Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation-Reference-Cited by-同舟云学术

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Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation

Published:2012-01-01 Issue:11-12 Volume:25 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Baş Veysel Nijat,Cangul Hakan,Agladioglu Sebahat Yilmaz,Kendall Michaela,Cetinkaya Semra,Aycan Zehra

Publisher

Walter de Gruyter GmbH

Subject

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

Link

https://www.degruyter.com/document/doi/10.1515/jpem-2012-0211/pdf

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital Hypothyroidism Patients With Thyroid Hormone Receptor Variants Are Not Rare: A Systematic Review;INQUIRY: The Journal of Health Care Organization, Provision, and Financing;2021-01

2. Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism;Clinica Chimica Acta;2017-05

3. Resistance to thyrotropin;Best Practice & Research Clinical Endocrinology & Metabolism;2017-03

4. Evaluation of the tshr gene reveals polymorphisms associated with typical symptoms in primary congenital hypothyroidism;Journal of Pediatric Endocrinology and Metabolism;2016-01-01

5. A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family;Journal of Clinical Research in Pediatric Endocrinology;2015-12-03

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