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Neuroimmunomodulation|December 13, 2007
From Neuroendocrinology to Neuroimmunomodulation - a tribute to Prof. Dr. Samuel McCannStefan R Bornstein
European Journal of Medical Genetics|January 2, 2014
Transforming growth factor-β (TGF-β) pathway abnormalities in tenascin-X deficiency associated with CAH-X syndromeRachel Morissette, Deborah P Merke, Nazli B McDonnell
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2005
Adrenocorticotropin hypersecretion and pituitary microadenoma following bilateral adrenalectomy in a patient with classic 21-hydroxylase deficiencyEvangelia Charmandari, George P Chrousos, Deborah P Merke
Lancet (London, England)|June 4, 2017
Congenital adrenal hyperplasiaDiala El-Maouche, Wiebke Arlt, Deborah P Merke
Endocrinology and Metabolism Clinics of North America|May 7, 2017
Genetics of Congenital Adrenal HyperplasiaFady Hannah-Shmouni, Wuyan Chen, Deborah P Merke
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice GuidelineStefan R Bornstein, Bruno Allolio, Wiebke Arlt, et al.
Reviews in Endocrine & Metabolic Disorders|November 18, 2022
The management of congenital adrenal hyperplasia during preconception, pregnancy, and postpartumJacqueline Yano Maher, Veronica Gomez-Lobo, Deborah P Merke
The Journal of Molecular Diagnostics : JMD|September 28, 2013
Comprehensive mutation analysis of the CYP21A2 gene: an efficient multistep approach to the molecular diagnosis of congenital adrenal hyperplasiaZhi Xu, Wuyan Chen, Deborah P Merke, et al.
Journal of the Endocrine Society|December 22, 2017
Congenital Adrenal Hyperplasia Presenting as an Adrenal Mass With Increased <sup>18</sup>F-FDG Positron Emission Tomography UptakeAshwini Mallappa, Corina M Millo, Martha Quezado, et al.
Reviews in Endocrine & Metabolic Disorders|November 19, 2024
GHRH in diabetes and metabolismCharlotte Steenblock, Stefan R Bornstein
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