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Journal of Clinical Endocrinology and Metabolism(10)
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scopus(20)
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: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:scopusRole of cytochrome b<inf>5</inf> in the 17,20-lyase activity of P450c17 [3]
OtherAbstract:Palabras claves:Autores:Miller W.L., Richard J. AuchusFuentes:scopusMedroxyprogesterone acetate and dexamethasone are competitive inhibitors of different human steroidogenic enzymes
ArticleAbstract: Medroxyprogesterone acetate (MPA), a widely used progestin, can suppress the hypothalamic-pituitary-Palabras claves:Autores:Lee T.C., Miller W.L., Richard J. AuchusFuentes:scopus