Unexpected Peripheral Markers of Thyroid Function in a Patient with a Novel Mutation of the MCT8 Thyroid Hormone Transporter Gene-Reference-Cited by-同舟云学术

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Unexpected Peripheral Markers of Thyroid Function in a Patient with a Novel Mutation of the MCT8 Thyroid Hormone Transporter Gene

Published:2006-09-15 Issue:1 Volume:67 Page:1-6
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Herzovich V.,Vaiani E.,Marino R.,Dratler G.,Lazzati J.M.,Tilitzky S.,Ramirez P.,Iorcansky S.,Rivarola M.A.,Belgorosky A.

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Reference21 articles.

1. Is Neuropsychological Development Related to Maternal Hypothyroidism or to Maternal Hypothyroxinemia?

2. Action of thyroid hormone in brain

3. Biochemistry, Cellular and Molecular Biology, and Physiological Roles of the Iodothyronine Selenodeiodinases

4. Iodothyronine Levels in the Human Developing Brain: Major Regulatory Roles of Iodothyronine Deiodinases in Different Areas

5. Identification of Monocarboxylate Transporter 8 as a Specific Thyroid Hormone Transporter

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1. Identification of a novel nonsense SLC16A2 gene mutation in an infant with severe neurologic phenotype: A case report;Medicine;2024-07-19

2. Treatment with TRIAC in pediatric patients with MCT8;Archivos Argentinos de Pediatria;2023-12-01

3. Allan-Herndon-Dudley syndrome in a female patient and related mechanisms;Molecular Genetics and Metabolism Reports;2022-06

4. Heterogeneous Clinical Characteristics of Allan-Herndon-Dudley Syndrome with SLC16A2 Mutations;Annals of Child Neurology;2021-10-01

5. Monocarboxylate Transporter 8 Deficiency: From Pathophysiological Understanding to Therapy Development;Frontiers in Endocrinology;2021-09-01

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