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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|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.
The Journal of Clinical Endocrinology and Metabolism|June 1, 2006
C-terminal amino acid alteration rather than late termination causes complete deficiency of thyroxine-binding globulin CD-NeuIsenburgLars C Moeller, Anja Fingerhut, Harald Lahner, 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.
Thyroid : Official Journal of the American Thyroid Association|May 25, 2022
A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital HypothyroidismMonica Malheiros França, Lucy Reeve, Alexandra M Dumitrescu, et al.
Endocrinology|May 20, 2006
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient miceAlexandra M Dumitrescu, Xiao-Hui Liao, Roy E Weiss, et al.
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