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6. Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome. Lee JW, Lee J, Heo NJ, Cheong HI, Han JS. J Korean Med Sci; 2016 Jan; 31(1):47-54. PubMed ID: 26770037 [Abstract] [Full Text] [Related]
8. A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene. Chen Q, Wu Y, Zhao J, Jia Y, Wang W. BMC Nephrol; 2018 Oct 19; 19(1):275. PubMed ID: 30340552 [Abstract] [Full Text] [Related]
10. Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing. Yang L, Fan J, Liu Y, Ren Y, Liu Z, Fu H, Qi H, Yang J. Medicine (Baltimore); 2023 Jun 16; 102(24):e33959. PubMed ID: 37327293 [Abstract] [Full Text] [Related]
11. [Pregnancy in a patient with Gitelman syndrome: a case report and review of literature]. Ducarme G, Davitian C, Uzan M, Belenfant X, Poncelet C. J Gynecol Obstet Biol Reprod (Paris); 2007 May 16; 36(3):310-3. PubMed ID: 17466223 [Abstract] [Full Text] [Related]
12. Systemic lupus erythematosus complicated by a Gitelman-like syndrome in an 8-year-old girl. Barathidasan GS, Krishnamurthy S, Karunakar P, Rajendran R, Ramya K, Dhandapany G, Ramamoorthy JG, Ganesh RN. CEN Case Rep; 2020 May 16; 9(2):129-132. PubMed ID: 31853802 [Abstract] [Full Text] [Related]
14. Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report. He G, Gang X, Sun Z, Wang P, Wang G, Guo W. Medicine (Baltimore); 2020 Jul 17; 99(29):e21123. PubMed ID: 32702863 [Abstract] [Full Text] [Related]
16. [A case of Gitelman syndrome with physical retardation]. Huang J, Zheng X, Guo D, Zhang G, Wang X, Liu C. Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2017 Oct 28; 42(10):1236-1238. PubMed ID: 29093260 [Abstract] [Full Text] [Related]
17. Hypokalaemic paralysis and metabolic alkalosis in a patient with Sjögren syndrome: a case report and literature review. Ranaweerage R, Perera S, Gunapala A. BMC Nephrol; 2021 Apr 30; 22(1):159. PubMed ID: 33931020 [Abstract] [Full Text] [Related]
18. Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome. Balavoine AS, Bataille P, Vanhille P, Azar R, Noël C, Asseman P, Soudan B, Wémeau JL, Vantyghem MC. Eur J Endocrinol; 2011 Oct 30; 165(4):665-73. PubMed ID: 21753071 [Abstract] [Full Text] [Related]
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20. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature. Koca O, Alay MT, Murt A, Kalayci Yigin A, Seven M, Bavunoglu I. CEN Case Rep; 2024 Oct 30; 13(5):330-338. PubMed ID: 38308744 [Abstract] [Full Text] [Related] Page: [Next] [New Search]