Documentos de El-Maouche D. | REDI

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Mostrando 4 resultados de: 4

Subtipo de publicación

Publisher

European Journal of Endocrinology(2)

Frontiers in Endocrinology(1)

Journal of Clinical Endocrinology and Metabolism(1)

Área temáticas

Enfermedades(4)

Farmacología y terapéutica(3)

Fisiología humana(2)

Ginecología, obstetricia, pediatría, geriatría(1)

Área de conocimiento

Medicina interna(2)

Ensayo clínico(1)

Año de Publicación

Origen

Palabras Claves

Clinical trial(1)

Congenital adrenal hyperplasia(1)

adrenal hypertrophy(1)

Androgen excess and diagnostic steroid biomarkers for nonclassic 21-hydroxylase deficiency without cosyntropin stimulation

Abstract: Objectives: The clinical presentation of patients with nonclassic 21-hydroxylase deficiency (N21OHD)

Palabras claves:

El-Maouche D., Gaynor A., Merke D.P., Nanba A.T., Richard J. Auchus, Turcu A.F., Veeraraghavan P., Zhao L.

A Phase 2, Multicenter Study of Nevanimibe for the Treatment of Congenital Adrenal Hyperplasia

Abstract: Context: Patients with classic congenital adrenal hyperplasia (CAH) often require supraphysiologic g

Palabras claves:

adrenal hypertrophy, ATR-101, Clinical trial, Congenital adrenal hyperplasia, nevanimibe

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.

Erratum: 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)

Abstract: The authors apologise for an error in Table 2 of the above article published in the July 2020 issue

Palabras claves:

El-Maouche D., Gaynor A., Merke D.P., Nanba A.T., Richard J. Auchus, Turcu A.F., Veeraraghavan P., Zhao L.

Treatment patterns and unmet needs in adults with classic congenital adrenal hyperplasia: A modified Delphi consensus study

Abstract: Background: Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a rare

Palabras claves:

classic CAH, classic congenital adrenal hyperplasia, glucocorticoid management, treatment complication, unmet needs

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.