Mostrando 10 resultados de: 215
Filtros aplicados
Publisher
Journal of Clinical Endocrinology and Metabolism(41)
Clinical Endocrinology(8)
Endocrinology(7)
European Journal of Endocrinology(7)
Hypertension(7)
Challenges in the assessment and diagnosis of polycystic ovary syndrome
OtherAbstract:Palabras claves:Autores:Chang A.Y., McCartney C., Richard J. Auchus, Straseski J., Wiencek J., Woodworth A.Fuentes:scopusClassics in cardiovascular endocrinology: Aldosterone action beyond electrolytes
OtherAbstract:Palabras claves:Autores:Richard J. AuchusFuentes:scopusClinical advances in the pharmacotherapy of congenital adrenal hyperplasia
ReviewAbstract: Background: Patients with 21-hydroxylase deficiency congenital adrenal hyperplasia (21OHD-CAH) havePalabras claves:Autores:Prete A., Richard J. Auchus, Ross R.J.Fuentes:scopusClinical and Hormonal Response to Mifepristone Therapy in 2 Patients with ACTH-Independent Cushing Syndrome
ArticleAbstract: Objective: Cushing syndrome is an endocrine disorder resulting from prolonged exposure to excess corPalabras claves:Autores:Moraitis A.G., Richard J. AuchusFuentes:scopusClinical and biochemical consequences of CYP17A1 inhibition with abiraterone given with and without exogenous glucocorticoids in castrate men with advanced prostate cancer
ArticleAbstract: Context: Abiraterone acetate is a small-molecule cytochrome P450 17A1 (CYP17A1) inhibitor that is acPalabras claves:Autores:Arlt W., Attard G., Cassidy A.M., De Bono J.S., Dowsett M., Folkerd E., Hughes B.A., Oommen N.B., Reid A.H.M., Richard J. Auchus, Thompson E.Fuentes:scopusClinical implications of androgen synthesis via 5α-reduced precursors
ReviewAbstract: During embryogenesis, the male external genitalia are formed by the action of the potent androgen, dPalabras claves:Autores:Ghayee H.K., Richard J. AuchusFuentes:scopusClinical significance of 11-oxygenated androgens
ReviewAbstract: Purpose of review The adrenal gland is considered a source of weak androgens, such as dehydroepiandrPalabras claves:11-ketotestosterone, 11-oxygenated 19-carbon steroids, 11β-hydroxyandrostenedione, Adrenal, Androgens, castration resistant prostate cancer, Congenital adrenal hyperplasia, polycystic ovarian syndromeAutores:Richard J. Auchus, Turcu A.F.Fuentes:scopusClinical syndromes of hormone receptor mutations: Hormone resistance and independence
ArticleAbstract: Clinical syndromes of hormone resistance or independence have baffled clinicians for decades. ThesePalabras claves:Glycollate, Hormone receptors, Sodium pentosan polysulphateAutores:Fuqua S.A.W., Richard J. AuchusFuentes:scopusClinical, 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:scopusCombined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patien
ArticleAbstract: Congenital adrenal hyperplasia (CAH) resulting from 17α-hydroxylase/17,20-lyase deficiency is a rarePalabras claves:Autores:Costenaro F., Czepielewski M., Kater C.E., Papari-Zareei M., Richard J. Auchus, Rodrigues T.Fuentes:scopus