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Biology, Geography & Health: Chapter 43112


Chapter 43112 provides bibliographic information on scholary research in the basic and applied life, earth and health sciences.





Cendrowski, W.S., 1966:
Familial multiple sclerosis in Poland. 1. Geographical distribution of the disease

Escalar, G.; Majeron, M.A., 1969:
Familial multiple sclerosis. Case report

Viparelli, U.; D.L.renzo, R.; Crispi, G.; Abbate, G., 1965:
Familial multiple sclerosis. Clinico-cytogenetic contribution. Considerations on the endogeno-constitutional factor

Kitamoto, T.; Neshige, R.; Kuroda, Y.; Noda, K.; Shibasaki, H., 1984:
Familial multiple sclerosis: report of two cases with immunogenetic studies

Mishalany, H.G.; Der Kaloustian, V.M., 1971:
Familial multiple-level intestinal atresias: report of two siblings

Baillet, J.; Gentit, F.; Quiret, J.C.; Lienart, J.; Descombes, P., 1970:
Familial mushroom poisoning. 3 cases


Warrier, C.B.; Pillai, T.D., 1967:
Familial myasthenia gravis

Yoshida, T.; Takino, Y.; Yarita, H.; Asato, H.; Ishibashi, H., 1982:
Familial myasthenia gravis occurring in a mother and her daughter

Rao, B.S.; Sateesh, S.; Baburaj, S.; Mohan Das, P.; Sarkar, N.K.; Arjun Das, G., 1985:
Familial myasthenia gravis--a case report

Sieff, C.A.; Malleson, P., 1980:
Familial myelofibrosis

Kolarz, G.; Pietschmann, H., 1972:
Familial myeloid leukaemias

Boga, M.; Jákó, J.; Domán, J.; Magyar, E.; Konyár, E., 1973:
Familial myeloma

Maldonado, J.E.; Kyle, R.A., 1974:
Familial myeloma. Report of eight families and a study of serum proteins in their relatives

Slee, P.H.; van Everdingen, J.J.; Geraedts, J.P.; te Velde, J.; den Ottolander, G.J., 1981:
Familial myeloproliferative disease. Hematological and cytogenetic studies

Tatti, V.; Marfurt, P.; Sirchia, G.; Pescia, G.; Luscieti, P.; Losa, G., 1984:
Familial myeloproliferative syndrome

Kelemen, J.; Rice, D.R.; Bradley, W.G.; Munsat, T.L.; DiMauro, S.; Hogan, E.L., 1982:
Familial myoadenylate deaminase deficiency and exertional myalgia

Nasser, W.K.; Williams, J.F.; Mishkin, M.E.; Childress, R.H.; Helmen, C.; Merritt, A.D.; Genovese, P.D., 1967:
Familial myocardial disease with and without obstruction to left ventricular outflow. Clinical, hemodynamic, and angiographic findings

Cristodorescu, R.; Ardeleanu, R.; Drăgulescu, I.; Coreanu, G., 1971:
Familial myocardial disease. On 2 clinical cases

Barriales Ardura, R., 1967:
Familial myocardial diseases

Zamora, C.; Eizaguirre, A.J.; Ruipérez, J.A.; Avecillas, E., 1970:
Familial myocardial diseases. Study of 14 members of a family

Takatsu, T.; Kitaura, Y.; Kurimoto, K.; Hori, K., 1974:
Familial myocardial diseases: clinical features and postpericardiotomy

Nieveen, J.; Huber, J., 1970:
Familial myocardial fibrosis

Noya Del Rio, A.; D.O.a, J.C., 1972:
Familial myocardiopathy with Wolff-Parkinson-White syndrome

Lucier, K.J.; Movilla, R.V.; Parvizian, M.K.; Siddiqui, R.; Gabriele, E.H.; Bourque, M.; MacIsaac, J.; Moorehead, P.C.; Chan, A.K.; Heddle, N.M.; Lane, S.J., 2018:
A brief survey of clinicians' perceptions of parent preferences for involvement in obstetrical and perinatal management decisions in haemophilia

Hall, J.G.; Preziosi, T.J., 1971:
Familial myoclonic epilepsy

Stuart, W.H.; Schwartz, J.F.; Mayer, W.B.; Karp, H.E., 1968:
Familial myoclonus

May, D.L.; White, H.H., 1968:
Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease

Christensen, T.E.; Saxtrup, O.; Hansen, T.I.; Kristensen, B.H.; Beck, B.L.; Plesner, T.; Krogh, I.M.; Andersen, V.; Strandgaard, S., 1983:
Familial myoglobinuria. A study of muscle and kidney pathophysiology in three brothers

Genge, A.; Karpati, G.; Arnold, D.; Shoubridge, E.A.; Carpenter, S., 1995:
Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease

Cancilla, P.A.; Kalyanaraman, K.; Verity, M.A.; Munsat, T.; Pearson, C.M., 1971:
Familial myopathy with probable lysis of myofibrils in type I fibers

Saunders, M.; Ashworth, B.; Emery, A.E.; Benedikz, J.E., 1968:
Familial myotonic periodic paralysis with muscle wasting

Sher, J.H.; Rimalovski, A.B.; Athanassiades, T.J.; Aronson, S.M., 1967:
Familial myotubular myopathy: a clinical, pathological, histochemical, and ultrastructural study

Monk, B.E.; Vollum, D.I., 1982:
Familial naevus sebaceus

Herrera Pombo, J.L.; Lozano, I.; Ruíz-Valdepeñas, P.; Arrieta, F.; Rodríguez-Miñon, J.L., 1973:
Familial nanism with high levels of immunoreactive STH

Igarashi, S.; Koyama, T.; Shimosaka, S.; Uchibori, M., 1982:
Familial narrow spinal canal (lumbar canal stenosis with narrow cervical canal): case reports of three brothers

Fischer, A.; Fischer, G.O.; Cooper, E., 1984:
Familial nasopharyngeal carcinoma

Reisberg, B.; deLeon, M.J.; Ferris, S.H., 1984:
Familial nature of Alzheimer's disease?

Dimitrov, T., 1983:
Familial nature of Balkan endemic nephropathy

Cazzato, G.; Zorzon, M., 1983:
Familial nature of acute cerebral vasculopathies of the ischemic type

Nora, J.J.; Meyer, T.C., 1966:
Familial nature of congenital heart diseases

Scarlato, G.; Pellegrini, G.; Moggio, M.; Meola, G.; Cordone, G.; Minetti, C.; Lester, A., 1982:
Familial nemaline myopathy

Vaudour, G.; Leballe, J.C.; Beauvais, P.; Costil, J.; Brissaud, H.E., 1974:
Familial neo-natal thrombopenic purpura with cerebro-meningeal hemorrhage by feto-maternal allo-immunization

Zonana, J.; Silvey, K.; Strimling, B., 1984:
Familial neonatal and infantile seizures: an autosomal-dominant disorder

Suton, R.A., 1968:
Familial neonatal hypoproteinaemia

Matsuura, N.; Yamada, Y.; Nohara, Y.; Konishi, J.; Kasagi, K.; Endo, K.; Kojima, H.; Wataya, K., 1980:
Familial neonatal transient hypothyroidism due to maternal TSH-binding inhibitor immunoglobulins

Caroti Ghelli, C.; Presciuttini, S.; Scarcello, E.; Vannucci, L.; Mosca, F., 1994:
Familial neoplasms: investigation of genealogic trees of patients surgically treated for colonic adenocarcinoma

D.V.gno, G.; Nacci, G.; Cormio, G.; Loverro, G., 1994:
Familial neoplastic syndromes of the ovary. A family study

Kusunoki, N.; Tamaki, S., 1966:
Familial nephritis

Oknińska, A.; Szotowa, W.; Szczypiorski, K.; Wróblewska, E., 1970:
Familial nephro-uropathies

Dyszy-Laube, B.; Glyda, J.; Sekowska-Zmuda, J.; Wojnarowski, M., 1971:
Familial nephronophthisis (medullary cystic disease)

Mayer, U.; Michalk, D., 1982:
Familial nephronophthisis. The Senior-Loken syndrome

Afanasenko, P.P., 1971:
Familial nephropathies

Ignatova, M.S.; Briskina, M.M.; Fokeeva, V.V.; Artemkina, L.N., 1970:
Familial nephropathies in children

Acecka, H.; Dowbor, B., 1972:
Familial nephropathy

Dubach, U.C.; Minder, F.C.; Antener, I., 1966:
Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland

Gekle, D.; Essler, H.; Brunner, H., 1969:
Familial nephropathy and impaired sound perception (Alport syndrome)

Kobierska-Szczepańska, A.; Jończyk, K.; Dziuba, P., 1974:
Familial nephropathy in the light of cases at the Department of Pediatrics at Zabrze

Pohorecka-Zagroba, L.; Twardowski, Z., 1974:
Familial nephropathy in the light of observed cases

Leumann, E.P.; Wegmann, W., 1983:
Familial nephropathy with hyperuricemia and gout

Hanicki, Z.; Hanicka, M.; Miezyński, W., 1970:
Familial nephropathy with neurogenic hypoacusia (Alport's syndrome)

Chandra, M.; Mouradian, J.; Hoyer, J.R.; Lewy, J.E., 1981:
Familial nephrotic syndrome and focal segmental glomerulosclerosis

Burke, E.C.; Holley, K.E.; Stickler, G.B., 1973:
Familial nephrotic syndrome with nephrocalcinosis and tubular dysfunction

Trefz, F.K.; Schmidt, H.; Hammersen, G.; Helmstädter, V.; Bolkenius, M., 1980:
Familial nesidioblastosis

Vance, J.E.; Stoll, R.W.; Kitabchi, A.E.; Buchanan, K.D.; Hollander, D.; Williams, R.H., 1972:
Familial nesidioblastosis as the predominant manifestation of multiple endocrine adenomatosis

Konigsmark, B.W.; Hollander, M.B.; Berlin, C.I., 1968:
Familial neural hearing loss and atopic dermatitis

Geiger, L.R.; Mancall, E.L.; Penn, A.S.; Tucker, S.H., 1974:
Familial neuralgic amyotrophy. Report of three families with review of the literature

Nakamura, Y., 1982:
Familial neuroaxonal dystrophy with principal lesions of nigro-pallido-subthalamic degeneration

Feingold, M.; Gheradi, G.J.; Simons, C., 1971:
Familial neuroblastoma and trisomy 13

Klein, H.; Plöchl, E., 1974:
Familial neuroblastoma of the suprarenal glands in the newborn

Griffin, M.E.; Bolande, R.P., 1969:
Familial neuroblastoma with regression and maturation to ganglioneurofibroma

Chatten, J.; Voorhess, M.L., 1967:
Familial neuroblastoma. Report of a kindred with multiple disorders, including neuroblastomas in four siblings

Hardy, P.C.; Nesbit, M.E., 1972:
Familial neuroblastoma: report of a kindred with a high incidence of infantile tumors

Willshaw, M.E.; Pérez, M.; Lacassie, Y., 1982:
Familial neurocutaneous melanosis

Iampol'skaia, G.I., 1972:
Familial neurofibromatosis with unusual clinical manifestations

Vital, C.; Julien, J.; Vallat, J.M.; L.B.anc, M., 1970:
Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study

Bank, W.J.; Morrow, G., 1971:
Familial neuromuscular disease with nonketotic hyperglycinemia

Meyers, K.R.; Golomb, H.M.; Hansen, J.L.; McKusick, V.A., 1974:
Familial neuromuscular disease with "myotubes"

D.P.azza, P.; Rasi, F.; Neri, W.; Govoni, E.; Martinelli, P., 1982:
Familial neuropathy with a tendency toward compression paralysis: problems in differential diagnosis from occupational neuropathies

Jedrzejowska, H.; Hausmanowa-Petrusewicz, I., 1981:
Familial neuropathy with liability to pressure palsies. Report of a case

Serrate, A., 1966:
Familial neuroses

Feroli, E.J., 1967:
Familial neutropenia. Report of six cases in one family

Chadfield, H.W., 1969:
Familial non-allergic angioneurotic oedema

van Baars, F.; van den Broek, P.; Cremers, C.; Veldman, J., 1981:
Familial non-chromaffinic paragangliomas (glomus tumors) : clinical aspects

Hooft, C.; D.H.uwere, R.; Van Acker, K.J., 1968:
Familial non-congenital microcephaly, peculiar appearance, mental and motor retardation, progressive evolution to spasticity and choreo-athetosis

Martoni, L.; Paolucci, G., 1968:
Familial non-hemolytic hyperbilirubinemia

Lucey, J.F., 1969:
Familial non-hemolytic jaundice: light therapy

Fielding, J.F., 1969:
Familial non-polypotic carcinoma of colon

Bethlem, J.; van Gool, J.; Hülsmann, W.C.; Meijer, A.E., 1966:
Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres

Austen, K.F., 1965:
Familial nonallergic angioneurotic edema (C'1 esterase inhibitor deficiency)

Blumenschein, S.D.; Kallen, R.J.; Storey, B.; Natzschka, J.C.; Odell, G.B.; Childs, B., 1968:
Familial nonhemolytic jaundice with late onset of neurological damage

Gardner, W.A.; Konigsmark, B.W., 1969:
Familial nonhemolytic jaundice: bilirubinosis and encephalopathy

Perona, G.; Frezza, M.; Leonardi, P.; D.S.ndre, G., 1967:
Familial nonhemolytic jaundice: clinical and morpho-functional observations on 20 patients

Gupta, K.; Chintu, C., 1982:
Familial nonhemolytic unconjugated hyperbilirubinemia (Crigler Najjar syndrome) with kernicterus - report of a case in Zambian child

Ito, T.; Suzuki, H.; Yamada, M.; Metoki, K.; Iinuma, K.; Ito, H., 1982:
Familial nonprogressive chorea: report of four cases in a family

Drets, M.E.; Cardoso, J.H.; Delfino, A.H.; Carrau, J., 1970:
Familial normal-partial trisomy 16 with selective endoreduplication in malformed proband

Bicanová, J.; Kelbich, J.; Scheihauer, E., 1981:
Familial normolipidemic dyslipoproteinemia

Laskarzewski, P.M.; Khoury, P.; Morrison, J.A.; Kelly, K.; Mellies, M.J.; Glueck, C.J., 1983:
Familial obesity and leanness

D'Emma, C.; Crippa, L.; Delozier, C.; Michail, E.; Graber, P., 1982:
Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation

Michel, M., 1970:
Familial obstructive myocardiopathy

Wośko, I.; Warda, E.; Borzecka, I.; Pietroń, K., 1968:
Familial occurence of Engelmann's disease

Oliva, H.; Rapado, A.; APADO.A.; D.L.B.rreda, P.; Casado Pérez, S.; Plaza Pérez, J.J.; Sabando Suárez, P.; THOL.L.MP.N.DES/PATHOL.S.LEEN/PATHOL.S.AIN, 1974:
Familial occurence of Hodgkin's disease

Wale, R.J.; Williams, J.A.; Beeley, A.H.; Hughes, E.S., 1983:
Familial occurrence in carcinoid tumours

Nowak, J.; Lastowska, M.; Jankowska, A., 1984:
Familial occurrence of Albers-Schoenberg disease

Miyazaki, T.; Shiomi, K.; Hachiya, T.; Yoshimura, M.; Ochi, Y., 1973:
Familial occurrence of Basedow's disease

Strik, W.O.; Strik, W., 1972:
Familial occurrence of Crohn's regional enteritis in binovular twins and 2 other siblings

Pecoldowa, K.; Warchalewska-Pykalowa, U., 1970:
Familial occurrence of Ekman-Lebstein-van der Hoeve syndrome

Pernhaupt, G.; Tschabitscher, H.; Wessely, P., 1974:
Familial occurrence of Fahr's syndrome

Riku, S.; Kumagai, T.; Sobue, I., 1983:
Familial occurrence of Fukuyama type congenital muscular dystrophy and limb-girdle syndrome

Friedman-Birnbaum, R.; Abraham, Z., 1983:
Familial occurrence of Kaposi's sarcoma. Report of two brothers

Berlin, S.O.; Odeberg, H.; Weingart, L., 1968:
Familial occurrence of M-components

Posselt, H.G.; Kohls, C.; Ball, F.; Bender, S.W., 1985:
Familial occurrence of Peutz-Jeghers syndrome and Crohn disease with manifestation of both diseases in the same patient

Czarnowski, J.; Gasiorek, J., 1984:
Familial occurrence of Quincke's edema

Netto, C.F.; Castro, R.M.; Gonçalves, A.P.; Dillon, N.L., 1965:
Familial occurrence of South American blastomycosis. Apropos of 14 cases

Fischer, P.R.; Shigeoka, A.O., 1983:
Familial occurrence of Stevens-Johnson syndrome

Schneider, R.G., 1969:
Familial occurrence of Wolff-Parkinson-White syndrome

Zoethout, H.E.; Ubbink, G.J., 1966:
Familial occurrence of a deficiency of immune globulins

Becker, W., 1983:
Familial occurrence of a glioblastoma multiforme. Computed tomographic and angiographic demonstration

Yoshida, M.C.; Honda, T., 1969:
Familial occurrence of a short arm deletion of a G-group chromosome

Passarge, E., 1983:
Familial occurrence of a short rib syndrome with hydrops fetalis but without polydactyly

Teja, K.; Cooper, P.H., 1981:
Familial occurrence of accessory tragus

von Studnitz, W.; Ljungberg, O., 1970:
Familial occurrence of adrenaline-producing pheochromocytoma associated with medullar thyroid carcinoma

Tobo, M.; Mitsuyama, Y.; Ikari, K.; Itoi, K., 1984:
Familial occurrence of adult-type neuronal ceroid lipofuscinosis

Breit, S.M.; Clark, P.; Robinson, J.P.; Luckhurst, E.; Dawkins, R.L.; Penny, R., 1983:
Familial occurrence of alpha 1-antitrypsin deficiency and Weber-Christian disease

Berlińska, A., 1982:
Familial occurrence of amyotrophic lateral sclerosis with a peculiar clinical picture

Goldschmidt, H.; Glöbl, H., 1972:
Familial occurrence of anorectal abnormalities associated with vertebral abnormalities

Fukamizu, H.; Matsumoto, K.; Inoue, K.; Moriguchi, T., 1982:
Familial occurrence of aplasia cutis congenita

Cihula, J.; Vortel, V.; Steiner, I.; Zizka, J.; Hametová, M., 1969:
Familial occurrence of aplasia of intrahepatic bile ducts with partial giant cell transformation of liver parenchyma in 2 siblings

Lockey, R.F.; Rucknagel, D.L.; Vanselow, N.A., 1973:
Familial occurrence of asthma, nasal polyps and aspirin intolerance

Navrátil, M.; Hanák, S., 1970:
Familial occurrence of benign jaundice in a 14-year-old boy

Gollop, T.R.; Lucchesi, E.; Martins, R.M.; Nione, A.S., 1980:
Familial occurrence of bifid femur and monodactylous ectrodactyly

Sakkonen, J.; Sääf, J., 1973:
Familial occurrence of breast cancer

Nakanishi, M., 1972:
Familial occurrence of bronchiectasis

Sroczyńska, F.; Dudkowski, L., 1970:
Familial occurrence of calcinosis of the pulmonary alveoli

Kesztele, V., 1974:
Familial occurrence of cancer

Maire, P.; Morichau-Beauchant, M.; Drucker, J.; Barboteau, M.A.; Barbier, J.; Matuchansky, C., 1984:
Familial occurrence of cancer of the colon and the rectum: results of a 3-year case-control survey

Burkland, C.E.; Juzek, R.H., 1966:
Familial occurrence of carcinoma of the ureter

Yamashita, J.; Handa, H.; Kim, C.; Kim, S., 1982:
Familial occurrence of cerebellar hemangioblastomas--analysis of five families

Marckwort, H.J.; Stapper, G., 1972:
Familial occurrence of cerebral palsy and changes in the eye with coloboma of the choroid

Prochorow, M.; Gidlecki, Z., 1972:
Familial occurrence of childhood diabetes

Kiszely, K., 1982:
Familial occurrence of childhood epilepsy and related clinical data

Perry, E.L.; Overholt, E.L.; Newcomer, K.L., 1969:
Familial occurrence of chondrocalcinosis (pseudogout syndrome)

Ming, P.M.; Parker, R.; Goodner, D.M., 1980:
Familial occurrence of chromosome 7/12 translocation

Philip, J., 1970:
Familial occurrence of chromosome abnormalities

Nekula, J.; Meduna, J.; Bruner, V., 1972:
Familial occurrence of cleidocranial dysostosis

Delaney, J.F., 1982:
Familial occurrence of coexistent periodic paralysis and spinal muscular atrophy: case reports

Schieche, M., 1970:
Familial occurrence of congenital angiocardiopathies

Gencík, A.; Moser, H.; Gencíkova, A.; Kehrer, B., 1982:
Familial occurrence of congenital diaphragmatic defect in three families

Ide, C.H.; Holt, R.; Holt, J.E., 1974:
Familial occurrence of congenital diffuse hemangiomatosis

Matsuki, H.; Iuchi, K.; Nishimura, M.; Chikamori, J.; Minami, S., 1970 :
Familial occurrence of congenital heart diseases

Rybak, K.; Zwierzchowska, D.; Zwierzchowski, H., 1984:
Familial occurrence of congenital hip dislocation

Jankowicz, E.; Banach, S.; Pikiel, L., 1971:
Familial occurrence of congenital intracranial aneurysf associated with cystic degeneration of the kidneys

Phelan, P.D.; Stocks, J.G.; Williams, H.E.; Danks, D.M., 1973:
Familial occurrence of congenital laryngeal clefts

Gacs, G.; Schuler, D.; Sellyei, M., 1970:
Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr)

Scott-Emuakpor, A.B.; Warren, S.T.; Kapur, S.; Quiachon, E.B.; Higgins, J.V., 1981:
Familial occurrence of congenital pulmonary lymphangiectasis. Genetic implications

Birõ, I.; Brittig, F.; Gottwald, G., 1971:
Familial occurrence of cryoglobulinemia

Pfitzer, P.; Splitt, M.; Müntefering, H.; Friesenecker, J.E., 1982:
Familial occurrence of cyclops over several generations

Chmielewski, J.; Stasikiewicz-Chmielewska, 1968:
Familial occurrence of cystic kidney

Bandura, A., 1971:
Familial occurrence of defective development of permanent teeth

Bruszt, P., 1971:
Familial occurrence of denticle

Nitscheff, W.; Stereff, S., 1966:
Familial occurrence of diffuse endoalveolar pulmolithiasis. Description of 3 cases in 1 family

Driessen, A.P.; Scherpenisse, L.A., 1970:
Familial occurrence of diffuse interstitial pulmonary fibrosis complicated by alveolar cell carcinoma

Danbara, T.; Matsuoka, R.; Nukiwa, T.; Natori, H.; Arai, T.; Kira, S., 1982:
Familial occurrence of diffuse panbronchiolitis accompanied with elevation of cold agglutinin titer in a father and his two daughters

Rosenkranz, W.; Holzer, S.; Scholz, H., 1971:
Familial occurrence of double satellites in group D chromosomes

Johnsonbaugh, R.E.; Drexler, H.G.; Light, I.J.; Sutherland, J.M., 1974:
Familial occurrence of drug-induced hearing loss

Vizkelety, T.; Szijj, E., 1964:
Familial occurrence of dysostosis enchondralis

Urbanová, O., 1973:
Familial occurrence of dysphonia

Lee, M.H.; Liebman, J.; Steinberg, A.G.; Perrin, E.V.; Whitman, V., 1973:
Familial occurrence of endocardial fibroelastosis in three siblings, including identical twins

Schwarz, E.; Meze, G., 1969:
Familial occurrence of endocardial fibrosis in 3 siblings

Beck, E., 1968:
Familial occurrence of epiphysiolysis capitis femoris

Arakawa, T.; Tamura, T.; Ohara, K.; Narisawa, K.; Tanno, K., 1968:
Familial occurrence of formiminotransferase deficiency of syndrome

van der Linden, W.; Simonson, N., 1973:
Familial occurrence of gallstone disease. Incidence in parents of young patients

Bergstrom, J.F.; Long, J.M., 1974:
Familial occurrence of ganglioneuromas

Veselinović, A.; Hofer, Z., 1973:
Familial occurrence of glaucoma

van Baars, F.M.; Cremers, C.W.; van den Broek, P.; Veldman, J.E., 1981:
Familial occurrence of glomus tumors; clinical and genetic aspects

Gasparová, D.; Szedélyová, L., 1980:
Familial occurrence of grouped pigmentation of the ocular fundus

Moeschler, J.; Clarren, S.K., 1982:
Familial occurrence of hemifacial microsomia with radial limb defects

Splino, M.; Peychl, L.; Kotrlík, J.; Kyntera, F., 1969:
Familial occurrence of human pseudotuberculosis caused by Pasteurella pseudotuberculosis

Hara, M.; Sato, Y.; Sato, T.; Izumi, M., 1970:
Familial occurrence of hyperthyroidism

Portenoy, R.K.; Berger, A.; Gross, E., 1984:
Familial occurrence of idiopathic normal-pressure hydrocephalus

Ottensooser, F.; de Araujo, J.T.; Rosales, T., 1970:
Familial occurrence of increased activity of blood-group A in serum

Pelikán, L.; Doubravský, J.; Mikes, K.; Cerný, M., 1967:
Familial occurrence of infantile cortical hyperostosis. (Caffey-de Toni-Silvermann syndrome)

Masár, I.; Puceková, G.; Stukovský, R., 1968:
Familial occurrence of infectious hepatitis under conditions of gamma globulin prophylaxis

Sakai, N.; Miwa, M.; Takada, M.; Yamada, H.; Sakata, K., 1974:
Familial occurrence of intracranial aneurysm. Report of 3 sibling cases and review of literature

Erickson, R.P.; Woolliscroft, J.; Allen, R.J., 1980:
Familial occurrence of intracranial arterial occlusive disease (Moyamoya) in neurofibromatosis

Grunert, V.; Horcajada, J.; Sunder-Plassmann, M., 1970:
Familial occurrence of intracranial meningiomas

Breebaart-de Miranda, J.G.; Velzeboer, C.M.; Delleman, J.W., 1970:
Familial occurrence of iris atrophy and cataract

van Loghem, E., 1974:
Familial occurrence of isolated IgA deficiency associated with antibodies to IgA. Evidence against a structural gene defect

Richards, B.W.; Sylvester, P.E.; Hodgson, S.J., 1965:
Familial occurrence of juvenile amaurotic family idiocy and phenylketonuria in the same subjects

Vogel, R.I.; Deasy, M.J., 1980:
Familial occurrence of juvenile periodontitis

Hoffman, I.D., 1983:
Familial occurrence of juvenile periodontitis with varied treatment of one of the siblings with five-year follow-up. Case report

Hellgren, L., 1983:
Familial occurrence of lichen ruber planus

Dziuba, P.; Jończyk, K.; Dziekanowska, D.; Bulsiewicz, H., 1972:
Familial occurrence of long arm deletion in chromosome 18 (46,18q-)

Boczkowski, K.; Wawryk, R.; Krupa, B.; Mickiewicz, E., 1972:
Familial occurrence of male pseudohermaphrodites with ambiguous external genitals

Vilcek, E., 1973:
Familial occurrence of malignant testicular tumors

Pamphlett, R.; Mackenzie, R.A., 1981:
Familial occurrence of meningioma: a case report

Sahar, A., 1965:
Familial occurrence of meningiomas. Case report

Neuhäuser, G., 1973:
Familial occurrence of meningomyeloceles

Miettinen, T.A.; Penttilä, I.M.; Lampainen, E., 1972:
Familial occurrence of mild hyperlipoproteinaemias

Nagae, K.; Goto, I.; Ueda, K.; Morotomi, Y., 1972:
Familial occurrence of multiple intracranial aneurysms. Case report

Ambrosetto, P.; Galassi, E., 1981:
Familial occurrence of multiple intracranial aneurysms. Case reports and review of the literature

Finke, J.; Schott, R., 1968:
Familial occurrence of multiple sclerosis

Johnson, E.R.; Gardner, D.M., 1981:
Familial occurrence of nonmedullary thyroid carcinoma. Experience at the University of Missouri Health Sciences Center

Svobodová, L.; Svoboda, J., 1973:
Familial occurrence of osteochondropathy of the child hip joint

Doktorczyk, H.; Knapikowa, D.; Mielecki, T.; Woźniak, J., 1970:
Familial occurrence of osteopoikilosis

Sarosi, G.; Doe, R.P., 1968:
Familial occurrence of parathyroid adenomas, pheochromocytoma, and medullary carcinoma of the thyroid with amyloid stroma (Sipple's syndrome)

Gencik, A.; Gencikova, A.; Pálova, A., 1982:
Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation

Niznikowska-Marks, M.J.; Wróblewska-Cieliszak, K., 1970:
Familial occurrence of patent ductus arteriosus

Rosner, J.; Peisert, E., 1974:
Familial occurrence of pemphigus vulgaris chronicus

Koziol, H.; Wlodarz, A., 1974:
Familial occurrence of peptic ulcer

Brook, C.G.; Wagner, H.; Zachmann, M.; Prader, A.; Armendares, S.; Frenk, S.; Alemán, P.; Najjar, S.S.; Slim, M.S.; Genton, N.; Bozic, C., 1973:
Familial occurrence of persistent Mullerian structures in otherwise normal males

Feltynowski, T.; Wieteska, A.; Januszewicz, A.; Wocial, B.; Szostek, M.; Januszewicz, W., 1995:
Familial occurrence of pheochromocytoma

Zák, M.; Mirejovský, P., 1969:
Familial occurrence of pneumocystis pneumonia due to congenital immunological deficiency

Schminda, R., 1973:
Familial occurrence of pneumoencephalographic changes in the course of chronic alcoholism

Chmielewski, J.; Jackowski, T.; Stasikiewicz-Chmielewska, 1966:
Familial occurrence of polycystic kidneys in association with other developmental abnormalities. (Report of a family)

Gram, B.R., 1983:
Familial occurrence of porphyria cutaneous tarda. The biochemical background and own clinical studies

Jaup, B.H.; Zettergren, L.S., 1980:
Familial occurrence of primary biliary cirrhosis associated with hypergammaglobulinemia in descendants: a family study

Sander, J., 1966:
Familial occurrence of primary pulmonary fibrosis

Ventruto, V.; Catani, L.; Celona, A.; Fioretti, G.; Stabile, M.; Gallo, G., 1980:
Familial occurrence of protrusio acetabuli (Otto's disease). Ten members affected in four generations

Szymczak, G.; Zawilska, K., 1970 :
Familial occurrence of pseudohypoparathyroidism

Florczak-Mikicińska, E.; Winnicki, S., 1982:
Familial occurrence of pseudohypoparathyroidism and pseudopseudohypoparathyroidism

Moll, J.M.; Wright, V., 1973:
Familial occurrence of psoriatic arthritis

Lisch, K., 1969:
Familial occurrence of relapsing facial paralysis with paralysis of the oculomotor muscles

Ellis, D.; Fisher, S.E.; Smith, W.I.; Jaffe, R., 1982:
Familial occurrence of renal and intestinal disease associated with tissue autoantibodies

de Die-Smulders, C.; Schrander-Stumpel, C.; Fryns, J.P., 1993:
Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay: a 4p deletion?

Azimi, F.; Bryan, P.J., 1974:
Familial occurrence of renal pseudotumour due to enlarged Column of Bertin in two brothers and their first cousin

Gumowska, M.; Czarnecka, D.; Czekalski, S.; Kosowicz, J., 1968:
Familial occurrence of renal tubular acidosis

Bartkowska-Orlowska, M.; Przybyl-Ereńska, K., 1970:
Familial occurrence of retinal detachment

Pasykowa, K., 1971:
Familial occurrence of ringed hair (thrix annulati)

Wiman, L.G., 1972:
Familial occurrence of sarcoidosis

Grönhagen-Riska, C.; Fyhrquist, F.; Hortling, L.; Koskimies, S., 1983:
Familial occurrence of sarcoidosis and Crohn's disease

Augustín, J.; Losonský, S.; Korcok, F., 1983:
Familial occurrence of sarcoma

Szczepanski, A.; Jakubowicz, K., 1972:
Familial occurrence of scleroderma

Stephenson, C.; Franken, E.A.; Ha-Upala, S.; Christian, J.C., 1971:
Familial occurrence of single ventricle

Fornatto, L.; Portaleone, P.; Schiffer, D., 1972:
Familial occurrence of solitary angioblastoma of the cerebellum and its relationship with von Hippel-Lindau disease

Witzel, L., 1967:
Familial occurrence of stomach carcinoma

Michałowicz, R.; Ignatowicz, R.; Kostrzewska, M., 1983:
Familial occurrence of subacute sclerosing panencephalitis (SSPE) in children

Biehl, G., 1971:
Familial occurrence of subperiostal bone fibroma

Novák, J., 1973:
Familial occurrence of supernumerary teeth

Weinhold, P.; Wegner, J.T.; Kane, J.M., 1981:
Familial occurrence of tardive dyskinesia

Gulley, R.M.; Kowalski, R.; Neuhoff, C.F., 1974:
Familial occurrence of testicular neoplasms: a case report

Bárta, M., 1970:
Familial occurrence of the Albers-Schönberg disease

Gross-Kieselstein, E.; Abrahamov, A.; Ben-Hur, N., 1971:
Familial occurrence of the Freeman-Sheldon syndrome: cranio-carpotarsal dysplasia

Homola, D.; Srnová, V., 1968:
Familial occurrence of the Wolff-Parkinson-White (WPW) syndrome

Rapant, V.; Dvorácek, C.; Turek, K.; Valach, V., 1965:
Familial occurrence of the Zollin ger-Ellison syndrome associated with diabetes

Yunis, J.J.; Ramsay, N.K., 1980:
Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1

Fixler, D.E.; Cole, R.B.; Paul, M.H.; Lev, M.; Girod, D.A., 1970:
Familial occurrence of the contracted form of endocardial fibroelastosis

Hogewind, B.L.; de la Rivière, G.B.; van Es, L.A.; Veltkamp, J.J., 1980:
Familial occurrence of the haemolytic uraemic syndrome

Walker, N., 1972:
Familial occurrence of the high scapula syndrome

Jørgensen, H.R.; Kristensen, B.; Mortensen, P.B., 1984:
Familial occurrence of the reduced activity of the pancreas correlated with amylase isoenzyme in the serum

McFadzean, A.J.; Yeung, R., 1969:
Familial occurrence of thyrotoxic periodic paralysis

Ziobrowski, S., 1985:
Familial occurrence of toxoplasmosis

Uchida, I.A.; Ray, M.; McRae, K.N.; Besant, D.F., 1968:
Familial occurrence of trisomy 22

Ambani, L.M.; Vaidya, R.A.; Rao, C.S.; Daftary, S.D.; Motashaw, N.D., 1980:
Familial occurrence of trophoblastic disease - report of recurrent molar pregnancies in sisters in three families

Horvat, Z.; Radosević, Z.; Ahmetović, S., 1970:
Familial occurrence of visceral erythematosus

Pelikán, L.; Hanák, S., 1970:
Familial occurrence of vitamin D resistant rickets (mother and 2 sons)

Ichihashi, T.; Harano, H.; Mizuno, J.; Kasahara, R.; Hoshino, D.; Nakagawa, H., 1995:
Familial occurrence of von Hippel-Lindau disease--a case report

Corder, M.P.; Culp, N.W.; Barrett, O., 1973:
Familial occurrence of von Willebrand's disease, thrombocytopenia, and severe gastrointestinal bleeding

Stokke, D.B.; Andresen, P., 1970:
Familial occurrence of "cryptothyroidism" with functioning ectopic thyroid tissue in solitary subhyoid localization

Krarup, N.B., 1969:
Familial occurrence of "palindromic rheumatism"

Lynch, H.T.; Krush, A.J.; Mulcahy, G.M.; Reed, W.B., 1974:
Familial occurrences of a variety of premalignant diseases and uncommon malignant neoplasms

Godel, V.; Iaina, A.; Goldman, B., 1980:
Familial ocular anomalies in juvenile nephronophthisis

Alberca, R.; Coca, M.C.; Gil Peralta, A.; Gómez Bosque, P.; Navarro, A., 1971:
Familial ocular myopathy. (Immunoelectrophoretic and electron microscopy studies)

Tamura, K.; Santa, T.; Kuroiwa, Y., 1974:
Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria

Tamura, K.; Santa, T.; Kuroiwa, Y., 1974:
Familial oculocraniosomatic neuromuscular disease with ragged red fibers

Goren, H.; Steinberg, M.C.; Farboody, G.H., 1980:
Familial oculoleptomeningeal amyloidosis

Currie, S., 1970:
Familial oculomotor palsy with Bell's palsy

Vita, G.; Dattola, R.; Santoro, M.; Messina, C., 1983:
Familial oculopharyngeal muscular dystrophy with distal spread

Roosen, N.; D.L.P.rte, C.; Van Vyve, M.; Solheid, C.; Selosse, P., 1984:
Familial oligodendroglioma. Case report

Tong, K.Q., 1983:
Familial oligodontia with ectodermal dysplasia: a sex-linked recessive hereditary disease

Berciano, J.; Ricoy, J.R.; Rebollo, M.; Combarros, O.; Coria, F.; Val, F., 1983:
Familial olivopontocerebellar atrophy (Menzel type). Apropos of a family followed for 46 years

Steele, K.; Nevin, N.C., 1985:
Familial omphalocele

Iwashita, H.; Inoue, N.; Kuroiwa, Y., 1969:
Familial optic and acoustic nerve degeneration with distal amyotrophy

Cordier, J.; Reny, A.; Raspiller, A., 1970:
Familial optic atrophy and juvenile diabetes

Wolf, M., 1995:
Familial oral Streptococcus mutans infections--a contribution to oral prophylaxis by pediatric nurses

Miranda-Nieves, G., 1967:
Familial orthochromatic leukodystrophy associated with complex abiotrophies, some classifiable as neuroaxonal degeneration. Resumption of the study of the Huys family published by van Bogaert, Edgar and Karcher, 1961

Andrew, T.A.; Spivey, J.; Lindebaum, R.H., 1981:
Familial osteochondritis dissecans and dwarfism

Anderson, L.G.; Cook, A.J.; Coccaro, P.J.; Coro, C.J.; Bosma, J.F., 1972:
Familial osteodysplasia

Niijima, K.H.; Kondo, A.; Ishikawa, J.; Kim, C.; Itoh, H., 1984:
Familial osteodysplasia associated with trigeminal neuralgia: case report

Swaney, J.J., 1973:
Familial osteogenic sarcoma

Chu, X.Y., 1984:
Familial osteomalacia

Cortina, H.; Vallcanera, A.; Vidal, J., 1981:
Familial osteopathia striata with cranial condensation

King, R.E.; Lovejoy, J.F., 1973:
Familial osteopetrosis with coxa vara. A case report

Forgács, S., 1970:
Familial osteopoikilosis

Kaposi, N.P., 1983:
Familial osteopoikilosis

Serre, H.; Simon, L.; Barjon, M.C.; Sany, J.; Privat, J.M., 1968:
Familial osteopoikilosis (3 cases)

Stelmasiak, Z.; Rozynkowa, D., 1973:
Familial osteosclerosis associated with facial hemispasm in 3 generations

Fára, M.; Chlupácková, V.; Hrivnákova, J., 1967:
Familial oto-facio-cervical dysmorphia

Koga, K.; Suzuki, Y.; Sakai, M.; Mukai, M., 1974:
Familial otosclerosis with chromosomal aberration

Matheson, J.A.; Matheson, H.; Anderson, S.A., 1981:
Familial ovarian cancer. How rare is it?

Franceschi, S.; L.V.cchia, C.; Mangioni, C., 1982:
Familial ovarian cancer: eight more families

Vesely, D.L.; Bower, R.H.; Kohler, P.O.; Char, F., 1980:
Familial ovarian dysgenesis in 46,XX females

Fienberg, R., 1972:
Familial ovarian hyperthecosis

Takahashi, A.; Saito, K.; Kondo, Y.; Kurosawa, T., 1973:
Familial oxalosis. Report of three cases and review of the literature

Mathieu, H.; Gagnadoux, M.F.; Mongour, P.; Czernichow, P.; Volter, F.; Kaplan, M., 1968:
Familial oxalosis. Study of 2 cases. Attempted treatment

Harbison, J.B.; Nice, C.M., 1971:
Familial pachydermoperiostosis presenting as an acromegaly-like syndrome

Tramier, G., 1969:
Familial palmo-plantar keratoderma of the Thost-Unna type

Grajower, M.M., 1983:
Familial pancreatic cancer

Lumadue, J.A.; Griffin, C.A.; Osman, M.; Hruban, R.H., 1995:
Familial pancreatic cancer and the genetics of pancreatic cancer

Mann, T.P.; Rubin, J., 1969:
Familial pancreatic exocrine dysfunction with pancreatic calcification

Bergström, K.; Hellström, K.; Kallner, M.; Lundh, G., 1973:
Familial pancreatitis associated with hyperglycinuria

Mian, T.A.; Zuberi, S.J., 1980:
Familial pancreatitis with lithiasis

Choudhry, V.P.; Srivastava, R.N.; Ghai, O.P., 1971:
Familial pancreatitis. (A case report)

Phade, V.R.; Lawrence, W.R.; Max, M.H., 1981:
Familial papillary carcinoma of the thyroid

Djalali, M.; Steinbach, P.; Barbi, G., 1984:
Familial paracentric inversion inv(3)(q21q25.1). Case report and review of the literature

Romain, D.R.; Columbano-Green, L.M.; Whyte, S.; Smythe, R.H.; Parfitt, R.G.; Gebbie, O.B.; Chapman, C.J., 1983:
Familial paracentric inversion of 1p

Del Porto, G.; D'Alessandro, E.; D.M.tteis, C.; D'Innocenzo, R.; Baldi, M.; Pachi, A.; Cappa, F., 1984:
Familial paracentric inversion of chromosome 15 (q15q24)

Delwaide, P.J.; Penders, C.A., 1971:
Familial paramyotonia and paretic crises with hypokalemia

Grant, J.A.; Blumenschein, G.R.; Buckley, C.E., 1971:
Familial paraproteinemia

Delacrétaz, J.; Maillard, G.F.; Emch, M.; Glauser, M.P., 1970:
Familial paraproteinemia and lichen myxedematosus. I. Clinical study

Glauser, M.P.; Maillard, G.F.; Emch, M.; Delacrétaz, J., 1970:
Familial paraproteinemia and lichen myxedematosus. II. Immunological study

Coca Martin, M.C., 1971:
Familial parasitologic study

Anonymous, 1968:
Familial parocystic rhabdomyolysis in children

Aimard, G.; Vighetto, A.; Trillet, M.; Ventre, J.J.; Devic, M., 1983:
Familial paroxysmal ataxia responsive to acetazolamide

de la Flor Bru, J.; Artigas Pallares, J.; Argemi Fontanet, J.; Salas Guzmán, S., 1985:
Familial paroxysmal choreoathetosis treated with carbamazepine

Zukerman, E.; Vilanova, L.C.; Seráfico, J., 1983:
Familial paroxysmal choreoathetosis. Report of 2 cases in one family

Kurlan, R.; Shoulson, I., 1983:
Familial paroxysmal dystonic choreoathetosis and response to alternate-day oxazepam therapy

Walker, E.S., 1981:
Familial paroxysmal dystonic choreoathetosis: a neurologic disorder simulating psychiatric illness

Barolin, G.S., 1967:
Familial paroxysmal hemilateral decrease of function with and without headache attacks

Garello, L.; Ottonello, G.A.; Regesta, G.; Tanganelli, P., 1983:
Familial paroxysmal kinesigenic choreoathetosis. Report of a pharmacological trial in 2 cases

Anonymous, 1967:
Familial paroxysmal polyserositis

Khachadurian, A.K.; Armenian, H.K., 1974:
Familial paroxysmal polyserositis (familial Mediterranean fever); incidence of amyloidosis and mode of inheritance

Mancini, J.L., 1973:
Familial paroxysmal polyserositis, phenotype I (familial Mediterranean fever). A rare cause of pleurisy. Case report and review of the literature

Armenian, H.K.; Khachadurian, A.K., 1973:
Familial paroxysmal polyserositis. Clinical and laboratory findings in 120 cases

Mignon, F.; Méry, J.P.; Cuvelier, R.; Delons, S.; Meyrier, A.; Rottembourg, J., 1981:
Familial paroxysmal polyserositis: modern therapeutic possibilities

Favara, B.E.; Vawter, G.F.; Wagner, R.; Kevy, S.; Porter, E.G., 1967:
Familial paroxysmal rhabdomyolysis in children. A myoglobinuric syndrome

Sacks, H.S.; Matisonn, R.; Kennelly, B.M., 1974:
Familial paroxysmal ventricular tachycardia in two sisters

Culbertson, W.W.; Giles, C.L.; West, C.; Stafford, T., 1983:
Familial pars planitis

Travi, V.H.; Ferreti, E., 1966:
Familial partial anodontia

Arya, B.S.; Savara, B.S., 1974:
Familial partial anodontia: report of a case

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

D.M.elenaere, A.; Fryns, J.P.; Van den Berghe, H., 1981:
Familial partial distal 18q (18q22-18q23) trisomy

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

Krzentowski, G.; Vandalem, J.L., 1981:
Familial partial resistance to thyroid hormones. A report on one case

de Nayer, P.; Oei, L.S.; Broeckx, J.; de Visscher, M., 1971:
Familial partial thyroxine-binding globulin deficiency

Orye, E.; van Caster, A., 1972:
Familial partial trisomy 18

Duca, D.; Bene, M.; Ioan, D.; Maximilian, C., 1980:
Familial partial trisomy: 6q25 leads to 6qter

Fischer, F., 1969:
Familial pathology of diabetic retinopathy

Kapoor, K.N.; Tandon, O.P., 1967:
Familial pattern of coronary artery disease

Ashworth, J.T., 1981:
Familial pattern of hypoglossal duct cysts

Suri, V.P.; Singh, D.; Tandon, O.P., 1966:
Familial patterns in coronary artery disease

Dumas, C.A.; Katerndahl, D.A.; Burge, S.K., 1995:
Familial patterns in patients with infrequent panic attacks

McClanahan, B.J.; Palmer, R.F.; Hackett, P.L., 1968:
Familial patterns in the development of hematopoietic disorders in 90Sr-fed swine. BNWL-714

Benjamin, S.D.; Baer, P.N., 1967:
Familial patterns of advanced alveolar bone loss in adolescence (periodontosis)

Mills, P.K.; Newell, G.R.; Johnson, D.E., 1984:
Familial patterns of testicular cancer

Freundlich, E.; Statter, M.; Yatziv, S., 1981:
Familial pellagra-like skin rash with neurological manifestations

Cousin, J.; Walbaum, R.; Cegarra, P.; Huguet, J.; Louis, J.; Pauli, A.; Fournier, A.; Fontaine, G., 1982:
Familial pelvi-scapulary dysplasia with anomalies of the epiphyses, dwarfism and dysmorphy: a new syndrome?

Cisárik, F.; Gavalec, M.; Hrbánová, Z., 1980:
Familial penetrance of familial hyperlipoproteinemias

Kronenfeld, J.J.; Ory, M.G., 1981:
Familial perceptions of juvenile diabetes

Goldman, H.; Perkins, H.A., 1984:
Familial pericarditis, arthritis, and camptodactyly

Rodriguez, M.T.; Martin, M.J.; Abrisqueta, J.A., 1984:
Familial pericentric inversion (10) and its effect on two offspring

Maltby, E.L., 1984:
Familial pericentric inversion (13) detected by antenatal diagnosis

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

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

Habedank, M., 1982:
Familial pericentric inversion of chromosome 13 resulting in duplication 13q22 to qter

Mattevi, M.S.; Pinheiro, C.E.; Erdtmann, B.; Flores, R.Z.; Salzano, F.M., 1981:
Familial pericentric inversion of chromosome 2

Sujansky, E.; Smith, A.C.; Peakman, D.C.; McConnell, T.S.; Baca, P.; Robinson, A., 1981:
Familial pericentric inversion of chromosome 8

Moedjono, S.J.; Sparkes, R.S., 1980:
Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?

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

Baumann, W.; Zabel, B.; Holl, M., 1984:
Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]

Dorf, G., 1965:
Familial periodic disease

Sandyk, R., 1980:
Familial periodic hypokalaemic paralysis

Sonkodi, S.; Szörényi, A.; Julesz, J.; Fazekas, T., 1980:
Familial periodic paralysis (hypopotassaemic form)

Gyntelberg, F.; Kjaer, C., 1967:
Familial periodic paralysis treated with triamterene

Johnsen, T., 1981:
Familial periodic paralysis with hypokalaemia. Experimental and clinical investigations

Libner, G.; Wandner, V.; Kray, H., 1973:
Familial periodic paralysis--misinterpreted for years

Marchiori, P.; Scaff, M.; Levy, J.A.; Callegaro, D.; de Assis, J.L., 1980:
Familial periodic paralysis: study of 8 cases

Haut, J.; Limon, S.; Offret, H.; Morax, S., 1973:
Familial peripheral retinal degenerescence and retinal detachment

Müller, D.; Castrillón-Oberndorfer; Orywall, D.; Genth, E., 1972:
Familial pernicious anemia

Beheshti, M.; Churchill, B.M.; Hardy, B.E.; Bailey, J.D.; Weksberg, R.; Rogan, G.F., 1984:
Familial persistent müllerian duct syndrome

Seringe, P.; Perelman, S.R.; Plainfosse, B.; Nathanson, M.; Allaneau, C.; Bertin, P.; Joron, F.; Belaisch, G., 1972:
Familial pheochromocytoma

Yan, C.L., 1983:
Familial pheochromocytoma (with report of 4 cases)

Huang, S.; McLeish, W.A., 1968:
Familial pheochromocytoma and amyloid-producing medullary carcinoma of thyroid

Carney, J.A.; Go, V.L.; Gordon, H.; Northcutt, R.C.; Pearse, A.G.; Sheps, S.G., 1980:
Familial pheochromocytoma and islet cell tumor of the pancreas

Mulholland, S.G.; Atuk, N.O.; Walzak, M.P., 1969:
Familial pheochromocytoma associated with cerebellar hemangioblastoma. A case history and review of the literature

Unsgård, G.; Kufaas, T.; Blika, S., 1984:
Familial pheochromocytoma associated with non Hippel-Lindau disease. A family study

Paloyan, E.; Scanu, A.; Straus, F.H.; Pickleman, J.R.; Paloyan, D., 1970:
Familial pheochromocytoma, medullary thyroid carcinoma, and parathyroid adenomas

Sharp, W.V.; Platt, R.L., 1971:
Familial pheochromocytoma. Association with von Hippel-Lindau's disease

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

Ginocchio, G.; Garavelli, G.; Boari, L.; Tenca, P.; Casiglia, E.; Pessina, A.C., 1995:
Familial pheochromocytoma: a family studied for 3 generations

Adachi, M.; Miura, Y.; Adachi, M.; Kimura, S.; Tomioka, H.; Nezu, M.; Yoshinaga, K.; Saito, K., 1983 :
Familial pheochromocytoma: case report and a review of literature in Japan

Funyu, T.; Shiraiwa, Y.; Nigawara, K.; Kudo, S.; Mikuni, S., 1973:
Familial pheochromocytoma: case report and review of the literature

Tank, E.S.; Gelbard, M.K.; Blank, B., 1982:
Familial pheochromocytomas

Pouches, H.; Tralli, F.; Mouniq, C., 1983:
Familial phobic rituals, methods of defense against an imagined adolescence

Sáenz-Lope, E.; Herranz-Tanarro, F.J.; Masdeu, J.C.; Bufil, J., 1984:
Familial photosensitive epilepsy: effectiveness of clonazepam

Díaz de la Vega, V.; Bialostosky, D.; Lupi, E.; Castro, G.; Barrios, R.; Reyes, P.A., 1980:
Familial pigeon breeder's disease. Possible association to HLA-Bw40 antigen

Volovich, L.E., 1966:
Familial pigmented urticaria

Ferrándiz, C.; Peyrí, J.; Henkes, J.; Ferrando, J.; Fontaranáu, R., 1980:
Familial pili canaliculi

Moulin, G., 1970:
Familial pilitortosis

Ferrier, P.E.; Stone, E.F., 1969:
Familial pituitary dwarfism associated with an abnormal sella turcica

Peter, B.; Schueller, H.; Sengler, J.; Zemp, A.; Vedrenne, C.; Laedlein-Greissammer, D.; Thierry, R., 1980:
Familial pituitary dwarfism due to isolated growth hormone deficiency (3 cases)

Ayala Ruiz, A.R.; Delgado Ochoa, D.; Vergara, M.D.; Loyo, M.; Matute Labrador, A.; Rosas, L.; Hernández Marín, I.; Cervera Aguilar, R., 1995:
Familial pituitary tumor with somatotropic compromise

Gjone, E.; Torsvik, H.; Norum, K.R., 1968:
Familial plasma cholesterol ester deficiency. A study of the erythrocytes

Hovig, T.; Gjone, E., 1973:
Familial plasma lecithin: cholesterol acyltransferase (LCAT) deficiency. Ultrastructural aspects of a new syndrome with particular reference to lesions in the kidneys and the spleen

Hamnström, B.; Gjone, E.; Norum, K.R., 1969:
Familial plasma lecithin: cholesterol acyltransferase deficiency

Sakuma, M.; Akanuma, Y.; Kodama, T.; Yamada, N.; Murata, S.; Murase, T.; Itakura, H.; Kosaka, K., 1982:
Familial plasma lecithin: cholesterol acyltransferase deficiency. A new family with partial LCAT activity

Nordöy, A.; Gjone, E., 1971:
Familial plasma lecithin: cholesterol acyltransferase deficiency. A study of the platelets

Bourlier, V.; Monnet, P.; Gauthier, J., 1965:
Familial poisoning by mushrooms. Helveolian Syndrome

Bermúdez de Rocha, M.V.; Lozano Meléndez, F.E.; Salazar Leal, M.E.; Waksman de Torres, N.; Piñeyro López, A., 1995:
Familial poisoning with Karwinskia humboldtiana

Frey, H.M.; Vogt, J.H.; Nerup, J., 1973:
Familial poly-endocrinopathy

Popa, M., 1980:
Familial polyadenomatoses of the endocrine glands

Poulsen, P.; Nielsen, O.H., 1980:
Familial polycystic syndrome. An unexpected finding at operation

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

Rafaillat, D.; Oules, O.; Vernet, G.; Bedu, M.; Galacteros, F.; Bardakdjian, J., 1985:
Familial polycythemia caused by high oxygen affinity hemoglobin. 2nd world case of hemoglobin J Providence

Wermer, P., 1973:
Familial polyendocrine adenomatous hyperplasia syndrome

Moutaffian, J.J.; Gabriel, B.; Carcassonne, Y.; Olmer, J., 1967:
Familial polyglobulia: apropos of 2 cases

Colomb, D.; Beyvin, A.J.; Battesti, M.R., 1969:
Familial polymorphous erythemato-squamous trichophytosis due to Trichophyton rubrum

Inokuchi, T.; Umezaki, H.; Onishi, A., 1972:
Familial polyneuropathy associated with elevated protein in the cerebrospinal fluid

Rocca, E.; Costantino, L.; D.L.llis, C.; Romano, D.; Rubino, R., 1980:
Familial polyposis and cancer. Apropos of 4 cases

Metzger, P.P.; Klainer, A.S.; Gainer, B.; Cadduck, W.M., 1974:
Familial polyposis and pituitary chromophobe adenoma

Berk, T.; Cohen, Z.; Cullen, J.B., 1981:
Familial polyposis and the role of the preventive registry

Pickens, D.R.; Farringer, J.L., 1969:
Familial polyposis and the spontaneous regression of polyps

Schier, J., 1974:
Familial polyposis as an obligatory cancer precursor

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

Gardner, E.J., 1983:
Familial polyposis coli and Gardner syndrome--is there a difference?

Alm, T., 1984:
Familial polyposis coli and associated lesions

Dowton, S.B., 1980:
Familial polyposis coli associated with familial meningiomas

Lyko, H.C.; Hartmann, J.X., 1981:
Familial polyposis coli plasma causes a transformation-associated morphology of cells in vitro: hyperproteinemia and colorectal polyps

Cole, C.W.; Meban, S., 1983:
Familial polyposis coli: an unusual family

Gonzaga, R.A.; Amarante, M.; Lima, F.R., 1984:
Familial polyposis coli: the difficult choice

Siegel, B.; Dror, Y.; Siegal, A., 1983:
Familial polyposis in Israel

Leggett, P.L.; Arensman, R.M.; Falterman, K.W., 1984:
Familial polyposis in children: early detection and preferred treatment

Moretti, G.; Bozic, C.; Genton, N., 1969:
Familial polyposis of Peutz-Jeghers type with malignant degeneration

Hantschmann, N.; Nemsmann, B., 1974:
Familial polyposis of colon and rectum

Falk, V.S.; Rogers, J.C., 1968:
Familial polyposis of colon. A twenty-five year follow-up study

Otnes, B.; Helsingen, N., 1969:
Familial polyposis of the colon in Norway

McQuaide, J.R.; Stewart, A.W., 1972:
Familial polyposis of the colon in the Bantu

Hayashi, F.; Nagakawa, T., 1970:
Familial polyposis of the colon, a case report

Sachatello, C.R., 1971:
Familial polyposis of the colon. A four-decade follow-up

Sachatello, C.R., 1970:
Familial polyposis of the colon. I. Leukocytic chromosome determinations--report of a patient with familial polyposis of the colon and Klinefelter's syndrome

Williams, J.L.; Wightman, J.A., 1966:
Familial polyposis of the colon. Report of a family with a 5-year follow-up of colectomy and ileorectal anastomosis

Yonemoto, R.H.; Slayback, J.B.; Byron, R.L.; Rosen, R.B., 1969:
Familial polyposis of the entire gastrointestinal tract

Yamada, S.; Takahashi, T., 1971:
Familial polyposis of the large intestine

Sztaba, R., 1968:
Familial polyposis of the large intestine in an 11-year old boy

Vecerina, S.; Fitting, J.V.; Saegesser, F.; Pettavel, J., 1973:
Familial polyposis, diffuse polyposis and cancer

King, R.M.; van Heerden, J.A.; Kvols, L.K., 1984:
Familial polyposis. A case report

Hootnick, D.; Holmes, L.B., 1972:
Familial polysyndactyly and craniofacial anomalies

Curth, H.O., 1969:
Familial pompholyx

Smit, L.M.; Barth, P.G.; Valk, J.; Njiokiktjien, C., 1984:
Familial porencephalic white matter disease in two generations

Sei, J.F.; Jeanmougin, M., 1983:
Familial portuguese type amyloid polyneuropathy. Attempt at a pathogenetic interpretation

Faulk, W.P.; Epstein, C.J.; Jones, M.D., 1970:
Familial posterior lumbosacral vertebral fusion and eyelid ptosis

Herishanu, Y.; Feldman, S., 1971:
Familial postero-lateral myelopathy and angiomatosis retinae

Sim, M.; Bale, R.N., 1973:
Familial pre-senile dementia: the revelance of a histological diagnosis of Pick's disease

Brown, A.R.; Rose, B.S., 1966:
Familial precocious polyarticular osteoarthrosis of chondrodysplastic type

Hopwood, N.J.; Kelch, R.P.; Helder, L.J., 1981:
Familial precocious puberty in a brother and sister

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

Edwards, J.H., 1969:
Familial predisposition in man

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

Freedman, B.I.; Tuttle, A.B.; Spray, B.J., 1995:
Familial predisposition to nephropathy in African-Americans with non-insulin-dependent diabetes mellitus

Fialkow, P.J.; Thuline, H.C.; Hecht, F.; Bryant, J., 1971:
Familial predisposition to thyroid disease in Down's syndrome: controlled immunoclinical studies

Simović, N., 1972:
Familial predisposition to urolithiasis in infants

van Gemund, J.J.; Laurent de Angulo, M.S.; van Gelderen, H.H., 1970:
Familial prenatal dwarfism with elevated serum immuno-reactive growth hormone levels and end-organ unresponsiveness

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

Mayberry, J.F.; Rhodes, J.; Newcombe, R.G., 1980:
Familial prevalence of inflammatory bowel disease in relatives of patients with Crohn's disease

Yamazaki, A.; Yoshizawa, O.; Shimano, K.; Beppu, H.; Yoshida, M., 1969:
Familial primary amyloidosis

Okayama, M.; Goto, I.; Tanaka, T.; Omae, T., 1974:
Familial primary amyloidosis with vitreous opacities and cognition disorder

Guénol, J.; Legrand, J.; Dubigeon, P.; Bureau, L.; Horeau, J.; Maury, P., 1969:
Familial primary amylosis with predominant renal and ocular localization

Gola, A.; Milewicz, A.; Turkiewicz, R., 1974:
Familial primary cardiomyopathy

Eisen, M.; Busse, K.; Beyer, J.; Grabs, V.; Happ, J.; Schäfer, R., 1974:
Familial primary hyperparathyroidism

Shimura, H.; Mihara, A.; Hashizume, Y., 1972:
Familial primary hyperparathyroidism--parathyroid adenoma in sisters

Wald, S.L.; Liwnicz, B.H.; Truman, T.A.; Khodadad, G., 1982:
Familial primary nervous system neoplasms in three generations

Hamel, B.C., 1995:
Familial primary pulmonary hypoplasia

Villamor, J.; Hita, J.; Barreiro, P.; Ortiz Vázquez, J.; Vãzquez, J.J., 1971:
Familial primary vasopressin resistant diabetes insipidus sensitive to biguanide

Sakhuja, V.; Ghosh, A.K.; Jha, V.; Pahwa, N.; Chugh, K.S., 1994:
Familial primary vesico-ureteric reflux

Schmidberger, H.; Grubbauer, H.M.; Holzer, H., 1974:
Familial primary vitamin D resistant rickets (phosphate diabetes). Observations of two cases--with and without therapy

Klinowska, W.; Morawska, Z.; Krzemień, K., 1973:
Familial proaccelerine (FV) deficiency

Van Laere, J., 1966:
Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems

Lehnhardt, E., 1967:
Familial progressive deafness and subclinical iodine metabolism disorder

Iannaccone, S.T.; Griggs, R.C.; Markesbery, W.R.; Joynt, R.J., 1974:
Familial progressive external ophthalmoplegia and ragged-red fibers

Chernosky, M.E.; Anderson, D.E.; Chang, J.P.; Shaw, M.W.; Romsdahl, M.M., 1971:
Familial progressive hyperpigmentation

Goutieres, F.; Aicardi, J.; Farkas-Bargeton, E., 1974 :
Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing encephalopathy

Rallo, E., 1969:
Familial progressive myoclonic epilepsy (Unverricht-Lundborg syndrome in five Valaisian families). A contribution to the research of its metabolic origin through the study of urinary excretion of mucopolysaccharides

Herbst, A., 1967:
Familial progressive myoclonus epilepsy (Unverricht/Lundborg)

Herbstund, A.; Schröter, P., 1973:
Familial progressive myoclonus epilepsy (pme) (type Unverricht)

Castaigne, P.; Cambier, J.; Brunet, P.; Schuller, E.; Chemaly, R., 1967:
Familial progressive myoclonus epilepsy, of a dominant heredity: clinical and biological study of a family

Simone, F., 1971:
Familial progressive rigidity of uncertain nosographic classification

Paparella, M.M.; Sugiura, S.; Hoshino, T., 1969:
Familial progressive sensorineural deafness

Soppi, E.; Lehtonen, A.; Toivanen, A., 1982:
Familial progressive systemic sclerosis (scleroderma): immunological analysis of two patients and six siblings from a single kindred

Hartemann, E., 1968:
Familial protein intolerance

Kekomäki, M.; Toivakka, E.; Häkkinen, V.; Salaspuro, M., 1968:
Familial protein intolerance with deficient transport of basic amino acids. Report on an adult patient with chronic hyperammonemia

Jagenburg, R.; Lindstedt, G.; Malmquist, J., 1970:
Familial protein intolerance with hyperammonemia

Rüster, M.; Rogner, G.; Kühn, R., 1966:
Familial proteinuria and hypercholisterinemia

François, R.; Bertrand, J.; Pellet; Salle, B.; Moreau, P.; Manuel, P., 1967:
Familial proteinuria of the tubular type with appearance of the Bartter syndrome in 1 of the members of the family: a new disease?

Armstrong, R.M.; Fogelson, M.H.; Silberberg, D.H., 1965:
Familial proximal spinal muscular atrophy. Study of a large pedigree

Sakaguchi, M.; Ishikawa, K.; Mizuta, H.; Kitagawa, T., 1982:
Familial pseudogout with destructive arthropathy

Luciani, J.C.; Lavabre-Bertrand, T.; Fourcade, J.; Barjon, P.; Mimran, A.; Callis, A., 1980:
Familial pseudohyperkalaemia

Hughes, J.D.; Meriwether, T.W., 1971:
Familial pseudohypertrophy of tendo-achillis with multisystem disease

Hamilton, D.V., 1980:
Familial pseudohypoparathyroidism presenting in adult life

Singleton, E.M.; Kinsbourne, M.; Anderson, W.B., 1973:
Familial pseudopapilledema

Shapiro, I.; Shapiro, S.K., 1980:
Familial pseudotumor cerebri and the empty sella syndrome

Pontalti, C.; Arnetoli, C.; Rodriguez, R., 1982:
Familial psychological picture and psychotherapy of 2 adolescent brothers with osteopetrosis

Carnevale, A.; López Hernández, A.; De los Cobos, L., 1973:
Familial pterygium syndrome with probably dominant transmission linked to the X chromosome

Schey, W.L.; Levin, B., 1971:
Familial pubic bone maldevelopment

Neubauer, I., 1972:
Familial pulmonary emphysema with lowered concentration of alpha-1-antitrypsin in the serum

McDonnell, L.; Sweeney, E.C.; Jagoe, W.S.; FitzGerald, M.X., 1982:
Familial pulmonary fibrosis and lung cancer

Hirsch, M.S.; Hong, C.K., 1973:
Familial pulmonary histiocytosis-X

Slotnick, E.A., 1971:
Familial pure gonadal dysgenesis with clitoral hypertrophy and a normal female karyotype

Fossati, P.; Pruvot, P.; Caridroit, M.; Buvat, J.; Montois, R.; Linquette, M., 1972:
Familial pyridoxine deficiency in a diabetic patient and her children. Infantile myoclonic encephalopathy with hypsarrhythmia cured with vitamin B 6 in one of them

Garbarz, M.; Bernard, J.F.; Boivin, P., 1980:
Familial pyridoxine-responsive sideroblastic anaemia. One case

Bjelle, A., 1981:
Familial pyrophosphate arthropathy. Occurrence and Crystal Identification

Lubahn, J.D.; Lister, G.D., 1983:
Familial radial nerve entrapment syndrome: a case report and literature review

Nábrády, J.; Bagdány, S., 1973:
Familial reciprocal translocation

Dugan, R.E., 1972:
Familial rectal pain

Soullard, J.; Potet, F.; Zeitoun, P.; Delineau, G., 1967:
Familial recto-colic polyposis. Nosologic and clinical study

Djeml, N.; Mestiri, S.; Gargouri, M.; Cammoun, M.; Hamza, R.; Ghrab, A., 1984:
Familial rectocolonic polyposis

Delamarre, J.; Dupas, J.L.; Capron, J.P.; Armand, A.; Hervé, M.; Descombes, P., 1982:
Familial rectocolonic polyposis, Gardner's syndrome and thyroid cancer : study of 2 cases

Koiffmann, C.P.; Wajntal, A.; Ursich, M.J.; Pupo, A.A., 1984:
Familial recurrence of geleophysic dysplasia

Kaláb, Z.; Fajt, M.; Steinerová, H., 1965:
Familial recurrent amyotrophic neuralgia in children

Shindo, S., 1968:
Familial recurrent corneal erosion

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

Brunner, F.X.; Herrmann, I.F., 1982:
Familial recurrent laryngeal nerve paralysis, a genetically fixed syndrome -- additional remark on linkage of deficiency gene and HLA

Prejac, M.; Ajduković, G.; Plasaj, M., 1966:
Familial recurrent paroxysmal polyserositis

Cole, M., 1984:
Familial recurrent peripheral facial palsy

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

Roos, D.; Thygesen, P., 1972:
Familial recurrent polyneuropathy. A family and a survey

Matiar-Vahar, H.; Rohrer, H., 1970:
Familial recurrent polytopic neuropathy

Galand, J.M., 1970:
Familial recurrent venous thrombosis

Dockter, G.; Müller, J., 1980:
Familial recurring intrahepatic cholestasis of the Tygstrup-Summerskill-Walshe type

Eckert, P.; Meyer-Wahl, L., 1982:
Familial recurring polytopic neuropathy. A case report

Graff, G.; Chemke, J.; Lancet, M., 1972:
Familial recurring thanatophoric dwarfism. A case report

Irvine, A.R.; Daroff, R.B.; Sanders, M.D.; Hoyt, W.F., 1968:
Familial reflex blepharospasm

Kiruluta, G.H.; Afridi, S.K.; Winsor, G.M., 1983:
Familial reflux in monozygotic twins

McConaghy, N.; Clancy, M., 1968:
Familial relationships of allusive thinking in university students and their parents

Roos, D., 1972:
Familial remitting polyneuropathy associated with partial immunoparesis

Pathak, S.; Strong, L.C.; Ferrell, R.E.; Trindade, A., 1982:
Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cells

Yao, M.; Shuin, T., 1995:
Familial renal cell carcinoma: review of recent molecular genetics

Krous, H.F.; Wenzl, J.E., 1980:
Familial renal cystic dysplasia associated with maternal diabetes mellitus

Berthoux, F.; Badinand, N.; Pellet, H.; François, R., 1972:
Familial renal cystic dysplasia with deafness and renal insufficiency

Kazi, Z.; Czakó, L., 1980:
Familial renal diabetes

Walker, S.H.; Firminger, H.I., 1974:
Familial renal dysplasia with sodium wasting and hypokalemic alkalosis

Miranda, D.; Schinella, R.A.; Finegold, M.J., 1972:
Familial renal dysplasia. Microdissection studies in siblings with associated central nervous system and hepatic malformations

Cazacu, B.; Zălaru, M.; Onete, I.; Maravei, E.; Udrea, T., 1965:
Familial renal glycosuria associated with maltosuria

Buckalew, V.M., 1968:
Familial renal tubular acidosis

Pearson, H.H., 1969:
Familial renal tumours

Eggert, W.; Hilgenfeld, E.; Reimann, J., 1980:
Familial renal-retinal dysplasia - a combination of eye and kidney malformations

Senior, B., 1973:
Familial renal-retinal dystrophy

Corley, R.P.; DeFries, J.C.; Kuse, A.R.; Vandenberg, S.G., 1980:
Familial resemblance for the Identical Blocks Test of spatial ability: no evidence for X linkage

Matthews, K.A.; Rosenman, R.H.; Dembroski, T.M.; Harris, E.L.; MacDougall, J.M., 1984:
Familial resemblance in components of the type A behavior pattern: a reanalysis of the California type A twin study

Nĕmec, J.; Kopecký, A.; Vána, S.; Bednár, J., 1984:
Familial resistance to thyroid hormones

McGee, M.G., 1981:
Familial response to chronic illness: the impact of home versus hospital dialysis

Weissbach, G.; Franz, H., 1970:
Familial reticuloendotheliosis in early infancy

Freeman, R.G., 1972:
Familial reticuloendotheliosis with eosinophilia and follicular mucinosis

Omenn, G.S., 1971:
Familial reticuloendotheliosis with eosinophilia: a follow-up

Miller, D.R., 1966:
Familial reticuloendotheliosis: concurrence of disease in five siblings

Bartlett, W.J.; Price, J., 1983:
Familial retinal arteriolar tortuosity with retinal hemorrhage

Gornig, H., 1966:
Familial retinal detachment

Brown, G.C.; Tasman, W.S., 1980:
Familial retinal dialysis

Weichselbaum, R.R.; Little, J.B., 1980:
Familial retinoblastoma and ataxia telangiectasia: human models for the study of DNA damage and repair

Strong, L.C.; Riccardi, V.M.; Ferrell, R.E.; Sparkes, R.S., 1981:
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation

Knight, L.A.; Gardner, H.A.; Gallie, B.L., 1980:
Familial retinoblastoma: segregation of chromosome 13 in four families

Zajícek, M.; Gájová, B., 1966:
Familial rheumatic fever and glomerulonephritis

Uribarri, G.; Martínez Gastey, A.; Fernández Pizarro, J.P., 1965:
Familial rheumatic fever. (Preliminary note)

Pinchuk, A.L., 1971:
Familial rheumatism and some problems of disability in rheumatism

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

Rossen, R.D.; Brewer, E.J.; Sharp, R.M.; Ott, J.; Templeton, J.W., 1980:
Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis

Palitzsch, D.; Scheffzek, A., 1981:
Familial right bundle branch block and left axis deviation without cardiac disorders

Steenkamp, W.F.; Combrink, J.M.; Myburgh, D.P., 1980:
Familial right bundle-branch block

Schaal, S.F.; Seidensticker, J.; Goodman, R.; Wooley, C.F., 1973:
Familial right bundle-branch block, left axis deviation, complete heart block, and early death. A heritable disorder of cardiac conduction

Goldstein, A.M.; Blot, W.J.; Greenberg, R.S.; Schoenberg, J.B.; Austin, D.F.; Preston-Martin, S.; Winn, D.M.; Bernstein, L.; McLaughlin, J.K.; Fraumeni, J.F., 1994:
Familial risk in oral and pharyngeal cancer

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

Robert, J.; Pernod, J.; Bonnet, R., 1974:
Familial sacro-coccygeal agenesis. Apropos of 6 cases in 2 families

Prieur, A.M.; Menkes, C.J.; Bessis, J.L.; Haquet, D.; Griscelli, C., 1982:
Familial sarcoid arthritis

Salm, R., 1969:
Familial sarcoidosis terminating as neurosarcoidosis

Sharma, O.P.; Johnson, C.S.; Balchum, O.J., 1971:
Familial sarcoidosis. Report of four siblings with acute sarcoidosis

Huan, P.; Hachulla, E.; Delaporte, E.; Piette, F.; Hatron, P.Y.; Devulder, B., 1995:
Familial sarcoidosis: 3 cases in the same family

Hutzler, R.U.; Shikanai, M.A., 1974:
Familial sarcoidosis: occurence in 3 sisters

Mandi, N., 1969:
Familial scarlet fever

Walker, E.; Shaye, J., 1982:
Familial schizophrenia. A predictor of neuromotor and attentional abnormalities in schizophrenia

Rendall, J.R.; McKenzie, A.W., 1974:
Familial scleroderma

Chekotilo, A.M.; Smerenskaia, A.V., 1970:
Familial scleroma (according to data from Transcarpathia)

Blankenship, R.M.; Greenburg, B.R.; Lucas, R.N.; Reynolds, R.D.; Beutler, E., 1973:
Familial sea-blue histiocytes with acid phosphatemia. A syndrome resembling Gaucher disease: the Lewis variant

Zina, A.M.; Bundino, S., 1983:
Familial sea-blue histiocytosis with cutaneous involvement. A case report with ultrastructural findings

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

Nell, P.A.; Ammann, A.J.; Hong, R.; Stiehm, E.R., 1972:
Familial selective IgA deficiency

Baird, W.M.; Ablin, R.J., 1971:
Familial selective deficiency of IgA

Goldberg, L.S.; Fudenberg, H.H., 1968:
Familial selective malabsorption of vitamin B 12. Re-evaluation of an in vivo intrinsic-factor inhibitor

Bell, M.; Harries, J.T.; Wolff, O.H.; Dawson, A.M.; Waters, A.H., 1973:
Familial selective malabsorption of vitamin B12

Gräsbeck, R., 1972:
Familial selective vitamin B 12 malabsorption

Shi, H.P.; Zhang, W.M.; Luo, H.Y.; Xue, G.R.; Zhu, C.Y.; Xu, J.Z.; He, B.Z., 1983:
Familial selective vitamin B12 malabsorption (Imerslund-Grasbeck syndrome)--a case report

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

Uzel, R., 1966:
Familial seminoma

Rosenmayr, F.; Weippl, G., 1969:
Familial septic granulomatosis

Noemi, I.; Rugiero, E.; Viovy, A.; Cortés, P.P.; Cerva, J.L.; González, M.; Back, S.; Gottlieb, B.; Herrera, M.E.; Cordovez, J., 1994:
Familial seroepidemiology of toxocariasis

Gjone, E.; Norum, K.R., 1968:
Familial serum cholesterol ester deficiency. Clinical study of a patient with a new syndrome

Arias, A.M.; Yung, C.W.; Rendler, S.; Soltani, K.; Lorincz, A.L., 1982:
Familial severe twenty-nail dystrophy

Hecht, F., 1981:
Familial sex chromosome mosaicism (yes) and interchromosomal effects (no)

Weatherall, D.J.; Pembrey, M.E.; Hall, E.G.; Sanger, R.; Tippett, P.; Gavin, J., 1970:
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation

Kardos, G.; Veerman, A.J.; de Waal, F.C.; van Oudheusden, L.J.; Slater, R., 1996:
Familial sideroblastic anemia with emergence of monosomy 5 and myelodysplastic syndrome

Yeo, R.A.; Cohen, D.B., 1983:
Familial sinistrality and sex differences in cognitive abilities

McKeever, W.F.; Hoff, A.L., 1982:
Familial sinistrality, sex, and laterality differences in naming and lexical decision latencies of right-handers

Zhu, J.M., 1980:
Familial sino-atrial node disease--report of 3 cases in one family

Livesley, B.; Catley, P.F.; Oram, S., 1972:
Familial sinuatrial disorder

Smolik, R.; Masior, J.; Stankiewicz, S.; Szymaniec, S.; Zienkowski, Z., 1968:
Familial sinus bradycardia

Spellberg, R.D., 1971:
Familial sinus node disease

Shao, D.Q., 1982:
Familial sinus node disease--report of 2 cases in a family

Antia, A.U., 1970:
Familial skeletal cardiovascular syndrome (Holt-Oram) in a polygamous African family

Holm-Bentzen, M.; Nielsen, C.B., 1982:
Familial slipped upper femoral epiphyses

Rennie, A.M., 1967:
Familial slipped upper femoral epiphysis

Zakut, H.; Mashiach, S.; Insler, V., 1974:
Familial solitary hypogonadotropism

Nehlil, J.; Dumont, G.; Doutre, J.C., 1973:
Familial spasmodic flexion paraplegia with important trophic bone disorders

Chouza, C.; Caamaño, J.L.; D.M.dina, O.; Bogacz, J.; Oehninger, C.; Vignale, R.; D.A.da, G.; Novoa, E.; D.B.llis, R.; Cardozo, H., 1984:
Familial spastic ataxia associated with Ehlers-Danlos syndrome with platelet dysfunction

Gamboa, I.; Hernández Peniche, J., 1973:
Familial spastic diplegia (study of a Mexican family)

Rodríguez-García, A.; Olmos-García de Alba, G.; Valarezo-Crespo, F., 1982:
Familial spastic diplegia and arginemia

Alberca-Serrano, R.; Fabiani, F.; Deneve, V.; Macken, J., 1965:
Familial spastic diplegia due to anoxic encephalopathy (Alpers). A contribution to the study of vascular fragilities of the nervous system of genetic type

Archambault, P., 1966:
Familial spastic paralysis

Losiowski, Z.; Wiszczor-Adamczyk, B., 1967:
Familial spastic paralysis in 3 siblings

Arjundas, G.; Ramamurthi, B.; Chettur, L., 1971:
Familial spastic paraplegia (a review with four case reports)

Tanaka, M.; Uchiyama, T.; Komatsu, M.; Morimatsu, M.; Hirai, S., 1982:
Familial spastic paraplegia associated with large stature and chromosomal abnormalities

Fujiwara, H.; Akabori, O.; Akashi, K.; Moriya, S., 1971:
Familial spastic paraplegia in 3 families

Ogawa, A.; Shiohira, A., 1965:
Familial spastic paraplegia occurring in siblings

Kuberski, T.; Tetava, P.; Koteka, G., 1981:
Familial spastic paraplegia on Mitiaro, Cook Islands

van Damme, J.; van Bogaert, L.; Verschueren, M., 1965:
Familial spastic paraplegia with chronic gouty arthropathy

Mahloudji, M.; Chuke, P.O., 1968:
Familial spastic paraplegia with retinal degeneration

Stewart, R.M.; Tunell, G.; Ehle, A., 1981:
Familial spastic paraplegia, peroneal neuropathy, and crural hypopigmentation: a new neurocutaneous syndrome

Gonçalves, A., 1980:
Familial spastic paraplegia. Genetic-scientific discussion apropos of an affected family

Owens, L.A.; Peterson, C.R.; Burdick, A.B., 1982:
Familial spastic paraplegia: a clinical and electrodiagnostic evaluation

Ozsváth, K., 1968:
Familial spastic spinal paralysis

Kozlowska, J.; Stawarczyk, W., 1973:
Familial spherocytic anemia in a 12-year-old boy

Walker, F.A., 1974:
Familial spina bifida associated with antiemetic ingestion in the first semester

Duke, R.J.; Hashimoto, S., 1973:
Familial spinal arachnoiditis--a new entity

Duke, R.J.; Hashimoto, S.A., 1974:
Familial spinal arachnoiditis. A new entity

Popov, I.; Nikolić, V.; Mitrović, D., 1983:
Familial spinal spastic paralysis--case study of the evolution of the disease through 5 generations

Gallai, V.; Borri, P.; Nenci, G.; Cianchetti, A.; Agostini, L., 1974:
Familial spino-cerebellar ataxia with megalocornea and stomatocytosis

Daras, M.; Tuchman, A.J.; David, S., 1983:
Familial spinocerebellar ataxia with skin hyperpigmentation

Richards, F.; Cooper, M.R.; Pearce, L.A.; Cowan, R.J.; Spurr, C.L., 1974:
Familial spinocerebellar degeneration, hemolytic anemia, and glutathione deficiency

Szappanos, L.; Czeizel, E.; Szepesi, K., 1984:
Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome

Asher, D.M.; Masters, C.L.; Gajdusek, D.C.; Gibbs, C.J., 1983:
Familial spongiform encephalopathies

Bohnert, B.; Noetzel, H., 1974:
Familial spongiform glioneuronal dystrophy

Gambetti, P.; Mellman, W.J.; Gonatas, N.K., 1969:
Familial spongy degeneration of the central nervous system (Van Bogaert-Bertrand disease). An ultrastructural study

Sharpe, I.K.; Ahmad, M.; Braun, W., 1980:
Familial spontaneous pneumothorax and HLA antigens

Schofield, P.F.; Macdonald, N.; Clegg, J.F., 1970:
Familial spontaneous rupture of the colon: report of two cases

Escat, J.; Carcy, J.B.; Gouzi, J.L.; Lazorthes, F.; Ribet, A.; Grimoud, M., 1970:
Familial spontaneous spleno-renal anastomosis

Bhigjee, A.I.; Bill, P.L.; Madurai, S.; York, D.; Thaler, D., 1995:
Familial spread of HTLV-I in KwaZulu/Natal

Bosch, J.; Brugera, M.; Rodes, J., 1973:
Familial spread of type-B hepatitis

Nishimura, T.; Masumura, M.; Nishina, S., 1966:
Familial staphylococcal infections, with special reference to a case with acute tibial osteomyelitis

Markand, O.N.; Garg, B.P.; Weaver, D.D., 1984:
Familial startle disease (hyperexplexia). Electrophysiologic studies

Cockel, R.; Hill, E.E.; Rushton, D.I.; Smith, B.; Hawkins, C.F., 1973:
Familial steatorrhoea with calcification of the basal ganglia and mental retardation

Ostrowski, J.E., 1972:
Familial sterility in a dairy shorthorn heard with frequent occurrence of segmental aplasia of the Wolffian duct

Donofrio, P.; Ayala, F., 1983:
Familial streblodactyly

Li, Y.M., 1981:
Familial streptomycin intoxication to the acoustic nerve

Aschoff-Pluta, R.; Bell, V.; Blumenthal, S.; Lungershausen, E.; Vogel, R., 1984:
Familial stresses as a sequel of psychiatric diseases in a relative. Results of an interview with relatives

Rice, G.P.; Boughner, D.R.; Stiller, C.; Ebers, G.C., 1980:
Familial stroke syndrome associated with mitral valve prolapse

Insley, J.; McDermott, A.; Parrington, J., 1968:
Familial structural chromosome abnormality with maternal mosaicism

Sönnichsen, N.; Apostoloff, G.; Randow, U.; Weidauer, S.; Zoellner, E., 1965:
Familial studies in lupus erythematosus

Woodtli, W.; Ziegler, W.H.; Dambacher, M.A., 1982:
Familial studies in medullary thyroid carcinoma and multiple endocrine adenomatosis

Hall, R.; Stanbury, J.B., 1967:
Familial studies of autoimmune thyroiditis

Amor, B., 1983:
Familial studies of reactive arthritis

Lange, G., 1966:
Familial studies on the heredity OF METRIC AND MORPHOLOGICAL TRAITS OF THE EXTERNAL EAR

Pawlak, A.; Szydlowski, E., 1966:
Familial study in a case of congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency

Baumann, R.; Straub, P.W., 1968:
Familial study in congenital Hageman factor deficiency (blood coagulation factor XII)

Anonymous, 1967:
Familial study in psychiatry

Bellon, R.; Pericarpin, S.; Fauran, P., 1965:
Familial study of SC hemoglobinopathies

Selman, E.; Mena, M.; Aracena, M.M.; Bancalari, A.; Nuñez, F.; Castro, H., 1982:
Familial study of extrinsic bronchial asthma

Liu, X.H., 1983:
Familial study of patients with psychosis, epilepsy and mental retardation

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

Addor, M.C.; Pescia, G.; Guignard, J.P.; Genton, N., 1984:
Familial study of vesico-ureteral reflux

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

Pagnan, A.; Kostner, G.; Braggion, M.; Ziron, L.; Bittolo Bon, G.; Avogaro, P., 1983:
Familial study on "sinking pre-beta", the Lp(a) lipoprotein, and its relationship with serum lipids, apolipoprotein A-I and B and clinical atherosclerosis

Kidd, K.K.; Heimbuch, R.C.; Records, M.A.; Oehlert, G.; Webster, R.L., 1980:
Familial stuttering patterns are not related to one measure of severity

Geisz, J.; Franzen, C.; Gekle, D., 1981:
Familial subsepsis allergica- a systemic form of chronic juvenile arthritis

August, G.J.; Stewart, M.A., 1983:
Familial subtypes of childhood hyperactivity

Critelli, G.; Gallagher, J.J.; Sealy, W.C.; Lanza, G.G.; Condorelli, M., 1981:
Familial sudden death in preexcitation syndrome. Surgical interruption of the anomalous pathways in two brothers

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

Sayag, J.; Fouque, R., 1972:
Familial superficial disseminated actinic porokeratosis

Chudley, A.E.; Zheng, H.Z.; Pabello, P.D.; Shia, G.; Wang, H.C., 1983:
Familial supernumerary microchromosome mosaicism: phenotypic effects and an attempt at characterization

Simon, M.; L.M.gnon, L., 1984:
Familial survey on a patient with idiopathic hemochromatosis. Therapeutic implications

Allannic, H.; Lorcy, Y.; Cornec, A.; L.M.rec, B.; Calmettes, C., 1980:
Familial surveys in screening for thyroid cancers with amyloid stroma. Report of a personal survey carried out on 80 members of the same family

Zimmerman, R.A.; Wilson, E., 1968:
Familial susceptibility to acquisition of group A B-hemolytic streptococci

Horn, Y., 1984:
Familial susceptibility to malignant tumors

Laplane, R.; Fontaine, J.L.; Lagardere, B.; Sambucy, F., 1972:
Familial syndesmodysplasic dwarfism. A new disease entity

Refetoff, S.; DeWind, L.T.; DeGroot, L.J., 1967 :
Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone

Balouet, G.; Daoulas, R.; Borel, J.; Labouche, F., 1967:
Familial syndrome of Gardner

Yvonneau, M.; Vital, C.; Belly, C.; Coquet, M., 1971:
Familial syndrome of amyotrophic lateral sclerosis with dementia

Chayasirisobhon, S.; Walters, B., 1984:
Familial syndrome of deafness, myoclonus, and cerebellar ataxia

Sauer, H.; Chüden, H.; Gottesbüren, H.; Schmitz-Valckenberg, P.; Seitz, D., 1973:
Familial syndrome of diabetes mellitus, primary optic nerve atrophy and inner-ear deafness

Castro-Gago, M.; Pombo, M.; Novo, I.; Tojo, R.; Peña, J., 1983:
Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies

Rizzon, P.; Biasco, G.; Brindicci, G.; Mauro, F., 1973:
Familial syndrome of midsystolic click and late systolic murmur

Strong, W.B., 1968:
Familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphism

Espiner, E.A.; Veale, A.M.; Sands, V.E.; Fitzgerald, P.H., 1970:
Familial syndrome of streak gonads and normal male karyotype in five phenotypic females

Monnet, P.; Paufique, L.; Salle, B.; Rosenberg, D.; Pasquier, N.; Picaud, S., 1969:
Familial syndrome of the Marinesco-Sjogren type with variations

Constantinidis, J.; de Ajuriaguerra, J., 1970:
Familial syndrome with parkinsonian tremor and anosmia and its therapy with L-dopa associated with a decarboxylase inhibitor

Habighorst, L.V.; Albers, P., 1965:
Familial synostosis of metacarpi IV and V

Jefferson, T.O.; Cohen, C., 1982:
Familial syringomyelia with mental impairment

Berliner, S.; Weinberger, A.; Zamir, R.; Salomon, F.; Joshua, H.; Pinkhas, J., 1981:
Familial systemic lupus erythematosus and C4 deficiency

Reveille, J.D.; Bias, W.B.; Winkelstein, J.A.; Provost, T.T.; Dorsch, C.A.; Arnett, F.C., 1983:
Familial systemic lupus erythematosus: immunogenetic studies in eight families

Meretoja, J., 1969:
Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome

Forabosco, A.; Cheli, E.; Marzona, L.; Temperani, P., 1973:
Familial t (22q Dq) translocation and free trisomy 21 in offspring

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

Najafzadeh, T.M.; Littman, V.A.; Dumars, K.W., 1983:
Familial t(4;13) with abnormal offspring in three generations

Yassa, R.; Ananth, J., 1981 :
Familial tardive dyskinesia

Taylor, J.C.; Colin, M.; Inamizu, T.; Mittman, C., 1980:
Familial temperature sensitive alpha 1 protease inhibitor (M1Anaheim)

Newcombe, H.B., 1966:
Familial tendencies in diseases of children

Cantoni, E.; Forabosco, A.; Santoro, L.; Romagnoli, R.; Marchetti, M.; Gallo, E., 1982:
Familial tendency in patients with compound odontomas

Surana, R.B.; Conen, P.E.; Braudo, M.; Keith, J.D., 1974:
Familial tertiary trisomy with t (14q-; 1 plus?)

Chandra, P.K.; Kalam, A.; Banerjee, P.; Bhattacharya, K.N.; Chowdhury, S., 1994:
Familial testotoxicosis

Chemke, J.; Graff, G.; Lancet, M., 1971:
Familial thanatophoric dwarfism

Searles, R.P.; Plymate, S.R.; Troup, G.M., 1981:
Familial thioamide-induced lupus syndrome in thyrotoxicosis

Raatikka, M.; Rapola, J.; Tuuteri, L.; Louhimo, I.; Savilahti, E., 1981:
Familial third and fourth pharyngeal pouch syndrome with truncus arteriosus: DiGeorge syndrome

Rohn, R.D.; Leffell, M.S.; Leadem, P.; Johnson, D.; Rubio, T.; Emanuel, B.S., 1984:
Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission

Kurstjens, R.; Bolt, C.; Haanen, C.A., 1967:
Familial thrombocytopenia

Helmerhorst, F.M.; Heaton, D.C.; Crossen, P.E.; von dem Borne, A.E.; Engelfriet, C.P.; Natarajan, A.T., 1984:
Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage

Gutenberger, J.; Trygstad, C.W.; Stiehm, E.R.; Opitz, J.M.; Thatcher, L.G.; Bloodworth, J.M., 1970:
Familial thrombocytopenia, elevated serum IgA levels and renal disease. A report of a kindred

Bentata-Pessayre, M.; Aurousseau, M.H.; Josso, F.; Delzant, G., 1980:
Familial thromboembolic disease associated with antithrombin III deficiency

Kurstjens, R.; Bolt, C.; Vossen, M.; Haanen, C., 1968:
Familial thrombopathic thrombocytopenia

Hofman, K.J.; Goldman, A.P.; Lurie, M.; Hockly, J.; Bradlow, B.A., 1980:
Familial thrombosis associated with antithrombin III deficiency in a young adult male. A case report

Marciniak, E.; Farley, C.H.; DeSimone, P.A., 1974:
Familial thrombosis due to antithrombin 3 deficiency

Buri, P., 1974:
Familial thrombosis of the mesenteric veins

Goldman, A.S.; Goldblum, R.M., 1973:
Familial thymic aplasia--genetic defect or maternal effect

Wuketich, S.; Zwintz, E., 1983:
Familial thymoma

Rais, N.; Kalra, P.; Bhandarkar, S.D.; Satoskar, R.S., 1983:
Familial thyroid disease: Grave's disease and non-toxic goitre (a case report)

Orti, E.; Castells, S.; Qazi, Q.H.; Inamdar, S., 1971:
Familial thyroid disease: lingual thyroid in two siblings and hypoplasia of a thyroid lobe in a third

Rosenberg, T.; Gilboa, Y., 1980:
Familial thyroid ectopy and hemiagenesis

Lisa Catón, V.; Peña Somovilla, J.L.; Ochoa Gómez, F.J.; Salcedo Aguilar, F.J.; Vilella Morato, A.; Campo Hernández, J.M., 1994:
Familial thyroid medullary carcinoma without associated neoplasms

O'Brien, P.K.; Wilansky, D.L., 1981:
Familial thyroid nodulation and arrhenoblastoma

Strunge, P., 1973:
Familial thyrosine-binding globulin deficiency. A genetic and biochemical assessment of 3 Danish families

Carta Sorcini, M.; Moschini, L.; Fiore, L.; Tomarchio, S.; D.I.io, M.G.; Gilardi, E.; Romagnoli, C.; Currò, V.; Carta, S., 1982:
Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidism

Refetoff, S.; Selenkow, H.A., 1968:
Familial thyroxine-binding globulin deficiency in a patient with Turner's syndrome (XO). Genetic study of a kindred

Shita, A.; Leroy, C.; Tagnon, A.; Chanoine, F.; Henoumont, Y.; Gillerot, Y., 1981:
Familial thyroxine-binding globulin deficiency with neurological abnormalities

Strunge, P., 1974:
Familial thyroxine-binding globulin deficiency. A study of three Danish families

Grant, D.B.; Clarke, H.G.; Putman, D., 1974:
Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups

Stockigt, J.R.; Barlow, J.W., 1982:
Familial thyroxine-excess syndrome

Costa, L.R.; D'Elia, P.R., 1970:
Familial tinea caused by Trichophyton verrucosum

Hoo, J.J.; Fischer, A.; Fuhrmann, W., 1982:
Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome

Schwanitz, G.; Keft, K.; Fleischer-Peters, A.; Zschiesche, S., 1983:
Familial tooth position anomalies in the Orangutang. Orthodontic, cytogenetic and anthropological studies

S.G.abski, R.; Nowicki, T., 1982:
Familial torticollis

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

Fried, K.; Bukovsky, J.; Rosenblatt, M.; Mundel, G., 1974:
Familial translocation 15-22. A possible cause for abortions in female carriers

Ricci, N.; Dallapiccola, B.; Cotti, G., 1968:
Familial translocation 2-D

Tancredi, F.; Ventruto, V., 1981:
Familial translocation 2; 17 with partial trisomy 2q32 to 2qter

Giliberti, P.; Celona, A.; Della Pietra, M.; D.M.si, R.V.; Fioretti, G.; Pagano, L.; Renda, S.; Vetrella, A.; Ventruto, V., 1980:
Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter

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

Tharapel, S.A.; Lewandowski, R.C.; Kukolich, M.K., 1984:
Familial translocation leading to partial trisomy 13: report of three cases

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

Dallapiccola, B., 1971:
Familial translocation t(2p-; 17p+)

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

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

Giovannelli, G.; Forabosco, A.; Dutrillaux, B., 1974:
Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters

Tenconi, R.; Baccichetti, C.; Dussini, N.; Panizza, G., 1974:
Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy

Henrot, H.; Aladenise, J.; Inghel, J., 1972 :
Familial transmission deafness

Loranger, A.W.; Oldham, J.M.; Tulis, E.H., 1982:
Familial transmission of DSM-III borderline personality disorder

Ricci, N.; Dallapiccola, B.; Preto, G., 1970:
Familial transmission of a Gq- (Ph1-like) chromosome

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

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

Smith, G.F.; Berg, J.M.; Ridler, M.A.; Faunch, J.A.; Farnham, F.N.; Pendrey, M.J., 1967:
Familial transmission of an aberrant submetacentric chromosome

Tuckerman, E.; Gray, J.E.; Salmon, J., 1970:
Familial transmission of an unusual variant of a group C chromosome

David, X.R.; Blanc, P.; Pageaux, G.P.; Desprez, D.; Diaz, D.; Lemaire, J.M.; Tognarelli, B.; Larrey, D.; Michel, H., 1995:
Familial transmission of hepatitis C virus

Berlin, I.N., 1981:
Familial treatment of severe adolescent problems

Bohlega, S.; Stigsby, B.; al-Kawi, M.Z.; McLean, D.R.; Ozand, P.; Omer, S.; Coates, P., 1995:
Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging

Johnstone, F.; Inglis, L., 1974 :
Familial trends in low birth weight

Witczuk, J.; Gruchała, E.; Stefańska, J., 1982:
Familial trichinosis after consumption of boar's meat

Murachi, S.; Nogami, H.; Oki, T.; Ogino, T., 1981:
Familial tricho-rhino-phalangeal syndrome Type II

Linn, H.W.; Hunter, G.A., 1970:
Familial trichoepithelioma of unusual distribution

Steenkamp, W.F., 1972:
Familial trifascicular block

Testa, D.; Milanese, C.; L.M.ntia, L.; Mastrangelo, M.; Crenna, P.; Negri, S., 1981:
Familial trigeminal neuralgia in Charcot-Marie-Tooth disease

van Genechten, F., 1982:
Familial trigger thumb in children

Cotta, H.; Jäger, M., 1965:
Familial triphalangism of the thumb and its surgical treatment

Stoll, C.; Roth, M.P., 1981:
Familial trisomy 10q

Parazzini, F.; L.V.cchia, C.; Franceschi, S.; Mangili, G., 1984:
Familial trophoblastic disease: case report

Mori, Y.; Mizutani, S., 1968:
Familial true hermaphroditism in genetic females

Grossiord, A.; Lacert, P.; Got, C.; Gaussel, J.J., 1973:
Familial truncular paralysis. A case with biopsy of a peripheral nerve. Histopathological lesions of a very peculiar type

Biscione, C.; Lamberti, A., 1972:
Familial tuberculosis at the present time. Clinico-statistical notes

Singh, S.V.; Goyal, S.K.; Chowdhury, B.L.; Shrimali, R.; Bansal, N.K., 1972:
Familial tuberous sclerosis (report of two cases in family with intra-abdominal tumors)

Serbănescu, G.; Neagoe, S.; Serbănescu, C.; Mălăescu, G.; Colceriu, N.; Davidescu, C.; Ruxanda, M., 1982:
Familial tuberous sclerosis in 2 successive generations with jacksonian crisis and grand-mal epilepsy

Bejar, R.L., 1966:
Familial tuberous sclerosis. A clinical reminder

Verma, B.S.; Tailor, M.H., 1965:
Familial tuberous sclerosis: a review with report of three cases

Ponz de Leon, M., 1994:
Familial tumors of other organs

Brusilovskiĭ, E.A., 1972:
Familial tumors of the stomach

O'Mahony, M.Y.; Ellis, J.P.; Hellier, M.; Mann, R.; Huddy, P., 1984:
Familial tylosis and carcinoma of the oesophagus

Herman, T.E.; M.A.ister, W.H., 1995:
Familial type 1 jejunal atresias and renal dysplasia

Dyerberg, J., 1974:
Familial type 3 hyperlipoproteinemia

Dyerberg, A.J., 1974:
Familial type I hyperlipoproteinemia

Khoo, K.L.; Chong, Y.H.; Pillay, R.P., 1973:
Familial type II hyperlipoproteinaemia in a Chinese family

Stein, E.A.; Mendelsohn, D.; Bersohn, I., 1974:
Familial type II hyperlipoproteinaemia. Clinical features and results of treatment in children and young adults

Aso, K.; Iitani, I.; Fujita, M., 1972:
Familial type II xanthoma

Akazawa, S.; Ikeda, Y.; Toyama, K.; Miyake, S.; Takamori, M.; Nagataki, S., 1984:
Familial type IIa hyperlipoproteinemia associated with a huge intracranial xanthoma

Schreibman, P.H.; Wilson, D.E.; Arky, R.A., 1969:
Familial type IV hyperlipoproteinemia

Scharf, Y.; Nahir, M.; Levy, N., 1974:
Familial ulcerative colitis associated with ankylosing spondylitis

Reichen, J., 1983:
Familial unconjugated hyperbilirubinemia syndromes

Tan, K.; Tominaga, S.; Hashimoto, A.; Mori, K.; Takao, A., 1973:
Familial upper-limb cardiovascular syndrome--ventriculo-radial dysplasia with pulmonary hypertension

Alexander, F.; Campbell, S., 1970:
Familial uremic medullary cystic disease

Srivastava, R.N., 1971:
Familial uremic medullary cystic disease or nephronophthisis?

Degos, R.; de Cinarca, O.C.; Méry, F., 1970:
Familial uroporphyrinuric pure late cutaneous porphyria

Castelain, P.Y., 1971:
Familial urticaria due to cold

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

James, M.P.; Eady, R.A., 1981:
Familial urticaria pigmentosa with giant mast cell granules. A clinical, light, and electron microscopic study

Castier, P.; François, M.; Duret, M.H., 1982:
Familial uveitis

Hemingway, A.P.; Leung, A.; Lavender, J.P., 1983:
Familial vanishing limbs: four generations of idiopathic multicentric osteolysis

Abramson, P.R., 1973:
Familial variables related to the expression of violent aggression in preschool-age children

Roberts, J.T.; Byrne, E.H.; Rosenthal, D., 1981:
Familial variant of dermatofibroma with malignancy in the proband

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

Galdston, M.; Janoff, A.; Davis, A.L., 1973:
Familial variation of leukocyte lysosomal protease and serum 1 -antitrypsin as determinants in chronic obstructive pulmonary disease

Ishii, Y.; Kato, K.; Fujimaki, T.; Narusawa, T.; Terao, T., 1968:
Familial variegate prophyria

Pasyk, K.A.; Argenta, L.C.; Erickson, R.P., 1984:
Familial vascular malformations. Report of 25 members of one family

Waynberger, M.; Coutadon, M.; Peltier, J.M.; Ducloux, G.; Jallut, H.; Slama, R., 1974:
Familial ventricular tachycardia. Apropos of 7 cases

Matsu, K.; Iseki, F.; Saigo, K.; Nagasawa, M.; Tomatsu, T., 1971:
Familial vertebral dysplasia: a case report

Jerkins, G.R.; Noe, H.N., 1982:
Familial vesicoureteral reflux: a prospective study

Gigliotti, R.; Harrison, H.; Reveley, R.A.; Drabkowski, A.J., 1971:
Familial vitamin D-refractory rickets

Falls, W.F.; Carter, N.W.; Rector, F.C.; Seldin, D.W., 1968:
Familial vitamin D-resistant rickets. Study of six cases with evaluation of the pathogenetic role of secondary hyperparathyroidism

Kosińska, D.; Szreterowa, M., 1984:
Familial vitreoretinal degeneration

Wright, R.L., 1969:
Familial von Hippel-Lindau's disease. Case report

Holt, R.J.; Freytes, C.O., 1983:
Familial warfarin resistance

Tamagna, J.A., 1965:
Familial white folded dysplasia of the oral mucous membranes

Kim, H.J.; Hsu, L.Y.; Hirschhorn, K., 1974:
Familial x/x translocation: t(x;x)(p22;q13)

Sawkar, L.A., 1971:
Familial xanthelasma, hyperlipidemia and multiple myeloma

Cifuentes Delatte, L.; Castro-Mendoza, H., 1967:
Familial xanthinuria

Pereg Macazaga, V.; García Fernández, H.; Regúlez, M.; Elorza Olabegoya, J.R.; Beitia Martín, J.J.; Vázquez García, J.A., 1984:
Familial xanthinuria, 2 new cases

Paget, M.; Routier, G.; Leuridan, B., 1965:
Familial xanthomatous hypercholesterolaemia. Apropos of a familial case

Paget, M.; Routier, G.; Leuridan, B., 1965:
Familial xanthomatous hypercholesterolemia. Apropos of a familial case

Gaburro, D.; Ripa, R.; Volpato, S., 1965:
Familial "chronic" hypoaldosteronism (a personal case)

Hudgson, P.; Bradley, W.G.; Jenkison, M., 1972 :
Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings

Worsfold, M.; Park, D.C.; Pennington, R.J., 1973:
Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings

van Wijngaarden, G.K.; Fleury, P.; Bethlem, J.; Meijer, A.E., 1969:
Familial "myotubular" myopathy

Barraquer-Bordas, L.; Peres-Serra, J.; Grau-Veciana, J.M.; Sagimon-Rabassa, E., 1970:
Familial "prosoplegic" migraine

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

Buksowicz, C.; Wochnik-Dyjas, D., 1966:
Familial, amyotrophic lateral sclerosis in childhood

Soto Melo, J.; Rodriguez Puchol, J.; Calderon, 1966:
Familial, circumscribed angiokeratoma of Fabry with visceral lesions

Grim, C.E.; Weinberger, M.H., 1980:
Familial, dexamethasone-suppressible, normokalemic hyperaldosteronism

Guérin, F., 1980:
Familial, educational and social integration of patients suffering from congenital heart disease

Hill, K.; Neidhardt, M., 1970:
Familial, infantile-septic chronic granulomatous disease: pathology and pathogenesis

Verhulst, J.; Portmann, M.; Boissiéras, P.; Deminière, C.; Piton, J., 1980:
Familial, malignant, chemodectoma bilateral in a 16-year-old girl

Adami, H.O.; Hansen, J.; Jung, B.; Rimsten, A., 1980:
Familiality in breast cancer: a case-control study in a Sweden population

Mauro, R.; Volpe, E.; Cataldi, V., 1968:
Familiality of Hodgkin's disease

Murata, M., 1982:
Familiality of breast cancer and hereditary factors

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

Lygonis, C.S., 1969:
Familiar absence of olfaction

Newman, C.V., 1972:
Familiar and relative size cues and surface texture as determinants of relative distance judgments

Korczowski, R., 1965:
Familiar appearance of Caffey's disease

Rocca, G.; Poli, G.; Gerardo, P.; Ascione, A.; Caporaso, N.; Craxi, A.; Dentico, P.; Marinucci, G.; Piccinino, F.; Raimondo, G., 1983:
Familiar clustering of delta infection

Semmence, A.M., 1972:
Familiar faces

McCormick, J.S., 1972:
Familiar faces--the constant attender

Semmence, A., 1972:
Familiar faces. Problems of identification

Gradowski, B., 1965:
Familiar food poisoning caused by Salmonella typhimurium

Jiménez Díaz, C.; Perianes, J.; Peláez, J.L.; Sánchez Villares, E.; Linazasoro, J.M.; Villalobos, E., 1964:
Familiar infantile haemochromatosis

Cole, F., 1974:
Familiar susceptibility to anesthesia

Howell, S.C., 1972:
Familiarity and complexity in perceptual recognition

Dale, H.C., 1967:
Familiarity and free recall

Epstein, A.; Giolas, T.G.; Owens, E., 1968:
Familiarity and intelligibility of monosyllabic word lists

Hake, H.W.; Myers, A.E., 1969:
Familiarity and shape constancy

Craven, E.E., 1972:
Familiarity breeds carelessness

Stirling, R.V.; Summerbell, D., 1983:
Familiarity breeds contempt: the behaviour of axons in foreign and familiar environments

Anonymous, 1972:
Familiarity breeds disease

Doni, A.; Brancato, R.; Bartoletti, L.; Berni, G., 1965:
Familiarity characteristics of Sjögren's disease. (Clinical contribution and considerations)

Young, A.W.; Hay, D.C.; McWeeny, K.H.; Ellis, A.W.; Barry, C., 1985:
Familiarity decisions for faces presented to the left and right cerebral hemispheres

Mewhort, D.J., 1967:
Familiarity of letter sequences, response uncertainty, and the tachistoscopic recognition experiment

Filip, M., 1966:
Familiarity of selected population groups with the main principles of socialist health services

Tateishi, Y., 1982:
Familiarity of the public health nurse with the public health clinic: a lesson in public health nursing activities at Kiyokawa-mura

Genskow, J.K.; Maglione, F.D., 1965:
Familiarity, dogmatism, and reported student attitudes toward the disabled

Crandall, J.E., 1967:
Familiarity, preference, and expectancy arousal

Flowers, J.H.; Polansky, M.L.; Kerl, S., 1981:
Familiarity, redundancy, and the spatial control of visual attention

Rosnow, R.L.; Goldstein, J.H., 1967:
Familiarity, salience, and the order of presentation of communications

Drake, R.A., 1984:
Familiarity-and-liking relationship under conditions of induced lateral orientation

Scandura, J.M., 1965:
Familiarization and one-trial learning: a positive interaction

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

Kaskirinne, L., 1972:
Familiarization programs for operating room nurses

Irwin, P.; Fink, M., 1983:
Familiarization session and placebo control in EEG studies of drug effects

Bruchác, D., 1974:
Familiarly reminiscence on the ancient school of midwifery

Hellner, K.A.; Rickers, J., 1973:
Familiary bilateral segmental retinopathia pigmentosa

Pavúr, J., 1973:
Familiary polyposis of the large intestine

Cleveland, M., 1981:
Families and adolescent drug abuse: structural analysis of children's roles

Glynn, T.J., 1982:
Families and drugs: a life-span research approach

Quinn, A.; Ford, J.; Mazzawy, M., 1981 :
Families and feelings: a time for sharing

Grace, J.T., 1995:
Families and nurses: building partnerships for growth and health

Parks, J.; Boyer, G.M., 1966:
Families and physicians (George M. Boyer)

Laing, R.D.; Esterson, A., 1967:
Families and schizophrenia

Reiss, D., 1995:
Families and schizophrenia redux

Mishler, E.G., 1966:
Families and schizophrenia; an experimental study

Molter, N.C., 1994:
Families are not visitors in the critical care unit

Player, M.L.; Frank, D.I., 1994:
Families as a source of AIDS information for school age children

Hatfield, A.B., 1981:
Families as advocates for the mentally ill: a growing movement

Garbarino, J.; Sebes, J.; Schellenbach, C., 1984:
Families at risk for destructive parent-child relations in adolescence

Herman, J.; Hirschman, L., 1981:
Families at risk for father-daughter incest

Ayoub, C.; Jacewitz, M.M., 1982:
Families at risk of poor parenting: a descriptive study of sixty at risk families in a model prevention program

Ayoub, C.; Jacewitz, M.M., 1982:
Families at risk of poor parenting: a model for service delivery, assessment, and intervention

Frommer, E.A., 1973:
Families at risk: help for those from broken homes

Lauridsen, V.; Jensen, E.L.; Sørensen, B.; Danfaer, L.; Pedersen, L.S., 1984:
Families caught in the squeeze because of inadequate teamwork

Lyden, C.J.; Robertson, J.G., 1970:
Families clinic, Limassol. A study of a unique British expatriate general practice in Cyprus

Anonymous, 1966:
Families do care

Vaughan, D.H., 1968:
Families experiencing a sudden, unexpected infant death

Dyregrov, A.; Hordvik, E.; Alsaker, T.G.; Finne, P.H., 1985:
Families experiencing the death of child. A model for support

Goldberg, B., 1995:
Families facing choices

Blackburn, R., 1971:
Families in Singapore

Krim, A.S., 1974:
Families in crisis. A cooperative project brings comprehensive on-site services to families living in an emergency relocation hotel

Christensen, E., 1995:
Families in distress, the development of children growing up with alcohol and violence

Power, J.G., 1968:
Families in flats

Moore, N.C., 1982:
Families in high-arise flats

Cook, D.A.; Morgan, H.G., 1982:
Families in high-rise flats

King, R.J., 1980:
Families in the eighties

Albertsen, C.S.; Lyngstad, G.D., 1971:
Families in the hospital

Dunkel, J.; Eisendrath, S., 1983:
Families in the intensive care unit: their effect on staff

Mackie, A.J., 1982:
Families of adopted adolescents

Miyake, Y., 1981:
Families of aged, demented patients being cared for at home and assistance extended to them--activities of an organization of families with aged demented patients

Quadrio, C., 1984:
Families of agoraphobic women

Rawlings, N.D.; Barrett, A.J., 1995:
Families of aspartic peptidases, and those of unknown catalytic mechanism

Feldman, R.B.; Guttman, H.A., 1984:
Families of borderline patients: literal-minded parents, borderline parents, and parental protectiveness

Jenkins, S.; Norman, E., 1969:
Families of children in foster care

Dar, H.; Winter, S.T.; Tal, Y., 1974:
Families of children with cleft lips and palates: concerns and counselling

Husband, P.; Hinton, P.E., 1972:
Families of children with repeated accidents

Axelrod, J.; Geismar, L.; Ross, R., 1994:
Families of chronically mentally ill patients: their structure, coping resources, and tolerance for deviant behavior

Rawlings, N.D.; Barrett, A.J., 1994:
Families of cysteine peptidases

Gallagher, J.J.; Beckman, P.; Cross, A.H., 1983:
Families of handicapped children: sources of stress and its amelioration

Selby, J.W.; Calhoun, L.G.; Jones, J.M.; Matthews, L., 1980:
Families of incest: a collation of clinical impressions

Hoover, C.F.; Insel, T.R., 1984:
Families of origin in obsessive-compulsive disorder

Rawlings, N.D.; Barrett, A.J., 1994:
Families of serine peptidases

Stevenson, A.C.; Davison, B.C., 1966:
Families referred for genetic advice

Crocker, A.C.; Cullinane, M.M., 1972:
Families under stress. The diagnosis of Hurler's syndrome

Noble, D.N.; Hamilton, A.K., 1981:
Families under stress: perinatal social work

Shuttlesworth, G.E.; Rubin, A.; Duffy, M., 1982:
Families versus institutions: incongruent role expectations in the nursing home

Humphry, R., 1995:
Families who live in chronic poverty: meeting the challenge of family-centered services

Marincheva, G.S., 1981:
Families with 2 oligophrenic siblings

Kaneko, M., 1968:
Families with a high incidence of cancer

Heap, K.K., 1984:
Families with abused children: a follow-up study of post-crisis support

Monvall, E., 1973:
Families with children and the employee get most in federal budget proposals

Stiksrud, A.; Margraf, J., 1982:
Families with drug-dependent adolescents

Mosher, L.R.; Pollin, W.; Stabenau, J.R., 1971:
Families with identical twins discordant for schizophrenia: some relationships between identification, thinking styles, psychopathology and dominance-submissiveness

Betancourt, G.L., 1971:
Families with suspected maltreated children

Wortis, H.; Pollack, M.; Wortis, J., 1966:
Families with two or more mentally retarded or mentally disturbed siblings: the preponderance of males

Herman, S.E.; Thompson, L., 1995:
Families' perceptions of their resources for caring for children with developmental disabilities

Incebük, B., 1983:
Families' problems over their hospitalized relatives in Gölbaşi Mental Hospital

Butler, M.C., 1984:
Families' responses to chemotherapy by an ambulatory infusion pump

High, D.M., 1994:
Families' roles in advance directives

Oliveri, M.E.; Reiss, D., 1982:
Families' schemata of social relationships

Vilain, R., 1982:
Families, I love you, or, a good understanding of hygiene

Pinkus, R.L., 1984:
Families, brain death, and traditional medical excellence

Gullotta, T.P.; Donohue, K.C., 1983:
Families, relocation, and the corporation

Jolly, H., 1974 :
Families--a nation's strength

Pearse, J., 1994:
Families--an important part of client care

Lamb, H.R., 1983:
Families: practical help replaces blame

Abasiekong, E.M., 1981:
Familism and hospital admission in rural Nigeria--a case study

Tamez, E.G., 1981:
Familism, machismo and child rearing practices among Mexican Americans

Brunschwig, H., 1982:
Familty Therapy


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