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List of PDF Full Texts available from EurekaMag Chapter 40129

Chapter 40129 contains a list of PDF Full Texts available from EurekaMag.





Starzycka, M., 1991:
Familial exudative vitreoretinopathy--vitreoretinopathia familiaris exsudative. I. Review of the literature

Zavalishin, I.A., 1975:
Familial facial neuritis

Forest, H.; Mardel, C.; Goujard, P.; Blum, F.; Diehly, A., 1979:
Familial facial paralysis. Generalised cortical hyperostosis

Meikle, A.W.; Smith, J.A.; West, D.W., 1985:
Familial factors affecting prostatic cancer risk and plasma sex-steroid levels

Pellegatta, B.; Sala, F.; Serafini, L.; Chiodini, E.; Merlo, M., 1988:
Familial factors and feeding modality in allergic pathology in childhood. Retrospective study

De Braekeleer, M.; Cholette, A.; Mathieu, J.; Boily, C.; Robitaille, Y.; Gauvreau, D., 1989:
Familial factors in Alzheimer's disease (IMAGE project). A case-control study in the Saguenay-Lac-St-Jean region (Quebec, Canada)

Iovkova, T., 1976:
Familial factors in coronary disease

Huckle, P.; McGuffin, P., 1991:
Familial factors in going to medical school

Perricone, G.; Paradiso, T., 1987 :
Familial factors in so-called idiopathic scoliosis

Yamamoto, H.; Inaba, S.; Tashiro, N.; Suzuki, A.; Akiyama, Y.; Kamishima, K.; Kishi, F.; Kawakami, Y., 1986:
Familial factors of airway reactivity and serum IgE levels in bronchial asthma

Kauffmann, F.; Tager, I.B.; Muñoz, A.; Speizer, F.E., 1989:
Familial factors related to lung function in children aged 6-10 years. Results from the PAARC epidemiologic study

Weinstein, A.G., 1987:
Familial factors responsible for persistent crying-induced asthma: a case report

Gilmartin, R.C.; Gooch, W.; Wilroy, R.S.; Stadlan, E., 1977:
Familial fatal neonatal radiculoneuropathy

Wening, J.V.; Thoma, G.; Mörl, F.K., 1986:
Familial fibroelastoma dorsi--first case report and review of literature

Meacham, P.W.; Brantley, B., 1987:
Familial fibromuscular dysplasia of the mesenteric arteries

Dominguez, F.E.; Tate, L.G.; Robinson, M.J., 1988:
Familial fibromuscular dysplasia presenting as sudden death

Simons, D.G., 1990:
Familial fibromyalgia and/or myofascial pain syndrome?

Ibaraki, K.; Arakaki, A.; Kayo, M.; Takeuchi, M.; Oroku, H.; Saito, H., 1986:
Familial flexion-supination deformity at the PIP joint of the finger

Constantiniu, S.; Teodorovici, G.; Oană, C.; Popovici, M.; Bercovici, C., 1979:
Familial focus of Yersinia enterocolitica

Michalska, Z., 1977:
Familial focus of hepatitis B infection in a pregnant woman and her 2 children: epidemiology and clinical manifestations

Loghin, L.; Coadă, S.; Lupu, A.; Botezat, R.; Apetroaia, D.; Roescu, F.; Albina, N.; Alexandru, I., 1985:
Familial focus of trichinelliasis

Pirozhenko, V.V.; Demirtasheva, N.G., 1978:
Familial form of Dercum's disease

Grabowska-Lubaszko, U.; Swiatkowska, A.; Balcerska, A., 1978:
Familial form of Holt-Oram syndrome

Ignatowicz, R.; Michałowicz, R.; Kmieć, T.; Jóźwiak, S., 1985:
Familial form of Parry-Romberg syndrome

Prier, S.; Tritschler, J.L.; Bricaire, F., 1979:
Familial form of bilateral acoustic neuroma

Mikol, J.; Bourdarias, H.; Dellanave, J.; Perie, G., 1988:
Familial form of bulbo-spinal amyotrophy in the adult

Baillet, J.; Ducroix, J.P.; Urruty, J.L., 1979:
Familial form of celiac disease. Apropos of 2 cases

Pépin, B.; Mikol, J.; Goldstein, B.; Haguenau, M.; Godlewski, S., 1976:
Familial form of centronuclear myopathy in the adult

Chateau, R.; Tommasi, M.; Groslambert, R.; Perret, J.; Pasquier, B., 1975 :
Familial form of cutaneous epitheliomatosis with complex neurological characteristics similar to hereditary spinocerebellar degeneration. Apropos of 4 cases including one case with anatomo-clinical description

Mil'gram, V.R.; Ievleva, V.G.; Penanen, L.A., 1978:
Familial form of fibrous osteodysplasia of the bones of the skull

Pradines, S.; Joannard, A.; Boujet, C.; Halimi, S.; Beaudoing, A., 1990:
Familial form of hypoglycemia due to leucine hypersensitivity

Pytel-Dabrowska, T.; Gidlecki, Z., 1985:
Familial form of hypoplastic anemia (Diamond-Blackfan syndrome)

Tieder, M.; Stark, H., 1979:
Familial form of idiopathic hypercalciuria with nanism, bone and renal involvement in children

Guzowski, K.; Paradowski, B., 1978:
Familial form of myasthenia

Cavallero, M.; Bonini, C.; Meriggi, F.; Scotti Foglieni, C., 1977:
Familial form of pilomatricoma: ultrastructural aspects

Gacyk, W.; Celińska, W.; Klimkiewicz, E.; Dybicki, J., 1977:
Familial form of portal hypertension

Popenko, S.E.; Khomasuridze, A.G., 1976:
Familial form of post-pubertal adrenogenital syndrome complicated by sterility

Visset, J.; Letessier, E.; Perchenet, A.S.; Fiche, M.; Hamy, A.; Paineau, J., 1992:
Familial form of primary cancer of the parathyroid glands. A disease entity or incidental association?

Swicowa, K.; Balcerska, A.; Szolc, A.; Mrygłodowicz, A.; Zawadzka, M., 1978:
Familial form of saccharase deficiency

Guseva, L.D., 1975:
Familial form of systemic lupus erythematosus

Ayed, K.; Ben Dridi, M.F.; Gorgi, Y.; Bardi, R.; Hamzaoui, K.; Dali, S., 1987:
Familial form of the Buckley syndrome with anomalies of cellular immunity

Pallardo Sánchez, L.F.; Montero, A.; Vidal, O.; Sánchez Sicilia, L.; Cerdán, A., 1977:
Familial form of type II pseuhypoparathyroidism

Tridon, P.; Picart, L.; Vidailhet, M., 1975:
Familial form of von Hippel-Lindau disease

Smadja, A.; Gontier, M.F., 1976:
Familial forms of Sipple's syndrome

Pernot, C.; Hoeffel, J.C.; Worms, A.M.; Perrot, B., 1978:
Familial forms of cardiopathies of Noonan's syndrome. Apropos of 3 families

Lejeune, J.P.; Combelles, G.; Christiaens, J.L., 1989:
Familial forms of cavernomas

Mathis, P.; Segal, S.; Beer Gabel, M.; Diebold, M.D.; Hochlaf, S., 1989:
Familial forms of endocrine tumors of the pancreas. Apropos of 4 cases in the same family

de Boissieu, D.; de Montis, G.; Badoual, J., 1990:
Familial forms of gastro-esophageal reflux

Thomas, D.; Lascault, G.; Caille, B.; Drobinski, G.; Huberman, J.P.; Shqueir, A.; Grosgogeat, Y., 1985:
Familial forms of interauricular communication of the ostium secundum type

Gorwood, P.; Leboyer, M.; Jay, M.; Hillaire, D.; Carteault, F.; Dugain, A.M.; Berg, S.; Des Lauriers, A.; Feingold, J., 1991:
Familial forms of schizophrenia. Cytogenetic study

Bareiss, P.; Christmann, D.; Beissel, J., 1976:
Familial forms of the mid-end systolic click and murmur syndrome with deviations of left ventricular kinetics

Noble, K.G.; Carr, R.E.; Siegel, I.M., 1978:
Familial foveal retinoschisis associated with a rod-cone dystrophy

Murthy, D.S.; Teebi, A.S.; Sundareshan, T.S.; al-Awadi, S.A., 1990:
Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardation

Shabtai, F.; Hart, J.; Klar, D.; Halbrecht, I., 1986:
Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22)

Levine, M.D.; Rimoin, D.L.; Lachman, R., 1975:
Familial frontal dysplasia

Ferraresi, S.; Servello, D.; De Lorenzi, L.; Allegranza, A., 1989:
Familial frontal lobe oligodendroglioma. Case report

Weiss, L.; Reynolds, W.A.; Szymanowski, R.T., 1975:
Familial frontometaphyseal dysplasia- evidence for dominant inheritance

Lira Pedrín, M.A.; Ramírez, A.; Lisker, R.; Villalobos, J.J.; Mutchinick, O.; Granados, J.; Angeles, A., 1987:
Familial gastric cancer

Seruca, R.; Carneiro, F.; Castedo, S.; David, L.; Lopes, C.; Sobrinho-Simões, M., 1991:
Familial gastric polyposis revisited. Autosomal dominant inheritance confirmed

Li, L., 1988:
Familial gastro-intestinal adenomatosis

Hadden, J.W., 1975:
Familial gastrointestinal cancer

Arvystas, M.G., 1976:
Familial generalized delayed eruption of the dentition with short stature

Eng, A.M.; Cogan, L.; Gunnar, R.M.; Blekys, I., 1976:
Familial generalized dyschromic amyloidosis cutis

Wall, P.; Platt, F.W., 1978:
Familial generalized lipodystrophy: a case report

Elte, J.W.; Bos, F.; Docter, R., 1987:
Familial generalized resistance to thyroid hormones--occurrence in three generations

Magner, J.A.; Petrick, P.; Menezes-Ferreira, M.M.; Stelling, M.; Weintraub, B.D., 1986:
Familial generalized resistance to thyroid hormones: report of three kindreds and correlation of patterns of affected tissues with the binding of [125I] triiodothyronine to fibroblast nuclei

Mieler, I.; Pistier, C., 1985:
Familial genetic research on the clinical picture in periodontal atrophy

Novak, M.A.; Green, W.R.; Miller, N.R., 1986:
Familial giant cell arteritis

Clayton, P.T.; Leonard, J.V.; Lawson, A.M.; Setchell, K.D.; Andersson, S.; Egestad, B.; Sjövall, J., 1987:
Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acids

Sándor, T.; Surinya, M.; Mónus, Z., 1975:
Familial giant cell hepatitis in infancy

Larsen, B.; Tarp, U.; Kristensen, E., 1987:
Familial giant hypertrophic gastritis (Ménétrier's disease)

Jones, G.; Wilroy, R.S.; McHaney, V., 1977:
Familial gingival fibromatosis associated with progressive deafness in five generations of a family

Katz, J.; Ben-Yehuda, A.; Machtei, E.; Goultschin, J.; Danon, Y.L., 1989:
Familial gingival fibromatosis; no correlation with HLA-antigen. A family study

Bozzo, L.; de Almeida, O.P.; Scully, C., 1992:
Familial gingival hyperplasia: a case of pseudo-Laband syndrome

Everson, R.B.; Fraumeni, J.F., 1976:
Familial glioblastoma with hepatic focal nodular hyperplasia

Hardman, P.D.; Bell, J.; Whittle, I.R.; Gregor, A., 1989:
Familial glioma: a report of glioblastoma in identical twins and oligo-astrocytoma in siblings

Malcoun, A.J., 1992:
Familial glomerular disease: it's all in the genes

Muszkowska-Penson, J.; Piotrowicz, E.; Chodorowski, Z.; Uszycka-Karcz, M.; Stolarczyk, J.; Stencel, H.; Suchecki, T.; Natoński, A.; Zygadłowski, J., 1976:
Familial glomerular nephropathy

Rambausek, M.; Hartz, G.; Waldherr, R.; Andrassy, K.; Ritz, E., 1987:
Familial glomerulonephritis

Vaĭshenker, P.G., 1979:
Familial glomus jugulare tumor

Imura, H., 1979:
Familial glucocorticoid deficiency

Grant, D.B.; Dunger, D.B.; Smith, I.; Hyland, K., 1992:
Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementia

Thistlethwaite, D.; Darling, J.A.; Fraser, R.; Mason, P.A.; Rees, L.H.; Harkness, R.A., 1975:
Familial glucocorticoid deficiency. Studies of diagnosis and pathogenesis

Petrykowski, W.; Burmeister, P.; Böhm, N., 1975:
Familial glucocorticoid insufficiency

Lloyd, H.J., 1975:
Familial goitrous cretinism associated with an abnormal haemoglobin

Kumei, Y.; Takasugi, Y.; Namiki, M., 1985:
Familial goitrous cretinism with giant goiter and hyperthyroglobulinemia: report of two siblings

Vilde, F.; Nezelof, C., 1976:
Familial granulomatous disease: histopathological and histogentic data

Braga, S.; Phillips, J.A.; Joss, E.; Schwarz, H.; Zuppinger, K., 1986:
Familial growth hormone deficiency resulting from a 7.6 kb deletion within the growth hormone gene cluster

Mintz, S.M., 1991:
Familial gynecologic malignancies

Hakala, T., 1991:
Familial gynecological cancer

Sadr, A.M.; Bahadori, M.; Manoochehri, H.A., 1977:
Familial gynecomastia

Berkovitz, G.D.; Guerami, A.; Brown, T.R.; MacDonald, P.C.; Migeon, C.J., 1985:
Familial gynecomastia with increased extraglandular aromatization of plasma carbon19-steroids

Say, B.; Carpenter, N.; Coldwell, J.G., 1979:
Familial gynecomastia without hypogonadism

Edelsten, A.D.; Tuck, S., 1978:
Familial haemolytic uraemic syndrome

Nespoli, L.; Locatelli, F.; Bonetti, F.; Porta, F.; Zecca, M.; Gibardi, A.; Gambarana, D.; Vitale, V.; Burgio, G.R.; Severi, F., 1991:
Familial haemophagocytic lymphohistiocytosis treated with allogeneic bone marrow transplantation

Botha, J.B.; Kahn, L.B.; Kaschula, R.O., 1975:
Familial haemophagocytic reticulosis. Report of 2 cases in sibs

Begley, C.G.; Tait, B.; Crapper, R.M.; Briggs, P.G.; Brodie, G.N.; Mackay, I.R., 1987:
Familial hairy cell leukemia

Kiriyama, T.; Mizutani, T.; Kakusui, K.; Wada, M.; Isoda, T.; Inoue, M.; Okabe, T.; Taniguchi, S.; Kuribayashi, T., 1979 :
Familial heart block and sick sinus syndrome of adult onset. Report to two families and review of the literature

Bilge, T.; Bilge, S.; Barut, S.; Cokneşeli, B., 1991:
Familial hemangioblastoma and von Hippel-Lindau's disease: case report

Cerdá-Nicolás, M.; Alemany, P.; Peydró, A.; Piquer, J.; Barberá, J.; Soler, F.; Barcia-Salorio, J.L., 1988:
Familial hemangioblastoma: morphological and ultrastructural study of 2 cases with spinal localization

Janda, J.; Rambousek, V., 1989:
Familial hematuria and Alport's syndrome

Boggi, R.; Carletti, P.; Bibiano, L.; Micucci, G.; Gaffi, G.; Mioli, V.; Greco, A., 1990:
Familial hematuric nephropathy: a review of thirty-four personal cases

Carter, J.B.; Patrinely, J.R.; Jankovic, J.; McCrary, J.A.; Boniuk, M., 1990:
Familial hemifacial spasm

Coad, J.E.; Wirtschafter, J.D.; Haines, S.J.; Heros, R.C.; Perrone, T., 1991:
Familial hemifacial spasm associated with arterial compression of the facial nerve. Case report

Müller, D.; Müller, J., 1977:
Familial hemiphegic migraine

Parrish, R.M.; Stevens, H., 1977:
Familial hemiplegia migraine

Glista, G.G.; Mellinger, J.F.; Rooke, E.D., 1975:
Familial hemiplegic migraine

Urbánek, K.; Myslivecek, M.; Simková, M., 1987 :
Familial hemiplegic migraine. Differential diagnosis of transitory ischemic attacks

Feller, E.R.; Pont, A.; Wands, J.R.; Carter, E.A.; Foster, G.; Kourides, I.A.; Isselbacher, K.J., 1977:
Familial hemochromatosis. Physiologic studies in the precirrhotic stage of the disease

Heilmann, E.; Wessels, G.; Loew, H., 1976:
Familial hemolytic anemia and terminal renal failure

Goodyer, P.R.; Fraser, F.C., 1990:
Familial hemolytic-uremic syndrome

Courtecuisse, V.; Dommergues, J.P.; Rivron, J.; Chaon, P., 1975:
Familial hemolytic-uremic syndrome with normal renal biopsy

Blättler, W.; Wegmann, W.; Herold, H.; Straub, P.W., 1975:
Familial hemolytic-uremic syndrome. Studies on pathogenesis in the survivors

Hesse, C.; Hansmann, M.L.; Janka-Schaub, G.E.; Rontogianni, D.; Radzun, H.J.; Fischer, R., 1991:
Familial hemophagocytic lymphohistiocytosis

Fuchs, W.A.; Guggenbichler, J.P., 1987:
Familial hemophagocytic lymphohistiocytosis (case report)

Hansmann, M.L.; Rontogianni, D.; Janka-Schaub, G.E.; Wacker, H.H.; Hinkeldey, K.; Radzun, H.J., 1989:
Familial hemophagocytic lymphohistiocytosis macrophages showing immunohistochemical properties of activated macrophages and T-accessory cells

Elinder, G.; Henter, J.; Söder, O., 1989:
Familial hemophagocytic lymphohistiocytosis--a hypercytokinemia?

Gilbert, E.F.; ZuRhein, G.M.; Wester, S.M.; Herrmann, J.; Hong, R.; Opitz, J.M., 1985:
Familial hemophagocytic lymphohistiocytosis: report of four cases in two families and review of the literature

Bezanilla Regato, J.L.; Estébanez Ruiz, S.; Navajas Gutiérrez, A.; Piñán Garcés, M.A.; Sojo Aguirre, A.; Moya Calderón, E., 1990:
Familial hemophagocytic lymphohistiocytosis: survival of a case treated by polychemotherapy

Bergholz, M.; Rahlf, G.; Doering, K.M., 1978:
Familial hemophagocytic reticulosis (Farquhar)

Prusek, W.; Kotschy, M.; Podwysocka-Harasimowicz, M., 1979:
Familial hemorrhagic diathesis caused by factor X deficiency

Mellis, C.; Bale, P.M., 1976:
Familial hepatic venoocclusive disease with probable immune deficiency

N'Dri, N.; Hadengue, A.; Benhamou, J.P., 1991:
Familial hepatocellular carcinoma in B or non-A non-B cirrhosis. Report of 4 families

Sanz Ortiz, J.; de la Gándara Porres, I.; Martino, E., 1985:
Familial hepatocellular carcinoma with positive surface antigen (HBsAg)

Dzys', I.P.; Moroz, A.D.; Skrypnychenko, L.S., 1979:
Familial hereditary hypoparathyroidism

Khaĭmin, V.M., 1977:
Familial hereditary nephropathies

Bititci, O.O., 1975:
Familial hereditary, progressive sensori-neural hearing loss with keratosis palmaris and plantaris

Mottironi, P.; Martinelli, M.M.; Palazzuolo, C.; Arturi, E.; Di Gregorio, A.; Alcini, E., 1986:
Familial heredity in hypertrophic cardiomyopathy. Review of hypertrophic cardiomyopathy. Review of the literature and presentation of personal case records

Leung, A.K., 1987:
Familial hiatal hernia

Bracco, G.; Dotti, G.; Levis, F.; David, E.; Saracco, G.; Rizzetto, M.; Verme, G., 1988:
Familial high-density lipoprotein deficiency (Tangier disease): the third Italian case

Kastelein, J.J.; Pritchard, P.H.; Erkelens, D.W.; Kuivenhoven, J.A.; Albers, J.J.; Frohlich, J.J., 1992:
Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent

Mau, H., 1988:
Familial hip dysplasia with short acetabular roofs

Valente, M.; Parenti, A.; Cipriani, R.; Peserico, A., 1987:
Familial histiocytic dermatoarthritis. Histologic and ultrastructural findings in two cases

Kubo, Y.; Hirano, H.; Ashiya, M.; Sato, Y.; Yamazaki, T.; Dan, S.; Sawada, U.; Okayasu, M.; Uchida, T., 1988:
Familial histiocytosis with aggressive clinical courses

Di Simone, A.; Riegler, G., 1987:
Familial histories in ulcerative colitis

Cardellicchio, A.; Lonardo, A.; Scuotto, A.; Viscardi, A.; Mazzacca, G., 1985:
Familial history in IBD

Yamaguchi, N.; Yamamura, J.; Takahashi, K.; Nakamura, R.; Okubo, T., 1990:
Familial history of cancer and dietary pattern, serum cholesterol, serum protein and blood hemoglobin

Chaudhry, H.R.; Arria, A.; Tarter, R.; Chaudhry, S.; Chaudhry, N., 1991:
Familial history of opium use and reported problems among opium addicts in Pakistan

Escobar, V.; Cantu, J.M.; Martin, A.O., 1979:
Familial holoprosencephaly

Lefrere, J.J.; Girot, R.; Courouce, A.M.; Maier-Redelsperger, M.; Cornu, P., 1986:
Familial human parvovirus infection associated with anemia in siblings with heterozygous beta-thalassemia

Lefrère, J.J.; Boutard, P.; Couroucé, A.M.; Lacaze, T.; Girot, R., 1985:
Familial human parvovirus infections

Berry, J.B.; Brighton, W.D., 1977:
Familial human short-term sensitizing (IgG S-TS) antibody

Avogaro, P.; Cazzolato, G., 1975:
Familial hyper-HDL-(a)-cholesterolemia

Avogaro, P.; Cazzolato, G.; Kostner, G.; Holasek, D.R., 1977:
Familial hyper-alpha-lipoproteinaemia. Further studies on serum lipoproteins and some serum enzymes

Glueck, C.J.; Fallat, R.W.; Millett, F.; Gartside, P.; Elston, R.C.; Go, R.C., 1975:
Familial hyper-alpha-lipoproteinemia: studies in eighteen kindreds

Okabe, T.; Fujisawa, M.; Watanabe, J.; Yotsumoto, H.; Takaku, F., 1987:
Familial hyper-angiotensin converting enzyme (ACE)-emia: increased production of ACE by monocyte-macrophage

Stowasser, M.; Gordon, R.D.; Tunny, T.J.; Klemm, S.A.; Finn, W.L.; Krek, A.L., 1992:
Familial hyperaldosteronism type II: five families with a new variety of primary aldosteronism

Glueck, C.J.; Fallat, R.W.; Millett, F.; Steiner, P.M., 1975:
Familial hyperalphalipoproteinemia

Terheggen, H.G.; Lowenthal, A.; Lavinha, F.; Colombo, J.P., 1975:
Familial hyperargininaemia

Sorrentino, D.; Jones, E.A.; Berk, P.D., 1989:
Familial hyperbilirubinaemia syndromes: kinetic approaches

Orellana, J.M., 1977:
Familial hyperbilirubinemia

Hamel, E.; Bedard, D.; Laviolette, F.; Butterworth, R.F.; Barbeau, A., 1978:
Familial hyperbilirubinemia in Friedreich's ataxia

Kassem, M.; Eriksen, E.F.; Mosekilde, L., 1991:
Familial hypercalciuric hypercalcemia

Kovanen, P.T., 1977:
Familial hypercholesteremia

Caturla Such, J.; Aguado Pérez, M.; Pedauye González, J.; López Martínez, M.; López, A.; Siles, A.; Pacheco, F.; Garcia romeu, C., 1977:
Familial hypercholesteremia caused by a homozygous gene. Review of the literature apropos of the study of a family

Cassi, E.; Massarotti, G.; Bernieri, A.; Cova, L.; Colombo, A.; Beretta, R.; Pagani, C., 1978:
Familial hypercholesteremia. Clinico-diagnostic and therapeutic aspects

Humphries, S.E., 1986:
Familial hypercholesterolaemia as an example of early diagnosis of coronary artery disease risk by DNA techniques

van Wingerden, J.J., 1991:
Familial hypercholesterolaemia in a black patient--completing the picture

Mittal, A.; Devgan, S.C.; Arora, S., 1991:
Familial hypercholesterolaemia in association with aortic stenosis

Victorino, R.; Silveira, J.C.; Geada, H.; Moura, M.C., 1978:
Familial hypercholesterolaemia with alpha 1-antitrypsin deficiency

Karnik, N.D.; Pandit, S.P.; Vyawahare, S.; Khokhani, R.C., 1990:
Familial hypercholesterolaemia--report of two cases

Hammond, K.D.; Khan, Q.; Laminski, N.A.; Mendelsohn, D.; Seftel, H.C., 1987:
Familial hypercholesterolaemia: effect of low density lipoproteins on esterification of cholesterol in lymphocytes from homozygous and heterozygous subjects

Jensen, L.T.; Skovby, F.; Andersen, G.E., 1988:
Familial hypercholesterolemia

Donadon, V.; Antonini Canterin, A.; De Paoli, P.; Borean, M.; Villalta, D.; Zanata, G.; Santini, G.F., 1986:
Familial hypercholesterolemia and HLA antigens

Eto, M.; Watanabe, K.; Chonan, N.; Ishii, K., 1988:
Familial hypercholesterolemia and apolipoprotein E4

Ravenholt, R.T., 1986:
Familial hypercholesterolemia and early coronary death

Brink, P.A.; Steyn, L.T.; Coetzee, G.A.; Van der Westhuyzen, D.R., 1987:
Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effect

Obando Santaella, I.; Fernández Gómez, E.; Mongil Ruiz, I.; Escobar Gallego, A.; Espino Aguilar, R., 1991:
Familial hypercholesterolemia in a homozygote and LDL kinetics

Nora, J.J.; Lortscher, R.M.; Spangler, R.D.; Bilheimer, D.W., 1985:
Familial hypercholesterolemia with "normal" cholesterol in obligate heterozygotes

Erkelens, D.W.; Sherwood, L.M.; Hals, F., 1989:
Familial hypercholesterolemia, tendinous xanthomas, and Frans Hals

Sobra, J.; Ceska, R., 1988:
Familial hypercholesterolemia--a receptor disease

Kontula, K., 1992:
Familial hypercholesterolemia--from gene defect to cholesterol accumulation

Stugaard, M.; Wiig, I.; Lund, H.; Ose, L.; Norseth, J., 1992:
Familial hypercholesterolemia--intensive diet therapy combined with drug therapy

Ose, L.; Tolleshaug, H., 1989:
Familial hypercholesterolemia. 50 years of research

Goldstein, J.L.; Brown, M.S., 1975:
Familial hypercholesterolemia. A genetic regulatory defect in cholesterol metabolism

Bellini, C.; Bonioli, E.; Ruffa, G.; Franchini, E.; Rivabella, L.; Cinollo, G.; Catapano, A.; Fumagalli, R.; Corsini, A.; Gemme, G., 1986 :
Familial hypercholesterolemia. Study of low-density lipoprotein receptors. Treatment with plasmapheresis

Bilheimer, D.W., 1987:
Familial hypercholesterolemia. There is a need for early detection and treatment

Brown, M.S.; Goldstein, J.L., 1976:
Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor

Goldstein, J.L.; Brown, M.S., 1985:
Familial hypercholesterolemia: a genetic receptor disease

Davignon, J., 1991:
Familial hypercholesterolemia: a treatable lethal disease

Ciarrocchi, A.; Gaddi, A.; Rimondi, S.; Mezzetti, M.; Scaramuzzino, G., 1988:
Familial hypercholesterolemia: clinical aspects

Kobierska-Szczepańska, A.; Dziuba, P.; Szczepański, Z., 1976:
Familial hypercholesterolemia: clinical findings and immunochemical studies of lipoproteins

Schneider, W.J., 1990:
Familial hypercholesterolemia: dissection of a receptor disease

Brown, M.S.; Goldstein, J.L., 1975:
Familial hypercholesterolemia: genetic, biochemical and pathophysiologic considerations

Brown, M.S.; Goldstein, J.L., 1979:
Familial hypercholesterolemia: model for genetic receptor disease

Goldstein, J.L.; Brown, M.S., 1978:
Familial hypercholesterolemia: pathogenesis of a receptor disease

Kovanen, P.T.; Tikkanen, M.J.; Pyörälä, K., 1992:
Familial hypercholesterolemia: treatable receptor disease

Brown, M.S.; Goldstein, J.L., 1977:
Familial hypercholesterolemia: unraveling a genetic receptor disease

Gagne, C.; Brun, D.; Moorjani, S.; Lupien, P.J., 1977:
Familial hyperchylomicronemia: study of lipolytic activity in a family

Boden, G.; Owen, O.E., 1977:
Familial hyperglucagonemia--an autosomal dominant disorder

Rose, C.I.; Haines, D.S., 1978:
Familial hyperglycerolemia

Farfel, Z.; Rosenthal, T.; Shibolet, S.; Iaina, A.; Gafni, J., 1976:
Familial hyperkalemia and hypertension

Baz, M.; Berland, Y.; Dussol, B.; Jaber, K.; Boobes, Y., 1990:
Familial hyperkalemia syndrome (Gordon's syndrome)

Brautbar, N.; Levi, J.; Rosler, A.; Leitesdorf, E.; Djaldeti, M.; Epstein, M.; Kleeman, C.R., 1978:
Familial hyperkalemia, hypertension, and hyporeninemia with normal aldosterone levels. A tubular defect in potassium handling

Sudo, M., 1978:
Familial hyperlipemia type II--its relation to juvenile atheromatous arteriosclersis

Bewsey, B., 1977:
Familial hyperlipidaemia

Singh, A., 1975:
Familial hyperlipoproteinemia and gallstones

Sobra, J., 1989:
Familial hyperlipoproteinemia and nationwide health programs

Rajagopal, G.; Chandrasekar, S.; Venugopala Rao, A.; Ramakrishnan, S., 1975:
Familial hyperlipoproteinemia in a South Indian family

Traurig, J.; Sobra, J.; Kvasilová, M.; Wildtová, Z., 1978:
Familial hyperlipoproteinemia type IIA with homozygotic manifestations in a heterozygote

Yamamura, T., 1992:
Familial hyperlipoproteinemia type III

Utermann, G.; Jaeschke, M.; Menzel, J., 1975:
Familial hyperlipoproteinemia type III: deficiency of a specific apolipoprotein (apo E-III) in the very-low-density lipoproteins

Kobayashi, T.; Ueno, E.; Fujita, T.; Yanagisawa, N.; Tsukagoshi, H., 1977:
Familial hyperlysinemia with mental retardation, convulsion & muscular hypertonia

Cox, R.P.; Markovitz, P.J.; Chuang, D.T., 1985:
Familial hyperlysinemias--multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase

Christensson, T., 1976:
Familial hyperparathyroidism

Warnakulasuriya, S.; Markwell, B.D.; Williams, D.M., 1985:
Familial hyperparathyroidism associated with cementifying fibromas of the jaws in two siblings

Macabeo, V.; David, L.; Frédérich, A.; François, R., 1975:
Familial hyperparathyroidism. Apropos of 3 observations

Goldsmith, R.E.; Sizemore, G.W.; Chen, I.W.; Zalme, E.; Altemeier, W.A., 1976:
Familial hyperparathyroidism. Description of a large kindred with physiologic observations and a review of the literature

Doury, P.; Pattin, S.; Eulry, F., 1988:
Familial hyperparathyroidism. Excluding polyendocrine adenomatosis

Farfel, Z.; Iaina, A.; Rosenthal, T.; Waks, U.; Shibolet, S.; Gafni, J., 1978:
Familial hyperpotassemia and hypertension accompanied by normal plasma aldosterone levels: possible hereditary cell membrane defect

Gabbay, K.H.; DeLuca, K.; Fisher, J.N.; Mako, M.E.; Rubenstein, A.H., 1976:
Familial hyperproinsulinemia. An autosomal dominant defect

Gabbay, K.H.; Bergenstal, R.M.; Wolff, J.; Mako, M.E.; Rubenstein, A.H., 1979:
Familial hyperproinsulinemia: partial characterization of circulating proinsulin-like material

Lee, P.A.; Migeon, C.J.; Bias, W.B.; Jones, G.S., 1987:
Familial hypersecretion of adrenal androgens transmitted as a dominant, non-HLA linked trait

Allen, D.H.; Basten, A.; Williams, G.V.; Woolcock, A.J., 1975:
Familial hypersensitivity pneumonitis

Blonde, L.; Bernene, J.L.; Goodman, A.D., 1975:
Familial hypertension

Bianchi, G.; Picotti, G.B.; Bracchi, G.; Cusi, D.; Gatti, M.; Lupi, G.P.; Ferrari, P.; Barlassina, C.; Colombo, G.; Gori, D., 1978 :
Familial hypertension and hormonal profile, renal haemodynamics and body fluids of young normotensive subjects

Staub, J.J.; Ryff-de Lèche, 1985:
Familial hyperthyroxinemia

Sapin, R.; Gasser, F.; Chambron, J., 1989:
Familial hyperthyroxinemia with dysalbuminemia: screening of 21,000 patients at the occasion of thyroid evaluation

Glueck, C.J.; Mellies, M.J.; Tsang, R.C.; Kashyap, M.L.; Steiner, P.M., 1977:
Familial hypertriglyceridemia in children: dietary management

Rozenberg, V.D., 1991:
Familial hypertrophic cardiomyopathy

Pochmalicki, G.; Duboc, D.; Toussaint, M.; Guérin, F., 1987:
Familial hypertrophic cardiomyopathy of early disclosure

Casanova, M.; Gamallo, C.; Quero-Jiménez, M.; García-Aguado, A.; Burgueros, M.; García, S.; Suarez, A., 1979:
Familial hypertrophic cardiomyopathy with unusual involvement of the right ventricle

Hopkins, B.E.; Taylor, R.R.; Robinson, J.S., 1975:
Familial hypertrophic cariomyopathy and lentiginosis

Pothen, P.; Cordiano, R.; Scanavacca, G.; Bongiovì, S.; Macor, F.; Palmieri, R.; Pigato, R.; Pessina, A.C.; Dal Palù, C., 1990:
Familial hypertrophic myocardiopathy: complex ventricular arrhythmias in healthy family members

Neoral, L.; Sýkora, J.; Kolembus, P., 1986:
Familial hypertrophic obstructive cardiomyopathy as a cause of sudden death

Sueoka, E.; Baba, N.; Kuroda, Y.; Oda, K.; Yamamoto, K.; Shibasaki, H., 1988:
Familial hypo-beta-lipoproteinemia associated with mental retardation and spastic paraparesis

Stein, E.A., 1977:
Familial hypo-beta-lipoproteinemia: a family detected by cord blood tests

Nizankowska-Błaz, T.; Korczowski, R.; Kanik, A., 1992:
Familial hypoadrenalism

Glueck, C.J.; Gartside, P.S.; Mellies, M.J.; Steiner, P.M., 1977:
Familial hypobeta-lipoproteinemia: studies in 13 kindreds

Araki, W.; Hirose, S.; Mimori, Y.; Nakamura, S.; Kimura, J.; Ohno, K.; Shimada, T., 1991:
Familial hypobetalipoproteinaemia complicated by cerebellar ataxia and steatocystoma multiplex

Yeshurun, D.; Taunton, O.D.; Gotto, A.M., 1978:
Familial hypobetalipoproteinemia

Young, S.G.; Hubl, S.T.; Chappell, D.A.; Smith, R.S.; Claiborne, F.; Snyder, S.M.; Terdiman, J.F., 1989:
Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46)

Young, S.G.; Hubl, S.T.; Smith, R.S.; Snyder, S.M.; Terdiman, J.F., 1990:
Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins

Kahn, J.A.; Glueck, C.J., 1978:
Familial hypobetalipoproteinemia. Absence of atherosclerosis in a postmortem study

Gay, G.; Pessah, M.; Bouma, M.E.; Roche, J.F.; Aymard, J.P.; Beucler, I.; Aggerbeck, L.P.; Infante, R., 1990:
Familial hypobetalipoproteinemia. Familial study of 4 cases

Muñoz Torres, M.; Cano Romera, A.; Domínguez, S.; Cano Parra, M.D.; Lobón, J.A.; Escobar Jiménez, F., 1991:
Familial hypobetalipoproteinemia: description of a heterozygous form with important biochemical alterations

Stuckey, B.G.; Gutteridge, D.H.; Kent, G.N.; Reed, W.D., 1990:
Familial hypocalciuric hypercalcaemia and pancreatitis: no causal link proven

Lyons, T.J.; Crookes, P.F.; Postlethwaite, W.; Sheridan, B.; Brown, R.C.; Atkinson, A.B., 1986:
Familial hypocalciuric hypercalcaemia as a differential diagnosis of hyperparathyroidism: studies in a large kindred and a review of surgical experience in the condition

Auwerx, J.; Brunzell, J.; Bouillon, R.; Demedts, M., 1987:
Familial hypocalciuric hypercalcaemia--familial benign hypercalcaemia: a review

Marx, S.J.; Fraser, D.; Rapoport, A., 1985:
Familial hypocalciuric hypercalcemia. Mild expression of the gene in heterozygotes and severe expression in homozygotes

Gilbert, F.; D'Amour, P.; Gascon-Barré, M.; Boutin, J.M.; Havramkova, J.; Bélanger, R.; Matte, R., 1985:
Familial hypocalciuric hypercalcemia: description of a new kindred with emphasis on its difference from primary hyperparathyroidism

Degli Esposti, A.; Ambrosioni, G.; Giardina, A.; Giovannini, G.; Laghi, M.G.; Molinari, P.P.; Salvatori, P.; Zaniboni, M.G., 1985:
Familial hypoglycocorticism syndrome unresponsive to ACTH, achalasia, alacrima, with associated distal neuromyopathy

Slti, I.S.; Salem, Z., 1979:
Familial hypogonadotropic hypogonadism with alopecia

Britton, W.J.; Satchell, P.M., 1977:
Familial hypokalaemic periodic paralysis in papua nuiginians--a reappraisal

Confavreux, C.; Garassus, P.; Vighetto, A.; Aimard, G., 1991:
Familial hypokalaemic periodic paralysis: prevention of paralytic attacks with lithium gluconate

Bernick, C., 1988:
Familial hypokalemic periodic paralysis

Cenac, A.; Develoux, M.; Touta, A.; Soumana, I., 1986:
Familial hypokalemic periodic paralysis (Westphal's disease) exists in Africa

Corbett, V.A.; Nuttall, F.Q., 1975:
Familial hypokalemic periodic paralysis in blacks

Buruma, O.J.; Bots, G.T.; Went, L.N., 1985:
Familial hypokalemic periodic paralysis. 50-year follow-up of a large family

Poll-The, B.T.; Bonnefont, J.P.; Ogier, H.; Charpentier, C.; Pelet, A.; L.F.r, J.M.; Jakobs, C.; Kok, R.M.; Duran, M.; Divry, P., 1988:
Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

Pronicka, E.; Gruszczyńska, B., 1991:
Familial hypomagnesaemia with secondary hypocalcaemia--autosomal or X-linked inheritance?

Seino, Y.; Shimotsuji, J.; Yabuuchi, M., 1978:
Familial hypophasphatemic vitamin D resistant rickets

López Vázquez, E.; Pérez Bañasco, V., 1977 :
Familial hypophosphatemia

Marie, P.J., 1986:
Familial hypophosphatemia and rickets caused by calcium deficiency

Kaitila, I.; Lachman, R.S.; Rimoin, D.L., 1975:
Familial hypophosphatemic rickets with resolution in childhood

Saggese, G.; Baroncelli, G.I.; Bertelloni, S.; Federico, G., 1987:
Familial hypophosphatemic rickets. Effects of treatment with 1,25-dihydroxycholecalciferol at supraphysiologic doses

Walton, J., 1976:
Familial hypophosphatemic rickets: a delineation of its subdivisions and pathogenesis

Chernov, A.P.; Loboreva, V.V., 1975:
Familial hypophosphatemic vitamin D-resistant rachitis

Hirschman, G.H.; Rao, D.D., 1976:
Familial hypophosphatemic vitamin D-resistant rickets

Fadavi, S.; Rowold, E., 1990:
Familial hypophosphatemic vitamin D-resistant rickets: review of the literature and report of case

Parks, J.S.; Tenore, A.; Bongiovanni, A.M.; Kirkland, R.T., 1978:
Familial hypopituitarism with large sella turcica

Van Egmond, H.; Defloor, E.; Kunnen, M.; Carton, D., 1976:
Familial hypoplastic left heart syndrome

Dacou-Voutetakis, C.; Feltquate, D.M.; Drakopoulou, M.; Kourides, I.A.; Dracopoli, N.C., 1990:
Familial hypothyroidism caused by a nonsense mutation in the thyroid-stimulating hormone beta-subunit gene

Kabadi, U.; Levine, L.H.; Krishnamurthy, P.S., 1977:
Familial hypothyroidism manifested by painful, swollen joints

Elpeleg, O.N.; Havkin, S.; Barash, V.; Jakobs, C.; Glick, B.; Shalev, R.S., 1992:
Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency

Akaoka, I.; Nishizawa, T.; Yano, E.; Takeuchi, A.; Nishida, Y., 1975:
Familial hypouricaemia due to renal tubular defect of urate transport

Benjamin, D.; Sperling, O.; Weinberg, A.; Pinkhas, J., 1978:
Familial hypouricemia due to isolated renal tubular abnormality

Benjamin, D.; Sperling, O.; Weinberger, A.; Pinkhas, J.; de Vries, A., 1977:
Familial hypouricemia due to isolated renal tubular defect. Attenuated response of uric acid clearance to probenecid and pyrazinamide

Ardiaca Capell, A.; Ibáñez Regales, M.; Rubio Caballero, M., 1987:
Familial idiopathic auricular fibrillation

Masuda, K.; Kawai, H.; Sebe, T.; Nishida, Y.; Takeda, M.; Masuda, T.; Yamasaki, M.; Saito, S., 1988:
Familial idiopathic basal ganglia calcification with dominant inheritance

Daskalov, T.R.; Kusitasev, G.; Mavrudieva, M.; Prodanov, A.; Boiadzhiev, K., 1986:
Familial idiopathic congestive cardiomyopathy in 2 brothers with a similar course

Vincenzo Fragola, P.; Autore, C.; Picelli, A.; Sommariva, L.; Cannata, D.; Sangiorgi, M., 1988:
Familial idiopathic dilated cardiomyopathy

Pelliccia, F.; Gaspardone, A.; Tomai, F.; Valente, A.; Romeo, F., 1987:
Familial idiopathic dilated cardiomyopathy. Description of 2 cases

Passa, P.; Zygelman, M.; Altman, J.J.; Fiet, J., 1978:
Familial idiopathic haemochromatosis with diabetes. Study of glucagon and growth hormone secretions

Bries, H., 1975:
Familial idiopathic hemochromatosis

Kocián, J.; Sotorník, I., 1976:
Familial idiopathic hypercalciuria

Cohen, R.D.; Blandy, J.P., 1979:
Familial idiopathic hypercalciuria

Shah, L.S.; Vengsarkar, A.S., 1979:
Familial idiopathic hypertrophic subaortic stenosis. (A case report)

Bétend, B.; Lebacq, E.; David, L.; Claustrat, B.; François, R., 1977:
Familial idiopathic hypogonadotrophic hypogonadism

Beckerman, R.C.; Taussig, L.M.; Pinnas, J.L., 1979:
Familial idiopathic pulmonary hemosiderosis

Aoki, K.; Washimi, Y.; Fujimori, N.; Maruyama, K.; Yanagisawa, N., 1990:
Familial idiopathic vitamin E deficiency associated with cerebellar atrophy

Statter, M.; Shina, A.; Schein, R.; Ben-Zvi, A.; Russell, A., 1975:
Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids

Statter, M.; Ben-Zvi, A.; Shina, A.; Schein, R.; Russell, A., 1976:
Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype"

Edwards, D.F.; Kennedy, J.R.; Patton, C.S.; Toal, R.L.; Daniel, G.B.; Lothrop, C.D., 1989:
Familial immotile-cilia syndrome in English springer spaniel dogs

Gajdos, A., 1978:
Familial immune deficit and genetic deficiency of adenosine deaminase or of nucleoside phosphorylase

Zawadzki, Z.A.; Aizawa, Y.; Kraj, M.A.; Haradin, A.R.; Fisher, B., 1977:
Familial immunopathies: report of nine families and survey of literature

Begleiter, M.L.; Harris, D.J., 1985:
Familial incidence of Crohn's disease

Sategna-Guidetti, C.; Bianco, L.; Bracco, E.; Marucco, E., 1986:
Familial incidence of Crohn's disease in Italy

Reddi, O.S.; Reddy, S.V.; Reddy, K.R., 1977:
Familial incidence of L-xylulosuria

Wu, R.K.; Trumble, T.E.; Ruwe, P.A., 1991:
Familial incidence of Paget's disease and secondary osteogenic sarcoma. A report of three cases from a single family

Herpertz-Dahlmann, B., 1988:
Familial incidence of affective diseases in patients with anorexia nervosa

Cerná, M.; Vosmík, F., 1978:
Familial incidence of basal cell naevus (Gorlin's syndrome). Review with case report.

Havelka, S.; Fáberová, R.; Gatterová, J.; Trnavský, K., 1990:
Familial incidence of diffuse idiopathic skeletal hyperostosis

Gatrad, A.R.; Gatrad, A.H., 1979:
Familial incidence of dystonic reactions to metoclopramide (maxolon)

Barczyk-Luczyk, K.; Debniak, Z.; Dryl, E.; Lisik, D.; Rudkowski, Z., 1992:
Familial incidence of hepatitis b

Vormittag, W.; Schwab, F.; Ferlitsch, A., 1978:
Familial incidence of juvenile diabetes mellitus and primary optic atrophy

Cheney, M.L.; Cheney, W.R.; LeJeune, F.E., 1986:
Familial incidence of labial pits

Wieczorek, V.; Tinschert, K.; Behrendt, W.; Besel, R.; Sölch, O.; Schreiber, D.; Hauschild, R., 1992:
Familial incidence of multiple, mainly spinal meningiomas

Hengrave, G.; De Grandi, P., 1986:
Familial incidence of ovarian cancer

Grunewald, A.M.; Gloor, M., 1992:
Familial incidence of postoperative Cullen gangrene

Acosta-Rua, G.J., 1978:
Familial incidence of ruptured intracranial aneurysms. Report of 12 cases

Vosmík, F.; Sluková, M., 1976:
Familial incidence of steatocystoma multiplex

Krízek, V.; Vondrová, M., 1986:
Familial incidence of urolithiasis

Veselova, T.M.; Kotova, N.G., 1976:
Familial incidents of meningococcal infection

Massa, R.; Weller, B.; Karpati, G.; Shoubridge, E.; Carpenter, S., 1991:
Familial inclusion body myositis among Kurdish-Iranian Jews

Perez-Palacios, G.; Ortiz, S.; López-Amor, E.; Morato, T.; Febres, F.; Lisker, R.; Scaglia, H., 1975:
Familial incomplete virilization due to partial end organ insensitivity to androgens

Köteles, G.; Kemény, P.; Reich, K., 1975:
Familial infantile achalasia in three siblings

Baldellou Vázquez, A.; Gomá Brufau, A.; Carreras Calvete, A.; Used Aznar, M.D.; Gómez Beltrán, J.L., 1979:
Familial infantile cortical hyperostosis

Snook, S.S.; King, N.W., 1989:
Familial infantile cortical hyperostosis (Caffey's disease) in rhesus monkeys (Macaca mulatta)

Lachaux, A.; Le Gall, C.; Loras Duclaux, I.; Hermier, M., 1992:
Familial infantile cortical hyperostosis (Caffey's disease) with osteolytic lesions of the skull

Gieron, M.A.; Korthals, J.K., 1985:
Familial infantile myasthenia gravis. Report of three cases with follow-up until adult life

Dambska, M.; Schmidt-Sidor, B., 1978:
Familial infantile spongy glio-neuronal dystrophy (progressive cerebral poliodystrophy)

Jensen, A.; Frederiksen, B., 1990:
Familial infection caused by Haemophilus influenzae

Joachim, G.; Hassall, E., 1992:
Familial inflammatory bowel disease in a paediatric population

Cederholm, J.; Wibell, L., 1991:
Familial influence on type 1 (insulin-dependent) diabetes mellitus by relatives with either insulin-treated or type 2 (non-insulin-dependent) diabetes mellitus

Oshima, T.; Matsuura, H.; Ishibashi, K.; Kainouchi, M.; Ishida, T.; Ozono, R.; Fujii, T.; Kajiyama, G., 1992:
Familial influence upon NaCl sensitivity in patients with essential hypertension

Kosnik, E.J.; Gilbert, G.; Sayers, M.P., 1975:
Familial inheritance of coronal craniosynostosis

Lugaresi, E.; Montagna, P.; Baruzzi, A.; Cortelli, P.; Tinuper, P.; Zucconi, M.; Gambetti, P.L.; Medori, R., 1986:
Familial insomnia with a malignant course: a new thalamic disease

Praptono, R.; Sunartini; Djunduah; Sadjimin, T., 1990:
Familial insulin resistance and acanthosis nigricans

Schwenk, W.F.; Rizza, R.A.; Mandarino, L.J.; Gerich, J.E.; Hayles, A.B.; Haymond, M.W., 1986:
Familial insulin resistance and acanthosis nigricans. Presence of a postbinding defect

Anonymous, 1991:
Familial insulin-dependent diabetes mellitus (IDDM) epidemiology: standardization of data for the DIAMOND Project. The WHO Multinational Project for Childhood Diabetes Group

Takumi, T.; Kodama, S.; Tsubota, T.; Nishio, H.; Takahashi, T.; Yokono, K.; Matsuo, T., 1988:
Familial insulin-resistant diabetes mellitus without acanthosis nigricans or androgenization

West, R.J.; Lloyd, J.K.; Turner, W.M., 1975:
Familial insulin-resistant diabetes, multiple somatic anomalies, and pineal hyperplasia

Bindoff, L.A.; Birch-Machin, M.A.; Farnsworth, L.; Gardner-Medwin, D.; Lindsay, J.G.; Turnbull, D.M., 1989:
Familial intermittent ataxia due to a defect of the E1 component of pyruvate dehydrogenase complex

Arias, M.; Zubimendi, J.A.; Val, F.; de Castro, S.; Llamazares, C., 1975:
Familial interstitial chronic nephropathy (nephronophthisis and tapeto-retiniana degeneration (Senior-Loken syndrome)

Coles, G.A.; Robinson, K.; Branch, R.A., 1976:
Familial interstitial nephritis

Brodsky, M.C.; Frenkel, R.E.; Spoor, T.C., 1988:
Familial intracranial aneurysm presenting as a subtle stable third nerve palsy. Case report

Andrews, R.J., 1979:
Familial intracranial aneurysms

Lozano, A.M.; Leblanc, R., 1987:
Familial intracranial aneurysms

Hashimoto, I., 1977:
Familial intracranial aneurysms and cerebral vascular anomalies

Fukawa, O.; Aihara, H., 1987:
Familial intracranial aneurysms--report of 20 cases in eight families and review of the literature

Lance, J.W.; Bassil, G.T., 1989:
Familial intractable hiccup relieved by baclofen

Aarabi, B.; Pasternak, G.; Hurko, O.; Long, D.M., 1979:
Familial intradural arachnoid cysts. Report of two cases

Mazurek, A.; Radwan, M.; Stolfa, W., 1979:
Familial intrahepatic cholestasis

Riely, C.A., 1979:
Familial intrahepatic cholestasis: an update

Latimer, C.A.; Rodríguez, W., 1989:
Familial intrahepatic cholestatic cirrhosis in a Puerto Rican family

Green, G.J.; Hong, W.K.; Everett, J.R.; Bhutani, R.; Amick, R.M., 1978:
Familial intraocular malignant melanoma: a case report

Cotton, J.B.; Rebelle, C.; Bosio, A.; Ladreyt-Ponchon, J.P.; Maillet, J., 1988:
Familial intrauterine nanism with constrictive pericarditis, the MuLiBrEy syndrome

Barros, A.; Tavares, M.C.; Gomes, M.P.; Tavares, M.P., 1986:
Familial inv(1)(p36.3q12) associated with sterility

Sole-Pujol, M.T.; Rivera, H.; Castro-Felix, L.P.; Moller, M.; Cantu, J.M., 1985:
Familial inv(2) (p2300q11.2)

Catti, A., 1975:
Familial inversions and other concomitant chromosome aberrations

Fisher, M.; Sargent, J.; Drachman, D., 1979:
Familial inverted choreoathetosis

Polak, B.C., 1977:
Familial investigation in Alport's syndrome

Hersh, J.H.; Douglas, C.; Houston, J.; Weisskopf, B., 1987:
Familial iridoplegia

Joondeph, B.C.; Goldberg, M.F., 1989:
Familial iris melanosis--a misnomer?

Hull, M.T.; Warfel, K.A.; Muller, J.; Higgins, J.T., 1979:
Familial islet cell tumors in Von Hippel-Lindau's disease

Moore, J.W.; Hyman, S.; Antonarakis, S.E.; Mules, E.H.; Thomas, G.H., 1986:
Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)

May, O., 1989:
Familial isolated thrombocytopenia. A family with autosomal dominant heredity

Velcek, F.T.; Coopersmith, I.S.; Chen, C.K.; Kassner, E.G.; Klotz, D.H.; kottmeier, P.K., 1976:
Familial juvenile adenomatous polyposis

Fukutake, T.; Hattori, T.; Kita, K.; Hirayama, K., 1985:
Familial juvenile encephalopathy (Binswanger type) with alopecia and lumbago--a syndrome

Dombrovskaia, E.A., 1990:
Familial juvenile nephronophthisis

Yoshida, A.; Morozumi, K.; Koyama, K.; Takeda, A.; Uchida, K.; Tominaga, Y.; Oikawa, T.; Fujinami, T.; Takagi, H., 1992:
Familial juvenile nephronophthisis and renal transplantation in two siblings

Matsubara, K.; Suzuki, K.; Lin, Y.W.; Yamamoto, T.; Ohta, S., 1991:
Familial juvenile nephronophthisis in two siblings--histological findings at an early stage

Vergesslich, K.A.; Ponhold, W.; Balzar, E.; Syrè, G.; Ulrich, W., 1986:
Familial juvenile nephronophthisis--a cause of chronic renal failure in childhood

Demuth, S.; August, C., 1990:
Familial juvenile nephronophthisis--a genetically-caused kidney disease

Cantani, A.; Bamonte, G.; Ceccoli, D.; Biribicchi, G.; Farinella, F., 1986:
Familial juvenile nephronophthisis. A review and differential diagnosis

August, C.; Demuth, S., 1990:
Familial juvenile nephronophthisis. Pathohistology of a rare genetic disease in three siblings

McCredie, D.A.; Baxter, T.J., 1976:
Familial juvenile nephronophthisis: report of a case including microdissection studies

Roberti, E.; Mota Hernández, F.; Sakihara, G.; Gordillo Paniagua, G., 1977:
Familial juvenile nephronopthisis

Rivero Puente, A.; Asin, J.L.; Reparaz, B.; García Carasusan, M.; Unzue, J.J., 1976:
Familial juvenile nephronopticic. Evolutive and clinico-pathological considerations on 4 cases

Itoyama, Y.; Shibasaki, H.; Goto, I.; Kuroiwa, Y.; Kawabuchi, M., 1976 :
Familial juvenile neuronal storage disease. Cherry red spots and dyssynergia cerebellaris myoclonica without dementia type

Mayer, J.M.; Mikol, J.; Haguenau, M.; Dellanave, J.; Pépin, B., 1986:
Familial juvenile parkinsonism with multiple systems degenerations. A clinicopathological study

Makishita, H.; Inoue, K.; Kagaya, H.; Yanagisawa, N.; Tsukagoshi, H., 1978:
Familial juvenile parkinsonism with retinitis pigmentosa and vitiligo

Nelson, P.G.; Arthur, L.J.; Gurling, K.J.; Gamble, D.R.; Taylor, K.W., 1977:
Familial juvenile-onset diabetes

Forstot, S.L.; Goldstein, J.H.; Damiano, R.E.; Dukes, D.K., 1988:
Familial keratoconus

Atherton, D.J.; Botcherby, P.K.; Francis, A.J.; Smith, N.P.; Wells, R.S.; Giannelli, F., 1989:
Familial keratoses of actinic distribution associated with internal malignancy and cellular hypersensitivity to UVA

Padilha-Gonçalves, A., 1986:
Familial keratotic papular lesions of the chin

Brenner, S.; Ilie, B., 1985:
Familial keratotic papular lesions on the chin

Lefranc, G.; Dumitresco, S.M.; Salier, J.P.; Rivat, L.; de Lange, G.; van Loghem, E.; Loiselet, J., 1979:
Familial lack of the IgG3 subclass: gene elimination or turning off expression and neutral evolution in the immune system

Shulman, J.B.; Hollister, D.W.; Thibeault, D.W.; Krugman, M.E., 1976:
Familial laryngomalacia: a case report

Fairfax, A.J.; Lambert, C.D., 1975:
Familial late onset heart block: a clinico-pathological study

Ríos, E.; Dal Borgo, P.; Riveros, A.; Díaz, S.M., 1989:
Familial lead poisoning

Luque Márquez, R.; Gutiérrez-Rave Pecero, M.; Pujol de la Llave, E., 1989:
Familial lead poisoning caused by the drinking of household water

Gil Llano, J.R.; Pérez de las Vacas, J.; Gaspar, G.; Solís Villa, F.J., 1985:
Familial lead poisoning from water of domestic use

Gjone, E., 1988:
Familial lecithin: cholesterol acyltransferase (LCAT) deficiency. An updated review Spring 1988

Iwamoto, A.; Naito, C.; Teramoto, T.; Kato, H.; Kako, M.; Kariya, T.; Shimizu, T.; Oka, H.; Oda, T., 1978:
Familial lecithin: cholesterol acyltransferase deficiency complicated with unconjugated hyperbilirubinemia and peripheral neuropathy. The first reported cases in the Far East

Winder, A.F.; Garner, A.; Sheraidah, G.A.; Barry, P., 1985:
Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea

Blomhoff, J.P.; Holme, R.; Sauar, J.; Gjone, E., 1978:
Familial lecithin:cholesterol acyltransferase deficiency. Further studies on plasma lipoproteins and plasma postheparin lipase activity of a patient with normal renal function

Hansen, E.; Jacobsen, B.B., 1985:
Familial leucine sensitive hypoglycemia

Ferraz, C.N.; Kerbauy, J.; Nazareth, H.; Matsumoto, M.; Pio da Silva, M., 1975 :
Familial leukaemia. A report of three cases of acute leukaemia in a Brazilian family

Gunz, F.W.; Gunz, J.P.; Veale, A.M.; Chapman, C.J.; Houston, I.B., 1975:
Familial leukaemia: a study of 909 families

Khitri, A.; Benlatrache, K.; Aouati, A.; Messerschmitt, J., 1977:
Familial leukemia

Hennekam, R.C.; Hofstee, N., 1990:
Familial liability to intrauterine vascular impairments

Valsecchi, R.; Bontempelli, M.; di Landro, A.; Barcella, A.; Lainelli, T., 1990:
Familial lichen planus

Sodaify, M.; Vollum, D.I., 1978:
Familial lichen planus. A case report

Copeman, P.W.; Tan, R.S.; Timlin, D.; Samman, P.D., 1978:
Familial lichen planus. Another disease or a distinct people?

Kofoed, M.L.; Wantzin, G.L., 1985:
Familial lichen planus. More frequent than previously suggested?

Urbina González, F.; Fernández-Cogolludo, E.; Abad, E.; Sánchez de Paz, F.; Sánchez Yus, E.; García-Pérez, A., 1987:
Familial lineal nevus of the connective tissue

Attal, H.C.; Jiwane, A.D.; Choubey, B.S., 1977:
Familial lipidosis--report of a rare form of Niemann Pick disease (type E) with a review of literature

Amirhakimi, G.H.; Haghighi, P.; Ghalambor, M.A.; Honari, S., 1976:
Familial lipogranulomatosis (Farber's disease)

Brun, L.D.; Gagné, C.; Julien, P.; Tremblay, A.; Moorjani, S.; Bouchard, C.; Lupien, P.J., 1989:
Familial lipoprotein lipase-activity deficiency: study of total body fatness and subcutaneous fat tissue distribution

Foster, J.H.; Donohue, T.A.; Berman, M.M., 1978:
Familial liver-cell adenomas and diabetes mellitus

Wadud, M.A.; Bose, B.K.; Al Nasir, T., 1989:
Familial localised scleroderma from Bangladesh: two case reports

Taj, M.; Ahmad, A., 1977:
Familial localized scleroderma (morphoea)

Androsoni, A.; Dolara, A.; Manetti, A.; Santoro, G.; Cecchi, F., 1979:
Familial long QT interval and sudden death

Dowgird, M.; Galar, B.; Sankowski, T.; Wasiluk, A., 1986:
Familial long QT syndrome

Pony, J.C.; Mattheyses, M.; Daubert, J.C.; Fourdilis, M.; Gouffault, J., 1977:
Familial long QT-syncope syndrome. 2 cases of Romano-Ward syndrome

Varughese, G.; Quartey, G.R., 1979:
Familial lumbar spinal stenosis with acute disc herniations. Case reports of four brothers

Postacchini, F.; Massobrio, M.; Ferro, L., 1985:
Familial lumbar stenosis. Case report of three siblings

Ooi, W.L.; Elston, R.C.; Chen, V.W.; Bailey-Wilson, J.E.; Rothschild, H., 1986:
Familial lung cancer--correcting an error in calculation

Herson, D.; Krivitzky, A.; Douche, C.; Jeantils; Lemaitre, M.O.; Delzant, G., 1989:
Familial lupus and Adie's tonic pupil

Anonymous, 1977:
Familial lupus and dogs

Moya Mir, M.S.; Mosquera, J.M.; Kreisler, M.; Barbadillo, R.; Martin Martin, F.; Cortejoso, E., 1978:
Familial lupus erythematosus disseminatus and HLA. Study of a family with 2 sisters affected with the disease

Cleland, L.G.; Bell, D.A.; Willans, M.; Saurino, B.C., 1978:
Familial lupus. Family studies of HLA and serologic findings

Barsky, S.; Knapp, D.; Bennin, B., 1977:
Familial lupus: spectrum of disease in one family

Cañadas, M.; Valladolid, J.M.; Villar, J.L.; Herrerías, J.M., 1987:
Familial lymphohistiocytosis with hepatic involvement: presentation of 2 cases

Trabelsi, M.; Bennaceur, B.; Damergi, R.; Gorji, Y.; Ben Jilani, S., 1990:
Familial lymphohistiocytosis--a second Tunisian case

Wright, J.A.; Pennington, J.E., 1987:
Familial lymphoid interstitial pneumonitis

Fradis, M.; Podoshin, L.; Zismann, D., 1978:
Familial lymphoma

Blattner, W.A.; Dean, J.H.; Fraumeni, J.F., 1979:
Familial lymphoproliferative malignancy: clinical and laboratory follow-up

Taleb, N.; Tohme, A.; Abi Jirgiss, D.; Kattan, J.; Salloum, E., 1991:
Familial macroglobulinemia in a Lebanese family with two sisters presenting Waldenström's disease

Chemke, J., 1976:
Familial macroglossia-omphalocele syndrome

Debicka, A., 1976:
Familial macular degeneration of the Stargardt type

Herzeel, R.; Brihaye-Van Geertruyden, M.; Verworst, F.; Bayet, T.; Nieus, C.; Kirckpatrick, C., 1979:
Familial maculopathy associated with endocrine disorders

Hauser, A.R.; Lerner, I.J.; King, R.A., 1992:
Familial male breast cancer

Hashishe, M.M.; Kohail, H.M., 1992:
Familial male breast cancer. A case report and review of the literature

Akgun, S.; Ertel, N.H.; Imperato-McGinley, J.; Sayli, B.S.; Shackleton, C., 1986:
Familial male pseudohermaphroditism due to 5-alpha-reductase deficiency in a Turkish village

Ganpathy, V.; Banerjee, P.; Dash, R.J., 1987:
Familial male pseudohermaphroditism with complete androgen insensitivity

Verma, I.C.; Sansi, P.K.; Kumar, V.; Ahuja, M.M., 1975:
Familial male pseudohermaphroditism with female external genitalia, presence of labial testes, male habitus and voice, and complete absence of Müllerian structures and lack of breast development

Sánchez Cascos, A., 1989:
Familial malformation recurrence in congenital heart disease

Habbema, L.; Kisch, L.S.; Starink, T.M., 1986:
Familial malignant atrophic papulosis (Degos' disease)--additional evidence for heredity and a benign course

Kopf, A.W.; Mintzis, M.; Grier, R.N.; Silvers, D.N.; Bart, R.S., 1976:
Familial malignant melanoma

Ghillani, M.; Caleffi, E., 1987:
Familial malignant melanoma and its relation to dysplastic nevus syndrome: considerations on 6 clinical cases

Muñoz, L.; Guzmán, J.; Ponce de León, S.; Mutchinick, O.; Arista, J.; Vázquez, J., 1988:
Familial malignant pleural mesothelioma. Report of 3 cases

Berlin, E.N., 1976:
Familial management of minimal brain dysfunction

el-Badramany, M.H.; Farag, T.I.; al-Awadi, S.A.; Hammad, I.M.; Abdelkader, A.; Murthy, D.S., 1989:
Familial manic-depressive illness with deleted short arm of chromosome 21: coincidental or causal?

Dubosson, J.D.; Schneider, P., 1978:
Familial manifestation of a circumscribed cutaneous aplasia of the vertex associated, in one case, with cardiac malformation

Gillor, A.; Korsch, E., 1992:
Familial manifestation of idiopathic atrial flutter

Winsor, E.J.; Van Allen, M.I., 1989:
Familial marker chromosome due to 3:1 disjunction of t(9;15) in a grandparent

Tal, A.; Carmi, R.; Chai-Am, E.; Zirkin, H.; Bar-Ziv, J.; Freud, E., 1985:
Familial meconium ileus with normal sweat electrolytes

Anonymous, 1978:
Familial mediterranean fever (periodic peritonitis)

Bonilla, F.; Enríquez, R.; Lacueva, J.; González, C., 1992:
Familial mediterranean fever or the need for an early diagnosis

Wolff, S.M., 1978:
Familial mediterranean fever: a status report

Gemme, G.; Ruffa, G.; Bonioli, E.; Mangiante, G., 1976:
Familial mediterreanean fever (periodic disease). Description of a case

Frei, D.; Briner, J.; Binswanger, U., 1979:
Familial medullary cystic kidney with progressive kidney failure

Houdent, C.; Avronsart, B.; Dubuisson, M.; Ozenne, G.; Testard, J.; Calmettes, C.; Chaventre, A.; Sobol, H.; Lenoir, G.M.; Wolf, L.M., 1990:
Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families

Lairmore, T.C.; Howe, J.R.; Korte, J.A.; Dilley, W.G.; Aine, L.; Aine, E.; Wells, S.A.; Donis-Keller, H., 1991:
Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A

Farndon, J.R.; Leight, G.S.; Dilley, W.G.; Baylin, S.B.; Smallridge, R.C.; Harrison, T.S.; Wells, S.A., 1986:
Familial medullary thyroid carcinoma without associated endocrinopathies: a distinct clinical entity

Hung, K.L., 1991:
Familial medulloblastoma in non-twin siblings

Tijssen, C.C., 1991:
Familial medulloblastoma in siblings: report in one family and review of the literature

Kirk, S.J.; Lawson, J.T.; Allen, I.V.; Parks, T.G., 1990:
Familial megaduodenum associated with hypoganglionosis

Kissel, P.; Andre, J.M.; Duc, M.L.; Jacquier, A., 1976:
Familial melkersson rosenthal syndrome

Herrin, J.T.; Bartsocas, C.S., 1989:
Familial membranoproliferative glomerulonephritis type 2 (MPGN-2)

Ferrante, L.; Acqui, M.; Mastronardi, L.; Nucci, F., 1987:
Familial meningiomas. Report of two cases

Sato, H.; Takaya, K.; Nihira, S.; Fujita, H., 1989:
Familial mental retardation associated with balanced chromosome rearrangement rcp t(8;11)(q24.3;p15.1)

Hess, O.M.; Goebel, N.H.; Streuli, R., 1978:
Familial mesomelial dwarfism (Nievergelt syndrome)

Li, F.P.; Lokich, J.; Lapey, J.; Neptune, W.B.; Wilkins, E.W., 1978:
Familial mesothelioma after intense asbestos exposure at home

Dawson, A.; Gibbs, A.; Browne, K.; Pooley, F.; Griffiths, M., 1992:
Familial mesothelioma. Details of 17 cases with histopathologic findings and mineral analysis

Gambardella, A.; Ciccarelli, R.; Pepe, A.; Mosca, A., 1990:
Familial metaphyseal dysplasia (Pyle's disease) versus craniometaphyseal dysplasia. Presentation of a case

Rosa, M.A.; Laudati, A.; Pannone, A., 1991:
Familial metaphyseal dysplasia: incidental detection of an osteochondroma

Guala, A.; Mittino, D.; Fabbrocini, P.; Ghini, T., 1992:
Familial metoclopramide-induced dystonic reactions

Lesný, I.; Seemanová, E., 1987:
Familial microcephaly with spasticity and epilepsy in 2 sisters

Vidal Pla, R.; Roca Tey, R.; Miravitlles, M.; de Gracia, J.; Nubiola, A.R., 1990:
Familial microepidemics of tuberculosis

Becker, A.; Delucchi, M.A.; Hodali, Y.; Taboada, H.; Valiente, N., 1986:
Familial microspherocytosis. A Study in 10 families

Schmid, M.; Schröder, M.; Langenbeck, U., 1985:
Familial microtia, meatal atresia, and conductive deafness in three siblings

Hoo, J.J., 1979:
Familial middle lobe bronchiectasis

Wallace, D.C.; Zheng, X.X.; Lott, M.T.; Shoffner, J.M.; Hodge, J.A.; Kelley, R.I.; Epstein, C.M.; Hopkins, L.C., 1988:
Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

Shimoji, A.; Katsuragi, S.; Miyakawa, T.; Hira, R.; Watanabe, K.; Miyakawa, K.; Ishitsu, T.; Miike, T., 1987:
Familial mitochondrial encephalomyopathy with stroke-like episodes and episodic disturbances of consciousness: a study of pedigree including three generations with multisystemic abnormalities

Estournet, B.; Duyckaerts, C.; Marsac, C.; Chabbi, N.; Bataille, J.; Barois, A.; Hauw, J.J.; Goulon, M., 1991:
Familial mitochondrial encephalopathy. A clinicopathologic study

Mizusawa, H.; Watanabe, M.; Kanazawa, I.; Nakanishi, T.; Kobayashi, M.; Tanaka, M.; Suzuki, H.; Nishikimi, M.; Ozawa, T., 1988:
Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IV

Bareiss, P.; Christmann, D.; Storck, D.; Warter, J., 1977:
Familial mitral valve prolapse and syncopes caused by ventricular tachycardia

Slack, R.W.; Phelps, P.D., 1985:
Familial mixed deafness with branchial arch defects (earpits-deafness syndrome)

Leblanc, R.; Lozano, A.; Robitaille, Y., 1986:
Familial mixed oligodendrocytic-astrocytic gliomas

Anonymous, 1986:
Familial moles and malignant melanoma in The Netherlands

Youinou, P.; Le Goff, P.; Saleun, J.P.; Fauchier, C.; Le Menn, G., 1977:
Familial monoclonal gammapathy. Preliminary results of a prospective survey

Kjellström, T.; Barkenius, G.; Malmquist, J.; Rausing, A., 1979:
Familial monocytic leukaemia. A report of two families

Shapiro, L.R.; Zemek, L.; Shulman, M.J., 1978:
Familial monozygotic twinning: an autosomal dominant form of monozygotic twinning with variable penetrance

Tranchant, C.; Dugay, M.H.; Mohr, M.; Wasser, P.; Warter, J.M., 1992:
Familial motor neuron disease with Lewy body-like inclusions in the substantia nigra, the subthalamic nucleus, and the globus pallidus

Horton, W.A.; Eldridge, R.; Brody, J.A., 1976:
Familial motor neuron disease. Evidence for at least three different types

Yoshimasu, F.; Tanaka, S.; Hayashi, T.; Iwata, K.; Oka, H., 1977:
Familial motor neuron disease: Autopsy findings in one of two brothers

Stopyrowa, J.; Pietrzyk, J.A.; Fyderek, K.; Spodaryk, M.; Barylak, A.; Miezyński, W.; Kaczmarski, F., 1988:
Familial mucolipidosis type II (I-cell disease)

Shul'ga, I.D.; Zharko, K.P., 1978:
Familial mucopolysaccharidosis

Gómez Sáez, J.M.; Valentines Pont, J.; Marigó Bertrán, M.; Boné Palomar, C.; Soler Ramón, J., 1985:
Familial mucosal neuromatosis: a minor form of multiple endocrine neoplasms II b?

Brownell, A.K., 1979:
Familial multicore disease

Char, F.; Douglas, J.E.; Dungan, W.T., 1975:
Familial multiforme ventricular extrasystoles with short stature, hyperpigmentation and microcephaly-a new syndrome

Blackford, S.; Roberts, D.L., 1991:
Familial multiple blue naevi

Bochnia, M.; Swiatkowska, M., 1978:
Familial multiple congenital anomalies of oto-cervical localization

Ballard, H.S.; Frame, B.; Hartsock, R.J.; Ballard, H.S., 1991:
Familial multiple endocrine adenoma-peptic ulcer complex. 1964

Gilmartin, D., 1978:
Familial multiple epidermoid cysts of the spleen

Hall, J.G.; Wilson, R.D.; Kalousek, D.; Beauchamp, R., 1985:
Familial multiple exostoses--no chromosome 8 deletion observed

Rogai, R.; Renai, P.; Benedetti, P.A., 1979:
Familial multiple exostoses. Presentation of a case

Kitano, K.; Kinoshita, K.; Fukumura, A.; Matsukado, Y., 1977:
Familial multiple hemangioblastomas--report of two cases in a family

Hilker, O.; Winterscheidt, M., 1987:
Familial multiple keratoacanthomas

Pasyk, K.A., 1992:
Familial multiple lateral telangiectatic nevi (port-wine stains or nevi flammei)

Schmid, M.; Boltshauser, E., 1989:
Familial multiple naevi flammei

Phillips, H.O.; Grubb, S.A., 1985:
Familial multiple osteochondritis dissecans. Report of a kindred

Eldridge, R.; McFarland, H.; Sever, J.; Sadowsky, D.; Krebs, H., 1978:
Familial multiple sclerosis: clinical, histocompatibility, and viral serological studies

Camarasa, J.G.; Calderon, P.; Moreno, A., 1988:
Familial multiple trichodiscomas

Su, C.C.; Su, W.T. , 1989:
Familial multiple-organ arterial ectasia with massive hemoptysis

Roy, E.P.; Riggs, J.E.; Crosby, T.W.; Gutmann, L.; Schochet, S.S., 1988:
Familial myalgic myopathy

Iyer, G.V.; Jayakumar, R.V., 1975:
Familial myasthenia gravis (case reports)

Lameatine De Assis, J.; Scaff, M., 1976:
Familial myasthenia gravis. Report of four cases

Dias-Tosta, E.; Aguiar, M.F.; Barbosa, H.; Vilela, S.S., 1989:
Familial myasthenia gravis: a case report in identical twins

Chin, D.; Gubbay, S.S., 1985:
Familial myasthenia gravis: a study of three families

de Freitas, M.R.; Gomes, S.E.; Cincinatus, D.; Garcia, J.M.; Nevares, M.T.; Hahn, M.D., 1985:
Familial myasthenia gravis: report of 2 brothers

Boudouresques, J.; Khalil, R.; Gosset, A.; Chérif, A.A.; Boudouresques, G.; Mortier, E., 1975:
Familial myasthenia. Observations in a father and his daughter

Hubert, D.; Thomas, M.; Krulik, M.; de Gramont, A.; Brissaud, P.; Sirinelli, A.; Debray, J., 1985:
Familial myeloma. Apropos of a case

Bondare, D.K.; Teĭlane, I.Ia.; Reĭskart, L.V.; Rotsena, A.Ia.; Grasmane, D.V., 1985:
Familial myeloproliferative syndrome (study of 4 families and review of the literature)

Kaufman, S.; Brière, J.; Bernard, J., 1978 :
Familial myeloproliferative syndromes. Study of 6 families and review of literature

Little, B.W.; Brown, P.W.; Rodgers-Johnson, P.; Perl, D.P.; Gajdusek, D.C., 1986:
Familial myoclonic dementia masquerading as Creutzfeldt-Jakob disease

Pérez Maiquez, F., 1976:
Familial myopathies (D.M.). Electroclinical study

Zagar, M.; Mohacek, I.; Jusić, A., 1979:
Familial myopathy of the shoulder and pelvic girdle associated with cardiomyopathy

Henze, T.; Bardosi, A.; Reichmann, H.R., 1991:
Familial myopathy with elevated serum angiotensin-converting enzyme, creatine kinase and lactate dehydrogenase isoenzyme 5

Morand, P.; Bienvenu, P.; Daumas, P.L.; Kieffer, A.; Muh, J.P.; Raynaud, R., 1977:
Familial myopathy with exclusively cardiac clinical expression

Chapon, F.; Viader, F.; Fardeau, M.; Tomé, F.; Daluzeau, N.; Berthelin, C.; Thénint, J.P.; Lechevalier, B., 1989:
Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency

Waldo, R., 1978:
Familial myopathy. Exacerbation by hypokalemia associated with colonic polyp

Rossi, B., 1976:
Familial myotonic syndrome with hyposthenia corrected with exercise

Liebler, G.A.; Magovern, G.J.; Park, S.B.; Cushing, W.J.; Begg, F.R.; Joyner, C.R., 1976:
Familial myxomas in four siblings

Rogan, K.M.; Sears-Rogan, P.; Virmani, R.; Pyeritz, R.E., 1989:
Familial myxomatous valvular disease

Cross, H.E.; Yoder, F., 1976:
Familial nanophthalmos

Hublin, C.; Partinen, M.; Koskimies, S., 1991:
Familial narcolepsy in Finland

Babin, R.W.; Kavanagh, K.T., 1985:
Familial nasal acilia syndrome

Levine, P.H.; Pocinki, A.G.; Madigan, P.; Bale, S., 1992:
Familial nasopharyngeal carcinoma in patients who are not Chinese

Bratov, R., 1979:
Familial nature of nephropathies in the village of Zidarovo, Burgas District

Frati, A.C.; Lugones, R.F.; Figueroa, J.A.; Criollos, O.; Martínez-Cairo, S., 1978:
Familial neoplasms and childhood dermatomyositis

Lawrence, J.R.; Robinson, M.F., 1978:
Familial nephritis in Adelaide

Hradcová, L.; Zajícek, M., 1977:
Familial nephrocalcinosis

Linnanvuo-Laitinen, M.; Pirttiaho, H.; Similä, S.; Lautala, P., 1985:
Familial nephrogenic diabetes insipidus and mental retardation

Freycon, M.T.; Lavocat, M.P.; Freycon, F., 1988 :
Familial nephrogenic diabetes insipidus with chronic hypernatremia and cerebral calcifications

Feest, T.G.; Wallis, J.P., 1985:
Familial nephropathic amyloidosis associated with indomethacin responsive fever

Zalin, A.M.; Jones, S.; Fitch, N.J.; Ramsden, D.B., 1991:
Familial nephropathic non-neuropathic amyloidosis: clinical features, immunohistochemistry and chemistry

Puig, J.G.; Miranda Carús, M.E.; Mateos, F.A.; Luz Picazo, M.; López Jiménez, M.; Ortíz Vázquez, J., 1991:
Familial nephropathy and gout: which comes first?

Nash, A.S.; Creswick, J.A., 1988:
Familial nephropathy in soft-coated wheaten terriers

Fiore, C.; Santoni, G.; Reggiani, F.M.; Buoncristiani, U.; Pasticci, B., 1985:
Familial nephropathy with retinitis pigmentosa and closed-angle glaucoma

Diekmann, L.; Louis, C.; Schulte-Kemna, E., 1977:
Familial nephropathy with retinitis pigmentosa and peripheral dysostosis

Barakat, A.Y.; D'Albora, J.B.; Martin, M.M.; Jose, P.A., 1977:
Familial nephrosis, nerve deafness, and hypoparathyroidism

Kim, P.K.; Pai, K.S.; Hwang, C.H.; Park, M.S.; Jeong, H.J.; Choi, I.J., 1991:
Familial nephrotic syndrome and HLA-DR5

Wojnarowski, M.; Wolff-Płodowska, A.; Trzebiński, A., 1979:
Familial nephrotic syndrome in the light of a case report in 2 twins

Schwarz, R.; Stögmann, W.; Fischbach, H., 1976:
Familial nephrotic syndrome with focal glomerular sclerosis

Schwartz, S.S.; Rich, B.H.; Lucky, A.W.; Straus, F.H.; Gonen, B.; Wolfsdorf, J.; Thorp, F.W.; Burrington, J.D.; Madden, J.D.; Rubenstein, A.H.; Rosenfield, R.L., 1979:
Familial nesidioblastosis: severe neonatal hypoglycemia in two families

Robertson, C.M.; Tyrrell, J.C.; Pritchard, J., 1991:
Familial neural crest tumours

Marangos, N.; Mausolf, A., 1990:
Familial neural mitochondrial deafness

Aver'ianov, I.N.; Iakhno, N.N.; Nechkina, N.P., 1992:
Familial neuralgic amyotrophy

Massi-Benedetti, F.; Angeletti, G.; de Giorgi, G.; Romagno, D.; Massi-Benedetti, M., 1978:
Familial neuro-hormonal diabetes insipidus. Study of 3 clinical cases

Pegelow, C.H.; Ebbin, A.J.; Powars, D.; Towner, J.W., 1975:
Familial neuroblastoma

Roberts, F.F.; Lee, K.R., 1975:
Familial neuroblastoma presenting as multiple tumors

Kushner, B.H.; Gilbert, F.; Helson, L., 1986:
Familial neuroblastoma. Case reports, literature review, and etiologic considerations

Klein, H.; Plöchl, E.; Lampert, F., 1975:
Familial neuroblastoma: cytogenetic investigation of the peripheral blood

Clausen, N., 1986:
Familial neuroblastomas. Predictors of heredity

Barson, A.J., 1979:
Familial neurodegenerative disorder associated with raised urinary VMA

Young, I.; Hosking, G.P., 1978:
Familial neurodegenerative disorder associated with raised urinary vanillylmandelic acid

Pedersen, O.D.; Bagger, H., 1991:
Familial neurofibromatosis and hypertrophic obstructive cardiomyopathy

Hofman, K.J.; Boehm, C.D., 1992:
Familial neurofibromatosis type 1: clinical experience with DNA testing

Sugiura, Y.; Sengoku, H., 1986:
Familial neurogenic acro-osteolysis, type Giaccai--report of two families

Dobkin, B.H.; Verity, M.A., 1978:
Familial neuromuscular disease with type 1 fiber hypoplasia, tubular aggregates, cardiomyopathy, and myasthenic features

Rosenfeld, N.; Harel, M.; Herman, S., 1977:
Familial neuropathy as a cause for distal thumb amputation. Case report

Merlob, P.; Reisner, S.H., 1985:
Familial nevus flammeus of the forehead and Unna's nevus

Jacobsen, J.H.; Rosenberg, R.S.; Huttenlocher, P.R.; Spire, J.P., 1986:
Familial nocturnal cramping

Greene, M.H.; Miller, R.W., 1978:
Familial non-Hodgkin lymphoma: histologic diversity and relation to other cancers

Perlman, M.; Williams, J.; Hirsch, M.; Bar-Ziv, J., 1975:
Familial non-cystic fibrosis mucus inspissation of respiratory tract

Ho, K.K.; O'Loughlin, S.; Powell, F.C., 1992:
Familial non-diabetic necrobiosis lipoidica

Singh, D.S.; Bisht, D.B.; Raju, S., 1978:
Familial non-haemolytic hyperbilirubinaemia

Crothers, D.C.; Harvey, T.C.; Faber, J.; Ramsden, D.B., 1992:
Familial non-toxic hyperthyroxinaemia: receptor or 5'-deiodinase defect or deficiency

Perret, B.; Gaze, H.; Zimmermann, A.; Oetliker, O., 1979:
Familial nonendemic hemolytic uremic syndrome: nephrectomy and transplantation

Mihas, A.A.; Kirby, J.D.; Hirschowitz, B.I., 1979:
Familial nonhemolytic jaundice with free and conjugated hyperbilirubinemia, elevated serum bile acids, and liver pigmentation

Singh, A.; Doyle, E.F.; Danilowicz, D.A.; Finegold, M.J., 1978:
Familial nonobstructive cardiomyopathy with endocardial fibroelastosis beyond infancy

Bonfils, S.; Vilotte, J., 1989:
Familial nonpolyposis colorectal cancers (Lynch syndrome). How to manage risk factors?

Hermier, M.; Beaupère, A., 1978:
Familial nonprogressive chorea; apropos of 1 case

Damasio, H.; Antunes, L.; Damasio, A.R., 1977:
Familial nonprogressive involuntary movements of childhood

Hammerstein, W.; Gebauer, H.J., 1989:
Familial nystagmus and hypoplasia of the macular in reciprocal, balanced translocation 5/16

Anonymous, 1979:
Familial obstructive sleep apnea

Piza-Katzer, H., 1976:
Familial occurence of Martin-Gruber anastomosis

Balícek, P.; Zizka, J., 1975:
Familial occurence of abnormal karyotype 14p+

Schnoy, N.; Bein, G.; Dumke, K., 1978:
Familial occurence of congenital short bowel

Zagórski, Z., 1978:
Familial occurence of membranous cataract

Matĕjovský, Z., 1977:
Familial occurence of osteosarcoma

Sangiorgi, M.; Fragola, P.V.; Capria, A., 1989:
Familial occurrence in cardiovascular diseases. Cardiovascular involvement in genetic disorders (2)

Sangiorgi, M.; Fragola, P.V.; Capria, A., 1989:
Familial occurrence in cardiovascular diseases. Familial cardiovascular diseases (1)

Korczowski, R.; Nizankowska-Błaz, T.; Watróbska, S., 1985 :
Familial occurrence of Addison's disease

Bidzan, L.; Kowalczuk-Zieleniec, E.; Motak, E., 1990:
Familial occurrence of Alzheimer's disease

Costa, J.M.; Osaho, N.K.; Vale, K.C.; Lago, E.L.; França, F.; Vexenat, J.A.; Marsden, P.D., 1986:
Familial occurrence of American cutaneous leishmaniasis in an endemic region, Corte de Pedra, Bahia

Bankier, A.; Haan, E.; Birrell, R., 1986:
Familial occurrence of Brachmann-de Lange syndrome

Madaliński, K.; Sabbouh, K.; Imielska, D.; Chorazykiewicz, M., 1989:
Familial occurrence of C1-inhibitor deficiency and the effect of treatment

Derkacz, Z.; Zaleski, J., 1975:
Familial occurrence of Crouzon's disease

Tomaszewska, B.; Zoch-Zwierz, W., 1988:
Familial occurrence of Crouzon's syndrome

Hunter, A., 1992:
Familial occurrence of Duchenne dystrophy through paternal lines in four families

Jakubowski, J., 1976:
Familial occurrence of Dupuytren's contracture

Hammerer, I.; Gassner, I.; Müller, W., 1979:
Familial occurrence of Elfin's face (Williams-Beurens Syndrome =wbs) and supravalvular aortic stenosis (= svas)

Musiał, J.; Krzanowski, M.; Judkiewicz, L.; Cierniewski, C., 1992:
Familial occurrence of Glanzmann thrombasthenia

Ujpál, M.; Szabó, G., 1992:
Familial occurrence of Gorlin-Goltz syndrome

Wójtowicz, S., 1977:
Familial occurrence of Grönblad-Strandberg syndrome

Mori, M.; Ban, N.; Kinoshita, K., 1988:
Familial occurrence of HTLV-I--associated myelopathy

Smakal, S.; Golán, T.; Bláha, M.; Dienstbier, Z.; Hermanská, Z., 1990:
Familial occurrence of Hodgkin's disease

Jójárt, G.; Fekete, F., 1977:
Familial occurrence of Ivemark's syndrome

Zeiler, K.; Mamoli, B.; Heiss, W.D., 1976:
Familial occurrence of Kugelberg-Welander pseudomyopathic spinal muscular atrophy

Juberg, R.C.; St Martin, E.C.; Hundley, J.R., 1975:
Familial occurrence of Wilms' tumor: nephroblastoma in one of monozygous twins and in another sibling

Mispireta, J.L.; Dumont, C.; Cárdenas, M.; de Micheli, A.; Martínez-Ríos, M.A., 1975:
Familial occurrence of Wolff-Parkinson-White syndrome. Report of a family group and review of the literature

Hancke, I.; Miller, K., 1985:
Familial occurrence of a pseudodicentric chromosome 21

Niikawa, N.; Matsuda, I.; Ohsawa, T.; Kajii, T., 1978:
Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblings

Schieche, M., 1975:
Familial occurrence of acquired heart valve defect

Kondo, H.; Ebara, M.; Oga, M.; Uchiyama, Y.; Yonemitsu, H., 1976:
Familial occurrence of aplastic anemia

Zerbe, F.; Dziegielewski, T., 1975:
Familial occurrence of atrioventricular block and supraventricular arrhythmia

Polgár, V.; Sándor, G., 1977:
Familial occurrence of balanced D/D translocation

Da Silva, J.A.; Da Silva, E.B.; de Souza, M.B., 1978:
Familial occurrence of basilar impression

Larrea, F.; Escorza, A.; Granados, J.; Valencia, X.; Valero, A.; Cravioto, M.C.; Pérez-Palacios, G., 1987:
Familial occurrence of big-big prolactin as the predominant immunoreactive human prolactin species in blood

Søgaard, I.; Jørgensen, J., 1975:
Familial occurrence of bilateral intracranial occlusion of the internal carotid arteries (Moya Moya)

Aragona, F.; Glazel, G.P.; Zacchello, G.; Andreetta, B., 1987:
Familial occurrence of blind-ending bifid and duplicated ureters

Misaki, T.; Hasegawa, M.; Tomita, F., 1975:
Familial occurrence of bradycardia

Rysz, A.; Gajkowski, K.; Empel, A., 1988:
Familial occurrence of calcinosis of the basal ganglia

Lengyel, G.; Kárteszi, M.; Vallent, K.; Makó, E.; Hídvégi, J.; Csóti, S.; Fehér, J., 1989:
Familial occurrence of carcinoid of the small intestine

Richter, G.; Zegelman, M.; Wagner, R.; Satter, P.; von Egidy, H., 1985:
Familial occurrence of cardiac myxomas

Ide, C.H.; Bingham, H.; Holt, J.E., 1975:
Familial occurrence of cebocephaly

Zoch-Zwierz, W.; Słowikowski, K.; Kadziela, H.; Lukaszewicz, D.; Biernacka, A., 1990:
Familial occurrence of central diabetes insipidus

Furgyik, S.; Grubb, R.; Kullander, S.; Sandahl, B.; Wingerup, L.; Eydal, A., 1986:
Familial occurrence of cervical cancer, stages 0-IV

Fazekas, T.; Bach, K.; Tóth, S.; Bodor, F., 1978:
Familial occurrence of chronic lymphatic leukemia. HL-A antigen and cytogenetic studies

Petzoldt, R.; Hartwich, G.; Demmler, K., 1976:
Familial occurrence of chronic lymphocytic leukemia: report of three siblings

Higgins, M.; Keller, J., 1975:
Familial occurrence of chronic respiratory disease and familial resemblance in ventilatory capacity

van Tilburg, A.J.; Lam, H.G.; Seldenrijk, C.A.; Stel, H.V.; Blok, P.; Dekker, W.; Meuwissen, S.G., 1990:
Familial occurrence of collagenous colitis. A report of two families

Law, I.P.; Hollinshead, A.C.; Whang-Peng, J.; Dean, J.H.; Oldham, R.K.; Herberman, R.B.; Rhode, M.C., 1977:
Familial occurrence of colon and uterine carcinoma and of lymphoproliferative malignancies. II. Chromosomal and immunologic abnormalities

Law, I.P.; Herberman, R.B.; Oldham, R.K.; Bouzoukis, J.; Hanson, S.M.; Rhode, M.C., 1977:
Familial occurrence of colon and uterine carcinoma and of lymphoproliferative malignancies: clinical description

Zalewska, R.; Midro, A.T.; Bakunowicz-Lazarczyk, A.; Proniewska-Skretek, E., 1992:
Familial occurrence of congenital aniridia

Oi, S.; Yamada, H.; Urui, S.; Matsumoto, S., 1988:
Familial occurrence of congenital anomalies of the central nervous system

Bochnia, M.; Ziemski, Z.; Rak, J., 1987:
Familial occurrence of congenital defects of the external ear

Oláh, Z., 1977:
Familial occurrence of congenital polycystic macular dystrophy

Rissanen, A.M., 1979:
Familial occurrence of coronary heart disease: effect of age at diagnosis

Egawa, K.; Johno, M.; Hayashibara, T.; Ono, T., 1992:
Familial occurrence of crusted (Norwegian) scabies with adult T-cell leukaemia

Duvie, S.O.; Evbuomwan, I.; Scott-Emuakpor, A.B.; Kadiri, I., 1990:
Familial occurrence of cryptorchidism

Rose, T.; Nothjunge, J.; Schlote, W., 1985:
Familial occurrence of dermatomyositis and progressive scleroderma after injection of a local anaesthetic for dental treatment

Brock, A.; Mortensen, P.B.; Mortensen, B.B.; Røge, H.R., 1988:
Familial occurrence of diminished pancreatic amylase in serum--a "silent" Amy-2 allelic variant?

Pelz, L.; Hille, J.M., 1977:
Familial occurrence of dorsal closure disorders of the neural tube

Jensen, I.W.; Faber, J.; Grunnet, N., 1990:
Familial occurrence of dysalbuminaemic hyperthyroxinaemia, lipomatosis and ankylosing spondylitis

Vallat, J.M.; Dunoyer, J., 1979:
Familial occurrence of entrapment neuropathies

Kostrzewski, J.M., 1976:
Familial occurrence of epidemic cerebrospinal meningitis

Mayron, R.; Grimwood, R.E., 1988:
Familial occurrence of eruptive vellus hair cysts

Pletcher, B.A.; Friedes, J.S.; Breg, W.R.; Touloukian, R.J., 1991:
Familial occurrence of esophageal atresia with and without tracheoesophagel fistula: report of two unusual kindreds

Zanghieri, G.; Di Gregorio, C.; Sacchetti, C.; Fante, R.; Sassatelli, R.; Cannizzo, G.; Carriero, A.; Ponz de Leon, M., 1990:
Familial occurrence of gastric cancer in the 2-year experience of a population-based registry

Salinas, C.F.; Bartoshesky, L.; Othersen, H.B.; Leape, L.; Feingold, M.; Jorgenson, R.J., 1979:
Familial occurrence of gastroschisis. Four new cases and review of the literature

Boczkowski, K., 1976:
Familial occurrence of gonadal tumors in XY females with breast development

Boczkowski, K.; Piatkowski, J., 1978:
Familial occurrence of gonadal tumors in women with a 46,XY karyotype

Matsubara, K.; Suzuki, K.; Lin, Y.W.; Yamamoto, T.; Ohta, S., 1992:
Familial occurrence of growth hormone deficiency and primary hypothyroidism

Eriksson, M.; Hållberg, B., 1992:
Familial occurrence of hematologic malignancies and other diseases in multiple myeloma: a case-control study

Plotz, R.D., 1985:
Familial occurrence of hemolytic disease of the newborn due to AO blood group incompatibility

Nikolopoulos, N.; Xynos, E.; Vassilakis, J.S., 1988:
Familial occurrence of hyperdynamic circulation status due to intrahepatic fistulae in hereditary hemorrhagic telangiectasia

Thompson, G.R.; Weiss, J.J.; Goldman, R.T.; Rigg, G.A., 1978:
Familial occurrence of hyperuricemia, gout, and medullary cystic disease

Bonuccelli, U.; Nuti, A.; Monzani, F.; De Negri, F.; Muratorio, A., 1991:
Familial occurrence of hypothyroidism and cerebellar ataxia

Mongird-Nakonieczna, J.; Kozlowski, B., 1976:
Familial occurrence of idiopathic scoliosis

Borkowski, Z., 1978:
Familial occurrence of idiopathic slipped proximal epiphysis of the hip

Sakane, T.; Murakawa, Y.; Suzuki, N.; Ueda, Y.; Tsuchida, T.; Takada, S.; Yamauchi, Y.; Tsunematsu, T., 1989:
Familial occurrence of impaired interleukin-2 activity and increased peripheral blood B cells actively secreting immunoglobulins in systemic lupus erythematosus

Topinková, M.; Kamarýt, J., 1988:
Familial occurrence of increased secretion of S alpha-amylase with recurrent swelling of the parotid glands in one member of the family

Ferreira, C.; Korkes, H.; Laredo, J.; Murad, N.; Pfeferman, A.; de Paola, A.A.; Borrotchin, L.; Kasinsky, N.; Buffolo, E.; Barcellini, A., 1977:
Familial occurrence of interatrial communication and pulmonary stenosis

Stavenow, L., 1979:
Familial occurrence of intracranial aneurysms

Midro, A.T.; Kulikowski, M.; Sawicka, A.; Panasiuk, B.; Korsak, E., 1988:
Familial occurrence of isodicentric X chromosomes with different breakpoints

Spanò, G.M.; Barletta, R.; Fiorentino, E.; De Pedrini, P.; Meloni, F.; Rapisarda, R.; Transi, M.G., 1989:
Familial occurrence of leukemia. Cytogenetic considerations apropos of 2 cases

Chrz, M.; Benesová, E.; Ceslar, P.; Trnĕný, M., 1992:
Familial occurrence of malignant hematologic diseases

Autio-Harmainen, H.; Pääkkö, P.; Alavaikko, M.; Karvonen, J.; Leisti, J., 1988:
Familial occurrence of malignant lymphoepithelial lesion of the parotid gland in a Finnish family with dominantly inherited trichoepithelioma

Massey, E.W., 1978:
Familial occurrence of meralgia paraesthetica

Kruk-Jeromin, J., 1986:
Familial occurrence of microtia

Biddison, J.H.; Dembo, D.H.; Spalt, H.; Hayes, M.G.; LeDoux, C.W., 1979:
Familial occurrence of mitral valve prolapse in X-linked muscular dystrophy

Kitahara, T.; Ariga, N.; Yamaura, A.; Makino, H.; Maki, Y., 1979:
Familial occurrence of moya-moya disease: report of three Japanese families

Ikeda, A.; Iguchi, I.; Hara, M.; Yamamoto, I.; Sato, O., 1990:
Familial occurrence of moyamoya disease with intracranial hemorrhage--report of two cases

Schramm, P.; Schmidt, K.L.; Rude, J., 1985:
Familial occurrence of multiple basalomas associated with hyperostotic spondylosis

Law, M.I., 1976:
Familial occurrence of multiple myeloma

Vassileva, S.; Krasteva, M., 1990:
Familial occurrence of multiple seborrheic keratoses and schizophrenia

Koui, F.; Yosida, M.; Maeda, T.; Mori, Y.; Fujiwara, Y.; Matsumura, T.; Yoshinaga, H., 1992:
Familial occurrence of myelodysplastic syndrome concomitant with monoclonal gammapathy

Clausen, N.; Andersson, P.; Tommerup, N., 1989:
Familial occurrence of neuroblastoma, von Recklinghausen's neurofibromatosis, Hirschsprung's agangliosis and jaw-winking syndrome

Tyagi, S.; Reddy, N.K.; Khalilullah, M., 1991:
Familial occurrence of non-specific aortoarteritis in two sisters

Lewy, P.R.; Belman, A.B., 1975:
Familial occurrence of nonobstructive, noninfectious vesicoureteral reflux with renal scarring

Havalad, S.; Noblett, H.; Speidel, B.D., 1979:
Familial occurrence of omphalocele suggesting sex-linked inheritance

Orstavik, K.H., 1989:
Familial occurrence of opioid-induced biliary colic

Suzuki, S.; Watanabe, I., 1985:
Familial occurrence of papillary thyroid carcinoma

Geysens, P.; D'Haenens, P.; Van Steenberge, R.; Wilms, G.; Baert, A.L., 1989:
Familial occurrence of paragangliomas

Himuro, H.; Kobayashi, E.; Kono, H.; Jinbo, M.; Kitamura, K., 1976:
Familial occurrence of pituitary adenoma

Höhle, B., 1978:
Familial occurrence of protrusio acetabuli

Napiontek, M.; Bernardczyk, K.; Kruczyński, J., 1986:
Familial occurrence of pseudoachondroplasia

Davee, M.A.; Moore, C.A.; Bull, M.J.; Hodes, M.E., 1992:
Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay

Biedrzyńska, B.; Blaszczyk, E.; Krajewska-Walasek, M., 1977:
Familial occurrence of severe pulmonary form of mucoviscidosis in early life

Gulotta, S.J.; Gupta, R.D.; Padmanabhan, V.T.; Morrison, J., 1977:
Familial occurrence of sinus bradycardia, short PR interval, intraventricular conduction defects, recurrent supraventricular tachycardia, and cardiomegaly

Rivera, H.; Zavala, C.; Hernándex-Franco, A.; Bustamante-Cruz, F.; Cantú, J.M., 1979:
Familial occurrence of supravalvular aortic stenosis

Molta, C.T.; Khan, M.A.; Aponte, C.J.; Reynolds, T.L.; Macintyre, S.S., 1989:
Familial occurrence of systemic sclerosis, rheumatoid arthritis and other immunological disorders: report of two kindreds with study of HLA antigens and review of the literature

Grabski, J.; Dziekanowska, D.; Buntner, B.; Panasiewicz, M., 1976:
Familial occurrence of testicular feminization

Sommer, A.; Cutler, E.A.; Cohen, B.L.; Harper, D.; Backes, C., 1977:
Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel

White, R.A.; Preus, M.; Watters, G.V.; Fraser, F.C., 1977:
Familial occurrence of the Williams syndrome

Mazurczak, T.; Stolarska, A.; Sito, A.; Mataszewska, K., 1977:
Familial occurrence of the cat's cry (cri du chat) syndrom resulting from a balanced t(5 : 12) translocation

Miernik, U.; Zielińska, B., 1988:
Familial occurrence of the orofaciodigital syndrome

Czerski, P.; Rogóyski, A.; Stolarska, A., 1977:
Familial occurrence of translocation (13q 14q) and 14q 21q)

Balícek, P.; Zizka, J., 1979:
Familial occurrence of translocation between chromosomes No. 3 and 4

Zwetsloot, C.P.; Kros, J.M.; Paz y Gueze, H.D., 1991:
Familial occurrence of tumours of the choroid plexus

Murata, I.; Makiyama, K.; Haga, H.; Iwanaga, S.; Yamasaki, K.; Mizuta, Y.; Kubo, K.; Senju, M.; Imanishi, T.; Hara, K., 1989:
Familial occurrence of ulcerative colitis--a case report with a review of the Japanese literature

Sonkodi, I.; Keszthelyi, G., 1977:
Familial occurrence of white spongy nevus

Frenk, E.; Calame, A., 1977:
Familial oculo-cutaneous hypopigmentation of dominant transmission due to a disorder in melanocyte formation. Association of Prader-Willi syndrome with a chromosome abnormality in one of the subjects involved

Uitti, R.J.; Donat, J.R.; Rozdilsky, B.; Schneider, R.J.; Koeppen, A.H., 1988:
Familial oculoleptomeningeal amyloidosis. Report of a new family with unusual features

Bonduelle, M.; Escourolle, R.; Bouygues, P.; Lormeau, G.; Gray, F., 1976:
Familial olivo-ponto-cerebellar atrophy with myoclonus. Limits of cerebellar myoclonic dyssynergia (Ramsay-Hunt syndrome)

Pryde, P.G.; Greb, A.; Isada, N.B.; Johnson, M.B.; Klein, M.; Evans, M.I., 1992:
Familial omphalocele: considerations in genetic counseling

Scott, H.; Moynahan, E.J.; Risdon, R.A.; Harvey, B.A.; Soothill, J.F., 1975:
Familial opsonization defect associated with fatal infantile dermatitis, infections, and histiocytosis

Wildberger, H., 1976:
Familial optic atrophy

Gorgone, G.; Li Volti, S.; Cavallaro, N.; Conti, L.; Profeta, G.M.; Mollica, F., 1986:
Familial optic atrophy with sex-influenced severity. A new variety of autosomal-dominant optic atrophy?

Morgan, M.K.; Onofrio, B.M.; Bender, C.E., 1989:
Familial os odontoideum. Case report

Dieppe, P., 1989:
Familial osteoarthrosis and type II collagen gene

Fonseca, A.S.; Keret, D.; MacEwen, G.D., 1990:
Familial osteochondritis dissecans

Auld, C.D.; Chesney, R.B., 1979:
Familial osteochondritis dissecans and carpal tunnel syndrome

Mubarak, S.J.; Carroll, N.C., 1979:
Familial osteochondritis dissecans of the knee

Kozlowski, K.; Middleton, R., 1985:
Familial osteochondritis dissecans: a dysplasia of articular cartilage?

Khaldi, F.; Bennaceur, B.; Gharbi, H.A., 1989:
Familial osteochondrodysplatic dwarfism associated with deafness and tapeto-retinal heredo-degeneration

Faccini, R.; Massari, L.; Chiarelli, G.M., 1986:
Familial osteochondrosis of the knee: etiological factors

Haddad, N.; Hila, A.; Amri, H.; Fourati, A., 1976:
Familial osteopoikilosis in a diabetic

Gilman, P.A.; Wang, N.; Fan, S.F.; Reede, J.; Khan, A.; Leventhal, B.G., 1985:
Familial osteosarcoma associated with 13;14 chromosomal rearrangement

Lehman, R.A.; Stears, J.C.; Wesenberg, R.L.; Nusbaum, E.D., 1977:
Familial osteosclerosis with abnormalities of the nervous system and meninges

Ferrer Marín-Blázquez, M.; Pérez de Lucas, N.; Alonso Salazar, M.T.; Latorre Rodríguez, O.; Riquelme Pérez, M.; Cirujano Pita, F.J., 1989:
Familial outbreak of Mycoplasma pneumoniae pneumonia

de Lalla, F.; Ezzell, J.W.; Pellizzer, G.; Parenti, E.; Vaglia, A.; Marranconi, F.; Tramarin, A., 1992:
Familial outbreak of agricultural anthrax in an area of northern Italy

Bañó Aracil, M.; González Morán, F.; Bertomeu Blanch, F.; Bellido Blasco, J.; Sánchez Linares, E.; Arnedo Pena, A.; Sieso Ibáñez, E.; Gil Alcamí, J.; Rico Verdú, J.C., 1992:
Familial outbreak of pneumonia by psittacosis

Cabañes Argudo, M.; Sánchez García, S.; Franco Serrano, J., 1991:
Familial outbreak of pulmonary tuberculosis

Makimoto, N.; Kajimoto, K.; Inoki, A.; Irie, S.; Naniwa, J.; Fujita, T.; Ueno, K.; Shiraishi, T.; Tada, S.; Kimura, I., 1991:
Familial outbreak with hypersensitivity pneumonitis

Freitas, R.B.; Gabbay, Y.B.; Pereira, J.D.; Linhares, A.C.; Lins, Z.C.; Fayal Neto, S., 1987:
Familial outbreaks of acute gastroenteritis associated with rotavirus in Belém, Pará

Schildkraut, J.M.; Thompson, W.D., 1988:
Familial ovarian cancer: a population-based case-control study

Skinner, J.L.; Oats, J.J.; Symonds, E.M., 1977:
Familial ovarian carcinoma

O'Mahony, D.; Whelton, M.J., 1989:
Familial pancreatic adenocarcinoma and HLA-typing

Ehrenthal, D.; Haeger, L.; Griffin, T.; Compton, C., 1987:
Familial pancreatic adenocarcinoma in three generations. A case report and a review of the literature

Lynch, H.T.; Lanspa, S.J.; Fitzgibbons, R.J.; Smyrk, T.; Fitzsimmons, M.L.; McClellan, J., 1989:
Familial pancreatic cancer (Part 1): Genetic pathology review

Lynch, H.T.; Fitzsimmons, M.L.; McClellan, J.; Lanspa, S.J.; Fitzgibbons, R.J.; Smyrk, T., 1990:
Familial pancreatic cancer (Part II): Surveillance, diagnostic tests, and surgical strategies

Robinson, A.E.; Kurtz, R.C., 1990:
Familial pancreatic cancer: insight into etiology or an interesting quirk of nature?

Swicowa, K.; Czauderna, A.; Langer, H.; Dziewicka, A., 1978:
Familial pancreatitis

Vulić, I.; Lukinović, N., 1977:
Familial pancytopenia of the Fanconi type

Schmid, M.; Hofmann, R.; Köhler, J.; Jannek, U., 1985:
Familial paracentric inversion inv(2)(q31q36)

Lin, C.C.; Bowen, P.; Hoo, J.J., 1987:
Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities

Carriero, A.; Rossner, G.; Nuzzo, A.; Basilico, L.; Bonomo, L., 1990:
Familial paragangliomas of the neck: integrated imaging and the planning of family screening

Lima, J.A.; Barbosa, J.; Lopes, A.S.; Lopes, J.S.; Ginefra, P.; Benchimol, A.B., 1976:
Familial paramyloidotic cardiomyopathy. Hemodynamic and cineangiocardiographic study

Lechevalier, B.; Schupp, C.; Fallet-Bianco, C.; Viader, F.; Eustache, F.; Chapon, F.; Morin, P., 1992:
Familial parkinsonian syndrome with athymhormia and hypoventilation

Roy, E.P.; Riggs, J.E.; Martin, J.D.; Ringel, R.A.; Gutmann, L., 1988:
Familial parkinsonism, apathy, weight loss, and central hypoventilation: successful long-term management

Ramo Tello, C.; González, J.L.; Hernández Gallego, J.; Calandre, L.; Bermejo, F., 1986:
Familial paroxysmal ataxia

Trillet, M.; Gouttard, M.; Schott, B., 1985:
Familial paroxysmal ataxia sensitive to acetazolamide. 3 cases in a new European family

Reitter, B.; Weisser, J., 1978:
Familial paroxysmal choreoathetosis. Clinical course, L-dopa-effect

Klinz, C.; Biesold, K.H., 1990:
Familial paroxysmal dystonic choreoathetosis

Lance, J.W., 1977:
Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes

Lance, J.W., 1977:
Familial paroxysmal dystonic choreoathetosis of Mount and Reback and its differentiation from related syndromes

Kurlan, R.; Behr, J.; Medved, L.; Shoulson, I., 1987:
Familial paroxysmal dystonic choreoathetosis: a family study

Szollár, J.; King, A.M.; Creasy, M.R.; Schwartz, F.; Insley, J.; Hulten, M., 1987:
Familial partial 17p duplication

Chen, H.; Tyrkus, M.; Cohen, F.; Woolley, P.V.; Mayeda, K.; Bhogaonker, A.; Espirtu, C.E.; Simpson, W., 1976:
Familial partial trisomy 6q syndromes resulting from inherited ins (5;6) (q33;q15q27)

Moreno-Fuenmayor, H.; Zackai, E.H.; Mellman, W.J.; Aronson, M., 1975:
Familial partial trisomy of the long arm of chromosome 10 (q24-26)

Chandrasekhar, K.P.; Dharmarajan, T.S., 1975:
Familial patent ductus arteriosus

Lee, C.C.; Wu, Y.C.; Lin, F.C., 1991:
Familial patent ductus arteriosus. Report of a family

Kumasaka, K.; Clarren, S.K., 1988:
Familial patterns of central nervous system dysfunction, growth deficiency, facial clefts and congenital megacolon: a specific disorder?

Foch, T.T.; DeFries, J.C.; McClearn, G.E.; Singer, S.M., 1977:
Familial patterns of impairment in reading disability

Cloutier, M.C.; Fajans, S.S., 1979:
Familial patterns of inheritance of diabetes mellitus. Maturity-onset type diabetes of young people (MODY)

Spitz, M.R.; Currier, R.D.; Fueger, J.J.; Babaian, R.J.; Newell, G.R., 1991:
Familial patterns of prostate cancer: a case-control analysis

Katzenelson, V.; David, M.; Zamir, R.; Mellibovsky, J.; Idises, C.; Sandbank, M., 1990:
Familial pemphigus vulgaris

Laskaris, G.; Sklavounou, A.; Stavrou, A.; Stavropoulou, K., 1989:
Familial pemphigus vulgaris with oral manifestations affecting two Greek families

Lazarovitch, I.; Koren, E.; Spirer, Z.; Solowiejczyk, M., 1976:
Familial peptic ulcer in childhood

Lindberg, L.; Pelto, K.; Borgström, G.H., 1992:
Familial pericentric inversion (3)(p12q24)

Ohnishi, Y.; Shigeto, M.; Ishibashi, T.; Hirata, J., 1990:
Familial pericentric inversion of chromosome 11 in a child with sporadic unilateral retinoblastoma

Spedicato, F.; D'Amore, A.; Gaudio, R., 1988:
Familial pericentric inversion of chromosome 13 associated with repeated early spontaneous abortions

Sutherland, G.R.; Gardiner, A.J.; Carter, R.F., 1976:
Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers

García Sagredo, J.M.; Morán Cabré, A.; San Román Cos-Gayón, C., 1975:
Familial pericentric inversion of y chromosome and Down's syndrome

Bjellerup, M.; Wallengren, J., 1990:
Familial perifolliculitis capitis abscedens et suffodiens in two brothers successfully treated with isotretinoin

Grotemeyer, K.H.; Jörg, J., 1979:
Familial periodic (hypokalaemic) paralysis: an unusual case report

Meana, C.R., 1975:
Familial periodic adynamia

Gamstorp, I., 1975:
Familial periodic paralysis

Kobayashi, A.L., 1975:
Familial periodic paralysis a report and review

Shah, N.; Kussman, M.J.; Tulgan, H., 1979:
Familial periodic paralysis and hyperthyroidism

Kashiwase, H.; Takagi, S.; Nakano, Y., 1977:
Familial periodic paralysis with hyper- and hypokalemic paralysis

Gérard, J.M.; Khoubesserian, P.; Telerman-Toppet, N.; De Barsy, T.; Coërs, C., 1978:
Familial periodic paralysis with hypokaliemia, hyperaldosteronism and extracellular vacuolization

Anmarkrud, N., 1976:
Familial periodic paralysis. Description of a family. Aspects of pathogenesis and treatment of the disease

Viana, J.P.; Coimbra, J.; Goulart, Z.; de Almeida, L.B.; Beirão, J.C., 1991:
Familial peripheral neuropathy caused by susceptibility to entrapment (tomaculous neuropathy)

Lin, A.E.; Milley, J.R.; Jaffe, R.; Medina, J., 1985:
Familial persistent pulmonary hypertension

Mendelow, A.D.; Kay, S.; Levin, E.; Mieny, C.J., 1978:
Familial phaeochromocytoma with von Hippel's disease in one sister and ectopic adrenal cortex in the kidney in another

Goncalves, E.; Ninane, J.; Wese, F.X.; Leonet, J.; Piret, L.; Cornu, G.; De Meyer, R., 1990:
Familial phaeochromocytoma: successful treatment with 131I-MIBG

Mennear, J.H., 1977:
Familial pharmacology

Gautier, J.F.; Schlumberger, M.; Fonseca, E.; Adotti, F.; Bosq, J.; Comoy, E.; Billebaud, T.; Parmentier, C., 1990:
Familial pheochromocytoma and Van Hippel-Lindau disease

Maurea, S.; Maurelli, L.; Lastoria, S.; Cuocolo, A.; Brunetti, A.; Pace, L.; Caracò, C.; Klain, M.; Lupoli, G.; Salvatore, M., 1992:
Familial pheochromocytoma in Sipple's syndrome. A comparison between scintigraphy with 131I-meta-iodobenzylguanidine, computed tomography and echography

Nakagawa, S.; Kojima, M.; Nakao, M.; Ohnishi, K.; Watanabe, H., 1987:
Familial pheochromocytoma in a daughter (extra-adrenal) and her mother

Atuk, N.O.; McDonald, T.; Wood, T.; Carpenter, J.T.; Walzak, M.P.; Donaldson, M.; Gillenwater, J.Y., 1979:
Familial pheochromocytoma, hypercalcemia, and von Hippel-Lindau disease. A ten year study of a large family

Spring, D.B.; Palubinskas, A.J., 1977:
Familial pheochromocytoma: a rare case of hydronephrosis and hydroureter in two generations

Kaufman, J.J.; Franklin, S., 1979:
Familial pheochromocytoma: a report of 2 cases in a kindred

Mori, Y.; Kiyohara, H.; Miki, T.; Horiuchi, N.; Kotake, T., 1977:
Familial pheochromocytoma: four cases in one kindred

Yu, T.L., 1992 :
Familial pheocromocytoma. Report of 4 families

Lesnick, J.E.; Chayt, K.J.; Bruce, D.A.; Rorke, L.B.; Trojanowski, J.; Savino, P.J.; Schatz, N.J., 1985:
Familial pineoblastoma. Report of two cases

Yuasa, H.; Tokito, S.; Nakagaki, H.; Kitamura, K., 1990:
Familial pituitary adenoma--report of four cases from two unrelated families

Samanta, B.C.; Panja, R.K., 1976:
Familial plantar keratoderma--a new entity

Kanoh, T.; Nakagawa, J.; Kajita, Y., 1986:
Familial plasma cell dyscrasia in mother and daughter

Gibson, G.J., 1977:
Familial pneumothoraces and bullae

Milosavljević, J.; Joksović, D., 1989:
Familial poisoning by carbon monoxide with different ECG changes

Hart, Z.H.; Chang, C.H.; Perrin, E.V.; Neerunjun, J.S.; Ayyar, R., 1977:
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia

Robinson, R.P.; Franck, W.A.; Carey, E.J.; Goldberg, E.B., 1978:
Familial polyarticular osteochondritis dissecans masquerading as juvenile rheumatoid arthritis

Adamson, J.W., 1975:
Familial polycythemia

Klingler, K.W.; Lengfelder, E.; Kohne, E.; Arnold, H., 1988:
Familial polyglobulism--a rare differential diagnosis of polycythemia vera

Kieny, J.R.; Stoll, C.; Roul, G.; Hessel, F.; Bareiss, P.; Sacrez, A., 1992:
Familial polymorph ventricular extrasystole associated with Pierre Robin syndrome

Badalian, L.O.; Temin, P.A.; Arkhipov, B.A.; Zavadenko, N.N.; Bulaeva, N.V., 1989:
Familial polymorphism of spinal amyotrophy in childhood

Juhlin, L.; Malmros-Enander, I., 1986:
Familial polymorphous light eruption with aquagenic urticaria: successful treatment with PUVA

Feistner, H.; Weissenborn, K.; Heinze, H.J.; Patzold, U., 1986:
Familial polyneuropathy with a disposition to pressure paralyses. A contribution to the differential diagnosis of mononeuropathies

Reitzik, M.; Lownie, J.F., 1975:
Familial polyostotic fibrous dysplasia

Bussey, H.J., 1979:
Familial polyposis coli

Nannery, W.M.; Barone, J.G.; Abouchedid, C., 1990:
Familial polyposis coli & Gardner's syndrome

Bussey, H.J., 1990:
Familial polyposis coli and hepatocellular neoplasms

Qizilbash, A.H., 1976:
Familial polyposis coli and periampullary carcinoma

Hooks, V.H.; Winters, P.M.; Ehleben, C.M., 1988:
Familial polyposis coli and the role of the polyposis registry

Jagannath, P.; Patil, P.; Dhir, V.; Desai, D.C.; Mohandas, K.M.; Swaroop, V.S.; Krishnamurthy, S.C.; DeSouza, L.J., 1991:
Familial polyposis coli with villous adenoma of ampulla of Vater

Anonymous, 1976:
Familial polyposis coli--pathomorphological studies

Lynch, H.T.; Boman, B.M.; Fitzgibbons, R.J., 1988:
Familial polyposis coli: genetics, surveillance, and treatment

Rider, S.H.; Mazzullo, H.A.; Davis, M.B.; Delhanty, J.D., 1986:
Familial polyposis coli: growth characteristics of karyotypically variable cultured fibroblasts, response to epidermal growth factor and the tumour promoter 12-0-tetradecanoyl phorbol-13-acetate

Geng, J.H., 1986:
Familial polyposis of colon (a study of 31 cases in 8 families)

Szklanny, J.; Załoga, K.; Kun, M.; Modzelewski, B., 1977:
Familial polyposis of the colon

Rubay, J.; Douniau, R.; Bouvy, P.; Parmentier, J., 1976:
Familial polyposis of the colon, associated with extracolic lesions and with a degenerated polyposis of the stomach

Sempé, J.; Bravo, J.L.; Eguiza, V.S.; Esesarte, G.; Lisker, R., 1977:
Familial polyposis of the colon. Analysis of 17 cases

Perry, R.E.; Christensen, M.A.; Thorson, A.G.; Williams, T., 1989:
Familial polyposis: colon cancer in the absence of rectal polyps

Crosignani, P.; Audisio, R.; Sant, M.; Gatta, G., 1989:
Familial polyposis: epidemiology

Arcuri, V.; Ceppa, P.; Lapertosa, G., 1979:
Familial polyposis: genetic and anatomo-pathological study of 2 families

Sensi, A.; Cerruti, S.; Calzolari, E.; Vesce, F., 1990:
Familial porencephaly

Lambert, D.G.; Beer, F.; Dalac, S.; Hourdain, M.J., 1988:
Familial porphyria cutanea tarda in a 7-year-old girl

D'Alessandro Gandolfo, L.; Griso, D.; Macri, A.; Biolcati, G.; Topi, G.C., 1989:
Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?

Best, L.G., 1991:
Familial posterior helical ear pits and Wiedemann-Beckwith syndrome

Ireland, A.J., 1991:
Familial posterior open bite: a primary failure of eruption

Rangasami, J.J.; Grant, D.B., 1992:
Familial precocious puberty in girls

Varlotta, G.P.; Brown, M.D.; Kelsey, J.L.; Golden, A.L., 1991:
Familial predisposition for herniation of a lumbar disc in patients who are less than twenty-one years old

Todd, N.W., 1987:
Familial predisposition for otitis media in Apache Indians at Canyon Day, Arizona

Schwartz, C.E.; Haber, D.A.; Stanton, V.P.; Strong, L.C.; Skolnick, M.H.; Housman, D.E., 1991:
Familial predisposition to Wilms tumor does not segregate with the WT1 gene

Murata, M.; Takayama, K.; Nagashima, Y.; Shimamura, K.; Fukuma, S., 1987:
Familial predisposition to cancer: a cohort study of participants in a cervical cancer screening program

Postacchini, F.; Lami, R.; Pugliese, O., 1988:
Familial predisposition to discogenic low-back pain. An epidemiologic and immunogenetic study

Shvedova, L.A., 1978:
Familial predisposition to endometrial cancer

Pettitt, D.J.; Saad, M.F.; Bennett, P.H.; Nelson, R.G.; Knowler, W.C., 1990:
Familial predisposition to renal disease in two generations of Pima Indians with type 2 (non-insulin-dependent) diabetes mellitus

Buletsa, B.A., 1990:
Familial predisposition to stroke in hypertension

Kienast, W.; Wagner, G.; Klaube, A.; Syska, J.; Wessel, H., 1976:
Familial preductal aortic coarctation. Report on a sibling observation

Ashcraft, K.W.; Holder, T.M.; Harris, D.J., 1975:
Familial presacral teratomas

Kosaka, K.; Arai, H.; Ikeda, K., 1985:
Familial presenile dementia with CJD-like lesions: preliminary results

Grove, W.M.; Lebow, B.S.; Clementz, B.A.; Cerri, A.; Medus, C.; Iacono, W.G., 1991:
Familial prevalence and coaggregation of schizotypy indicators: a multitrait family study

Tsuji, H.; Murai, K.; Akagi, K.; Fujishima, M., 1992:
Familial primary biliary cirrhosis associated with impaired concanavalin A-induced lymphocyte transformation in relatives. Two family studies

Rutishauser, M.; Feldges, A., 1977:
Familial primary chronic type ventilation

Vasily, D.B.; Bhatia, S.G.; Uhlin, S.R., 1978:
Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies

Ostinelli, J.; Valeyre, D.; Turbie, P.; Clerici, C.; Battesti, J.P., 1986:
Familial primary diffuse interstitial pulmonary fibrosis with bullous emphysema

Moulin, G.; Cognat, T.; Delaye, J.; Ferrier, E.; Wagschal, D., 1988:
Familial primary disseminated amyloidosis (a new clinical form?)

Colliot, S.; Heim, M.; Vincentelli, J.M.; Jaquet, P.; Simonin, R., 1990:
Familial primary empty sella turcica. Apropos of a family with 3 cases

Brady, J., 1990:
Familial primary failure of eruption of permanent teeth

Quietzsch, J.; Baumgarten, C., 1992:
Familial primary generalized epilepsy and drug (anticonvulsant)-induced systemic lupus erythematosus--a family study

Oon, C.J.; Yo, S.L.; Chua, D.; Chio, L.F.; Tan, L.; Chang, C.H.; Chan, S.H., 1978:
Familial primary hepatocellular carcinoma

Ikeda, M.; Ishikura, A.; Kogure, Y., 1989:
Familial primary intracranial malignant lymphoma

Vazhenin, A.V.; Bekhtereva, E.I.; Rask, R.E.; Kotliarov, E.V., 1986 :
Familial primary multiple cancer of the respiratory organs

Poissonnier, M.; Gruyer, P.; Noël, L.; Brière, J.; Tulliez, M.; Castaigne, S., 1988:
Familial primary myeloproliferative syndrome. Three cases in the same family

Wettstein, A.; Colombo, J.P., 1986:
Familial primary ornithine carbamoyltransferase defect

Fried, K.; Yuval, E.; Eidelman, A.; Beer, S., 1975:
Familial primary vesicoureteral reflux

Cusano, F.; Scarano, G., 1991:
Familial progeria or mandibulo-acral dysplasia?

Dobkin, B.H.; Verity, M.A., 1976:
Familial progressive bulbar and spinal muscular atrophy. Juvenile onset and late morbidity with ragged-red fibers

Kurihara, T.; Araki, S.; Okamoto, S.; Shirabe, T., 1977:
Familial progressive bulbar-spinal muscular atrophy: case report with muscle biopsy study

Qu, H., 1985:
Familial progressive diaphyseal dysplasia (Engelmann's disease)

Schenck, E.; Kruschke, U., 1975:
Familial progressive dystonia with diurnal fluctuation. Case report. Remarkable therapeutic effect of 1-dopa

Ling, D.B.; Lo, T., 1991:
Familial progressive hyperpigmentation: a family study in China

Lovisetto, P.; Ferraris, R.; Marchi, L.; Mairano, D.; Colombo, M.L.; Magnetti, L., 1979 :
Familial progressive intrahepatic cholestasis. Byler's disease

Guazzi, G.C.; Federico, A., 1985:
Familial progressive myoclonus epilepsies

Verhagen, W.I.; Huygen, P.L., 1991:
Familial progressive vestibulocochlear dysfunction

Densen, P.; Weiler, J.M.; Griffiss, J.M.; Hoffmann, L.G., 1987:
Familial properdin deficiency and fatal meningococcemia. Correction of the bactericidal defect by vaccination

Brottier, L.; Vergnes, C.; Bonnet, J.; Boisseau, M.; Bricaud, H., 1987:
Familial protein C deficiency and venous thrombosis

Hole, T.; Gjøen, O.I.; Stenvaag, J.P., 1991:
Familial protein C-deficiency--a clinical presentation

D'Angelo, A.; Mari, G.; Della Valle, P.; Marassi, A.; D'Angelo, S.V., 1990:
Familial protein S deficiency presenting as deep vein thrombosis occurring during pregnancy

Brenes, L.G.; Brenes, J.N.; Hernandez, M.M., 1977:
Familial proximal renal tubular acidosis. A distinct clinical entity

James, D.R.; Stansbie, D., 1987:
Familial pseudohyperkalaemia: inhibition of erythrocyte K+ efflux at 4 degrees C by quinine

Roy, C., 1977:
Familial pseudohypoaldosteronism (apropos of 5 cases)

Dinno, N.D.; Shearer, L.; Weisskopf, B., 1979:
Familial pseudomarfanism, a new syndrome?

Neil, J.F.; Glew, R.H.; Peters, S.P., 1979:
Familial psychosis and diverse neurologic abnormalities in adult-onset Gaucher's disease

Youssef, H.; Lyster, G.; Youssef, F., 1989:
Familial psychosis and vulnerability to tardive dyskinesia

Davies, B.H.; Tuddenham, E.G., 1976:
Familial pulmonary fibrosis associated with oculocutaneous albinism and platelet function defect. A new syndrome

Boccon-Gibod, L.; Just, J.; Grimfeld, A.; Tournier, G., 1989:
Familial pulmonary hemorrhage and lupus syndrome with C4 deficiency

Boylan, P.; Howe, A.; Gearty, J.; O'Brien, N.G., 1977:
Familial pulmonary hypoplasia

Klinge, T.; Laursen, H.B., 1975:
Familial pulmonary stenosis with underdeveloped or normal right ventricle

Manetti, A.; Favilli, S.; Mandorla, S.; De Simone, L.; Dolara, A., 1990:
Familial pulmonary stenosis: considerations on genetic aspects

Voordes, C.G.; Kuipers, J.R.; Elema, J.D., 1977:
Familial pulmonary veno-occlusive disease: a case report

Balgir, R.S., 1986:
Familial pure depressive disorder versus sporadic depressive disorder: a dermatoglyphic study

Szalay, G.C., 1979:
Familial pyloric atresia

Spritz, R.A., 1978:
Familial radioulnar synostosis