Showing results (141-150 of 252) with videos related to

Sort By:
Pageof 26
Clinical Endocrinology|March 27, 2007
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in IsraelisYardena Tenenbaum-Rakover, Sunee Mamanasiri, Carrie Ris-Stalpers, et al.
Molecular Endocrinology (Baltimore, Md.)|December 13, 2005
Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I)Usanee Ringkananont, Joost Van Durme, Lucia Montanelli, et al.
Endocrinology|July 23, 2014
Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
Thyroid : Official Journal of the American Thyroid Association|October 31, 2018
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese FamiliesYui Watanabe, Ryan J Bruellman, Reham S Ebrhim, et al.
Thyroid : Official Journal of the American Thyroid Association|July 29, 2020
Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone MetabolismMonica M França, Alina German, Gustavo W Fernandes, et al.
The Journal of Clinical Endocrinology and Metabolism|June 29, 2024
A Phase I/II Trial of Sapanisertib in Advanced Anaplastic and Radioiodine Refractory Differentiated Thyroid CarcinomaKartik Sehgal, Anthony Serritella, Mofei Liu, et al.
Thyroid : Official Journal of the American Thyroid Association|February 6, 2014
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extractionSolomon Maximo Greenberg, Alfonso Massimiliano Ferrara, Everton S Nicholas, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2023
Identifying and Predicting Diverse Patterns of Benign Nodule GrowthPingPing Xiang, Sara Ahmadi, Alexandra Coleman, et al.
Pageof 26