Long-Term Follow-Up of a Patient with Sporadic Nonautoimmune Hyperthyroidism Due to a Thyrotropin-Receptor Mutation (D619G)-Reference-Cited by-同舟云学术

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Long-Term Follow-Up of a Patient with Sporadic Nonautoimmune Hyperthyroidism Due to a Thyrotropin-Receptor Mutation (D619G)

Published:2018-01 Issue:1 Volume:4 Page:84-89
ISSN:2376-0605
Container-title:AACE Clinical Case Reports
language:en
Short-container-title:AACE Clinical Case Reports

Author:

Nishihara Eijun,Tsugawa Mamiko,Ozaki Yoshikazu,Nagayama Yuji,Fukata Shuji,Hirokawa Mitsuyoshi,Ito Mitsuru,Nishikawa Mitsushige,Nakamura Hirotoshi,Ito Yoshiya,Miyauchi Akira

Publisher

Elsevier BV

Reference20 articles.

1. Genetic hyperthyroidism: hyperthyroidism due to activating TSHR mutations;Hébrant;Eur J Endocrinol,2011

2. Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor gene;Aycan;J Clin Res Pediatr Endocrinol,2010

3. Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene;Agretti;Eur J Pediatr,2012

4. Sporadic congenital hyperthyroidism due to a germline mutation in the thyrotropin receptor gene (Leu 512 Gln) in a Japanese patient;Nishihara;Endocr J,2006

5. Shared sporadic and somatic thyrotropin receptor mutations display more active in vitro activities than familial thyrotropin receptor mutations;Lueblinghoff;Thyroid,2011

Cited by 1 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. Familial neonatal nonautoimmune hyperthyroidism due to a gain-of-function (D619G) thyrotropin-receptor mutation;Journal of Pediatric Endocrinology and Metabolism;2020-11-13

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