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Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene productHOFMANN, Sabine; PHILBROOK, Christine; GERBITZ, Klaus-Dieter et al.Human molecular genetics (Print). 2003, Vol 12, Num 16, pp 2003-2012, issn 0964-6906, 10 p.Article

First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 geneDOMENECH, Enric; KRUYER, Helena; GOMEZ, Carolina et al.Prenatal diagnosis. 2004, Vol 24, Num 10, pp 787-789, issn 0197-3851, 3 p.Article

No association of mutations and mRNA expression of WFS1/wolframin with bipolar disorder in humansKATO, Tadafumi; IWAMOTO, Kazuya; WASHIZUKA, Shinsuke et al.Neuroscience letters. 2003, Vol 338, Num 1, pp 21-24, issn 0304-3940, 4 p.Article

Severe orthostatic dysregulation associated with Wolfram syndromeSYNOFZIK, Matthis; WEISS, Daniel; ERHARHAGHEN, Jite et al.Journal of neurology. 2010, Vol 257, Num 10, pp 1751-1753, issn 0340-5354, 3 p.Article

Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 MutationBONNYCASTLE, Lori L; CHINES, Peter S; NARISU, Narisu et al.Diabetes (New York, NY). 2013, Vol 62, Num 11, pp 3943-3950, issn 0012-1797, 8 p.Article

Síndrome de Wolfram. Estudio clînico y genético en dos familias = WOLFRAM SYNDROME. CLINICAL AND GENETIC STUDY IN TWO FAMILIESLOU FRANCES, G; SOTO DE RUIZ, S; LOPEZ-MADRAZO HERNANDEZ, M. J et al.Anales de pediatria (2003. Ed. impresa). 2008, Vol 68, Num 1, pp 54-57, issn 1695-4033, 4 p.Article

A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for wolfram syndrome 2AMR, Sami; HEISEY, Cindy; MIN ZHANG et al.American journal of human genetics. 2007, Vol 81, Num 4, pp 673-683, issn 0002-9297, 11 p.Article

DIDMOAD syndrome: A diagnostic as well as therapeutic dilemmaAYYUB, Muhammad; ANWAR, Masood; ALI, Waqar et al.International journal of hematology. 2004, Vol 80, Num 2, pp 197-198, issn 0925-5710, 2 p.Article

Phenoty e-genotype correlations in a series of Wolfram syndrome familiesSMITH, Casey J. A; CROCK, Patricia A; KING, Bruce R et al.Diabetes care. 2004, Vol 27, Num 8, pp 2003-2009, issn 0149-5992, 7 p.Article

Wolfram syndrome in the Polish population: novel mutations and genotype―phenotype correlationZMYSLOWSKA, A; BOROWIEC, M; ANTOSIK, K et al.Clinical endocrinology (Oxford. Print). 2011, Vol 75, Num 5, pp 636-641, issn 0300-0664, 6 p.Article

Wolfram syndrome: Identification of a phenotypic and genotypic variant from JordanAJLOUNI, Kamel; JARRAH, Nadim; EL-KHATEEB, Mohammed et al.American journal of medical genetics. 2002, Vol 115, Num 1, pp 61-65, issn 0148-7299Article

Prevalence of monogenic diabetes amongst Polish children after a nationwide genetic screening campaignFENDLER, W; BOROWIEC, M; ZMYSLOWSKA, A et al.Diabetologia (Berlin). 2012, Vol 55, Num 10, pp 2631-2635, issn 0012-186X, 5 p.Article

Wolfram syndrome associated with leukoencephalopathyLABAUGE, Pierre; RENARD, Dimitri; CHAUSSENOT, Annabelle et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 8, issn 0022-3050, p. 928Article

Neurologic Features and Genotype-Phenotype Correlation in Wolfram SyndromeCHAUSSENOT, Annabelle; BANNWARTH, Sylvie; ROUZIER, Cecile et al.Annals of neurology. 2011, Vol 69, Num 3, pp 501-508, issn 0364-5134, 8 p.Article

Radiological findings in Wolfram syndromeHADIDY, Azmy M; JARRAH, Nadim S; AL-TILL, Maha I et al.Saudi medical journal. 2004, Vol 25, Num 5, pp 638-641, issn 0379-5284, 4 p.Article

Hearing Impairment in Genotyped Wolfram Syndrome PatientsPLANTINGA, Rutger F; PENNINGS, Ronald J. E; HUYGEN, Patrick L. M et al.The Annals of otology, rhinology & laryngology. 2008, Vol 117, Num 7, pp 494-500, issn 0003-4894, 7 p.Article

Syndrome de wolfram. À propos de deux cas = Two cases of Wolfram syndromeSAYOUTI, A; BENHADDOU, R; KHOUMIRI, R et al.Journal français d'ophtalmologie. 2007, Vol 30, Num 6, pp 607-609, issn 0181-5512, 3 p.Article

Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome familiesDOMENECH, E; GOMEZ-ZAERA, M; NUNES, V et al.Clinical genetics. 2004, Vol 65, Num 6, pp 463-469, issn 0009-9163, 7 p.Article

Wolfram syndrome and WFS1 geneRIGOLI, L; LOMBARDO, F; DI BELLA, C et al.Clinical genetics. 2011, Vol 79, Num 2, pp 103-117, issn 0009-9163, 15 p.Article

Identification of novel mutations in WFS1 and genotype-phenotype correlation in wolfram syndromeCANO, A; ROUZIER, C; PAQUIS-FLUCKLINGER, V et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 14, pp 1605-1612, issn 1552-4825, 8 p.Article

Ataxie cérébelleuse révélant un syndrome de Wolfram = Wolfram's syndrome presenting as a cerebellar ataxiaMATHIS, S; PAQUIS, V; MESNAGE, V et al.Revue neurologique (Paris). 2007, Vol 163, Num 2, pp 197-204, issn 0035-3787, 8 p.Article

Wolframin mutations and hospitalization for psychiatric illnessSWIFT, M; SWIFT, R. G.Molecular psychiatry. 2005, Vol 10, Num 8, pp 799-803, issn 1359-4184, 5 p.Article

Identification of a male schizophrenic patient carrying a de novo balanced translocation, t(4;13)(p16.1; q21.31)ITOKAWA, Masanari; KASUGA, Takehiko; YOSHIKAWA, Takeo et al.Psychiatry and clinical neurosciences (Carlton. Print). 2004, Vol 58, Num 3, pp 333-337, issn 1323-1316, 5 p.Article

Wolfram syndrome and suicide: Evidence for a role of WFS1 in suicidal and impulsive behaviorSEQUEIRA, Adolfo; KIM, Caroline; ROULEAU, Guy et al.American journal of medical genetics. 2003, Vol 119B, Num 1, pp 108-113, issn 0148-7299, 6 p.Article

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