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Journal of Clinical Endocrinology and Metabolism(5)
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scopus(7)
11-Ketotestosterone Is the Dominant Circulating Bioactive Androgen during Normal and Premature Adrenarche
ArticleAbstract: Context: Adrenarche refers to the rise of dehydroepiandrosterone sulfate (DHEA-S) associated with thPalabras claves:Autores:Auchus G.C., Kasa-Vubu J.Z., Lerario A.M., Rainey W.E., Rege J., Richard J. Auchus, Smith J.M., Turcu A.F., White P.C.Fuentes:scopusCongenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
ReviewAbstract: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders affecting cortisolPalabras claves:21-hydroxylase deficiency, aldosterone, cortisol, CYP21A2, Glucocorticoid, mineralocorticoid, Steroid biosynthesisAutores:Arlt W., Faisal Ahmed S., Falhammar H., Flück C.E., Guasti L., Huebner A., Kortmann B.B.M., Krone N., Merke D.P., Miller W.L., Nordenström A., Reisch N., Richard J. Auchus, Sandberg D.E., Speiser P.W., Stikkelbroeck N.M.M.L., Touraine P., Utari A., van der Grinten H.L.C., White P.C., Wudy S.A.Fuentes:scopusCongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society* clinical practice guideline
ArticleAbstract: Objective: To update the congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency cliPalabras claves:Autores:Arlt W., Baskin L.S., Conway G.S., Merke D.P., Meyer-Bahlburg H.F.L., Miller W.L., Murad M.H., Oberfield S.E., Richard J. Auchus, Speiser P.W., White P.C.Fuentes:scopusAge-dependent increases in adrenal cytochrome b5 and serum 5-androstenediol-3-sulfate
ArticleAbstract: Context: Adrenal production of dehydroepiandrosterone sulfate (DHEA-S) increases throughout childhooPalabras claves:Autores:Karashima S., Kasa-Vubu J.Z., Lerario A.M., Nakamura Y., Rainey W.E., Rege J., Richard J. Auchus, Sasano H., Smith J.M., White P.C.Fuentes:scopusAldosterone Synthase Promoter Polymorphism and Cardiovascular Phenotypes in a Large, Multiethnic Population-Based Study
ArticleAbstract: Background A single-nucleotide polymorphism in the aldosterone synthase gene (CYP11B2) promoter [-34Palabras claves:aldosterone, Genetics, glucose, Hypertension, left ventricular massAutores:Byrd J.B., Richard J. Auchus, White P.C.Fuentes:scopusErratum: Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society clinical practice guideline (The Journal of Clinical Endocrinology and Metabolism (2018) 103:11 (4043-4088) DOI: 10.1210/jc.2018-01865)
OtherAbstract: The above-mentioned guideline by Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, MePalabras claves:Autores:Arlt W., Baskin L.S., Conway G.S., Merke D.P., Meyer-Bahlburg H.F.L., Miller W.L., Murad M.H., Oberfield S.E., Richard J. Auchus, Speiser P.W., White P.C.Fuentes:scopusResponse to letter to the editor: “Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society clinical practice guideline”
OtherAbstract:Palabras claves:Autores:Merke D.P., Miller W.L., Richard J. Auchus, Speiser P.W., White P.C.Fuentes:scopus