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Barry Rich

Showing results (1-10 of 5) with videos related to

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CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|April 9, 2015
Better treatment for depressionBarry Rich
Archives of Pediatrics & Adolescent Medicine|September 10, 2003
Self-reported social class, self-management behaviors, and the effect of diabetes mellitus in urban, minority young people and their familiesRebecca Lipton, Melinda Drum, Deborah Burnet, et al.
Pediatrics|May 4, 2005
Obesity at the onset of diabetes in an ethnically diverse population of children: what does it mean for epidemiologists and clinicians?Rebecca B Lipton, Melinda Drum, Deborah Burnet, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiencyChantal Lutfallah, Weihua Wang, J Ian Mason, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasiaSongya Pang, Weihua Wang, Barry Rich, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|April 9, 2015
Better treatment for depressionBarry Rich
Archives of Pediatrics & Adolescent Medicine|September 10, 2003
Self-reported social class, self-management behaviors, and the effect of diabetes mellitus in urban, minority young people and their familiesRebecca Lipton, Melinda Drum, Deborah Burnet, et al.
Pediatrics|May 4, 2005
Obesity at the onset of diabetes in an ethnically diverse population of children: what does it mean for epidemiologists and clinicians?Rebecca B Lipton, Melinda Drum, Deborah Burnet, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiencyChantal Lutfallah, Weihua Wang, J Ian Mason, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasiaSongya Pang, Weihua Wang, Barry Rich, et al.
Pageof 1