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Deborah P Merke

Showing results (41-50 of 112) with videos related to

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Clinical Endocrinology|January 28, 2009
Quality of life in children and adolescents 1-year after cure of Cushing syndrome: a prospective studyMargaret F Keil, Deborah P Merke, Roma Gandhi, et al.
Journal of Child and Adolescent Psychopharmacology|February 24, 2009
Early hyperandrogenism affects the development of hippocampal function: preliminary evidence from a functional magnetic resonance imaging study of boys with familial male precocious pubertySven C Mueller, Darcy Mandell, Ellen W Leschek, et al.
The Journal of Clinical Endocrinology and Metabolism|May 31, 2007
Patients with classic congenital adrenal hyperplasia have decreased epinephrine reserve and defective glycemic control during prolonged moderate-intensity exerciseLiza Green-Golan, Catherine Yates, Bart Drinkard, 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.
American Journal of Medical Genetics. Part A|November 19, 2009
The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: quadricuspid aortic valve and other midline defectsWuyan Chen, Mimi S Kim, Sujata Shanbhag, et al.
The Journal of Clinical Endocrinology and Metabolism|March 23, 2023
Interpretation of Steroid Biomarkers in 21-Hydroxylase Deficiency and Their Use in Disease ManagementKyriakie Sarafoglou, Deborah P Merke, Nicole Reisch, et al.
CPT: Pharmacometrics & Systems Pharmacology|July 27, 2025
Predicting Residual 21-Hydroxylase Enzymatic Activity in Pediatric and Adult Congenital Adrenal Hyperplasia Patients: Towards Individualized TherapyDavide Bindellini, Robin Michelet, Yersultan Mirasbekov, et al.
The Journal of Clinical Endocrinology and Metabolism|October 6, 2025
Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-Hydroxylase Deficiency in 457 IndividualsQizong Lao, Annie Schulman, Sarah Kulkarni, 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.
Clinical Endocrinology|June 28, 2016
Androgens correlate with increased erythropoiesis in women with congenital adrenal hyperplasiaNayananjani Karunasena, Thang S Han, Ashwini Mallappa, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

Sort By:
Pageof 12
Clinical Endocrinology|January 28, 2009
Quality of life in children and adolescents 1-year after cure of Cushing syndrome: a prospective studyMargaret F Keil, Deborah P Merke, Roma Gandhi, et al.
Journal of Child and Adolescent Psychopharmacology|February 24, 2009
Early hyperandrogenism affects the development of hippocampal function: preliminary evidence from a functional magnetic resonance imaging study of boys with familial male precocious pubertySven C Mueller, Darcy Mandell, Ellen W Leschek, et al.
The Journal of Clinical Endocrinology and Metabolism|May 31, 2007
Patients with classic congenital adrenal hyperplasia have decreased epinephrine reserve and defective glycemic control during prolonged moderate-intensity exerciseLiza Green-Golan, Catherine Yates, Bart Drinkard, 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.
American Journal of Medical Genetics. Part A|November 19, 2009
The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: quadricuspid aortic valve and other midline defectsWuyan Chen, Mimi S Kim, Sujata Shanbhag, et al.
The Journal of Clinical Endocrinology and Metabolism|March 23, 2023
Interpretation of Steroid Biomarkers in 21-Hydroxylase Deficiency and Their Use in Disease ManagementKyriakie Sarafoglou, Deborah P Merke, Nicole Reisch, et al.
CPT: Pharmacometrics & Systems Pharmacology|July 27, 2025
Predicting Residual 21-Hydroxylase Enzymatic Activity in Pediatric and Adult Congenital Adrenal Hyperplasia Patients: Towards Individualized TherapyDavide Bindellini, Robin Michelet, Yersultan Mirasbekov, et al.
The Journal of Clinical Endocrinology and Metabolism|October 6, 2025
Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-Hydroxylase Deficiency in 457 IndividualsQizong Lao, Annie Schulman, Sarah Kulkarni, 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.
Clinical Endocrinology|June 28, 2016
Androgens correlate with increased erythropoiesis in women with congenital adrenal hyperplasiaNayananjani Karunasena, Thang S Han, Ashwini Mallappa, et al.
Pageof 12