 1969: Familial pathology of diabetic retinopathy. Deutsche Zeitschrift für Verdauungs- und Stoffwechselkrankheiten 22: 97-100

Kapoor, K.N.; Tandon, O.P. 1967: Familial pattern of coronary artery disease. Journal of the Indian Medical Association 48(12): 586-590

Ashworth, J.T. 1981: Familial pattern of hypoglossal duct cysts. JAMA 245(7): 705

Suri, V.P.; Singh, D.; Tandon, O.P. 1966: Familial patterns in coronary artery disease. Indian Journal of Medical Sciences 20(5): 321-328

Dumas, C.A.; Katerndahl, D.A.; Burge, S.K. 1995: Familial patterns in patients with infrequent panic attacks. Archives of Family Medicine 4(10): 863-867

McClanahan, B.J.; Palmer, R.F.; Hackett, P.L. 1968: Familial patterns in the development of hematopoietic disorders in 90Sr-fed swine. BNWL-714. Bnwl Reports . U.S. Atomic Energy Commission 1968: 2.21

Benjamin, S.D.; Baer, P.N. 1967: Familial patterns of advanced alveolar bone loss in adolescence (periodontosis). Periodontics 5(2): 82-88

Mills, P.K.; Newell, G.R.; Johnson, D.E. 1984: Familial patterns of testicular cancer. Urology 24(1): 1-7

Freundlich, E.; Statter, M.; Yatziv, S. 1981: Familial pellagra-like skin rash with neurological manifestations. Archives of Disease in Childhood 56(2): 146-148

Cousin, J.; Walbaum, R.; Cegarra, P.; Huguet, J.; Louis, J.; Pauli, A.; Fournier, A.; Fontaine, G. 1982: Familial pelvi-scapulary dysplasia with anomalies of the epiphyses, dwarfism and dysmorphy: a new syndrome?. Archives Francaises de Pediatrie 39(3): 173-175

Cisárik, F.; Gavalec, M.; Hrbánová, Z. 1980: Familial penetrance of familial hyperlipoproteinemias. Vnitrni Lekarstvi 26(5): 457-461

Kronenfeld, J.J.; Ory, M.G. 1981: Familial perceptions of juvenile diabetes. Postgraduate Medicine 70(4): 83-95

Goldman, H.; Perkins, H.A. 1984: Familial pericarditis, arthritis, and camptodactyly. New England Journal of Medicine 310(2): 127-128

Rodriguez, M.T.; Martin, M.J.; Abrisqueta, J.A. 1984: Familial pericentric inversion (10) and its effect on two offspring. Journal of Medical Genetics 21(4): 317-319

Maltby, E.L. 1984: Familial pericentric inversion (13) detected by antenatal diagnosis. Journal of Medical Genetics 21(2): 149-151

Kaiser, P.; Förster, W.; Steuernagel, P.; Hillig, U.; Herberg, K.P. 1984: Familial pericentric inversion (14) (p11;q24) with a rec dup(q) in one offspring. Clinical Genetics 26(1): 73-76

Stahl-Maugé, C.; Weiss-Wichert, P.; Propping, P. 1982: Familial pericentric inversion of chromosome 1 in a boy with Goldenhar's syndrome. Human Genetics 61(1): 78

Habedank, M. 1982: Familial pericentric inversion of chromosome 13 resulting in duplication 13q22 to qter. Journal of Medical Genetics 19(3): 227-229

Mattevi, M.S.; Pinheiro, C.E.; Erdtmann, B.; Flores, R.Z.; Salzano, F.M. 1981: Familial pericentric inversion of chromosome 2. Journal de Genetique Humaine 29(2): 161-169

Sujansky, E.; Smith, A.C.; Peakman, D.C.; McConnell, T.S.; Baca, P.; Robinson, A. 1981: Familial pericentric inversion of chromosome 8. American Journal of Medical Genetics 10(3): 229-235

Moedjono, S.J.; Sparkes, R.S. 1980: Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?. Annales de Genetique 23(4): 235-237

Mattei, J.F.; Mattei, M.G.; Balestrazzi, P.; Giraud, F. 1983: Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion. Clinical Genetics 24(3): 220-222

Baumann, W.; Zabel, B.; Holl, M. 1984: Familial pericentric inversion of the X chromosome [inv(X)(p11q28). Annales de Genetique 27(2): 106-108

Dorf, G. 1965: Familial periodic disease. Gazette Medicale de France 72(8): 1613-1614

Sonkodi, S.; Szörényi, A.; Julesz, J.; Fazekas, T. 1980: Familial periodic paralysis (hypopotassaemic form). Wiener Klinische Wochenschrift 92(17): 610-613

Gyntelberg, F.; Kjaer, C. 1967: Familial periodic paralysis treated with triamterene. Ugeskrift for Laeger 129(16): 522-523

Johnsen, T. 1981: Familial periodic paralysis with hypokalaemia. Experimental and clinical investigations. Danish Medical Bulletin 28(1): 1-27

Libner, G.; Wandner, V.; Kray, H. 1973: Familial periodic paralysis--misinterpreted for years. Das Deutsche Gesundheitswesen 28(2): 61-64

Marchiori, P.; Scaff, M.; Levy, J.A.; Callegaro, D.; de Assis, J.L. 1980: Familial periodic paralysis: study of 8 cases. Arquivos de Neuro-Psiquiatria 38(4): 391-398

Haut, J.; Limon, S.; Offret, H.; Morax, S. 1973: Familial peripheral retinal degenerescence and retinal detachment. Bulletin des Societes d'Ophtalmologie de France 73(1): 27-37

Müller, D.; Castrillón-Oberndorfer; Orywall, D.; Genth, E. 1972: Familial pernicious anemia. Klinische Wochenschrift 50(23): 1085-1091

Beheshti, M.; Churchill, B.M.; Hardy, B.E.; Bailey, J.D.; Weksberg, R.; Rogan, G.F. 1984: Familial persistent müllerian duct syndrome. Journal of Urology 131(5): 968-969

Seringe, P.; Perelman, S.R.; Plainfosse, B.; Nathanson, M.; Allaneau, C.; Bertin, P.; Joron, F.; Belaisch, G. 1972: Familial pheochromocytoma. Annales D'endocrinologie 33(5): 529-530

Yan, C.L. 1983: Familial pheochromocytoma (with report of 4 cases). Zhonghua Yi Xue Za Zhi 63(4): 232-234

Huang, S.; McLeish, W.A. 1968: Familial pheochromocytoma and amyloid-producing medullary carcinoma of thyroid. Laval Medical 39(1): 22-23

Carney, J.A.; Go, V.L.; Gordon, H.; Northcutt, R.C.; Pearse, A.G.; Sheps, S.G. 1980: Familial pheochromocytoma and islet cell tumor of the pancreas. American Journal of Medicine 68(4): 515-521

Mulholland, S.G.; Atuk, N.O.; Walzak, M.P. 1969: Familial pheochromocytoma associated with cerebellar hemangioblastoma. A case history and review of the literature. JAMA 207(9): 1709-1711

Paloyan, E.; Scanu, A.; Straus, F.H.; Pickleman, J.R.; Paloyan, D. 1970: Familial pheochromocytoma, medullary thyroid carcinoma, and parathyroid adenomas. JAMA 214(8): 1443-1447

Sharp, W.V.; Platt, R.L. 1971: Familial pheochromocytoma. Association with von Hippel-Lindau's disease. Angiology 22(3): 141-146

Donath, A.; Käser, H.; Roos, B.; Ziegler, W.; Oetliker, O.; Colombo, J.P.; Bettex, M. 1965: Familial pheochromocytoma. Discussion of its malignancy and hereditary character: apropos of a case in a child with peculiar secretion. Helvetica Paediatrica Acta 20(1): 1-18

Ginocchio, G.; Garavelli, G.; Boari, L.; Tenca, P.; Casiglia, E.; Pessina, A.C. 1995: Familial pheochromocytoma: a family studied for 3 generations. Giornale Italiano di Cardiologia 25(3): 281-288

Adachi, M.; Miura, Y.; Adachi, M.; Kimura, S.; Tomioka, H.; Nezu, M.; Yoshinaga, K.; Saito, K. 1983: Familial pheochromocytoma: case report and a review of literature in Japan. Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 72(12): 1740-1748

Funyu, T.; Shiraiwa, Y.; Nigawara, K.; Kudo, S.; Mikuni, S. 1973: Familial pheochromocytoma: case report and review of the literature. Journal of Urology 110(2): 151-154

Tank, E.S.; Gelbard, M.K.; Blank, B. 1982: Familial pheochromocytomas. Journal of Urology 128(5): 1013-1016

Pouches, H.; Tralli, F.; Mouniq, C. 1983: Familial phobic rituals, methods of defense against an imagined adolescence. Neuropsychiatrie de l'Enfance et de l'Adolescence 31(8-9): 435-436

Sáenz-Lope, E.; Herranz-Tanarro, F.J.; Masdeu, J.C.; Bufil, J. 1984: Familial photosensitive epilepsy: effectiveness of clonazepam. Clinical Eeg 15(1): 47-52

Díaz de la Vega, V.; Bialostosky, D.; Lupi, E.; Castro, G.; Barrios, R.; Reyes, P.A. 1980: Familial pigeon breeder's disease. Possible association to HLA-Bw40 antigen. Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 32(4): 401-407

Volovich, L.E. 1966: Familial pigmented urticaria. Vestnik Dermatologii i Venerologii 40(2): 75

Ferrándiz, C.; Peyrí, J.; Henkes, J.; Ferrando, J.; Fontaranáu, R. 1980: Familial pili canaliculi. Actas Dermo-Sifiliograficas 71(5-6): 225-228

Moulin, G. 1970: Familial pilitortosis. Lyon Medical 223(14): 759-760

Ferrier, P.E.; Stone, E.F. 1969: Familial pituitary dwarfism associated with an abnormal sella turcica. Pediatrics 43(5): 858-865

Peter, B.; Schueller, H.; Sengler, J.; Zemp, A.; Vedrenne, C.; Laedlein-Greissammer, D.; Thierry, R. 1980: Familial pituitary dwarfism due to isolated growth hormone deficiency (3 cases). La Revue de Medecine Interne 1(2): 181-184

Ayala Ruiz, A.R.; Delgado Ochoa, D.; Vergara, M.D.; Loyo, M.; Matute Labrador, A.; Rosas, L.; Hernández Marín, I.; Cervera Aguilar, R. 1995: Familial pituitary tumor with somatotropic compromise. Ginecologia y Obstetricia de Mexico 63: 163-165

Gjone, E.; Torsvik, H.; Norum, K.R. 1968: Familial plasma cholesterol ester deficiency. a study of the erythrocytes. Scandinavian Journal of Clinical and Laboratory Investigation 21(4): 327-332

Hovig, T.; Gjone, E. 1973: Familial plasma lecithin: cholesterol acyltransferase (LCAT) deficiency. Ultrastructural aspects of a new syndrome with particular reference to lesions in the kidneys and the spleen. Acta Pathologica et Microbiologica Scandinavica. Section A Pathology 81(5): 681-697

Hamnström, B.; Gjone, E.; Norum, K.R. 1969: Familial plasma lecithin: cholesterol acyltransferase deficiency. British Medical Journal 2(5652): 283-286

Sakuma, M.; Akanuma, Y.; Kodama, T.; Yamada, N.; Murata, S.; Murase, T.; Itakura, H.; Kosaka, K. 1982: Familial plasma lecithin: cholesterol acyltransferase deficiency. a new family with partial LCAT activity. Acta Medica Scandinavica 212(4): 225-232

Nordöy, A.; Gjone, E. 1971: Familial plasma lecithin: cholesterol acyltransferase deficiency. a study of the platelets. Scandinavian Journal of Clinical and Laboratory Investigation 27(3): 263-268

Bourlier, V.; Monnet, P.; Gauthier, J. 1965: Familial poisoning by mushrooms. Helveolian Syndrome. Pediatrie 20(4): 461-464

Bermúdez de Rocha, M.V.; Lozano Meléndez, F.E.; Salazar Leal, M.E.; Waksman de Torres, N.; Piñeyro López, A. 1995: Familial poisoning with Karwinskia humboldtiana. Gaceta Medica de Mexico 131(1): 100-106

Frey, H.M.; Vogt, J.H.; Nerup, J. 1973: Familial poly-endocrinopathy. Acta Endocrinologica 72(2): 401-416

Popa, M. 1980: Familial polyadenomatoses of the endocrine glands. Endocrinologie 18(1): 61-63

Poulsen, P.; Nielsen, O.H. 1980: Familial polycystic syndrome. An unexpected finding at operation. Ugeskrift for Laeger 142(18): 1150-1151

White, J.M.; Szur, L.; Gillies, I.D.; Lorkin, P.A.; Lehmann, H. 1973: Familial polycythaemia caused by a new haemoglobin variant: Hb Heathrow, beta 103 (G5) phenylalanine leads to leucine. British Medical Journal 3(5882): 665-667

Rafaillat, D.; Oules, O.; Vernet, G.; Bedu, M.; Galacteros, F.; Bardakdjian, J. 1985: Familial polycythemia caused by high oxygen affinity hemoglobin. 2nd world case of hemoglobin J Providence. Revue de Pneumologie Clinique 41(4): 259-263

Wermer, P. 1973: Familial polyendocrine adenomatous hyperplasia syndrome. Actualites Endocrinologiques 13: 5-13

Moutaffian, J.J.; Gabriel, B.; Carcassonne, Y.; Olmer, J. 1967: Familial polyglobulia: apropos of 2 cases. Marseille Medical 104(2): 107-115

Colomb, D.; Beyvin, A.J.; Battesti, M.R. 1969: Familial polymorphous erythemato-squamous trichophytosis due to Trichophyton rubrum. Lyon Medical 221(17): 1024

Inokuchi, T.; Umezaki, H.; Onishi, A. 1972: Familial polyneuropathy associated with elevated protein in the cerebrospinal fluid. Rinsho Shinkeigaku 12(4): 179-184

Rocca, E.; Costantino, L.; De Lellis, C.; Romano, D.; Rubino, R. 1980: Familial polyposis and cancer. Apropos of 4 cases. Minerva Dietologica E Gastroenterologica 26(3): 223-226

Metzger, P.P.; Klainer, A.S.; Gainer, B.; Cadduck, W.M. 1974: Familial polyposis and pituitary chromophobe adenoma. West Virginia Medical Journal 70(10): 256-258

Berk, T.; Cohen, Z.; Cullen, J.B. 1981: Familial polyposis and the role of the preventive registry. Canadian Medical Association Journal 124(11): 1427-1428

Pickens, D.R.; Farringer, J.L. 1969: Familial polyposis and the spontaneous regression of polyps. American Surgeon 35(5): 361-365

Schier, J. 1974: Familial polyposis as an obligatory cancer precursor. Langenbecks Archiv für Chirurgie 337: 771-775

Weston, S.D.; Wiener, M. 1967: Familial polyposis associated with a new type of soft-tissue lesion (skin pigmentation): report of three cases and a review of the literature. Diseases of the Colon and Rectum 10(4): 311-321

Gardner, E.J. 1983: Familial polyposis coli and Gardner syndrome--is there a difference?. Progress in Clinical and Biological Research 115: 39-60

Alm, T. 1984: Familial polyposis coli and associated lesions. Acta Gastro-Enterologica Belgica 47(5): 469-475

Dowton, S.B. 1980: Familial polyposis coli associated with familial meningiomas. Medical Journal of Australia 1(12): 615

Lyko, H.C.; Hartmann, J.X. 1981: Familial polyposis coli plasma causes a transformation-associated morphology of cells in vitro: hyperproteinemia and colorectal polyps. Cancer Detection and Prevention 4(1-4): 401-405

Cole, C.W.; Meban, S. 1983: Familial polyposis coli: an unusual family. Canadian Journal of Surgery. Journal Canadien de Chirurgie 26(4): 374-376

Gonzaga, R.A.; Amarante, M.; Lima, F.R. 1984: Familial polyposis coli: the difficult choice. Lancet 1(8373): 402-403

Siegel, B.; Dror, Y.; Siegal, A. 1983: Familial polyposis in Israel. Harefuah 105(5-6): 101-103

Leggett, P.L.; Arensman, R.M.; Falterman, K.W. 1984: Familial polyposis in children: early detection and preferred treatment. Southern Medical Journal 77(4): 462-464

Moretti, G.; Bozic, C.; Genton, N. 1969: Familial polyposis of Peutz-Jeghers type with malignant degeneration. Annales de Chirurgie Infantile 10(3): 243-248

Falk, V.S.; Rogers, J.C. 1968: Familial polyposis of colon. a twenty-five year follow-up study. Archives of Surgery 96(6): 967-969

Otnes, B.; Helsingen, N. 1969: Familial polyposis of the colon in Norway. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 89(19): 1481-1483

McQuaide, J.R.; Stewart, A.W. 1972: Familial polyposis of the colon in the Bantu. South African Medical Journal 46(35): 1241-1246

Hayashi, F.; Nagakawa, T. 1970: Familial polyposis of the colon, a case report. Saishin Igaku. Modern Medicine 25(12): 2561-2568

Sachatello, C.R. 1971: Familial polyposis of the colon. A four-decade follow-up. Cancer 28(3): 581-587

Sachatello, C.R. 1970: Familial polyposis of the colon. I. Leukocytic chromosome determinations--report of a patient with familial polyposis of the colon and Klinefelter's syndrome. Diseases of the Colon and Rectum 13(5): 368-371

Williams, J.L.; Wightman, J.A. 1966: Familial polyposis of the colon. Report of a family with a 5-year follow-up of colectomy and ileorectal anastomosis. British Journal of Surgery 53(9): 780-784

Yonemoto, R.H.; Slayback, J.B.; Byron, R.L.; Rosen, R.B. 1969: Familial polyposis of the entire gastrointestinal tract. Archives of Surgery 99(4): 427-434

Yamada, S.; Takahashi, T. 1971: Familial polyposis of the large intestine. Gan no Rinsho. Japan Journal of Cancer Clinics 17(9): 676-686

Sztaba, R. 1968: Familial polyposis of the large intestine in an 11-year old boy. Wiadomosci Lekarskie 21(22): 2051-2053

Vecerina, S.; Fitting, J.V.; Saegesser, F.; Pettavel, J. 1973: Familial polyposis, diffuse polyposis and cancer. Schweizerische Rundschau für Medizin Praxis 62(34): 1036-1039

King, R.M.; van Heerden, J.A.; Kvols, L.K. 1984: Familial polyposis. A case report. South African Journal of Surgery. Suid-Afrikaanse Tydskrif Vir Chirurgie 22(2): 103-107

Hootnick, D.; Holmes, L.B. 1972: Familial polysyndactyly and craniofacial anomalies. Clinical Genetics 3(2): 128-134

Curth, H.O. 1969: Familial pompholyx. Archives of Dermatology 100(4): 520

Smit, L.M.; Barth, P.G.; Valk, J.; Njiokiktjien, C. 1984: Familial porencephalic white matter disease in two generations. Brain and Development 6(1): 54-58

Sei, J.F.; Jeanmougin, M. 1983: Familial portuguese type amyloid polyneuropathy. Attempt at a pathogenetic interpretation. Annales de Medecine Interne 134(4): 320-322

Faulk, W.P.; Epstein, C.J.; Jones, M.D. 1970: Familial posterior lumbosacral vertebral fusion and eyelid ptosis. American Journal of Diseases of Children 119(6): 510-512

Herishanu, Y.; Feldman, S. 1971: Familial postero-lateral myelopathy and angiomatosis retinae. Confinia Neurologica 33(3): 186-190

Sim, M.; Bale, R.N. 1973: Familial pre-senile dementia: the revelance of a histological diagnosis of Pick's disease. British Journal of Psychiatry: the Journal of Mental Science 122(571): 671-673

Brown, A.R.; Rose, B.S. 1966: Familial precocious polyarticular osteoarthrosis of chondrodysplastic type. New Zealand Medical Journal 65(407): 449-461

Hopwood, N.J.; Kelch, R.P.; Helder, L.J. 1981: Familial precocious puberty in a brother and sister. American Journal of Diseases of Children 135(1): 78-79

Dorofeeva, G.D.; Degonskaia, I.V.; Dorofeev, A.E. 1981: Familial predisposition in juvenile rheumatoid arthritis. Pediatriia 5: 50-51

Edwards, J.H. 1969: Familial predisposition in man. British Medical Bulletin 25(1): 58-64

Ottesen, E.A.; Mendell, N.R.; MacQueen, J.M.; Weller, P.F.; Amos, D.B.; Ward, F.E. 1981: Familial predisposition to filarial infection--not linked to HLA-A or-B locus specificities. Acta Tropica 38(3): 205-216

Freedman, B.I.; Tuttle, A.B.; Spray, B.J. 1995: Familial predisposition to nephropathy in African-Americans with non-insulin-dependent diabetes mellitus. American Journal of Kidney Diseases: the Official Journal of the National Kidney Foundation 25(5): 710-713

Fialkow, P.J.; Thuline, H.C.; Hecht, F.; Bryant, J. 1971: Familial predisposition to thyroid disease in Down's syndrome: controlled immunoclinical studies. American Journal of Human Genetics 23(1): 67-86

Simović, N. 1972: Familial predisposition to urolithiasis in infants. Lijecnicki Vjesnik 94(10): 506-508

Van Gemund, J.J.; Laurent de Angulo, M.S.; van Gelderen, H.H. 1970: Familial prenatal dwarfism with elevated serum immuno-reactive growth hormone levels and end-organ unresponsiveness. Maandschrift Voor Kindergeneeskunde 37(11): 372-382

Warter, J.M.; Steinmetz, G.; Heldt, N.; Rumbach, L.; Marescaux, C.; Eber, A.M.; Collard, M.; Rohmer, F.; Floquet, J.; Guedenet, J.C.; Gehin, P.; Weber, M. 1982: Familial presenile dementia: Gerstmann-Sträussler-Scheinker's syndrome. Revue Neurologique (Paris) 138(2): 107-121

Mayberry, J.F.; Rhodes, J.; Newcombe, R.G. 1980: Familial prevalence of inflammatory bowel disease in relatives of patients with Crohn's disease. British Medical Journal 280(6207): 84

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Okayama, M.; Goto, I.; Tanaka, T.; Omae, T. 1974: Familial primary amyloidosis with vitreous opacities and cognition disorder. Rinsho Shinkeigaku 14(3): 293-299

Guénol, J.; Legrand, J.; Dubigeon, P.; Bureau, L.; Horeau, J.; Maury, P. 1969: Familial primary amylosis with predominant renal and ocular localization. Annales de Medecine Interne 120(3): 207-219

Gola, A.; Milewicz, A.; Turkiewicz, R. 1974: Familial primary cardiomyopathy. Polski Tygodnik Lekarski 29(15): 613-614

Eisen, M.; Busse, K.; Beyer, J.; Grabs, V.; Happ, J.; Schäfer, R. 1974: Familial primary hyperparathyroidism. Deutsche Medizinische Wochenschrift 99(21): 1128 Passim

Shimura, H.; Mihara, A.; Hashizume, Y. 1972: Familial primary hyperparathyroidism--parathyroid adenoma in sisters. Nihon Rinsho. Japanese Journal of Clinical Medicine 30(3): 838-844

Wald, S.L.; Liwnicz, B.H.; Truman, T.A.; Khodadad, G. 1982: Familial primary nervous system neoplasms in three generations. Neurosurgery 11(1 Part 1): 12-15

Hamel, B.C. 1995: Familial primary pulmonary hypoplasia. European Journal of Pediatrics 154(4): 336

Villamor, J.; Hita, J.; Barreiro, P.; Ortiz Vázquez, J.; Vãzquez, J.J. 1971: Familial primary vasopressin resistant diabetes insipidus sensitive to biguanide. Revista Clinica Espanola 121(1): 51-62

Sakhuja, V.; Ghosh, A.K.; Jha, V.; Pahwa, N.; Chugh, K.S. 1994: Familial primary vesico-ureteric reflux. Journal of the Association of Physicians of India 42(1): 74-75

Schmidberger, H.; Grubbauer, H.M.; Holzer, H. 1974: Familial primary vitamin D resistant rickets (phosphate diabetes). Observations of two cases--with and without therapy. Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 120(2): 200-209

Klinowska, W.; Morawska, Z.; Krzemień, K. 1973: Familial proaccelerine (FV) deficiency. Polski Tygodnik Lekarski 28(49): 1919-1922

Van Laere, J. 1966: Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems. Revue Neurologique (Paris) 115(2): 289-295

Lehnhardt, E. 1967: Familial progressive deafness and subclinical iodine metabolism disorder. Zeitschrift für Laryngologie Rhinologie Otologie und ihre Grenzgebiete 46(4): 260-270

Iannaccone, S.T.; Griggs, R.C.; Markesbery, W.R.; Joynt, R.J. 1974: Familial progressive external ophthalmoplegia and ragged-red fibers. Neurology 24(11): 1033-1038

Chernosky, M.E.; Anderson, D.E.; Chang, J.P.; Shaw, M.W.; Romsdahl, M.M. 1971: Familial progressive hyperpigmentation. Archives of Dermatology 103(6): 581-91 Passim

Goutieres, F.; Aicardi, J.; Farkas-Bargeton, E. 1974: Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing encephalopathy. Acta Neuropathologica 28(2): 143-150

Rallo, E. 1969: Familial progressive myoclonic epilepsy (Unverricht-Lundborg syndrome in five Valaisian families). a contribution to the research of its metabolic origin through the study of urinary excretion of mucopolysaccharides. Acta Geneticae Medicae et Gemellologiae 18(3): 231-270

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Herbstund, A.; Schröter, P. 1973: Familial progressive myoclonus epilepsy (pme) (type Unverricht). Psychiatrie Neurologie und Medizinische Psychologie. Beihefte 17-18: 100-117

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Simone, F. 1971: Familial progressive rigidity of uncertain nosographic classification. Rivista di Neurologia 41(3): 170-181

Paparella, M.M.; Sugiura, S.; Hoshino, T. 1969: Familial progressive sensorineural deafness. Archives of Otolaryngology 90(1): 44-51

Soppi, E.; Lehtonen, A.; Toivanen, A. 1982: Familial progressive systemic sclerosis (scleroderma): immunological analysis of two patients and six siblings from a single kindred. Clinical and Experimental Immunology 50(2): 275-282

Hartemann, E. 1968: Familial protein intolerance. Pediatrie 23(8): 960-961

Kekomäki, M.; Toivakka, E.; Häkkinen, V.; Salaspuro, M. 1968: Familial protein intolerance with deficient transport of basic amino acids. Report on an adult patient with chronic hyperammonemia. Acta Medica Scandinavica 183(4): 357-359

Jagenburg, R.; Lindstedt, G.; Malmquist, J. 1970: Familial protein intolerance with hyperammonemia. Lakartidningen 67(45): 5255-5260

Rüster, M.; Rogner, G.; Kühn, R. 1966: Familial proteinuria and hypercholisterinemia. Klinische Wochenschrift 44(22): 1284-1289

François, R.; Bertrand, J.; Pellet; Salle, B.; Moreau, P.; Manuel, P. 1967: Familial proteinuria of the tubular type with appearance of the Bartter syndrome in 1 of the members of the family: a new disease?. Journal d'Urologie et de Nephrologie 73(10): 829-839

Armstrong, R.M.; Fogelson, M.H.; Silberberg, D.H. 1965: Familial proximal spinal muscular atrophy. Study of a large pedigree. Transactions of the American Neurological Association 90: 207-210

Sakaguchi, M.; Ishikawa, K.; Mizuta, H.; Kitagawa, T. 1982: Familial pseudogout with destructive arthropathy. Ryumachi 22(1): 4-13

Luciani, J.C.; Lavabre-Bertrand, T.; Fourcade, J.; Barjon, P.; Mimran, A.; Callis, A. 1980: Familial pseudohyperkalaemia. Lancet 1(8166): 491

Hughes, J.D.; Meriwether, T.W. 1971: Familial pseudohypertrophy of tendo-achillis with multisystem disease. Southern Medical Journal 64(3): 311-316

Hamilton, D.V. 1980: Familial pseudohypoparathyroidism presenting in adult life. Journal of the Royal Society of Medicine 73(10): 724-726

Singleton, E.M.; Kinsbourne, M.; Anderson, W.B. 1973: Familial pseudopapilledema. Southern Medical Journal 66(7): 796-802

Shapiro, I.; Shapiro, S.K. 1980: Familial pseudotumor cerebri and the empty sella syndrome. Annals of Ophthalmology 12(9): 1045-1048

Pontalti, C.; Arnetoli, C.; Rodriguez, R. 1982: Familial psychological picture and psychotherapy of 2 adolescent brothers with osteopetrosis. Minerva Psichiatrica 23(1): 55-58

Carnevale, A.; López Hernández, A.; De los Cobos, L. 1973: Familial pterygium syndrome with probably dominant transmission linked to the X chromosome. Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 25(3): 237-244

Schey, W.L.; Levin, B. 1971: Familial pubic bone maldevelopment. Radiology 101(1): 147-149

Neubauer, I. 1972: Familial pulmonary emphysema with lowered concentration of alpha-1-antitrypsin in the serum. Ugeskrift for Laeger 134(25): 1335-1337

McDonnell, L.; Sweeney, E.C.; Jagoe, W.S.; FitzGerald, M.X. 1982: Familial pulmonary fibrosis and lung cancer. Irish Journal of Medical Science 151(10): 315-317

Hirsch, M.S.; Hong, C.K. 1973: Familial pulmonary histiocytosis-X. American Review of Respiratory Disease 107(5): 831-835

Slotnick, E.A. 1971: Familial pure gonadal dysgenesis with clitoral hypertrophy and a normal female karyotype. Journal of the American Osteopathic Association 70(11): 1167-1178

Fossati, P.; Pruvot, P.; Caridroit, M.; Buvat, J.; Montois, R.; Linquette, M. 1972: Familial pyridoxine deficiency in a diabetic patient and her children. Infantile myoclonic encephalopathy with hypsarrhythmia cured with vitamin B 6 in one of them. Lille Medical: Journal de la Faculte de Medecine et de Pharmacie de l'Universite de Lille 17(5): 719-729

Garbarz, M.; Bernard, J.F.; Boivin, P. 1980: Familial pyridoxine-responsive sideroblastic anaemia. one case. La Nouvelle Presse Medicale 9(44): 3345-3347

Bjelle, A. 1981: Familial pyrophosphate arthropathy. Occurrence and Crystal Identification. Scandinavian Journal of Rheumatology 10(3): 209-214

Lubahn, J.D.; Lister, G.D. 1983: Familial radial nerve entrapment syndrome: a case report and literature review. Journal of Hand Surgery 8(3): 297-299

Nábrády, J.; Bagdány, S. 1973: Familial reciprocal translocation. Orvosi Hetilap 114(41): 2489-2491

Dugan, R.E. 1972: Familial rectal pain. Lancet 1(7755): 854

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Djeml, N.; Mestiri, S.; Gargouri, M.; Cammoun, M.; Hamza, R.; Ghrab, A. 1984: Familial rectocolonic polyposis. La Tunisie Medicale 62(4): 289-295

Koiffmann, C.P.; Wajntal, A.; Ursich, M.J.; Pupo, A.A. 1984: Familial recurrence of geleophysic dysplasia. American Journal of Medical Genetics 19(3): 483-486

Kaláb, Z.; Fajt, M.; Steinerová, H. 1965: Familial recurrent amyotrophic neuralgia in children. Ceskoslovenska Pediatrie 20(10): 883-886

Shindo, S. 1968: Familial recurrent corneal erosion. Nippon Ganka Gakkai Zasshi 72(7): 998-1004

Holzbach, R.T.; Sivak, D.A.; Braun, W.E. 1983: Familial recurrent intrahepatic cholestasis of pregnancy: a genetic study providing evidence for transmission of a sex-limited, dominant trait. Gastroenterology 85(1): 175-179

Brunner, F.X.; Herrmann, I.F. 1982: Familial recurrent laryngeal nerve paralysis, a genetically fixed syndrome -- additional remark on linkage of deficiency gene and HLA. Laryngologie Rhinologie Otologie 61(4): 186-188

Prejac, M.; Ajduković, G.; Plasaj, M. 1966: Familial recurrent paroxysmal polyserositis. Lijecnicki Vjesnik 88(9): 1041-1051

Cole, M. 1984: Familial recurrent peripheral facial palsy. American Journal of Otolaryngology 5(6): 432

Caillé, J.P.; Sarrade-Loucheur, C.; Ferrer, F.; Vergoz, D. 1980: Familial recurrent phlebitis due to deficiency of antithrombin III. Apropos of a case. Phlebologie 33(1): 131-137

Roos, D.; Thygesen, P. 1972: Familial recurrent polyneuropathy. a family and a survey. Brain: a Journal of Neurology 95(2): 235-248

Matiar-Vahar, H.; Rohrer, H. 1970: Familial recurrent polytopic neuropathy. Fortschritte der Neurologie Psychiatrie und Ihrer Grenzgebiete 38(10): 493-523

Galand, J.M. 1970: Familial recurrent venous thrombosis. Phlebologie 23(3): 221-224

Dockter, G.; Müller, J. 1980: Familial recurring intrahepatic cholestasis of the Tygstrup-Summerskill-Walshe type. Monatsschrift für Kinderheilkunde 128(5): 326-328

Eckert, P.; Meyer-Wahl, L. 1982: Familial recurring polytopic neuropathy. A case report. Der Nervenarzt 53(10): 598-602

Graff, G.; Chemke, J.; Lancet, M. 1972: Familial recurring thanatophoric dwarfism. A case report. Obstetrics and Gynecology 39(4): 515-520

Irvine, A.R.; Daroff, R.B.; Sanders, M.D.; Hoyt, W.F. 1968: Familial reflex blepharospasm. American Journal of Ophthalmology 65(6): 889-890

Kiruluta, G.H.; Afridi, S.K.; Winsor, G.M. 1983: Familial reflux in monozygotic twins. Urology 21(3): 298-299

McConaghy, N.; Clancy, M. 1968: Familial relationships of allusive thinking in university students and their parents. British Journal of Psychiatry: the Journal of Mental Science 114(514): 1079-1087

Roos, D. 1972: Familial remitting polyneuropathy associated with partial immunoparesis. Acta Neurologica Scandinavica 48(2): 133-147

Pathak, S.; Strong, L.C.; Ferrell, R.E.; Trindade, A. 1982: Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cells. Science 217(4563): 939-941

Yao, M.; Shuin, T. 1995: Familial renal cell carcinoma: review of recent molecular genetics. International Journal of Urology: Official Journal of the Japanese Urological Association 2(2): 61-70

Krous, H.F.; Wenzl, J.E. 1980: Familial renal cystic dysplasia associated with maternal diabetes mellitus. Southern Medical Journal 73(1): 85-86

Berthoux, F.; Badinand, N.; Pellet, H.; François, R. 1972: Familial renal cystic dysplasia with deafness and renal insufficiency. Archives Francaises de Pediatrie 29(4): 438

Kazi, Z.; Czakó, L. 1980: Familial renal diabetes. Orvosi Hetilap 121(15): 901-903

Walker, S.H.; Firminger, H.I. 1974: Familial renal dysplasia with sodium wasting and hypokalemic alkalosis. American Journal of Diseases of Children 127(6): 882-887

Miranda, D.; Schinella, R.A.; Finegold, M.J. 1972: Familial renal dysplasia. Microdissection studies in siblings with associated central nervous system and hepatic malformations. Archives of Pathology 93(6): 483-491

Cazacu, B.; Zălaru, M.; Onete, I.; Maravei, E.; Udrea, T. 1965: Familial renal glycosuria associated with maltosuria. Medicina Interna 17(7): 845-850

Buckalew, V.M. 1968: Familial renal tubular acidosis. Annals of Internal Medicine 68(6): 1367-1368

Eggert, W.; Hilgenfeld, E.; Reimann, J. 1980: Familial renal-retinal dysplasia - a combination of eye and kidney malformations. Zeitschrift für Arztliche Fortbildung 74(12): 575-577

Senior, B. 1973: Familial renal-retinal dystrophy. American Journal of Diseases of Children 125(3): 442-447

Corley, R.P.; DeFries, J.C.; Kuse, A.R.; Vandenberg, S.G. 1980: Familial resemblance for the Identical Blocks Test of spatial ability: no evidence for X linkage. Behavior Genetics 10(2): 211-215

Matthews, K.A.; Rosenman, R.H.; Dembroski, T.M.; Harris, E.L.; MacDougall, J.M. 1984: Familial resemblance in components of the type a behavior pattern: a reanalysis of the California type a twin study. Psychosomatic Medicine 46(6): 512-522

Nĕmec, J.; Kopecký, A.; Vána, S.; Bednár, J. 1984: Familial resistance to thyroid hormones. Ceskoslovenska Pediatrie 39(1): 36-39

McGee, M.G. 1981: Familial response to chronic illness: the impact of home versus hospital dialysis. Journal of the American Association of Nephrology Nurses and Technicians 8(4): 9-12

Weissbach, G.; Franz, H. 1970: Familial reticuloendotheliosis in early infancy. Folia Haematologica 93(2): 196-209

Freeman, R.G. 1972: Familial reticuloendotheliosis with eosinophilia and follicular mucinosis. Archives of Dermatology 105(5): 737-738

Omenn, G.S. 1971: Familial reticuloendotheliosis with eosinophilia: a follow-up. Birth Defects Original Article Series 7(8): 196

Miller, D.R. 1966: Familial reticuloendotheliosis: concurrence of disease in five siblings. Pediatrics 38(6): 986-995

Bartlett, W.J.; Price, J. 1983: Familial retinal arteriolar tortuosity with retinal hemorrhage. American Journal of Ophthalmology 95(4): 556-558

Gornig, H. 1966: Familial retinal detachment. Das Deutsche Gesundheitswesen 21(35): 1662-1665

Brown, G.C.; Tasman, W.S. 1980: Familial retinal dialysis. Canadian Journal of Ophthalmology. Journal Canadien d'Ophtalmologie 15(4): 193-195

Weichselbaum, R.R.; Little, J.B. 1980: Familial retinoblastoma and ataxia telangiectasia: human models for the study of DNA damage and repair. Cancer 45(4): 775-779

Strong, L.C.; Riccardi, V.M.; Ferrell, R.E.; Sparkes, R.S. 1981: Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation. Science 213(4515): 1501-1503

Knight, L.A.; Gardner, H.A.; Gallie, B.L. 1980: Familial retinoblastoma: segregation of chromosome 13 in four families. American Journal of Human Genetics 32(2): 194-201

Zajícek, M.; Gájová, B. 1966: Familial rheumatic fever and glomerulonephritis. Ceskoslovenska Pediatrie 21(3): 250-252

Uribarri, G.; Martínez Gastey, A.; Fernández Pizarro, J.P. 1965: Familial rheumatic fever. (Preliminary note). Revista Clinica Espanola 97(6): 410-412

Pinchuk, A.L. 1971: Familial rheumatism and some problems of disability in rheumatism. Terapevticheskii Arkhiv 43(1): 47-49

Rossen, R.D.; Brewer, E.J.; Sharp, R.M.; Yunis, E.J.; Schanfield, M.S.; Birdsall, H.H.; Ferrell, R.E.; Templeton, J.W. 1982: Familial rheumatoid arthritis: a kindred identified through a proband with seronegative juvenile arthritis includes members with seropositive, adult-onset disease. Human Immunology 4(3): 183-196

Rossen, R.D.; Brewer, E.J.; Sharp, R.M.; Ott, J.; Templeton, J.W. 1980: Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis. Journal of Clinical Investigation 65(3): 629-642

Palitzsch, D.; Scheffzek, A. 1981: Familial right bundle branch block and left axis deviation without cardiac disorders. Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 129(5): 300-302

Steenkamp, W.F.; Combrink, J.M.; Myburgh, D.P. 1980: Familial right bundle-branch block. South African Medical Journal 58(10): 393

Schaal, S.F.; Seidensticker, J.; Goodman, R.; Wooley, C.F. 1973: Familial right bundle-branch block, left axis deviation, complete heart block, and early death. a heritable disorder of cardiac conduction. Annals of Internal Medicine 79(1): 63-66

Goldstein, A.M.; Blot, W.J.; Greenberg, R.S.; Schoenberg, J.B.; Austin, D.F.; Preston-Martin, S.; Winn, D.M.; Bernstein, L.; McLaughlin, J.K.; Fraumeni, J.F. 1994: Familial risk in oral and pharyngeal cancer. European Journal of Cancer. Part B Oral Oncology 30b (5): 319-322

Andrieu, N.; Duffy, S.W.; Rohan, T.E.; Lê, M.G.; Luporsi, E.; Gerber, M.; Renaud, R.; Zaridze, D.G.; Lifanova, Y.; Day, N.E. 1995: Familial risk, abortion and their interactive effect on the risk of breast cancer--a combined analysis of six case-control studies. British Journal of Cancer 72(3): 744-751

Robert, J.; Pernod, J.; Bonnet, R. 1974: Familial sacro-coccygeal agenesis. Apropos of 6 cases in 2 families. Journal de Genetique Humaine 22(1): 45-60

Prieur, A.M.; Menkes, C.J.; Bessis, J.L.; Haquet, D.; Griscelli, C. 1982: Familial sarcoid arthritis. Archives Francaises de Pediatrie 39(5): 311-313

Salm, R. 1969: Familial sarcoidosis terminating as neurosarcoidosis. Postgraduate Medical Journal 45(528): 668-674

Sharma, O.P.; Johnson, C.S.; Balchum, O.J. 1971: Familial sarcoidosis. Report of four siblings with acute sarcoidosis. American Review of Respiratory Disease 104(2): 255-257

Huan, P.; Hachulla, E.; Delaporte, E.; Piette, F.; Hatron, P.Y.; Devulder, B. 1995: Familial sarcoidosis: 3 cases in the same family. La Revue de Medecine Interne 16(4): 280-282

Hutzler, R.U.; Shikanai, M.A. 1974: Familial sarcoidosis: occurence in 3 sisters. Revista do Hospital das Clinicas 29(1): 57-60

Mandi, N. 1969: Familial scarlet fever. Medicinski Pregled 22(9): 513-515

Walker, E.; Shaye, J. 1982: Familial schizophrenia. a predictor of neuromotor and attentional abnormalities in schizophrenia. Archives of General Psychiatry 39(10): 1153-1156

Rendall, J.R.; McKenzie, A.W. 1974: Familial scleroderma. British Journal of Dermatology 91(5): 517-522

Chekotilo, A.M.; Smerenskaia, A.V. 1970: Familial scleroma (according to data from Transcarpathia). Zhurnal Mikrobiologii Epidemiologii i Immunobiologii 47(2): 120-123

Blankenship, R.M.; Greenburg, B.R.; Lucas, R.N.; Reynolds, R.D.; Beutler, E. 1973: Familial sea-blue histiocytes with acid phosphatemia. a syndrome resembling Gaucher disease: the Lewis variant. JAMA 225(1): 54-56

Zina, A.M.; Bundino, S. 1983: Familial sea-blue histiocytosis with cutaneous involvement. A case report with ultrastructural findings. British Journal of Dermatology 108(3): 355-361

Carpentier, S.; Dutrillaux, B.; Lafourcade, J.; Berger, R.; Rethoré, M.O.; Lejeune, J. 1972: Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen. Annales de Genetique 15(1): 57-60

Nell, P.A.; Ammann, A.J.; Hong, R.; Stiehm, E.R. 1972: Familial selective IgA deficiency. Pediatrics 49(1): 71-79

Baird, W.M.; Ablin, R.J. 1971: Familial selective deficiency of IgA. Journal of Pediatrics 79(5): 877-878

Goldberg, L.S.; Fudenberg, H.H. 1968: Familial selective malabsorption of vitamin B 12. Re-evaluation of an in vivo intrinsic-factor inhibitor. New England Journal of Medicine 279(8): 405-407

Bell, M.; Harries, J.T.; Wolff, O.H.; Dawson, A.M.; Waters, A.H. 1973: Familial selective malabsorption of vitamin B12. Archives of Disease in Childhood 48(11): 896-900

Gräsbeck, R. 1972: Familial selective vitamin B 12 malabsorption. New England Journal of Medicine 287(7): 358

Shi, H.P.; Zhang, W.M.; Luo, H.Y.; Xue, G.R.; Zhu, C.Y.; Xu, J.Z.; He, B.Z. 1983: Familial selective vitamin B12 malabsorption (Imerslund-Grasbeck syndrome)--a case report. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae 5(1): 54-56

Altay, C.; Cetin, M.; Gümrük, F.; Irken, G.; Yetgin, S.; Laleli, Y. 1995: Familial selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome) in a pool of Turkish patients. Pediatric Hematology and Oncology 12(1): 19-28

Uzel, R. 1966: Familial seminoma. Turk Tip Cemiyeti Mecmuasi 32(12): 715-719

Rosenmayr, F.; Weippl, G. 1969: Familial septic granulomatosis. Wiener Klinische Wochenschrift 81(36): 635

Noemi, I.; Rugiero, E.; Viovy, A.; Cortés, P.P.; Cerva, J.L.; González, M.; Back, S.; Gottlieb, B.; Herrera, M.E.; Cordovez, J. 1994: Familial seroepidemiology of toxocariasis. Boletin Chileno de Parasitologia 49(3-4): 52-59

Gjone, E.; Norum, K.R. 1968: Familial serum cholesterol ester deficiency. Clinical study of a patient with a new syndrome. Acta Medica Scandinavica 183(1-2): 107-112

Arias, A.M.; Yung, C.W.; Rendler, S.; Soltani, K.; Lorincz, A.L. 1982: Familial severe twenty-nail dystrophy. Journal of the American Academy of Dermatology 7(3): 349-352

Hecht, F. 1981: Familial sex chromosome mosaicism (yes) and interchromosomal effects (no). Clinical Genetics 19(1): 77-78

Weatherall, D.J.; Pembrey, M.E.; Hall, E.G.; Sanger, R.; Tippett, P.; Gavin, J. 1970: Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation. Lancet 2(7676): 744-748

Kardos, G.; Veerman, A.J.; de Waal, F.C.; van Oudheusden, L.J.; Slater, R. 1996: Familial sideroblastic anemia with emergence of monosomy 5 and myelodysplastic syndrome. Medical and Pediatric Oncology 26(1): 54-56

Yeo, R.A.; Cohen, D.B. 1983: Familial sinistrality and sex differences in cognitive abilities. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior 19(1): 125-130

McKeever, W.F.; Hoff, A.L. 1982: Familial sinistrality, sex, and laterality differences in naming and lexical decision latencies of right-handers. Brain and Language 17(2): 225-239

Zhu, J.M. 1980: Familial sino-atrial node disease--report of 3 cases in one family. Zhonghua Nei Ke Za Zhi 19(6): 446-448

Livesley, B.; Catley, P.F.; Oram, S. 1972: Familial sinuatrial disorder. British Heart Journal 34(7): 668-670

Smolik, R.; Masior, J.; Stankiewicz, S.; Szymaniec, S.; Zienkowski, Z. 1968: Familial sinus bradycardia. Kardiologia Polska 11(1): 59-62

Spellberg, R.D. 1971: Familial sinus node disease. Chest 60(3): 246-251

Shao, D.Q. 1982: Familial sinus node disease--report of 2 cases in a family. Zhonghua Xin Xue Guan Bing Za Zhi 10(3): 203-204

Antia, A.U. 1970: Familial skeletal cardiovascular syndrome (Holt-Oram) in a polygamous African family. British Heart Journal 32(2): 241-244

Holm-Bentzen, M.; Nielsen, C.B. 1982: Familial slipped upper femoral epiphyses. Ugeskrift for Laeger 144(10): 717-718

Rennie, A.M. 1967: Familial slipped upper femoral epiphysis. Journal of Bone and Joint Surgery. British Volume 49(3): 535-539

Zakut, H.; Mashiach, S.; Insler, V. 1974: Familial solitary hypogonadotropism. Harefuah 87(8): 356-358

Nehlil, J.; Dumont, G.; Doutre, J.C. 1973: Familial spasmodic flexion paraplegia with important trophic bone disorders. Revue Neurologique (Paris) 128(2): 132-133

Chouza, C.; Caamaño, J.L.; De Medina, O.; Bogacz, J.; Oehninger, C.; Vignale, R.; De Anda, G.; Novoa, E.; De Bellis, R.; Cardozo, H. 1984: Familial spastic ataxia associated with Ehlers-Danlos syndrome with platelet dysfunction. Canadian Journal of Neurological Sciences. le Journal Canadien des Sciences Neurologiques 11(4 Suppl): 541-549

Gamboa, I.; Hernández Peniche, J. 1973: Familial spastic diplegia (study of a Mexican family). Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 25(1): 47-50

Rodríguez-García, A.; Olmos-García de Alba, G.; Valarezo-Crespo, F. 1982: Familial spastic diplegia and arginemia. Boletin Medico del Hospital Infantil de Mexico 39(10): 675-679

Alberca-Serrano, R.; Fabiani, F.; Deneve, V.; Macken, J. 1965: Familial spastic diplegia due to anoxic encephalopathy (Alpers). a contribution to the study of vascular fragilities of the nervous system of genetic type. Journal of the Neurological Sciences 2(5): 419-433

Archambault, P. 1966: Familial spastic paralysis. Journal of the Maine Medical Association 57(3): 52

Losiowski, Z.; Wiszczor-Adamczyk, B. 1967: Familial spastic paralysis in 3 siblings. Pediatria Polska 42(2): 219-221

Arjundas, G.; Ramamurthi, B.; Chettur, L. 1971: Familial spastic paraplegia (a review with four case reports). Journal of the Association of Physicians of India 19(9): 653-657

Tanaka, M.; Uchiyama, T.; Komatsu, M.; Morimatsu, M.; Hirai, S. 1982: Familial spastic paraplegia associated with large stature and chromosomal abnormalities. Rinsho Shinkeigaku 22(10): 940-946

Fujiwara, H.; Akabori, O.; Akashi, K.; Moriya, S. 1971: Familial spastic paraplegia in 3 families. Seikeigeka. Orthopedic Surgery 22(6): 471-476

Ogawa, A.; Shiohira, A. 1965: Familial spastic paraplegia occurring in siblings. Nihon Shonika Gakkai Zasshi. Acta Paediatrica Japonica 69(10): 884-888

Kuberski, T.; Tetava, P.; Koteka, G. 1981: Familial spastic paraplegia on Mitiaro, Cook Islands. New Zealand Medical Journal 93(680): 187-188

Van Damme, J.; van Bogaert, L.; Verschueren, M. 1965: Familial spastic paraplegia with chronic gouty arthropathy. Verhandelingen - Koninklijke Vlaamse Academie Voor Geneeskunde van Belgie 27(6): 727-764

Mahloudji, M.; Chuke, P.O. 1968: Familial spastic paraplegia with retinal degeneration. Johns Hopkins Medical Journal 123(3): 142-144

Stewart, R.M.; Tunell, G.; Ehle, A. 1981: Familial spastic paraplegia, peroneal neuropathy, and crural hypopigmentation: a new neurocutaneous syndrome. Neurology 31(6): 754-757

Gonçalves, A. 1980: Familial spastic paraplegia. Genetic-scientific discussion apropos of an affected family. Arquivos de Neuro-Psiquiatria 38(2): 144-149

Owens, L.A.; Peterson, C.R.; Burdick, A.B. 1982: Familial spastic paraplegia: a clinical and electrodiagnostic evaluation. Archives of Physical Medicine and Rehabilitation 63(8): 357-361

Ozsváth, K. 1968: Familial spastic spinal paralysis. Deutsche Zeitschrift für Nervenheilkunde 193(4): 287-323

Kozlowska, J.; Stawarczyk, W. 1973: Familial spherocytic anemia in a 12-year-old boy. Pediatria Polska 48(5): 627-630

Walker, F.A. 1974: Familial spina bifida associated with antiemetic ingestion in the first semester. Birth Defects Original Article Series 10(7): 17-21

Duke, R.J.; Hashimoto, S. 1973: Familial spinal arachnoiditis--a new entity. Transactions of the American Neurological Association 98: 98-102

Duke, R.J.; Hashimoto, S.A. 1974: Familial spinal arachnoiditis. a new entity. Archives of Neurology 30(4): 300-303

Popov, I.; Nikolić, V.; Mitrović, D. 1983: Familial spinal spastic paralysis--case study of the evolution of the disease through 5 generations. Medicinski Pregled 36(11-12): 515-517

Gallai, V.; Borri, P.; Nenci, G.; Cianchetti, A.; Agostini, L. 1974: Familial spino-cerebellar ataxia with megalocornea and stomatocytosis. Rivista di Patologia Nervosa E Mentale 95(5): 481-494

Daras, M.; Tuchman, A.J.; David, S. 1983: Familial spinocerebellar ataxia with skin hyperpigmentation. Journal of Neurology Neurosurgery and Psychiatry 46(8): 743-744

Richards, F.; Cooper, M.R.; Pearce, L.A.; Cowan, R.J.; Spurr, C.L. 1974: Familial spinocerebellar degeneration, hemolytic anemia, and glutathione deficiency. Archives of Internal Medicine 134(3): 534-537

Szappanos, L.; Czeizel, E.; Szepesi, K. 1984: Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome. Orvosi Hetilap 125(11): 633-638

Asher, D.M.; Masters, C.L.; Gajdusek, D.C.; Gibbs, C.J. 1983: Familial spongiform encephalopathies. Research Publications - Association for Research in Nervous and Mental Disease 60: 273-291

Bohnert, B.; Noetzel, H. 1974: Familial spongiform glioneuronal dystrophy. Archiv für Psychiatrie und Nervenkrankheiten 218(4): 353-368

Gambetti, P.; Mellman, W.J.; Gonatas, N.K. 1969: Familial spongy degeneration of the central nervous system (van Bogaert-Bertrand disease). An ultrastructural study. Acta Neuropathologica 12(2): 103-115

Sharpe, I.K.; Ahmad, M.; Braun, W. 1980: Familial spontaneous pneumothorax and HLA antigens. Chest 78(2): 264-268

Schofield, P.F.; Macdonald, N.; Clegg, J.F. 1970: Familial spontaneous rupture of the colon: report of two cases. Diseases of the Colon and Rectum 13(5): 394-396

Escat, J.; Carcy, J.B.; Gouzi, J.L.; Lazorthes, F.; Ribet, A.; Grimoud, M. 1970: Familial spontaneous spleno-renal anastomosis. Archives Francaises des Maladies de l'Appareil Digestif 59(9): 597-600

Bhigjee, A.I.; Bill, P.L.; Madurai, S.; York, D.; Thaler, D. 1995: Familial spread of HTLV-i in KwaZulu/Natal. South African Medical Journal 85(3): 186-187

Bosch, J.; Brugera, M.; Rodes, J. 1973: Familial spread of type-B hepatitis. Lancet 2(7826): 457

Nishimura, T.; Masumura, M.; Nishina, S. 1966: Familial staphylococcal infections, with special reference to a case with acute tibial osteomyelitis. Nihon Shonika Gakkai Zasshi. Acta Paediatrica Japonica 70(6): 479-484

Markand, O.N.; Garg, B.P.; Weaver, D.D. 1984: Familial startle disease (hyperexplexia). Electrophysiologic studies. Archives of Neurology 41(1): 71-74

Cockel, R.; Hill, E.E.; Rushton, D.I.; Smith, B.; Hawkins, C.F. 1973: Familial steatorrhoea with calcification of the basal ganglia and mental retardation. Quarterly Journal of Medicine 42(168): 771-783

Ostrowski, J.E. 1972: Familial sterility in a dairy shorthorn heard with frequent occurrence of segmental aplasia of the Wolffian duct. Deutsche Tierärztliche Wochenschrift 79(19): 473-475

Donofrio, P.; Ayala, F. 1983: Familial streblodactyly. Acta Dermato-Venereologica 63(4): 361-363

Li, Y.M. 1981: Familial streptomycin intoxication to the acoustic nerve. Zhonghua Yi Xue Za Zhi 61(11): 668-669

Rice, G.P.; Boughner, D.R.; Stiller, C.; Ebers, G.C. 1980: Familial stroke syndrome associated with mitral valve prolapse. Annals of Neurology 7(2): 130-134

Insley, J.; McDermott, A.; Parrington, J. 1968: Familial structural chromosome abnormality with maternal mosaicism. Annales de Genetique 11(3): 138-144

Sönnichsen, N.; Apostoloff, G.; Randow, U.; Weidauer, S.; Zoellner, E. 1965: Familial studies in lupus erythematosus. Dermatologische Wochenschrift 151(30): 883-884

Woodtli, W.; Ziegler, W.H.; Dambacher, M.A. 1982: Familial studies in medullary thyroid carcinoma and multiple endocrine adenomatosis. Schweizerische Medizinische Wochenschrift 112(49): 1780-1784

Hall, R.; Stanbury, J.B. 1967: Familial studies of autoimmune thyroiditis. Clinical and Experimental Immunology 2(Suppl): 719-725

Amor, B. 1983: Familial studies of reactive arthritis. Revue du Rhumatisme et des Maladies Osteo-Articulaires 50(11): 771-775

Lange, G. 1966: Familial Studies on the Heredity of Metric and Morphological Traits of the External Ear. Zeitschrift fur Morphologie und Anthropologie 57(2): 111-167

Pawlak, A.; Szydlowski, E. 1966: Familial study in a case of congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency. Polskie Archiwum Medycyny Wewnetrznej 36(6): 863-868

Baumann, R.; Straub, P.W. 1968: Familial study in congenital Hageman factor deficiency (blood coagulation factor XII). Schweizerische Medizinische Wochenschrift 98(42): 1653-1655

Utena, H. 1967: Behavioral studies in psychiatry. Seishin Shinkeigaku Zasshi 69(9): 893-900

Bellon, R.; Pericarpin, S.; Fauran, P. 1965: Familial study of SC hemoglobinopathies. Journal de Medecine de Bordeaux et du Sud-Ouest 142(6): 953-955

Selman, E.; Mena, M.; Aracena, M.M.; Bancalari, A.; Nuñez, F.; Castro, H. 1982: Familial study of extrinsic bronchial asthma. Revista Chilena de Pediatria 53(2): 101-105

Liu, X.H. 1983: Familial study of patients with psychosis, epilepsy and mental retardation. Zhonghua Shen Jing Jing Shen Ke Za Zhi 16(2): 99-102

Guijarro-Merino, R.; Villar-Ortiz, J.; Pérez-Vega, E.; García-Donas, M.A.; Carneado de la Fuente, J. 1984: Familial study of porphyria variegata through its presentation in an adolescent. Medicina Clinica 83(4): 160-163

Addor, M.C.; Pescia, G.; Guignard, J.P.; Genton, N. 1984: Familial study of vesico-ureteral reflux. Journal de Genetique Humaine 32(2): 91-100

Pagnan, A.; Zanetti, G.; Guarini, P. 1980: Familial study on the "double pre-beta lipoproteinemia" and on a polymorphic pattern of apolipoprotein e (EIV "variant" pattern) from human very low density lipoproteins (VLDL). Atherosclerosis 35(4): 351-361

Pagnan, A.; Kostner, G.; Braggion, M.; Ziron, L.; Bittolo Bon, G.; Avogaro, P. 1983: Familial study on "sinking pre-beta", the Lp(a) lipoprotein, and its relationship with serum lipids, apolipoprotein A-i and B and clinical atherosclerosis. Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift für Klinische Chemie und Klinische Biochemie 21(5): 267-272

Kidd, K.K.; Heimbuch, R.C.; Records, M.A.; Oehlert, G.; Webster, R.L. 1980: Familial stuttering patterns are not related to one measure of severity. Journal of Speech and Hearing Research 23(3): 539-545

Geisz, J.; Franzen, C.; Gekle, D. 1981: Familial subsepsis allergica- a systemic form of chronic juvenile arthritis. Helvetica Paediatrica Acta 36(2): 159-164

August, G.J.; Stewart, M.A. 1983: Familial subtypes of childhood hyperactivity. Journal of Nervous and Mental Disease 171(6): 362-368

Critelli, G.; Gallagher, J.J.; Sealy, W.C.; Lanza, G.G.; Condorelli, M. 1981: Familial sudden death in preexcitation syndrome. Surgical interruption of the anomalous pathways in two brothers. Giornale Italiano di Cardiologia 11(12): 1883-1894

Federico, A.; Turchiaro, G.; Carlomagno, S.; Valerio, P.; Stefani, M.; Del Vacchio, M.; Balbi, R.; Guazzi, G.C. 1974: Familial sulfatidosis associated with systemic ponto-cerebellar atrophy: clinical, biochemical, genetic and anatomo-pathological study. Acta Neurologica 29(3): 314-342

Sayag, J.; Fouque, R. 1972: Familial superficial disseminated actinic porokeratosis. Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 79(3): 290

Chudley, A.E.; Zheng, H.Z.; Pabello, P.D.; Shia, G.; Wang, H.C. 1983: Familial supernumerary microchromosome mosaicism: phenotypic effects and an attempt at characterization. American Journal of Medical Genetics 16(1): 89-97

Simon, M.; Le Mignon, L. 1984: Familial survey on a patient with idiopathic hemochromatosis. Therapeutic implications. Diabete and Metabolisme 10(3): 223-224

Allannic, H.; Lorcy, Y.; Cornec, A.; Le Marec, B.; Calmettes, C. 1980: Familial surveys in screening for thyroid cancers with amyloid stroma. Report of a personal survey carried out on 80 members of the same family. Annales d'Endocrinologie 41(1): 31-41

Zimmerman, R.A.; Wilson, E. 1968: Familial susceptibility to acquisition of group a B-hemolytic streptococci. American Journal of Diseases of Children 116(3): 292-300

Horn, Y. 1984: Familial susceptibility to malignant tumors. Harefuah 106(11): 531-533

Laplane, R.; Fontaine, J.L.; Lagardere, B.; Sambucy, F. 1972: Familial syndesmodysplasic dwarfism. a new disease entity. Archives Francaises de Pediatrie 29(8): 831-838

Refetoff, S.; DeWind, L.T.; DeGroot, L.J. 1967: Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone. Journal of Clinical Endocrinology and Metabolism 27(2): 279-294

Balouet, G.; Daoulas, R.; Borel, J.; Labouche, F. 1967: Familial syndrome of Gardner. Archives d'Anatomie Pathologique 15(4): 318-321

Yvonneau, M.; Vital, C.; Belly, C.; Coquet, M. 1971: Familial syndrome of amyotrophic lateral sclerosis with dementia. L'Encephale 60(6): 449-462

Chayasirisobhon, S.; Walters, B. 1984: Familial syndrome of deafness, myoclonus, and cerebellar ataxia. Neurology 34(1): 78-79

Castro-Gago, M.; Pombo, M.; Novo, I.; Tojo, R.; Peña, J. 1983: Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies. Anales Espanoles de Pediatria 19(2): 128-131

Rizzon, P.; Biasco, G.; Brindicci, G.; Mauro, F. 1973: Familial syndrome of midsystolic click and late systolic murmur. British Heart Journal 35(3): 245-259

Strong, W.B. 1968: Familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphism. Journal of Pediatrics 73(6): 882-888

Espiner, E.A.; Veale, A.M.; Sands, V.E.; Fitzgerald, P.H. 1970: Familial syndrome of streak gonads and normal male karyotype in five phenotypic females. New England Journal of Medicine 283(1): 6-11

Monnet, P.; Paufique, L.; Salle, B.; Rosenberg, D.; Pasquier, N.; Picaud, S. 1969: Familial syndrome of the Marinesco-Sjogren type with variations. Archives Francaises de Pediatrie 26(1): 87-95

Constantinidis, J.; de Ajuriaguerra, J. 1970: Familial syndrome with parkinsonian tremor and anosmia and its therapy with L-dopa associated with a decarboxylase inhibitor. Therapeutique 46(3): 263-269

Habighorst, L.V.; Albers, P. 1965: Familial synostosis of metacarpi IV and V. Zeitschrift für Orthopadie und ihre Grenzgebiete 100(4): 521-525

Jefferson, T.O.; Cohen, C. 1982: Familial syringomyelia with mental impairment. Journal of the Royal Army Medical Corps 128(1): 41-42

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

Reveille, J.D.; Bias, W.B.; Winkelstein, J.A.; Provost, T.T.; Dorsch, C.A.; Arnett, F.C. 1983: Familial systemic lupus erythematosus: immunogenetic studies in eight families. Medicine 62(1): 21-35

Meretoja, J. 1969: Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. a previously unrecognized heritable syndrome. Annals of Clinical Research 1(4): 314-324

Forabosco, A.; Cheli, E.; Marzona, L.; Temperani, P. 1973: Familial t (22q Dq) translocation and free trisomy 21 in offspring. Minerva Pediatrica 25(31): 1289-1299

Kitsiou-Tzeli, S.; Hallett, J.J.; Atkins, L.; Latt, S.A.; Holmes, L.B. 1984: Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the down syndrome. American Journal of Medical Genetics 18(4): 725-729

Najafzadeh, T.M.; Littman, V.A.; Dumars, K.W. 1983: Familial t(4;13) with abnormal offspring in three generations. American Journal of Medical Genetics 16(1): 15-22

Yassa, R.; Ananth, J. 1981: Familial tardive dyskinesia. American Journal of Psychiatry 138(12): 1618-1619

Taylor, J.C.; Colin, M.; Inamizu, T.; Mittman, C. 1980: Familial temperature sensitive alpha 1 protease inhibitor (M1Anaheim). Clinica Chimica Acta; International Journal of Clinical Chemistry 104(3): 301-308

Newcombe, H.B. 1966: Familial tendencies in diseases of children. British Journal of Preventive and Social Medicine 20(2): 49-57

Cantoni, E.; Forabosco, A.; Santoro, L.; Romagnoli, R.; Marchetti, M.; Gallo, E. 1982: Familial tendency in patients with compound odontomas. Rivista di Odontostomatologia e Implantoprotesi 4: 26-27

Surana, R.B.; Conen, P.E.; Braudo, M.; Keith, J.D. 1974: Familial tertiary trisomy with t (14q-; 1 plus?). Birth Defects Original Article Series 10(8): 53-65

Chandra, P.K.; Kalam, A.; Banerjee, P.; Bhattacharya, K.N.; Chowdhury, S. 1994: Familial testotoxicosis. Indian Pediatrics 31(4): 448-451

Chemke, J.; Graff, G.; Lancet, M. 1971: Familial thanatophoric dwarfism. Lancet 1(7713): 1358

Searles, R.P.; Plymate, S.R.; Troup, G.M. 1981: Familial thioamide-induced lupus syndrome in thyrotoxicosis. Journal of Rheumatology 8(3): 498-500

Raatikka, M.; Rapola, J.; Tuuteri, L.; Louhimo, I.; Savilahti, E. 1981: Familial third and fourth pharyngeal pouch syndrome with truncus arteriosus: DiGeorge syndrome. Pediatrics 67(2): 173-175

Rohn, R.D.; Leffell, M.S.; Leadem, P.; Johnson, D.; Rubio, T.; Emanuel, B.S. 1984: Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission. Journal of Pediatrics 105(1): 47-51

Kurstjens, R.; Bolt, C.; Haanen, C.A. 1967: Familial thrombocytopenia. Nederlands Tijdschrift Voor Geneeskunde 111(42): 1897-1898

Helmerhorst, F.M.; Heaton, D.C.; Crossen, P.E.; von dem Borne, A.E.; Engelfriet, C.P.; Natarajan, A.T. 1984: Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage. Human Genetics 65(3): 252-256

Gutenberger, J.; Trygstad, C.W.; Stiehm, E.R.; Opitz, J.M.; Thatcher, L.G.; Bloodworth, J.M. 1970: Familial thrombocytopenia, elevated serum IgA levels and renal disease. A report of a kindred. American Journal of Medicine 49(6): 729-741

Bentata-Pessayre, M.; Aurousseau, M.H.; Josso, F.; Delzant, G. 1980: Familial thromboembolic disease associated with antithrombin IIi deficiency. Annales de Medecine Interne 131(6): 378-382

Kurstjens, R.; Bolt, C.; Vossen, M.; Haanen, C. 1968: Familial thrombopathic thrombocytopenia. British Journal of Haematology 15(3): 305-317

Hofman, K.J.; Goldman, A.P.; Lurie, M.; Hockly, J.; Bradlow, B.A. 1980: Familial thrombosis associated with antithrombin III deficiency in a young adult male. A case report. South African Medical Journal 58(13): 531-533

Marciniak, E.; Farley, C.H.; DeSimone, P.A. 1974: Familial thrombosis due to antithrombin 3 deficiency. Blood 43(2): 219-231

Buri, P. 1974: Familial thrombosis of the mesenteric veins. Helvetica Chirurgica Acta 41(1-2): 85-87

Goldman, A.S.; Goldblum, R.M. 1973: Familial thymic aplasia--genetic defect or maternal effect. New England Journal of Medicine 288(2): 108

Wuketich, S.; Zwintz, E. 1983: Familial thymoma. Wiener Klinische Wochenschrift 95(12): 424-428

Rais, N.; Kalra, P.; Bhandarkar, S.D.; Satoskar, R.S. 1983: Familial thyroid disease: Grave's disease and non-toxic goitre (a case report). Journal of Postgraduate Medicine 29(4): 253-254

Orti, E.; Castells, S.; Qazi, Q.H.; Inamdar, S. 1971: Familial thyroid disease: lingual thyroid in two siblings and hypoplasia of a thyroid lobe in a third. Journal of Pediatrics 78(4): 675-677

Rosenberg, T.; Gilboa, Y. 1980: Familial thyroid ectopy and hemiagenesis. Archives of Disease in Childhood 55(8): 639-641

Lisa Catón, V.; Peña Somovilla, J.L.; Ochoa Gómez, F.J.; Salcedo Aguilar, F.J.; Vilella Morato, A.; Campo Hernández, J.M. 1994: Familial thyroid medullary carcinoma without associated neoplasms. Anales de Medicina Interna 11(9): 452-454

O'Brien, P.K.; Wilansky, D.L. 1981: Familial thyroid nodulation and arrhenoblastoma. American Journal of Clinical Pathology 75(4): 578-581

Strunge, P. 1973: Familial thyrosine-binding globulin deficiency. a genetic and biochemical assessment of 3 Danish families. Ugeskrift for Laeger 135(19): 857-861

Carta Sorcini, M.; Moschini, L.; Fiore, L.; Tomarchio, S.; Di Irio, M.G.; Gilardi, E.; Romagnoli, C.; Currò, V.; Carta, S. 1982: Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidism. Journal of Endocrinological Investigation 5(1): 21-25

Refetoff, S.; Selenkow, H.A. 1968: Familial thyroxine-binding globulin deficiency in a patient with Turner's syndrome (XO). Genetic study of a kindred. New England Journal of Medicine 278(20): 1081-1087

Shita, A.; Leroy, C.; Tagnon, A.; Chanoine, F.; Henoumont, Y.; Gillerot, Y. 1981: Familial thyroxine-binding globulin deficiency with neurological abnormalities. Acta Clinica Belgica 36(6): 313-314

Strunge, P. 1974: Familial thyroxine-binding globulin deficiency. a study of three Danish families. Acta Medica Scandinavica 195(1-2): 5-9

Grant, D.B.; Clarke, H.G.; Putman, D. 1974: Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups. Journal of Medical Genetics 11(3): 271-274

Stockigt, J.R.; Barlow, J.W. 1982: Familial thyroxine-excess syndrome. Annals of Internal Medicine 97(1): 143-144

Costa, L.R.; D'Elia, P.R. 1970: Familial tinea caused by Trichophyton verrucosum. Hospital 77(4): 1347-1354

Hoo, J.J.; Fischer, A.; Fuhrmann, W. 1982: Familial tiny 9p/20p translocation: 9p24. the critical segment for monosomy 9p syndrome. Annales de Genetique 25(4): 249-252

Schwanitz, G.; Keft, K.; Fleischer-Peters, A.; Zschiesche, S. 1983: Familial tooth position anomalies in the Orangutang. Orthodontic, cytogenetic and anthropological studies. Fortschritte der Kieferorthopadie 44(3): 172-183

St Grabski, R.; Nowicki, T. 1982: Familial torticollis. Chirurgia Narzadow Ruchu i Ortopedia Polska 47(1-2): 135-138

Soikup, S.W.; Passarge, E.; Becroft, S.M.; Shaw, R.L.; Young, L.G. 1969: Familial translocation (3?--;G?q+) and nondisjunction of chromosome in group G in two unrelated families. Cytogenetics 8(4): 315-325

Fried, K.; Bukovsky, J.; Rosenblatt, M.; Mundel, G. 1974: Familial translocation 15-22. a possible cause for abortions in female carriers. Journal of Medical Genetics 11(3): 280-282

Ricci, N.; Dallapiccola, B.; Cotti, G. 1968: Familial translocation 2-D. Annales de Genetique 11(2): 111-113

Tancredi, F.; Ventruto, V. 1981: Familial translocation 2; 17 with partial trisomy 2q32 to 2qter. La Pediatria 89(1): 35-40

Giliberti, P.; Celona, A.; Della Pietra, M.; De Masi, R.V.; Fioretti, G.; Pagano, L.; Renda, S.; Vetrella, A.; Ventruto, V. 1980: Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter. Annales de Genetique 23(4): 249-250

Tal'vik, T.A.; Mikel'saar, A.V.; Mikel'saar, R.V. 1974: Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+). Soviet Genetics 8(5): 651-657

Tharapel, S.A.; Lewandowski, R.C.; Kukolich, M.K. 1984: Familial translocation leading to partial trisomy 13: report of three cases. Indian Journal of Pediatrics 51(411): 481-487

Huang, T.H.; Peckham, D.; Batanian, J.R.; Martin, M.B.; Kouba, M.; Caldwell, C.W.; Miles, J.H. 1994: Familial translocation t(10;14) (q26.1;q32.3): report of three offspring with 10q deletion and 14q duplication. Clinical Genetics 46(4): 299-303

Dallapiccola, B. 1971: Familial translocation t(2p-; 17p+). Annales de Genetique 14(2): 153-155

Gregori Romero, M.; Gil Benso, R.; López Ginés, C.; Pellín Pérez, A.; Barberá Guillem, E. 1984: Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities. Anales Espanoles de Pediatria 21(6): 593-596

Del Amo, A.; Gullón, A. 1972: Familial translocation t(3p+;8q-) studied by banding with giemsa staining. Humangenetik 15(1): 14-19

Giovannelli, G.; Forabosco, A.; Dutrillaux, B. 1974: Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters. Annales de Genetique 17(2): 119-124

Tenconi, R.; Baccichetti, C.; Dussini, N.; Panizza, G. 1974: Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy. Annales de Genetique 17(4): 275-277

Henrot, H.; Aladenise, J.; Inghel, J. 1972: Familial transmission deafness. Annales d'Oto-Laryngologie et de Chirurgie Cervico Faciale: Bulletin de la Societe d'Oto-Laryngologie des Hopitaux de Paris 89(3): 176-180

Loranger, A.W.; Oldham, J.M.; Tulis, E.H. 1982: Familial transmission of DSM-IIi borderline personality disorder. Archives of General Psychiatry 39(7): 795-799

Ricci, N.; Dallapiccola, B.; Preto, G. 1970: Familial transmission of a Gq- (Ph1-like) chromosome. Annales de Genetique 13(4): 263-264

Lozzio, C.B.; Kattine, A.A. 1969: Familial transmission of a chromosomal translocation t(2q+;Cp-). Journal of Medical Genetics 6(2): 174-179

Cohen, M.M.; Lockwood, M.A. 1967: Familial transmission of a presumptive D/E (13-15/17-18) short arm translocation. Pediatric Research 1(2): 104-109

Smith, G.F.; Berg, J.M.; Ridler, M.A.; Faunch, J.A.; Farnham, F.N.; Pendrey, M.J. 1967: Familial transmission of an aberrant submetacentric chromosome. Journal of Mental Deficiency Research 11(1): 58-68

Tuckerman, E.; Gray, J.E.; Salmon, J. 1970: Familial transmission of an unusual variant of a group C chromosome. Annales de Genetique 13(3): 183-186

David, X.R.; Blanc, P.; Pageaux, G.P.; Desprez, D.; Diaz, D.; Lemaire, J.M.; Tognarelli, B.; Larrey, D.; Michel, H. 1995: Familial transmission of hepatitis C virus. Gastroenterologie Clinique et Biologique 19(2): 150-155

Berlin, I.N. 1981: Familial treatment of severe adolescent problems. Current Psychiatric Therapies 20: 61-69

Bohlega, S.; Stigsby, B.; al-Kawi, M.Z.; McLean, D.R.; Ozand, P.; Omer, S.; Coates, P. 1995: Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging. Movement Disorders: Official Journal of the Movement Disorder Society 10(4): 513-517

Johnstone, F.; Inglis, L. 1974: Familial trends in low birth weight. British Medical Journal 3(5932): 659-661

Witczuk, J.; Gruchała, E.; Stefańska, J. 1982: Familial trichinosis after consumption of boar's meat. Przeglad Epidemiologiczny 36(1-2): 181-184

Murachi, S.; Nogami, H.; Oki, T.; Ogino, T. 1981: Familial tricho-rhino-phalangeal syndrome Type Ii. Clinical Genetics 19(3): 149-155

Linn, H.W.; Hunter, G.A. 1970: Familial trichoepithelioma of unusual distribution. Australasian Journal of Dermatology 11(2): 101-103

Steenkamp, W.F. 1972: Familial trifascicular block. American Heart Journal 84(6): 758-760

Testa, D.; Milanese, C.; La Mantia, L.; Mastrangelo, M.; Crenna, P.; Negri, S. 1981: Familial trigeminal neuralgia in Charcot-Marie-Tooth disease. Journal of Neurology 225(4): 283-287

Van Genechten, F. 1982: Familial trigger thumb in children. Hand 14(1): 56-58

Cotta, H.; Jäger, M. 1965: Familial triphalangism of the thumb and its surgical treatment. Archiv für Orthopadische und Unfall-Chirurgie 58(4): 282-290

Stoll, C.; Roth, M.P. 1981: Familial trisomy 10q. Archives Francaises de Pediatrie 38(4): 273-274

Parazzini, F.; La Vecchia, C.; Franceschi, S.; Mangili, G. 1984: Familial trophoblastic disease: case report. American Journal of Obstetrics and Gynecology 149(4): 382-383

Mori, Y.; Mizutani, S. 1968: Familial true hermaphroditism in genetic females. Nihon Hinyokika Gakkai Zasshi. Japanese Journal of Urology 59(10): 857-864

Grossiord, A.; Lacert, P.; Got, C.; Gaussel, J.J. 1973: Familial truncular paralysis. A case with biopsy of a peripheral nerve. Histopathological lesions of a very peculiar type. Revue Neurologique (Paris) 128(6): 426-428

Biscione, C.; Lamberti, A. 1972: Familial tuberculosis at the present time. Clinico-statistical notes. Rassegna Internazionale di Clinica E Terapia 52(7): 383-395

Singh, S.V.; Goyal, S.K.; Chowdhury, B.L.; Shrimali, R.; Bansal, N.K. 1972: Familial tuberous sclerosis (report of two cases in family with intra-abdominal tumors). Journal of the Association of Physicians of India 20(7): 529-532

Serbănescu, G.; Neagoe, S.; Serbănescu, C.; Mălăescu, G.; Colceriu, N.; Davidescu, C.; Ruxanda, M. 1982: Familial tuberous sclerosis in 2 successive generations with jacksonian crisis and grand-mal epilepsy. Revista de Medicina Interna Neurologie Psihiatrie Neurochirurgie Dermato-Venerologie. Neurologie Psihiatrie Neurochirurgie 27(2): 119-124

Bejar, R.L. 1966: Familial tuberous sclerosis. a clinical reminder. Clinical Pediatrics 5(2): 127-129

Verma, B.S.; Tailor, M.H. 1965: Familial tuberous sclerosis: a review with report of three cases. Indian Pediatrics 2(11): 401-410

Ponz de Leon, M. 1994: Familial tumors of other organs. Recent Results in Cancer Research. Fortschritte der Krebsforschung. Progres Dans les Recherches sur le Cancer 136: 332-340

Brusilovskiĭ, E.A. 1972: Familial tumors of the stomach. Klinicheskaia Meditsina 50(6): 103-104

O'Mahony, M.Y.; Ellis, J.P.; Hellier, M.; Mann, R.; Huddy, P. 1984: Familial tylosis and carcinoma of the oesophagus. Journal of the Royal Society of Medicine 77(6): 514-517

Herman, T.E.; Mc Alister, W.H. 1995: Familial type 1 jejunal atresias and renal dysplasia. Pediatric Radiology 25(4): 272-274

Dyerberg, J. 1974: Familial type 3 hyperlipoproteinemia. Ugeskrift for Laeger 136(12): 652-653

Dyerberg, A.J. 1974: Familial type i hyperlipoproteinemia. Ugeskrift for Laeger 136(52): 2932

Khoo, K.L.; Chong, Y.H.; Pillay, R.P. 1973: Familial type Ii hyperlipoproteinaemia in a Chinese family. Medical Journal of Australia 1(21): 1048-1050

Stein, E.A.; Mendelsohn, D.; Bersohn, I. 1974: Familial type Ii hyperlipoproteinaemia. Clinical features and results of treatment in children and young adults. South African Medical Journal 48(4): 135-138

Aso, K.; Iitani, I.; Fujita, M. 1972: Familial type Ii xanthoma. Nihon Hifuka Gakkai Zasshi. Japanese Journal of Dermatology 82(9): 739-748

Akazawa, S.; Ikeda, Y.; Toyama, K.; Miyake, S.; Takamori, M.; Nagataki, S. 1984: Familial type IIa hyperlipoproteinemia associated with a huge intracranial xanthoma. Archives of Neurology 41(7): 793-794

Schreibman, P.H.; Wilson, D.E.; Arky, R.A. 1969: Familial type IV hyperlipoproteinemia. New England Journal of Medicine 281(18): 981-985

Scharf, Y.; Nahir, M.; Levy, N. 1974: Familial ulcerative colitis associated with ankylosing spondylitis. Harefuah 86(1): 30-31

Tan, K.; Tominaga, S.; Hashimoto, A.; Mori, K.; Takao, A. 1973: Familial upper-limb cardiovascular syndrome--ventriculo-radial dysplasia with pulmonary hypertension. Kyobu Geka. Japanese Journal of Thoracic Surgery 26(12): 851-856

Alexander, F.; Campbell, S. 1970: Familial uremic medullary cystic disease. Pediatrics 45(6): 1024-1028

Srivastava, R.N. 1971: Familial uremic medullary cystic disease or nephronophthisis?. Pediatrics 47(2): 477-478

Degos, R.; de Cinarca, O.C.; Méry, F. 1970: Familial uroporphyrinuric pure late cutaneous porphyria. Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 77(1): 26-28

Castelain, P.Y. 1971: Familial urticaria due to cold. Bulletin de la Societe Francaise de Dermatologie et de Syphiligraphie 78(5): 525-526

Pachón Díaz, J.; Cuello Contreras, J.A.; Gómez Camacho, E.; Creagh Cerquera, R.; López Cortés, L.; Viciana Fernández, P. 1984: Familial urticaria induced by cold. Medicina Clinica 82(4): 183

James, M.P.; Eady, R.A. 1981: Familial urticaria pigmentosa with giant mast cell granules. a clinical, light, and electron microscopic study. Archives of Dermatology 117(11): 713-718

Castier, P.; François, M.; Duret, M.H. 1982: Familial uveitis. Bulletin des Societes d'Ophtalmologie de France 82(10): 1277-1279

Hemingway, A.P.; Leung, A.; Lavender, J.P. 1983: Familial vanishing limbs: four generations of idiopathic multicentric osteolysis. Clinical Radiology 34(5): 585-588

Abramson, P.R. 1973: Familial variables related to the expression of violent aggression in preschool-age children. Journal of Genetic Psychology 122(2d Half): 345-346

Roberts, J.T.; Byrne, E.H.; Rosenthal, D. 1981: Familial variant of dermatofibroma with malignancy in the proband. Archives of Dermatology 117(1): 12-15

Zharko, K.P.; el-Khelu, G.E. 1981: Familial variants of cardiac rhythm and conductivity disorders. Vrachebnoe Delo 11: 67-68

Galdston, M.; Janoff, A.; Davis, A.L. 1973: Familial variation of leukocyte lysosomal protease and serum 1 -antitrypsin as determinants in chronic obstructive pulmonary disease. American Review of Respiratory Disease 107(5): 718-727

Ishii, Y.; Kato, K.; Fujimaki, T.; Narusawa, T.; Terao, T. 1968: Familial variegate prophyria. Saishin Igaku. Modern Medicine 23(11): 2405-2410

Pasyk, K.A.; Argenta, L.C.; Erickson, R.P. 1984: Familial vascular malformations. Report of 25 members of one family. Clinical Genetics 26(3): 221-227

Waynberger, M.; Coutadon, M.; Peltier, J.M.; Ducloux, G.; Jallut, H.; Slama, R. 1974: Familial ventricular tachycardia. Apropos of 7 cases. La Nouvelle Presse Medicale 3(30): 1857-1860

Matsu, K.; Iseki, F.; Saigo, K.; Nagasawa, M.; Tomatsu, T. 1971: Familial vertebral dysplasia: a case report. Seikeigeka. Orthopedic Surgery 22(2): 110-114

Jerkins, G.R.; Noe, H.N. 1982: Familial vesicoureteral reflux: a prospective study. Journal of Urology 128(4): 774-778

Gigliotti, R.; Harrison, H.; Reveley, R.A.; Drabkowski, A.J. 1971: Familial vitamin D-refractory rickets. Journal of the American Dental Association 82(2): 383-387

Falls, W.F.; Carter, N.W.; Rector, F.C.; Seldin, D.W. 1968: Familial vitamin D-resistant rickets. Study of six cases with evaluation of the pathogenetic role of secondary hyperparathyroidism. Annals of Internal Medicine 68(3): 553-560

Kosińska, D.; Szreterowa, M. 1984: Familial vitreoretinal degeneration. Klinika Oczna 86(7): 307-308

Wright, R.L. 1969: Familial von Hippel-Lindau's disease. Case report. Journal of Neurosurgery 30(3): 281-285

Holt, R.J.; Freytes, C.O. 1983: Familial warfarin resistance. Drug Intelligence and Clinical Pharmacy 17(4): 281-283

Tamagna, J.A. 1965: Familial white folded dysplasia of the oral mucous membranes. Journal of Clinical Stomatology Conferences 6(3): 56-57

Kim, H.J.; Hsu, L.Y.; Hirschhorn, K. 1974: Familial x/x translocation: t(x;x)(p22;q13). Cytogenetics and Cell Genetics 13(5): 454-464

Sawkar, L.A. 1971: Familial xanthelasma, hyperlipidemia and multiple myeloma. Journal of the Association of Physicians of India 19(4): 329-334

Cifuentes Delatte, L.; Castro-Mendoza, H. 1967: Familial xanthinuria. Revista Clinica Espanola 107(4): 244-256

Pereg Macazaga, V.; García Fernández, H.; Regúlez, M.; Elorza Olabegoya, J.R.; Beitia Martín, J.J.; Vázquez García, J.A. 1984: Familial xanthinuria, 2 new cases. Medicina Clinica 82(8): 364-365

Paget, M.; Routier, G.; Leuridan, B. 1965: Familial xanthomatous hypercholesterolaemia. Apropos of a familial case. Annales de Biologie Clinique 23(5): 679-697

Paget, M.; Routier, G.; Leuridan, B. 1965: Familial xanthomatous hypercholesterolemia. Apropos of a familial case. Journal des Sciences Medicales de Lille 83(10): 543-560

Gaburro, D.; Ripa, R.; Volpato, S. 1965: Familial "chronic" hypoaldosteronism (a personal case). La Medecine Infantile 72(8): 553-557

Hudgson, P.; Bradley, W.G.; Jenkison, M. 1972: Familial "mitochondrial" myopathy. a myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings. Journal of the Neurological Sciences 16(3): 343-370

Worsfold, M.; Park, D.C.; Pennington, R.J. 1973: Familial "mitochondrial" myopathy. a myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings. Journal of the Neurological Sciences 19(3): 261-274

Van Wijngaarden, G.K.; Fleury, P.; Bethlem, J.; Meijer, A.E. 1969: Familial "myotubular" myopathy. Neurology 19(9): 901-908

Barraquer-Bordas, L.; Peres-Serra, J.; Grau-Veciana, J.M.; Sagimon-Rabassa, E. 1970: Familial "prosoplegic" migraine. Acta Neurologica Belgica 70(3): 301-308

Connolly, M.J.; Payne, R.H.; Johnson, G.; Gallie, B.L.; Allderdice, P.W.; Marshall, W.H.; Lawton, R.D. 1983: Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity. Human Genetics 65(2): 122-124

Buksowicz, C.; Wochnik-Dyjas, D. 1966: Familial, amyotrophic lateral sclerosis in childhood. Neurologia Neurochirurgia i Psychiatria Polska 16(7): 865-867

Soto Melo, J.; Rodriguez Puchol, J.; Calderon 1966: Familial, circumscribed angiokeratoma of Fabry with visceral lesions. Actas Dermo-Sifiliograficas 57(7): 181-192

Grim, C.E.; Weinberger, M.H. 1980: Familial, dexamethasone-suppressible, normokalemic hyperaldosteronism. Pediatrics 65(3): 597-604

Guérin, F. 1980: Familial, educational and social integration of patients suffering from congenital heart disease. La Revue du Praticien 30(21): 1403-1406

Verhulst, J.; Portmann, M.; Boissiéras, P.; Deminière, C.; Piton, J. 1980: Familial, malignant, chemodectoma bilateral in a 16-year-old girl. Revue de Laryngologie - Otologie - Rhinologie 101(5-6): 251-261

Adami, H.O.; Hansen, J.; Jung, B.; Rimsten, A. 1980: Familiality in breast cancer: a case-control study in a Sweden population. British journal of cancer 42(1): 71-77

Mauro, R.; Volpe, E.; Cataldi, V. 1968: Familiality of Hodgkin's disease. Rassegna Internazionale di Clinica E Terapia 48(4): 199-206

Murata, M. 1982: Familiality of breast cancer and hereditary factors. Gan to Kagaku Ryoho. Cancer and ChemoTherapy 9(5): 808-814

Pethö, B.; Karczag, I.; Czeizel, A. 1982: Familially accumulated schizophrenia (folie à cinq) in association with Stein-Leventhal syndrome. Psychiatria Clinica 15(4): 206-211

Lygonis, C.S. 1969: Familiar absence of olfaction. Hereditas 61(3): 413-416

Newman, C.V. 1972: Familiar and relative size cues and surface texture as determinants of relative distance judgments. Journal of Experimental Psychology 96(1): 37-42

Korczowski, R. 1965: Familiar appearance of Caffey's disease. Wiadomosci Lekarskie 18(19): 1551-1552

Rocca, G.; Poli, G.; Gerardo, P.; Ascione, A.; Caporaso, N.; Craxi, A.; Dentico, P.; Marinucci, G.; Piccinino, F.; Raimondo, G. 1983: Familiar clustering of delta infection. Progress in Clinical and Biological Research 143: 133-137

Semmence, A.M. 1972: Familiar faces. Practitioner 208(244): 286-287

McCormick, J.S. 1972: Familiar faces--the constant attender. Proceedings of the Royal Society of Medicine 65(6): 507-509

Semmence, A. 1972: Familiar faces. Problems of identification. Proceedings of the Royal Society of Medicine 65(6): 505-507

Gradowski, B. 1965: Familiar food poisoning caused by Salmonella typhimurium. Przeglad Epidemiologiczny 19(2): 249-250

Jiménez Díaz, C.; Perianes, J.; Peláez, J.L.; Sánchez Villares, E.; Linazasoro, J.M.; Villalobos, E. 1964: Familiar infantile haemochromatosis. Bulletin of the Institute for Medical Research University of Madrid 17(4): 173-185

Cole, F. 1974: Familiar susceptibility to anesthesia. Nebraska Medical Journal 59(12): 469-470

Howell, S.C. 1972: Familiarity and complexity in perceptual recognition. Journal of Gerontology 27(3): 364-371

Dale, H.C. 1967: Familiarity and free recall. Quarterly Journal of Experimental Psychology 19(2): 103-108

Epstein, A.; Giolas, T.G.; Owens, E. 1968: Familiarity and intelligibility of monosyllabic word lists. Journal of Speech and Hearing Research 11(2): 435-438

Hake, H.W.; Myers, A.E. 1969: Familiarity and shape constancy. Journal of Experimental Psychology 80(2): 205-214

Craven, E.E. 1972: Familiarity breeds carelessness. Tic 31(3): 14-16

Stirling, R.V.; Summerbell, D. 1983: Familiarity breeds contempt: the behaviour of axons in foreign and familiar environments. Progress in Clinical and Biological Research 110 Pt A: 217-226

Couldridge, R. 1972: One jigger, no complications. Nursing Mirror and Midwives Journal 134(9): 31

Doni, A.; Brancato, R.; Bartoletti, L.; Berni, G. 1965: Familiarity characteristics of Sjögren's disease. (Clinical contribution and considerations). Rivista Critica di Clinica Medica 65(6): 750-759

Young, A.W.; Hay, D.C.; McWeeny, K.H.; Ellis, A.W.; Barry, C. 1985: Familiarity decisions for faces presented to the left and right cerebral hemispheres. Brain and Cognition 4(4): 439-450

Mewhort, D.J. 1967: Familiarity of letter sequences, response uncertainty, and the tachistoscopic recognition experiment. Canadian Journal of Psychology 21(4): 309-321

Filip, M. 1966: Familiarity of selected population groups with the main principles of socialist health services. Ceskoslovenske Zdravotnictvi 14(7): 441-445

Tateishi, Y. 1982: Familiarity of the public health nurse with the public health clinic: a lesson in public health nursing activities at Kiyokawa-mura. Japanese Journal for Public Health Nurse 38(4): 281-284

Genskow, J.K.; Maglione, F.D. 1965: Familiarity, dogmatism, and reported student attitudes toward the disabled. Journal of Social Psychology 67(2): 329-341

Crandall, J.E. 1967: Familiarity, preference, and expectancy arousal. Journal of Experimental Psychology 73(3): 374-381

Flowers, J.H.; Polansky, M.L.; Kerl, S. 1981: Familiarity, redundancy, and the spatial control of visual attention. Journal of Experimental Psychology. Human Perception and Performance 7(1): 157-166

Rosnow, R.L.; Goldstein, J.H. 1967: Familiarity, salience, and the order of presentation of communications. Journal of Social Psychology 73(1): 97-110

Drake, R.A. 1984: Familiarity-and-liking relationship under conditions of induced lateral orientation. International Journal of Neuroscience 23(3): 195-198

Scandura, J.M. 1965: Familiarization and one-trial learning: a positive interaction. Psychological Reports 17(1): 27-38

Cherniakov, I.N.; Prodin, V.I.; Shishov, A.A. 1994: Familiarization drills with barochamber ascents for flight personnel as an element in their psychophysiological training for high-altitude flights. Voenno-MeditsinskiiZhurnal 1994(8): 51

Kaskirinne, L. 1972: Familiarization programs for operating room nurses. Sairaanhoidon Vuosikirja 9: 169-183

Irwin, P.; Fink, M. 1983: Familiarization session and placebo control in EEG studies of drug effects. Neuropsychobiology 10(2-3): 173-177

Bruchác, D. 1974: Familiarly reminiscence on the ancient school of midwifery. Ceskoslovenska Gynekologie 39(4): 256-257

Hellner, K.A.; Rickers, J. 1973: Familiary bilateral segmental retinopathia pigmentosa. Ophthalmologica. Journal International d'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift für Augenheilkunde 166(5): 327-341

Pavúr, J. 1973: Familiary polyposis of the large intestine. Rozhledy V Chirurgii: Mesicnik Ceskoslovenske Chirurgicke Spolecnosti 52(5): 318-322

Cleveland, M. 1981: Families and adolescent drug abuse: structural analysis of children's roles. Family Process 20(3): 295-304

Glynn, T.J. 1982: Families and drugs: a life-span research approach. American Journal of Drug and Alcohol Abuse 9(4): 397-412

Quinn, A.; Ford, J.; Mazzawy, M. 1981: Families and feelings: a time for sharing. Journal of Neurosurgical Nursing 13(4): 217-218

Grace, J.T. 1995: Families and nurses: building partnerships for growth and health. Journal of Obstetric Gynecologic and Neonatal Nursing: Jognn 24(4): 298-300

Parks, J.; Boyer, G.M. 1966: Families and physicians (George M. Boyer). Maryland State Medical Journal 15(7): 39-45

Laing, R.D.; Esterson, A. 1967: Families and schizophrenia. International Journal of Psychiatry 4(1): 65-71

Reiss, D. 1995: Families and schizophrenia redux. Psychiatry 58(1): 1-5

Mishler, E.G. 1966: Families and schizophrenia; an experimental study. Mental Hygiene 50(4): 552-556

Molter, N.C. 1994: Families are not visitors in the critical care unit. Dimensions of Critical Care Nursing: Dccn 13(1): 2-3

Player, M.L.; Frank, D.I. 1994: Families as a source of AIDS information for school age children. Clinical Nurse Specialist Cns 8(6): 321-327

Hatfield, A.B. 1981: Families as advocates for the mentally ill: a growing movement. Hospital and Community Psychiatry 32(9): 641-642

Garbarino, J.; Sebes, J.; Schellenbach, C. 1984: Families at risk for destructive parent-child relations in adolescence. Child Development 55(1): 174-183

Herman, J.; Hirschman, L. 1981: Families at risk for father-daughter incest. American Journal of Psychiatry 138(7): 967-970

Ayoub, C.; Jacewitz, M.M. 1982: Families at risk of poor parenting: a descriptive study of sixty at risk families in a model prevention program. Child Abuse and Neglect 6(4): 413-422

Ayoub, C.; Jacewitz, M.M. 1982: Families at risk of poor parenting: a model for service delivery, assessment, and intervention. Child Abuse and Neglect 6(3): 351-358

Frommer, E.A. 1973: Families at risk: help for those from broken homes. Nursing Times 69(43): 1408-1409

Lauridsen, V.; Jensen, E.L.; Sørensen, B.; Danfaer, L.; Pedersen, L.S. 1984: Families caught in the squeeze because of inadequate teamwork. Sygeplejersken 84(34): 12-13

Lyden, C.J.; Robertson, J.G. 1970: Families clinic, Limassol. a study of a unique British expatriate general practice in Cyprus. Journal of the Royal College of General Practitioners 20(99): 212-223

Collins, V.J. 1966: Positioning of the patient for surgery. AORN Journal 4(6): 55-66

Vaughan, D.H. 1968: Families experiencing a sudden, unexpected infant death. Journal of the Royal College of General Practitioners 16(5): 359-367

Dyregrov, A.; Hordvik, E.; Alsaker, T.G.; Finne, P.H. 1985: Families experiencing the death of child. a model for support. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 105(33): 2391-2395

Goldberg, B. 1995: Families facing choices. Asha 37(5): 38-45

Blackburn, R. 1971: Families in Singapore. Journal of the Royal College of General Practitioners 21(104): 168-182

Krim, A.S. 1974: Families in crisis. a cooperative project brings comprehensive on-site services to families living in an emergency relocation hotel. Children Today 3(1): 2-6 Passim

Christensen, E. 1995: Families in distress, the development of children growing up with alcohol and violence. Arctic Medical Research 54(Suppl 1): 53-59

Power, J.G. 1968: Families in flats. British Medical Journal 1(5590): 516

Moore, N.C. 1982: Families in high-arise flats. British Medical Journal 285(6336): 215-216

Cook, D.A.; Morgan, H.G. 1982: Families in high-rise flats. British Medical Journal 284(6319): 846

King, R.J. 1980: Families in the eighties. Australian Family Physician 9(11): 786-792

Albertsen, C.S.; Lyngstad, G.D. 1971: Families in the hospital. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 91(12): 879-882

Dunkel, J.; Eisendrath, S. 1983: Families in the intensive care unit: their effect on staff. Heart and Lung: the Journal of Critical Care 12(3): 258-261

Mackie, A.J. 1982: Families of adopted adolescents. Journal of Adolescence 5(2): 167-178

Miyake, Y. 1981: Families of aged, demented patients being cared for at home and assistance extended to them--activities of an organization of families with aged demented patients. Nursing Technique 27(3): 329-334

Quadrio, C. 1984: Families of agoraphobic women. Australian and New Zealand Journal of Psychiatry 18(2): 164-170

Rawlings, N.D.; Barrett, A.J. 1995: Families of aspartic peptidases, and those of unknown catalytic mechanism. Methods in Enzymology 248: 105-120

Feldman, R.B.; Guttman, H.A. 1984: Families of borderline patients: literal-minded parents, borderline parents, and parental protectiveness. American Journal of Psychiatry 141(11): 1392-1396

Jenkins, S.; Norman, E. 1969: Families of children in foster care. Children 16(4): 155-159

Dar, H.; Winter, S.T.; Tal, Y. 1974: Families of children with cleft lips and palates: concerns and counselling. Developmental Medicine and Child Neurology 16(4): 513-517

Husband, P.; Hinton, P.E. 1972: Families of children with repeated accidents. Archives of Disease in Childhood 47(253): 396-400

Axelrod, J.; Geismar, L.; Ross, R. 1994: Families of chronically mentally ill patients: their structure, coping resources, and tolerance for deviant behavior. Health and Social Work 19(4): 271-278

Rawlings, N.D.; Barrett, A.J. 1994: Families of cysteine peptidases. Methods in Enzymology 244: 461-486

Gallagher, J.J.; Beckman, P.; Cross, A.H. 1983: Families of handicapped children: sources of stress and its amelioration. Exceptional Children 50(1): 10-19

Selby, J.W.; Calhoun, L.G.; Jones, J.M.; Matthews, L. 1980: Families of incest: a collation of clinical impressions. International Journal of Social Psychiatry 26(1): 7-16

Hoover, C.F.; Insel, T.R. 1984: Families of origin in obsessive-compulsive disorder. Journal of Nervous and Mental Disease 172(4): 207-215

Rawlings, N.D.; Barrett, A.J. 1994: Families of serine peptidases. Methods in Enzymology 244: 19-61

Stevenson, A.C.; Davison, B.C. 1966: Families referred for genetic advice. British Medical Journal 2(5521): 1060-1062

Crocker, A.C.; Cullinane, M.M. 1972: Families under stress. The diagnosis of Hurler's syndrome. Postgraduate Medicine 51(3): 223-229

Noble, D.N.; Hamilton, A.K. 1981: Families under stress: perinatal social work. Health and Social Work 6(1): 28-35

Shuttlesworth, G.E.; Rubin, A.; Duffy, M. 1982: Families versus institutions: incongruent role expectations in the nursing home. Gerontologist 22(2): 200-208

Marincheva, G.S. 1981: Families with 2 oligophrenic siblings. Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 81(3): 383-387

Kaneko, M. 1968: Families with a high incidence of cancer. Nihon Rinsho. Japanese Journal of Clinical Medicine 26(9): 2108-2109

Heap, K.K. 1984: Families with abused children: a follow-up study of post-crisis support. Child Abuse and Neglect 8(4): 467-472

Monvall, E. 1973: Families with children and the employee get most in federal budget proposals. Tidskrift for Sveriges Sjukskoterskor 40(3): 12-18

Stiksrud, A.; Margraf, J. 1982: Families with drug-dependent adolescents. Praxis der Kinderpsychologie und Kinderpsychiatrie 31(7): 271-277

Mosher, L.R.; Pollin, W.; Stabenau, J.R. 1971: Families with identical twins discordant for schizophrenia: some relationships between identification, thinking styles, psychopathology and dominance-submissiveness. British Journal of Psychiatry: the Journal of Mental Science 118(542): 29-42

Betancourt, G.L. 1971: Families with suspected maltreated children. Boletin de la Asociacion Medica de Puerto Rico 63(9): 216-218

Wortis, H.; Pollack, M.; Wortis, J. 1966: Families with two or more mentally retarded or mentally disturbed siblings: the preponderance of males. American Journal of Mental Deficiency 70(5): 745-752

Herman, S.E.; Thompson, L. 1995: Families' perceptions of their resources for caring for children with developmental disabilities. Mental Retardation 33(2): 73-83

Incebük, B. 1983: Families' problems over their hospitalized relatives in Gölbaşi Mental Hospital. Turk Hemsireler Dergisi 33(2): 33-35

Butler, M.C. 1984: Families' responses to chemotherapy by an ambulatory infusion pump. Nursing Clinics of North America 19(1): 139-144

High, D.M. 1994: Families' roles in advance directives. Hastings Center Report 24(6): S16-S18

Oliveri, M.E.; Reiss, D. 1982: Families' schemata of social relationships. Family Process 21(3): 295-311

Vilain, R. 1982: Families, i love you, or, a good understanding of hygiene. Revue de l'Infirmiere 32(20): 10-11

Pinkus, R.L. 1984: Families, brain death, and traditional medical excellence. Journal of Neurosurgery 60(6): 1192-1194

Gullotta, T.P.; Donohue, K.C. 1983: Families, relocation, and the corporation. New Directions for Mental Health Services 20: 15-24

Jolly, H. 1974: Families--a nation's strength. Health Visitor 47(7): 216-222

Pearse, J. 1994: Families--an important part of client care. Contemporary Nurse 3(3): 132-133

Lamb, H.R. 1983: Families: practical help replaces blame. Hospital and Community Psychiatry 34(10): 893

Abasiekong, E.M. 1981: Familism and hospital admission in rural Nigeria--a case study. Social Science and Medicine. Medical Anthropology 15b (1): 45-50

Tamez, E.G. 1981: Familism, machismo and child rearing practices among Mexican Americans. Journal of Psychosocial Nursing and Mental Health Services 19(9): 21-25

Brunschwig, H. 1982: Familty Therapy. SOINS. Psychiatrie 16: 47-49