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Article(2)
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Arquivos Brasileiros de Endocrinologia e Metabologia(1)
Journal of Clinical Endocrinology and Metabolism(1)
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scopus(2)
Distinctive profile of the 17-hydroxylase and 17,20-lyase activities revealed by urinary steroid metabolomes of patients with CYP17 deficiency
ArticleAbstract: Objectives: (1) Characterize serum (S) and urinary (U) steroid metabolites in complete CYP17 deficiePalabras claves:17, 17-hydroxylase deficiency, 20-lyase deficiency, Congenital adrenal hyperplasia, Corticosterone, CYP17, Urinary steroid metabolomeAutores:Kater C.E., Neres M.S., Richard J. Auchus, Shackleton C.H.L.Fuentes:scopusTwo Prevalent CYP17 Mutations and Genotype-Phenotype Correlations in 24 Brazilian Patients with 17-Hydroxylase Deficiency
ArticleAbstract: We performed molecular genetic analysis of 24 subjects from 19 families with 17-hydroxylase deficienPalabras claves:Autores:Costa-Santos M., Kater C.E., Richard J. AuchusFuentes:scopus