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Deborah P Merke

Showing results (61-70 of 112) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|May 6, 2024
CAHQL: A Patient-Reported Outcome Instrument to Assess Health-Related Quality of Life in Congenital Adrenal HyperplasiaMyrto Eleni Flokas, Li Yang, Kimberly R Middleton, et al.
European Journal of Endocrinology|September 3, 2010
Psychiatric characterization of children with genetic causes of hyperandrogenismSven C Mueller, Pamela Ng, Ninet Sinaii, et al.
Journal of the Endocrine Society|December 22, 2017
Alterations in Hydrocortisone Pharmacokinetics in a Patient With Congenital Adrenal Hyperplasia Following Bariatric SurgeryAshwini Mallappa, Aikaterini A Nella, Parag Kumar, et al.
Psychoneuroendocrinology|December 29, 2007
Steroid abnormalities and the developing brain: declarative memory for emotionally arousing and neutral material in children with congenital adrenal hyperplasiaFrançoise S Maheu, Deborah P Merke, Elizabeth A Schroth, 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.
Human Mutation|June 15, 2016
Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal HyperplasiaWuyan Chen, Ashley F Perritt, Rachel Morissette, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2004
Endocrinologic and psychologic evaluation of 21-hydroxylase deficiency carriers and matched normal subjects: evidence for physical and/or psychologic vulnerability to stressEvangelia Charmandari, Deborah P Merke, Paulo J Negro, et al.
Psychoneuroendocrinology|August 25, 2012
Incentive processing in Congenital Adrenal Hyperplasia (CAH): a reward-based antisaccade studySven C Mueller, Teresa Daniele, Jessica MacIntyre, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiencyEvangelia Charmandari, Graeme Eisenhofer, Sarah L Mehlinger, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2017
11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase DeficiencyAdina F Turcu, Ashwini Mallappa, Meredith S Elman, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

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Pageof 12
The Journal of Clinical Endocrinology and Metabolism|May 6, 2024
CAHQL: A Patient-Reported Outcome Instrument to Assess Health-Related Quality of Life in Congenital Adrenal HyperplasiaMyrto Eleni Flokas, Li Yang, Kimberly R Middleton, et al.
European Journal of Endocrinology|September 3, 2010
Psychiatric characterization of children with genetic causes of hyperandrogenismSven C Mueller, Pamela Ng, Ninet Sinaii, et al.
Journal of the Endocrine Society|December 22, 2017
Alterations in Hydrocortisone Pharmacokinetics in a Patient With Congenital Adrenal Hyperplasia Following Bariatric SurgeryAshwini Mallappa, Aikaterini A Nella, Parag Kumar, et al.
Psychoneuroendocrinology|December 29, 2007
Steroid abnormalities and the developing brain: declarative memory for emotionally arousing and neutral material in children with congenital adrenal hyperplasiaFrançoise S Maheu, Deborah P Merke, Elizabeth A Schroth, 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.
Human Mutation|June 15, 2016
Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal HyperplasiaWuyan Chen, Ashley F Perritt, Rachel Morissette, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2004
Endocrinologic and psychologic evaluation of 21-hydroxylase deficiency carriers and matched normal subjects: evidence for physical and/or psychologic vulnerability to stressEvangelia Charmandari, Deborah P Merke, Paulo J Negro, et al.
Psychoneuroendocrinology|August 25, 2012
Incentive processing in Congenital Adrenal Hyperplasia (CAH): a reward-based antisaccade studySven C Mueller, Teresa Daniele, Jessica MacIntyre, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiencyEvangelia Charmandari, Graeme Eisenhofer, Sarah L Mehlinger, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2017
11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase DeficiencyAdina F Turcu, Ashwini Mallappa, Meredith S Elman, et al.
Pageof 12