Graves’ disease and Gitelman syndrome
Author:
Affiliation:
1. Tajiri Thyroid Clinic; Kumamoto Japan
2. Department of Infection Control and Clinical Laboratory Medicine; Dokkyo Medical University; Tochigi Japan
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Reference5 articles.
1. Coexistence of Graves’ disease in a 14-year-old young girl with Gitelman syndrome;Zha;Clinical Endocrinology (Oxford),2015
2. Rare independent mutations in renal salt handling genes contribute to blood pressure variation;Ji;Nature Genetics,2008
3. Mutational analysis of SLC12A3 gene in a Japanese general population of northern Japan;Tsutaya;Hirosaki Medical Journal,2011
4. Gitelman's syndrome: towards genotype-phenotype correlations?;Riveira-Munoz;Pediatric Nephrology,2007
5. Concurrence of thyrotoxicosis and Gitelman's syndrome-associated hypokalemia-induced periodic paralysis;Imashuku;Pediatric Reports,2012
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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 SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome;Clinical Endocrinology;2022-12-28
4. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review;WORLD J CLIN CASES;2022
5. 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
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