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Biochimica Et Biophysica Acta|September 19, 2012
The syndromes of reduced sensitivity to thyroid hormoneAlexandra M Dumitrescu, Samuel RefetoffEndocrine Development|August 9, 2007
Novel biological and clinical aspects of thyroid hormone metabolismAlexandra M Dumitrescu, Samuel RefetoffCurrent Opinion in Endocrinology, Diabetes, and Obesity|August 27, 2013
Inherited defects of thyroid hormone-cell-membrane transport: review of recent findingsJiao Fu, Samuel Refetoff, Alexandra M DumitrescuThe Journal of Clinical Endocrinology and Metabolism|July 9, 2010
Approach to the patient with resistance to thyroid hormone and pregnancyRoy E Weiss, Alexandra Dumitrescu, Samuel RefetoffThe Journal of Clinical Endocrinology and Metabolism|November 1, 2014
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancerAlfonso Massimiliano Ferrara, Theodora Pappa, Jiao Fu, et al.Thyroid : Official Journal of the American Thyroid Association|August 5, 2020
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene MutationSamuel Refetoff, Theodora Pappa, Meredith K Williams, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 26, 2014
Familial dysalbuminemic hyperthyroxinemia in a 4-year-old girl with hyperactivity, palpitations and advanced dental age: how gold standard assays may be misleadingAbha Choudhary, Chutintorn Sriphrapradang, Samuel Refetoff, et al.Thyroid : Official Journal of the American Thyroid Association|November 1, 2016
A Novel Thyroid Hormone Receptor Beta Gene Mutation (G251V) in a Thai Patient with Resistance to Thyroid Hormone Coexisting with Pituitary IncidentalomaChutintorn Sriphrapradang, Panudda Srichomkwun, Samuel Refetoff, et al.Molecular Endocrinology (Baltimore, Md.)|July 30, 2005
Cytosolic action of thyroid hormone leads to induction of hypoxia-inducible factor-1alpha and glycolytic genesLars C Moeller, Alexandra M Dumitrescu, Samuel RefetoffThe Journal of Clinical Endocrinology and Metabolism|April 1, 2011
Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesisPia Hermanns, Helmut Grasberger, Samuel Refetoff, et al.Pageof 26