Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2009
A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiencyKristian Løvås, Ian McFarlane, Huy-Hoang Nguyen, et al.
The Journal of Biological Chemistry|January 10, 2002
The structural basis for the specificity of retinoid-X receptor-selective agonists: new insights into the role of helix H12James D Love, John T Gooch, Szilvia Benko, et al.
The Journal of Clinical Endocrinology and Metabolism|November 15, 2007
Long-term DHEA replacement in primary adrenal insufficiency: a randomized, controlled trialEleanor M Gurnell, Penelope J Hunt, Suzanne E Curran, et al.
European Journal of Endocrinology|March 14, 2009
Glucocorticoid replacement therapy and pharmacogenetics in Addison's disease: effects on boneKristian Løvås, Clara G Gjesdal, Monika Christensen, et al.
The Journal of Clinical Endocrinology and Metabolism|November 18, 2011
Quality of life in European patients with Addison's disease: validity of the disease-specific questionnaire AddiQoLMarianne Øksnes, Sophie Bensing, Anna-Lena Hulting, et al.
Clinical Endocrinology|December 15, 2012
Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous communityHakan Cangul, Zehra Aycan, Alvaro Olivera-Nappa, et al.
Nature Genetics|July 16, 2002
Digenic inheritance of severe insulin resistance in a human pedigreeDavid B Savage, Maura Agostini, Inês Barroso, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
Pageof 2