Mostrando 10 resultados de: 18
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Journal of Clinical Endocrinology and Metabolism(9)
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scopus(18)
Clinical, biochemical, and molecular characterization of macronodular adrenocortical hyperplasia of the zona reticularis: A new syndrome
ArticleAbstract: Context: Macronodular adrenocortical hyperplasia classically presents with progressive hypercortisolPalabras claves:Autores:Carrick K., Ghayee H.K., Miller W.L., Nwariaku F.E., Rainey W.E., Rege J., Richard J. Auchus, Watumull L.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 - More dogma bites the dust
OtherAbstract:Palabras claves:Autores:Miller W.L., Richard J. AuchusFuentes: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:scopusCortisol response to operative stress with anesthesia in healthy children
ArticleAbstract: Background: Supraphysiological "stress dosing" is generally given to adrenally insufficient patientsPalabras claves:Autores:Baskin L.S., Miller W.L., Richard J. Auchus, Taylor L.Fuentes:scopusEnzymatic activities of P450c17 stably expressed in fibroblasts from patients with the polycystic ovary syndrome
ArticleAbstract: Polycystic ovary syndrome (PCOS) is a common endocrine disorder affecting approximately 5-10% of womPalabras claves:Autores:Arlt W., Dunaif A., Geller D.H., Martens J.W.M., Miller W.L., Ossovskaya V.S., Richard J. Auchus, Rodriguez H.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:scopusThe 17, 20-lyase activity of cytochrome P450c17 from human fetal testis favors the Δ<sup>5</sup> steroidogenic pathway
ArticleAbstract: Cytochrome P450c17 catalyzes both 17α-hydroxylation and 17,20-lyase conversion of 21-carbon steroidsPalabras claves:Autores:Flück C.E., Miller W.L., Richard J. AuchusFuentes:scopusThe genetic and functional basis of isolated 17, 20-lyase deficiency
OtherAbstract: Human male sexual differentiation requires production of fetal testicular testosterone, whose biosynPalabras claves:Autores:Geller D.H., Mendonça B.B., Miller W.L., Richard J. AuchusFuentes:scopusThe molecular basis of isolated 17,20 lyase deficiency
Conference ObjectAbstract: Human P450c17 catalyzes the 17α-hydroxylation of pregnenolone to 17OH pregnenolone and of progesteroPalabras claves:Autores:Geller D.H., Miller W.L., Richard J. AuchusFuentes:scopus