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Results 1 to 25 of 137596

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Fatal acute encephalopathy in two siblings: A distinct hereditary entity?PRASUN, Pankaj; STOCKTON, David W.Journal of the neurological sciences. 2012, Vol 314, Num 1-2, pp 155-157, issn 0022-510X, 3 p.Article

Multivariate prediction of emerging psychosis in adolescents at high risk for schizophreniaSHAH, Jai; EACK, Shaun M; MONTROSE, Debra M et al.Schizophrenia research. 2012, Vol 141, Num 2-3, pp 189-196, issn 0920-9964, 8 p.Article

Familial Ménière's disease: clinical and genetic aspectsMORRISON, A. W; BAILEY, M. E. S; MORRISON, G. A. J et al.Journal of laryngology and otology. 2009, Vol 123, Num 1, pp 29-37, issn 0022-2151, 9 p.Article

Mesial temporal lobe epilepsy : Clinical and neuropathologic findings of familial and sporadic formsANDRADE-VALENCA, Luciana Patriziaa; MORAES VALENCA, Marcelo; RODRIGUES VELASCO, Tonicarlo et al.Epilepsia (Copenhagen). 2008, Vol 49, Num 6, pp 1046-1054, issn 0013-9580, 9 p.Article

Natural history of familial myomasUIMARI, Outi; SUOMALAINEN-KÖNIG, Sanna; SAKKINEN, Nina et al.European journal of obstetrics, gynecology, and reproductive biology. 2006, Vol 125, Num 2, pp 255-258, issn 0301-2115, 4 p.Article

Genetics of fibrosing lung diseasesGRUTTERS, J. C; DU BOIS, R. M.The European respiratory journal. 2005, Vol 25, Num 5, pp 915-927, issn 0903-1936, 13 p.Article

Visual scanpath dysfunction in first-degree relatives of schizophrenia probands: evidence for a vulnerability marker?LOUGHLAND, Carmel M; WILLIAMS, Leanne M; HARRIS, Anthony W et al.Schizophrenia research. 2004, Vol 67, Num 1, pp 11-21, issn 0920-9964, 11 p.Article

Special features of familial intracranial aneurysms : report of 215 familial aneurysms. CommentariesRONKAINEN, A; HERNESNIEMI, J; TROMP, G et al.Neurosurgery. 1995, Vol 37, Num 1, pp 43-47, issn 0148-396XArticle

Sixteen years of plasma exchange in a homozygote for familial hypecholesterolaemiaLEREN, T. P; FAGERHOL, M. K; LEREN, P et al.Journal of internal medicine. 1993, Vol 233, Num 2, pp 195-200, issn 0954-6820Article

Intrauterine growth retardation and familial short statureHEINRICH, U. E.Baillière's clinical endocrinology and metabolism. 1992, Vol 6, Num 3, pp 589-601, issn 0950-351XArticle

Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patient with heterozygous familial hypercholesterolemiaLELLI, N; GHISELLINI, M; CALANDRA, S et al.Human genetics. 1991, Vol 86, Num 4, pp 359-362, issn 0340-6717Article

LDL-apheresis : results of longterm treatment and vascular outcomeKELLER, C.Atherosclerosis. 1991, Vol 86, Num 1, pp 1-8, issn 0021-9150Article

Comparison of the effects of a low-fat, high-carbohydrate diet at low levels of polyunsaturates on plasma lipids of patients with familial endogenous hypertriglyceridemiaCOMINACINI, L; BOSELLO, O; GARBIN, U et al.Journal of nutritional medicine. 1990, Vol 1, Num 2, pp 95-105, 11 p.Article

Incidence of sporadic and familial medullary thyroid carcinoma in Sweden 1959 through 1981 : a nationwide study in 126 patientsBERGHOLM, U; ADAMI, H.-O; TELENIUS-BERG, M et al.Acta oncologica (Stockholm). 1990, Vol 29, Num 1, pp 9-15, issn 0284-186X, 7 p.Article

Excess breast cancer risk in first degree relatives of CHEK2*1100delC positive familial breast cancer casesADANK, Muriel A; VERHOEF, Senno; JONKER, Marianne A et al.European journal of cancer (1990). 2013, Vol 49, Num 8, pp 1993-1999, issn 0959-8049, 7 p.Article

Malondialdehyde (MDA) and protein carbonyl (PCO) levels as biomarkers of oxidative stress in subjects with familial hypercholesterolemiaPIRINCCIOGLU, Ayfer Gözü; GÖKALP, Deniz; PIRINCCIOGLU, Mihdiye et al.Clinical biochemistry. 2010, Vol 43, Num 15, pp 1220-1224, issn 0009-9120, 5 p.Article

Sisters with clinically mild encephalopathy with a reversible splenial lesion (MERS)-like features; Familial MERS?IMAMURA, Takuji; TAKANASHI, Jun-Ichi; YASUGI, Jun et al.Journal of the neurological sciences. 2010, Vol 290, Num 1-2, pp 153-156, issn 0022-510X, 4 p.Article

The association of psychosocial and familial factors with adolescent suicidal ideation: A population-based studyAN, Hoyoung; AHN, Joon-Ho; BHANG, Soo-Young et al.Psychiatry research (Print). 2010, Vol 177, Num 3, pp 318-322, issn 0165-1781, 5 p.Article

The effect of seasons and seasonal variation on neuropsychological test performance in patients with bipolar I disorder and their first-degree relativesRAJAJÄRVI, Elina; ANTILA, Mervi; KIESEPPÄ, Tuula et al.Journal of affective disorders. 2010, Vol 127, Num 1-3, pp 58-65, issn 0165-0327, 8 p.Article

Cognitive functioning of bipolar I patients and relatives from families with or without schizophrenia or schizoaffective disorderANTILA, Mervi; PARTONEN, Timo; KIESEPPÄ, Tuula et al.Journal of affective disorders. 2009, Vol 116, Num 1-2, pp 70-79, issn 0165-0327, 10 p.Article

Twin study of illness history variables in psychosisALLAN, Charlotte L; CARDNO, Alastair G; RIJSDIJK, Frühling V et al.Schizophrenia research. 2009, Vol 115, Num 2-3, pp 237-244, issn 0920-9964, 8 p.Article

Familial and hereditary prostate cancer by definition in an italian surgical series : Clinical features and outcomeSACCO, Emilio; PRAYER-GALETTI, Tommaso; PINTO, Francesco et al.European urology. 2005, Vol 47, Num 6, pp 761-768, issn 0302-2838, 8 p.Article

Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in Chinese Patients with hypokalemic periodic paralysisLIN, Shih-Hua; HSU, Yaw-Don; CHENG, Nai-Lin et al.The American journal of the medical sciences. 2005, Vol 329, Num 2, pp 66-70, issn 0002-9629, 5 p.Article

Lipoprotein(a) plasma concentrations associated with lipolytic activities in eight kindreds with familial combined hyperlipidemia and normolipidemic subjectsCABEZAS, M. C; DE BRUIN, T. W. A; VAN LINDE-SIBENIUS TRIP, M et al.Metabolism, clinical and experimental. 1993, Vol 42, Num 6, pp 756-762, issn 0026-0495Article

Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementiaGRANT, D. B; DUNGER, D. B; SMITH, I et al.European journal of pediatrics. 1992, Vol 151, Num 2, pp 85-89, issn 0340-6199Article

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