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The Journal of Clinical Endocrinology and Metabolism|May 7, 2010
Autoimmunity in patients with resistance to thyroid hormoneMarla S Barkoff, Masha Kocherginsky, João Anselmo, et al.
JCI Insight|February 20, 2024
Impaired T3 uptake and action in MCT8-deficient cerebral organoids underlie Allan-Herndon-Dudley syndromeFederico Salas-Lucia, Sergio Escamilla, Antonio C Bianco, et al.
Thyroid : Official Journal of the American Thyroid Association|April 21, 2018
Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid TestsMizuho S Mimoto, Anara Karaca, Neal Scherberg, et al.
Thyroid : Official Journal of the American Thyroid Association|May 19, 2009
Comparison of thyroidectomized calf serum and stripped serum for the study of thyroid hormone action in human skin fibroblasts in vitroLars C Moeller, Craig Wardrip, Marek Niekrasz, et al.
Thyroid : Official Journal of the American Thyroid Association|February 5, 2009
A somatic gain-of-function mutation in the thyrotropin receptor gene producing a toxic adenoma in an infantBrenda Kohn, Helmut Grasberger, Leslie L Lam, et al.
Thyroid : Official Journal of the American Thyroid Association|May 8, 2015
A TSHβ Variant with Impaired Immunoreactivity but Intact Biological Activity and Its Clinical ImplicationsTheodora Pappa, Jesper Johannesen, Neal Scherberg, et al.
Journal of Neurology|April 19, 2005
X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 geneKnut Brockmann, Alexandra M Dumitrescu, Thomas T Best, et al.
American Journal of Human Genetics|December 9, 2003
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter geneAlexandra M Dumitrescu, Xiao-Hui Liao, Thomas B Best, et al.
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