Documentos de Falhammar H. | REDI

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Área de conocimiento: "Medicina interna"

Subtipo de publicación

Publisher

Frontiers in Endocrinology(1)

Área temáticas

Enfermedades(2)

Área de conocimiento

Año de Publicación

Origen

Palabras Claves

21-hydroxylase deficiency(1)

Co-morbidities(1)

Congenital adrenal hyperplasia(1)

classic congenital adrenal hyperplasia(1)

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Abstract: Purpose: To study the current practice for assessing comorbidity in adults with 21-hydroxylase CAH a

Palabras claves:

21-hydroxylase deficiency, Co-morbidities, Congenital adrenal hyperplasia, outcome, registry

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.

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.