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European Journal of Endocrinology(3)
Journal of Clinical Endocrinology and Metabolism(3)
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scopus(9)
11-Oxygenated Androgens Useful in the Setting of Discrepant Conventional Biomarkers in 21-Hydroxylase Deficiency
ArticleAbstract: Context: Serum 17-hydroxyprogesterone (17OHP) and androstenedione (A4) are the conventional biomarkePalabras claves:alternate androgens, androgen excess, Biomarkers, Congenital adrenal hyperplasia, monitoring therapy, steroidogenesisAutores:Brookner B., Jha S., Merke D.P., Richard J. Auchus, Sinaii N., 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: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: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: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:scopusCorrection to: Tildacerfont in Adults With Classic Congenital Adrenal Hyperplasia: Results from Two Phase 2 Studies (The Journal of Clinical Endocrinology and Metabolism (2021) 106:11 (e4666-e4679) DOI: 10.1210/clinem/dgab438)
OtherAbstract: Table 2 contained an error in the listed dose. For cohort B, the dose was incorrectly listed as 200Palabras claves:Autores:Barnes C.N., Huang M., Imel E.A., Madu I.J., Merke D.P., Moriarty D., Nakhle S., Newfield R.S., Richard J. Auchus, Sarafoglou K., Vogiatzi M.G.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: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:scopusExcess 11-Oxygenated Androgens in Women With Severe Insulin Resistance Are Mediated by Adrenal Insulin Receptor Signaling
ArticleAbstract: Context: Syndromes of severe insulin resistance (SIR) include insulin receptoropathy, in which all sPalabras claves:11-oxygenated androgens, hyperandrogenism, insulin receptor, Lipodystrophy, ovaries, severe insulin resistanceAutores:Abel B.S., Brown R.J., Jha S., Merke D.P., Richard J. Auchus, Turcu A.F., Walzer D.Fuentes:scopus