Coexistence of Graves' Disease in a 14-year-old young girl with Gitelman Syndrome-Reference-Cited by-同舟云学术

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Coexistence of Graves' Disease in a 14-year-old young girl with Gitelman Syndrome

Published:2015-05-07 Issue:6 Volume:83 Page:995-997
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Zha Bingbing¹,Zheng Pengxi¹,Liu Jun¹,Huang Xinmei¹

Affiliation:

1. Department of Endocrinology; Shanghai Fifth People's Hospital; Fudan University; Shanghai China

Funder

Natural Science Foundation of Shanghai

Minhang District Natural Science Foundation of Shanghai

National Natural Science Foundation of China

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference5 articles.

1. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter;Simon;Nature Genetics,1996

2. Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome;Balavoine;European Journal of Endocrinology,2011

3. A single nucleotide polymorphism alters the activity of the renal Na+:Cl− cotransporter and reveals a role for transmembrane segment 4 in chloride and thiazide affinity;Moreno;Journal of Biological Chemistry,2004

4. Clinical severity of Gitelman syndrome determined by serum magnesium;Jiang;American Journal of Nephrology,2014

5. Indomethacin, Amiloride, or Eplerenone for Treating Hypokalemia in Gitelman Syndrome;Blanchard;Journal of the American Society of Nephrology,2015

Cited by 17 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. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature;CEN Case Reports;2024-02-03

2. Gitelman syndrome with Graves’ disease leading to rhabdomyolysis: a case report and literature review;BMC Nephrology;2023-05-02

3. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review;WORLD J CLIN CASES;2022

4. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review;World Journal of Clinical Cases;2022-07-26

5. Inherited Disorders of Sodium and Potassium Handling;Pediatric Nephrology;2022

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