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au.\*:("HOUANG, Muriel")

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IGF type 1 receptor ligand binding characteristics are altered in a subgroup of children with intrauterine growth retardationDUCOS, Bertrand; CABROL, Sylvie; HOUANG, Muriel et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 11, pp 5516-5524, issn 0021-972XArticle

Serum adiponectin and leptin concentrations in HIV-infected children with fat redistribution syndromeVERKAUSKIENE, Rasa; DOLLFUS, Catherine; LEVINE, Martine et al.Pediatric research. 2006, Vol 60, Num 2, pp 225-230, issn 0031-3998, 6 p.Article

11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical russell-silver syndrome : Clinical scoring system and epigenetic-phenotypic correlationsNETCHINE, Irène; ROSSIGNOL, Sylvie; RAUX DEMAY, Marie-Charles et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 8, pp 3148-3154, issn 0021-972X, 7 p.Article

Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain DevelopmentNETCHINE, Irène; AZZI, Salah; GODEAU, François et al.The Journal of clinical endocrinology and metabolism. 2009, Vol 94, Num 10, pp 3913-3921, issn 0021-972X, 9 p.Article

Autoimmune polyendocrinopathy-candidiasis- ectodermal dystrophy syndrome with renal failure : Impact of posttransplant immunosuppression on disease activityULINSKI, Tim; PERRIN, Laurence; MORRIS, Michael et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 1, pp 192-195, issn 0021-972X, 4 p.Article

Longitudinal evaluation and risk factors of lipodystrophy and associated metabolic changes in HIV-infected childrenBEREGSZASZI, Marta; DOLLFUS, Catherine; BLANCHE, Stéphane et al.Journal of acquired immune deficiency syndromes (1999). 2005, Vol 40, Num 2, pp 161-168, issn 1525-4135, 8 p.Article

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populationsALBERT, Sébastien; BLONS, Hélène; DELOBEL, Bruno et al.European journal of human genetics. 2006, Vol 14, Num 6, pp 773-779, issn 1018-4813, 7 p.Article

Perrault Syndrome : Report of Four New Cases, Review and Exclusion of Candidate GenesMARLIN, Sandrine; LACOMBE, Didier; FELDMANN, Delphine et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 5, pp 661-664, issn 1552-4825, 4 p.Article

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndromeGICQUEL, Christine; ROSSIGNOL, Sylvie; BERTRAND, Anne-Marie et al.Nature genetics. 2005, Vol 37, Num 9, pp 1003-1007, issn 1061-4036, 5 p.Article

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