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Journal of Clinical Endocrinology and Metabolism(15)
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scopus(49)
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: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 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:scopusAssociation of Maternal-Neonatal Steroids with Early Pregnancy Endocrine Disrupting Chemicals and Pregnancy Outcomes
ArticleAbstract: Context: Steroids play an important role in fetal development and parturition. Gestational exposuresPalabras claves:Developmental programming, Endocrine disrupting chemical, Estradiol, Pregnancy, steroids, TestosteroneAutores:Banker M., Dolinoy D.C., Domino S.E., Goodrich J.M., Kelley A.S., O'Day P.J., Padmanabhan V., Puttabyatappa M., Richard J. Auchus, Smith Y.R., Song P.X.K.Fuentes:scopus11-Oxygenated C<inf>19</inf> Steroids Do Not Decline with Age in Women
ArticleAbstract: The ovaries and adrenals are sources of androgens in women. Although dehydroepiandrosterone (DHEA),Palabras claves:Autores:Nanba A.T., Rainey W.E., Rege J., Ren J., Richard J. Auchus, Turcu A.F.Fuentes:scopus11-Oxygenated androgens are biomarkers of adrenal volume and testicular adrenal rest tumors in 21-hydroxylase deficiency
ArticleAbstract: Context: Patients with 21-hydroxylase deficiency (21OHD) have long-term complications, resulting froPalabras claves:Autores:Avila N.A., Elman M.S., Mallappa A., Marko J., Merke D.P., Rao H., Richard J. Auchus, Tsodikov A., Turcu A.F.Fuentes:scopus46,XX DSD: The masculinised female
ReviewAbstract: The 46,XX disorders of sex development (DSDs) cause virilisation or masculinisation of the female foPalabras claves:46,XX DSD, Adrenal gland, androgen, Congenital adrenal hyperplasia, steroidogenesis, VirilisationAutores:Chang A.Y., Richard J. AuchusFuentes:scopusA Phase 2, Multicenter Study of Nevanimibe for the Treatment of Congenital Adrenal Hyperplasia
ArticleAbstract: Context: Patients with classic congenital adrenal hyperplasia (CAH) often require supraphysiologic gPalabras claves:adrenal hypertrophy, ATR-101, Clinical trial, Congenital adrenal hyperplasia, nevanimibeAutores:Chang A.Y., El-Maouche D., Joyal E.G., Lin V.H., Merke D.P., Mohideen P., Plaunt M.R., Richard J. Auchus, Turcu A.F., Vogiatzi M.G., Weintraub L.Fuentes:scopusA novel point mutation in P450c17 (CYP17) causing combined 17α-hydroxylase/17,20-lyase deficiency
ArticleAbstract: Context: Combined 17α-hydroxylase/17,20-lyase deficiency is a rare cause of congenital adrenal hyperPalabras claves:Autores:Achermann J.C., Ahmad T., Brooke A.M., Gore M.E., Lin L., Monson J.P., Papari-Zareei M., Richard J. Auchus, Rumsby G., Shepherd J.H., Taylor N.F.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:scopus