Mostrando 10 resultados de: 10
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Enfermedades(7)
Fisiología humana(6)
Farmacología y terapéutica(5)
Ginecología, obstetricia, pediatría, geriatría(2)
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scopus(10)
Circadian rhythms of 11-oxygenated C19 steroids and Δ5-steroid sulfates in healthy men
ArticleAbstract: Background: Many hormones display distinct circadian rhythms, driven by ce ntral regulators, hormonaPalabras claves:Autores:Chen X., Rainey W.E., Rege J., Richard J. Auchus, Turcu A.F., Veldhuis J.D., Yang R., Zhao L.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: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:scopusAbiraterone acetate treatment lowers 11-oxygenated androgens
ArticleAbstract: Context: The human adrenal is the dominant source of androgens in castration-resistant prostate cancPalabras claves:Autores:Alyamani M., O'Day P.J., Richard J. Auchus, Sharifi N., Wright C.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:scopusGene expression profiles in aldosterone-producing adenomas and adjacent adrenal glands
ArticleAbstract: Background: Primary aldosteronism (PA) is the most common form of endocrine hypertension affecting ∼Palabras claves:Autores:Edwards M.A., Morimoto R., Nakamura Y., Rainey W.E., Richard J. Auchus, Sasano H., Satoh F., Wang T.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:scopusLevoketoconazole treatment in endogenous Cushing’s syndrome: extended evaluation of clinical, biochemical, and radiologic outcomes
ArticleAbstract: Objective: This extended evaluation (EE) of the SONICS study assessed the effects of levoketoconazolPalabras claves:Autores:Biller B.M.K., Buchfelder M., Cohen F., Feldt-Rasmussen U., Fleseriu M., Geer E.B., Greenman Y., Heaney A.P., Kennedy L., Pivonello R., Richard J. Auchus, Salvatori R., Zacharieva S.Fuentes:scopusLong-term outcomes of osilodrostat in Cushing’s disease: LINC 3 study extension
ArticleAbstract: Objective: To investigate the long-term efficacy and tolerability of osilodrostat, a potent oral 11βPalabras claves:Autores:Belaya Z., Biller B.M.K., Feelders R.A., Fleseriu M., Houde G., Izquierdo M., Newell-Price J., Pedroncelli A.M., Pivonello R., Richard J. Auchus, Roughton M., Scaroni C., Shimatsu A., Vila G., Walia R.Fuentes:scopusPuberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair
ArticleAbstract: Objective: 17-Hydroxylase/17,20-lyase deficiency (17OHD) results from mutations in the CYP17A1 gene,Palabras claves:Autores:Akcay T., Bereket A., Guran T., Papari-Zareei M., Richard J. Auchus, Turan S.Fuentes:scopus