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Lancet (London, England)|June 21, 2005
Congenital adrenal hyperplasiaDeborah P Merke, Stefan R BornsteinAnnals of Internal Medicine|February 19, 2002
NIH conference. Future directions in the study and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyDeborah P Merke, Stefan R Bornstein, Nilo A Avila, et al.The Journal of Clinical Endocrinology and Metabolism|May 8, 2002
Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: potential clinical implicationsEvangelia Charmandari, Martina Weise, Stefan R Bornstein, 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 MerkeNature Reviews. Endocrinology|April 12, 2022
Management challenges and therapeutic advances in congenital adrenal hyperplasiaAshwini Mallappa, Deborah P MerkeSeminars in Reproductive Medicine|June 17, 2009
Cardiovascular disease risk in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMimi S Kim, Deborah P MerkeThe Lancet. Diabetes & Endocrinology|March 14, 2014
Management of adolescents with congenital adrenal hyperplasiaDeborah P Merke, Dix P PoppasHormone Research in Paediatrics|May 8, 2018
Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X SyndromeWalter L Miller, Deborah P MerkeThe Journal of Molecular Diagnostics : JMD|June 24, 2019
High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal HyperplasiaQizong Lao, Brittany Brookner, Deborah P MerkeThe Journal of Clinical Endocrinology and Metabolism|November 5, 2002
Pubertal and gender-related changes in the sympathoadrenal system in healthy childrenMartina Weise, Graeme Eisenhofer, Deborah P MerkePageof 56