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The Journal of Clinical Endocrinology and Metabolism
|
March 8, 2008
Approach to the adult with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Deborah P Merke
Nature Reviews. Endocrinology
|
April 12, 2022
Management challenges and therapeutic advances in congenital adrenal hyperplasia
Ashwini Mallappa, Deborah P Merke
Seminars in Reproductive Medicine
|
June 17, 2009
Cardiovascular disease risk in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Mimi S Kim, Deborah P Merke
The Lancet. Diabetes & Endocrinology
|
March 14, 2014
Management of adolescents with congenital adrenal hyperplasia
Deborah P Merke, Dix P Poppas
Hormone Research in Paediatrics
|
May 8, 2018
Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome
Walter L Miller, Deborah P Merke
Lancet (London, England)
|
June 21, 2005
Congenital adrenal hyperplasia
Deborah P Merke, Stefan R Bornstein
The 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 Hyperplasia
Qizong Lao, Brittany Brookner, Deborah P Merke
The Journal of Clinical Endocrinology and Metabolism
|
November 5, 2002
Pubertal and gender-related changes in the sympathoadrenal system in healthy children
Martina Weise, Graeme Eisenhofer, Deborah P Merke
European Journal of Medical Genetics
|
January 2, 2014
Transforming growth factor-β (TGF-β) pathway abnormalities in tenascin-X deficiency associated with CAH-X syndrome
Rachel 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 deficiency
Evangelia Charmandari, George P Chrousos, Deborah P Merke
Page
of 12
Search research articles
Search
Showing results (1-10 of 112) with videos related to
Sort By:
Page
of 12
The Journal of Clinical Endocrinology and Metabolism
|
March 8, 2008
Approach to the adult with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Deborah P Merke
Nature Reviews. Endocrinology
|
April 12, 2022
Management challenges and therapeutic advances in congenital adrenal hyperplasia
Ashwini Mallappa, Deborah P Merke
Seminars in Reproductive Medicine
|
June 17, 2009
Cardiovascular disease risk in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Mimi S Kim, Deborah P Merke
The Lancet. Diabetes & Endocrinology
|
March 14, 2014
Management of adolescents with congenital adrenal hyperplasia
Deborah P Merke, Dix P Poppas
Hormone Research in Paediatrics
|
May 8, 2018
Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome
Walter L Miller, Deborah P Merke
Lancet (London, England)
|
June 21, 2005
Congenital adrenal hyperplasia
Deborah P Merke, Stefan R Bornstein
The 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 Hyperplasia
Qizong Lao, Brittany Brookner, Deborah P Merke
The Journal of Clinical Endocrinology and Metabolism
|
November 5, 2002
Pubertal and gender-related changes in the sympathoadrenal system in healthy children
Martina Weise, Graeme Eisenhofer, Deborah P Merke
European Journal of Medical Genetics
|
January 2, 2014
Transforming growth factor-β (TGF-β) pathway abnormalities in tenascin-X deficiency associated with CAH-X syndrome
Rachel 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 deficiency
Evangelia Charmandari, George P Chrousos, Deborah P Merke
Page
of 12