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Androgen 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: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:scopusRefining the Definitions of Biochemical and Clinical Cure for Primary Aldosteronism Using the Primary Aldosteronism Surgical Outcome (PASO) Classification System
ArticleAbstract: Introduction: Determination of outcomes after adrenalectomy for primary aldosteronism (PA) is limitePalabras claves:Autores:Cohen M.S., Gauger P.G., Hughes D.T., Miller B.S., Nanba A.T., Richard J. Auchus, Turcu A.F.Fuentes:scopusThe Rise, Fall, and Resurrection of 11-Oxygenated Androgens in Human Physiology and Disease
ReviewAbstract: The 11-oxyandrogens, particularly 11-ketotestosterone, have been recognized as a biologically importPalabras claves:11-Hydroxylase, 21-hydroxylase deficiency, adrenal glands, adrenarche, androgenAutores:Nanba A.T., Richard J. Auchus, Turcu A.F.Fuentes:scopusThree Discrete Patterns of Primary Aldosteronism Lateralization in Response to Cosyntropin during Adrenal Vein Sampling
ArticleAbstract: Cosyntropin [ACTH (1-24)] stimulation during adrenal vein (AV) sampling (AVS) enhances the confidencPalabras claves:Autores:Nanba A.T., Nanba K., Rainey W.E., Richard J. Auchus, Shields J.J., Turcu A.F., Wannachalee T., Zhao L.Fuentes:scopus