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Lancet (London, England)|June 4, 2017
Congenital adrenal hyperplasiaDiala El-Maouche, Wiebke Arlt, Deborah P MerkeClinical Endocrinology|May 28, 2014
Cortical bone mineral density in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyDiala El-Maouche, Suzanne Collier, Mala Prasad, et al.Journal of the Endocrine Society|November 21, 2019
Individualizing Management of Infertility in Classic Congenital Adrenal Hyperplasia and Testicular Adrenal Rest TumorsSmita Jha, Diala El-Maouche, Jamie Marko, et al.The Journal of Clinical Endocrinology and Metabolism|March 28, 2018
Longitudinal Assessment of Illnesses, Stress Dosing, and Illness Sequelae in Patients With Congenital Adrenal HyperplasiaDiala El-Maouche, Courtney J Hargreaves, Ninet Sinaii, et al.The Journal of Clinical Endocrinology and Metabolism|March 7, 2021
Cardiovascular Disease Risk Factors and Metabolic Morbidity in a Longitudinal Study of Congenital Adrenal HyperplasiaAhmed Torky, Ninet Sinaii, Smita Jha, et al.Clinical Endocrinology|April 20, 2019
Adrenal morphology and associated comorbidities in congenital adrenal hyperplasiaDiala El-Maouche, Fady Hannah-Shmouni, Ashwini Mallappa, et al.European Journal of Endocrinology|June 4, 2020
Androgen excess and diagnostic steroid biomarkers for nonclassic 21-hydroxylase deficiency without cosyntropin stimulationAdina F Turcu, Diala El-Maouche, Lili Zhao, et al.Pharmacotherapy|November 25, 2005
Decreased persistence to cholinesterase inhibitor therapy with concomitant use of drugs that can impair cognitionStephen J Kogut, Diala El-Maouche, Susan M AbughoshThe Journal of Clinical Endocrinology and Metabolism|June 27, 2020
A Phase 2, Multicenter Study of Nevanimibe for the Treatment of Congenital Adrenal HyperplasiaDiala El-Maouche, Deborah P Merke, Maria G Vogiatzi, et al.The Journal of Clinical Endocrinology and Metabolism|March 8, 2008
Approach to the adult with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyDeborah P MerkePageof 40