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The Journal of Clinical Endocrinology and Metabolism|June 29, 2006
Mosaicism of a thyroid hormone receptor-beta gene mutation in resistance to thyroid hormoneSunee Mamanasiri, Sena Yesil, Alexandra M Dumitrescu, et al.
Thyroid : Official Journal of the American Thyroid Association|December 31, 2021
Severe Resistance to Thyroid Hormone Beta in a Patient with AthyreosisFederico Salas-Lucia, Monica M França, James A Amrhein, et al.
The Journal of Clinical Endocrinology and Metabolism|May 7, 2023
Effect of the Fetal THRB Genotype on the PlacentaFederico Salas-Lucia, Marius N Stan, Haleigh James, 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.
Endocrinology|September 14, 2013
Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levelsCaterina Di Cosmo, Xiao-Hui Liao, Honggang Ye, 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.
Thyroid : Official Journal of the American Thyroid Association|January 8, 2020
Nonautoimmune Hyperthyroidism Caused by a Somatic Mosaic GNAS Mutation Involving Part of the Thyroid GlandMonica M França, Robert L Levine, Theodora Pappa, et al.
Endocrinology|January 17, 2009
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronineAinhoa Ceballos, Monica M Belinchon, Eduardo Sanchez-Mendoza, et al.
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