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Pediatric Endocrinology
Contributing journals to this collection:
Journal of Clinical Endocrinology & Metabolism,
Molecular Endocrinology,
Endocrinology,
Endocrine Reviews,
and Endocrine Society Journals
Citations 51-60 of 803 total displayed.
- Article
Duplications of the Functional CYP21A2 Gene Are Primarily Restricted to Q318X Alleles: Evidence for a Founder Effect
- S. Kleinle, R. Lang, G. F. Fischer, H. Vierhapper, F. Waldhauser, M. Födinger, and S. M. Baumgartner-Parzer
J. Clin. Endocrinol. Metab. published September 22, 2009, doi:10.1210/jc.2009-0487
[Abstract]
- Article
Hypogonadotropic Hypogonadism due to a Novel Missense Mutation in the First Extracellular Loop of the Neurokinin B Receptor
- Tulay Guran, Gwen Tolhurst, Abdullah Bereket, Nuno Rocha, Keith Porter, Serap Turan, Fiona M. Gribble, L. Damla Kotan, Teoman Akcay, Zeynep Atay, Husniye Canan, Ayse Serin, Stephen O'Rahilly, Frank Reimann, Robert K. Semple, and A. Kemal Topaloglu
J. Clin. Endocrinol. Metab. published September 15, 2009, doi:10.1210/jc.2009-0551
[Abstract]
- Article
Low-Birth Weight Children Develop Lower Sex Hormone Binding Globulin and Higher Dehydroepiandrosterone Sulfate Levels and Aggravate their Visceral Adiposity and Hypoadiponectinemia between Six and Eight Years of Age
- Lourdes Ibáñez, Abel Lopez-Bermejo, Marta Díaz, Larisa Suárez, and Francis de Zegher
J. Clin. Endocrinol. Metab. published September 8, 2009, doi:10.1210/jc.2009-0789
[Abstract]
- Article
Experience with Intraamniotic Thyroxine Treatment in Nonimmune Fetal Goitrous Hypothyroidism in 12 Cases
- Virginie Ribault, Mireille Castanet, Anne-Marie Bertrand, Jean Guibourdenche, Edith Vuillard, Dominique Luton, Michel Polak the French Fetal Goiter Study Group
J. Clin. Endocrinol. Metab. published September 8, 2009, doi:10.1210/jc.2008-2681
[Abstract]
- Article
Heritability of Childhood Weight Gain from Birth and Risk Markers for Adult Metabolic Disease in Prepubertal Twins
- Kathryn Beardsall, Ken K. Ong, Nuala Murphy, M. Lynn Ahmed, Jing Hua Zhao, Maarten W. Peeters, and David B. Dunger
J. Clin. Endocrinol. Metab. published September 1, 2009, doi:10.1210/jc.2009-0757
[Abstract]
- Article
A Missense GATA3 Mutation, Thr272Ile, Causes the Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome
- Katherine U. Gaynor, Irina V. Grigorieva, M. Andrew Nesbit, Treena Cranston, Thushari Gomes, Ludwig Gortner, and Rajesh V. Thakker
J. Clin. Endocrinol. Metab. published September 1, 2009, doi:10.1210/jc.2009-0717
[Abstract]
- Article
Influence of Duration of Diabetes, Glycemic Control, and Traditional Cardiovascular Risk Factors on Early Atherosclerotic Vascular Changes in Adolescents and Young Adults with Type 2 Diabetes Mellitus
- Amy S. Shah, Lawrence M. Dolan, Thomas R. Kimball, Zhiqian Gao, Philip R. Khoury, Stephen R. Daniels, and Elaine M. Urbina
J. Clin. Endocrinol. Metab. published September 1, 2009, doi:10.1210/jc.2008-2039
[Abstract]
- Editorials
Adult Care of Pediatric Conditions: Lessons from Turner’s Syndrome
- Gerard S. Conway
J. Clin. Endocrinol. Metab. 2009; 94: 3185-3187, doi:10.1210/jc.2009-1457
[Full text]
- Editorials
What Do We Know about Iodine Supplementation in Pregnancy?
- Elizabeth N. Pearce
J. Clin. Endocrinol. Metab. 2009; 94: 3188-3190, doi:10.1210/jc.2009-1512
[Full text]
- Endocrine Care
Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency
- Kyriaki S. Alatzoglou, James P. Turton, Daniel Kelberman, Peter E. Clayton, Ameeta Mehta, Charles Buchanan, Simon Aylwin, Elisabeth C. Crowne, Henrik T. Christesen, Niels T. Hertel, Peter J. Trainer, Martin O. Savage, Jamal Raza, Kausik Banerjee, Sunil K. Sinha, Svetlana Ten, Talat Mushtaq, Raja Brauner, Timothy D. Cheetham, Peter C. Hindmarsh, Primus E. Mullis, and Mehul T. Dattani
J. Clin. Endocrinol. Metab. 94: 3191 -3199; published online before print as doi:10.1210/jc.2008-2783
[Abstract]
[Full text]
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