Mostrando 10 resultados de: 15
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Journal of Clinical Endocrinology and Metabolism(4)
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scopus(15)
Androgen biosynthesis and gene defects
Book PartAbstract: Formation of the male external genitalia in human beings requires the production of dihydrotestosterPalabras claves:androgen, Cytochrome p450, Dehydrogenase, Dihydrotestosterone, Disorder of sex development, External genitalia, Hydroxysteroid, Hypogonadism, steroidogenesis, Testis, Testosterone, VirilizationAutores:Richard J. Auchus, Turcu A.F.Fuentes:scopusAndrogen excess and diagnostic steroid biomarkers for nonclassic 21-hydroxylase deficiency without cosyntropin stimulation
ArticleAbstract: Objectives: The clinical presentation of patients with nonclassic 21-hydroxylase deficiency (N21OHD)Palabras claves:Autores:El-Maouche D., Gaynor A., Merke D.P., Nanba A.T., Richard J. Auchus, Turcu A.F., Veeraraghavan P., Zhao L.Fuentes:scopus24-Hour Profiles of 11-Oxygenated C<inf>19</inf> Steroids and Δ<sup>5</sup>-Steroid Sulfates during Oral and Continuous Subcutaneous Glucocorticoids in 21-Hydroxylase Deficiency
ArticleAbstract: Background: Optimal management of androgen excess in 21-hydroxylase deficiency (21OHD) remains challPalabras claves:11-oxyandrogens, 21-hydroxylase deficiency, CAH, Circadian hormones, Congenital adrenal hyperplasia, cortisol 24-hour profileAutores:Byrd J.B., Chen X., Mallappa A., Merke D.P., Nanba A.T., Nella A.A., Richard J. Auchus, Turcu A.F., Zhao L.Fuentes: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:scopusCytochrome b<inf>5</inf> Activates the 17,20-Lyase Activity of Human Cytochrome P450 17A1 by Increasing the Coupling of NADPH Consumption to Androgen Production
ArticleAbstract: Human cytochrome P450 17A1 is required for all androgen biosynthesis and is the target of abirateronPalabras claves:Autores:Im S.C., Pearl N.M., Peng H.M., Rege J., Richard J. Auchus, Turcu A.F., Waskell L.Fuentes:scopusApproach to the Patient with Primary Aldosteronism: Utility and Limitations of Adrenal Vein Sampling
ArticleAbstract: Several studies over the past 3 decades document a higher prevalence of primary aldosteronism (PA) aPalabras claves:Adrenal, Adrenal vein sampling, aldosterone, Hypertension, primary aldosteronismAutores:Richard J. Auchus, Turcu A.F.Fuentes:scopusAdrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency
ArticleAbstract: Objective: To comprehensively characterize androgens and androgen precursors in classic 21-hydroxylaPalabras claves:Autores:Chomic R., Giordano T.J., Merke D.P., Nanba A.T., Rainey W.E., Richard J. Auchus, Shields J.J., Turcu A.F., Upadhyay S.K.Fuentes:scopusAdrenocorticotropin acutely regulates pregnenolone sulfate production by the human adrenal in vivo and in vitro
ArticleAbstract: Background: Dehydroepiandrosterone sulfate (DHEAS) is the most abundant steroid in human circulationPalabras claves:Autores:Nanba A.T., Peng H.M., Rainey W.E., Rege J., Ren J., Richard J. Auchus, Turcu A.F.Fuentes:scopusErratum: Androgen excess and diagnostic steroid biomarkers for nonclassic 21-hydroxylase deficiency without cosyntropin stimulation (European Journal of Endocrinology (2020) 18:1 (63-71) DOI: 10.1530/EJE-20-0129)
OtherAbstract: The authors apologise for an error in Table 2 of the above article published in the July 2020 issuePalabras claves:Autores:El-Maouche D., Gaynor A., Merke D.P., Nanba A.T., Richard J. Auchus, Turcu A.F., Veeraraghavan P., Zhao L.Fuentes:scopusNovel treatment strategies in congenital adrenal hyperplasia
ReviewAbstract: Purpose of review In recent years, important steps have been taken to improve the treatment of congePalabras claves:21-hydroxylase deficiency, Abiraterone acetate, Congenital adrenal hyperplasia, glucocorticoidsAutores:Richard J. Auchus, Turcu A.F.Fuentes:scopus