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The Journal of Clinical Endocrinology and Metabolism|December 24, 2019
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital HypothyroidismRyan J Bruellman, Yui Watanabe, Reham S Ebrhim, et al.
Thyroid : Official Journal of the American Thyroid Association|July 20, 2016
Adeno Associated Virus 9-Based Gene Therapy Delivers a Functional Monocarboxylate Transporter 8, Improving Thyroid Hormone Availability to the Brain of Mct8-Deficient MiceHideyuki Iwayama, Xiao-Hui Liao, Lyndsey Braun, et al.
The Journal of Clinical Endocrinology and Metabolism|September 26, 2025
Functional Domain Mapping of TPO: Insights from Six Variants in Sudanese Kindreds with Congenital HypothyroidismMohammad S Islam, Ruy Andrade Louzada Neto, Jessica Bouviere, et al.
The Journal of Clinical Endocrinology and Metabolism|April 15, 2011
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlationChutintorn Sriphrapradang, Yardena Tenenbaum-Rakover, Mia Weiss, et al.
Neurosurgery|July 21, 2011
Transsphenoidal surgery for Cushing disease: experience with 136 patientsIvan Ciric, Jin-Cheng Zhao, Hongyan Du, et al.
The Journal of Clinical Endocrinology and Metabolism|November 29, 2007
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidismIlaria Zamproni, Helmut Grasberger, Francesca Cortinovis, et al.
The Journal of Biological Chemistry|December 13, 2005
Dominant role of thyrotropin-releasing hormone in the hypothalamic-pituitary-thyroid axisAmisra A Nikrodhanond, Tania M Ortiga-Carvalho, Nobuyuki Shibusawa, et al.
Thyroid : Official Journal of the American Thyroid Association|July 25, 2019
A Liver-Specific Thyromimetic, VK2809, Decreases Hepatosteatosis in Glycogen Storage Disease Type IaJin Zhou, Lauren R Waskowicz, Andrea Lim, et al.
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