Mostrando 10 resultados de: 12
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Journal of Clinical Endocrinology and Metabolism(6)
Endocrine Reviews(2)
Journal of Steroid Biochemistry and Molecular Biology(1)
Nature Genetics(1)
Seminars in Reproductive Medicine(1)
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Fisiología humana(7)
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scopus(12)
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:scopusDefects in androgen biosynthesis causing 46,XY disorders of sexual development
ArticleAbstract: At least one genetic defect in each reaction of the classical androgen biosynthesis pathway has beenPalabras claves:46 XY DSD, androgen, Congenital adrenal hyperplasia, Enzyme, Steroid, steroidogenesis, Testis, TestosteroneAutores:Miller W.L., Richard J. AuchusFuentes:scopusAdrenocortical carcinoma in a 17th-century girl
ReviewAbstract: Adrenocortical carcinoma (ACC) is a rare, often fatal disease, that may be seen sporadically or withPalabras claves:Adrenal, AUTOPSY, Cáncer, Cushing syndrome, PediatricsAutores:Else T., Miller W.L., Richard J. AuchusFuentes: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: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: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:scopus