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Congenital 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:scopusLong-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia
ArticleAbstract: Purpose: To study the current practice for assessing comorbidity in adults with 21-hydroxylase CAH aPalabras claves:21-hydroxylase deficiency, Co-morbidities, Congenital adrenal hyperplasia, outcome, registryAutores:Ahmed S.F., Ali S.R., Bachega T.A.S.S., Baronio F., Bonfig W., Bryce J., Ceccato F., Cools M., Costa E.C., Daniel E., Falhammar H., Guaragna-Filho G., Iotova V., Markosyan R., Miranda M.C., Richard J. Auchus, Righi B., Ross R.J., Russo G., Stancampiano M.R., Tomlinson J.W., T’Sjoen G.Fuentes:scopusTreatment patterns and unmet needs in adults with classic congenital adrenal hyperplasia: A modified Delphi consensus study
ArticleAbstract: Background: Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a rarePalabras claves:classic CAH, classic congenital adrenal hyperplasia, glucocorticoid management, treatment complication, unmet needsAutores:Anatchkova M., Courtillot C., Cutts K., Dobs A., El-Maouche D., Falhammar H., Farrar M., Lacroix A., Lamotte M., O’Donoghue C., Richard J. Auchus, Taylor N., Touraine P., Yonan C.Fuentes:scopus