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For: Melander O, Orho-Melander M, Bengtsson K, Lindblad U, Râstam L, Groop L, Hulthén UL. Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension. Hypertension 2000;36:389-94. [PMID: 10988270 DOI: 10.1161/01.hyp.36.3.389] [Cited by in Crossref: 58] [Cited by in F6Publishing: 16] [Article Influence: 2.6] [Reference Citation Analysis]
Number Citing Articles
1 Huang K, Dai YL, Zhang JW, Zhang L, Wu W, Dong GP, Ullah R, Fei Y, Fu JF. Gitelman syndrome combined with growth hormone deficiency: Three cases report. Medicine (Baltimore) 2019;98:e17244. [PMID: 31577716 DOI: 10.1097/MD.0000000000017244] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
2 Chen SY, Jie N. Gitelman syndrome: A case report. World J Clin Cases 2022; 10(17): 5893-5898 [DOI: 10.12998/wjcc.v10.i17.5893] [Reference Citation Analysis]
3 Garneau AP, Marcoux AA, Noël M, Frenette-Cotton R, Drolet MC, Couet J, Larivière R, Isenring P. Ablation of Potassium-Chloride Cotransporter Type 3 (Kcc3) in Mouse Causes Multiple Cardiovascular Defects and Isosmotic Polyuria. PLoS One 2016;11:e0154398. [PMID: 27166674 DOI: 10.1371/journal.pone.0154398] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
4 Pearce D, Manis AD, Nesterov V, Korbmacher C. Regulation of distal tubule sodium transport: mechanisms and roles in homeostasis and pathophysiology. Pflugers Arch 2022;474:869-84. [PMID: 35895103 DOI: 10.1007/s00424-022-02732-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Zhang JH, Ruan DD, Hu YN, Ruan XL, Zhu YB, Yang X, Wu JB, Lin XF, Luo JW, Tang FQ. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations. Biomed Res Int 2021;2021:9973161. [PMID: 34046503 DOI: 10.1155/2021/9973161] [Reference Citation Analysis]
6 Zhang R, Zhuang L, Li M, Zhang J, Zhao W, Ge X, Chen Y, Wang F, Wang N, Bao Y, Liu L, Liu Y, Jia W. Arg913Gln of SLC12A3 gene promotes development and progression of end-stage renal disease in Chinese type 2 diabetes mellitus. Mol Cell Biochem 2018;437:203-10. [PMID: 28744814 DOI: 10.1007/s11010-017-3120-z] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
7 Lü Q, Dong Y, Wan H, Zhang Y, Tang L, Zhang F, Yan Z, Tong N. Consideration of the diagnosis of hypertension accompanied with hypokalaemia: monism or dualism? J Int Med Res 2018;46:2944-53. [PMID: 29808706 DOI: 10.1177/0300060518768154] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
8 Lee JW, Lee J, Heo NJ, Cheong HI, Han JS. Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome. J Korean Med Sci. 2016;31:47-54. [PMID: 26770037 DOI: 10.3346/jkms.2016.31.1.47] [Cited by in Crossref: 20] [Cited by in F6Publishing: 11] [Article Influence: 2.9] [Reference Citation Analysis]
9 Luo JW, Meng XR, Yang X, Liang JX, Hong FY, Zheng XY, Li WH. Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine. Chin J Integr Med 2017;23:461-8. [PMID: 26825084 DOI: 10.1007/s11655-016-2461-x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
10 Glaudemans B, Yntema HG, San-Cristobal P, Schoots J, Pfundt R, Kamsteeg EJ, Bindels RJ, Knoers NV, Hoenderop JG, Hoefsloot LH. Novel NCC mutants and functional analysis in a new cohort of patients with Gitelman syndrome. Eur J Hum Genet. 2012;20:263-270. [PMID: 22009145 DOI: 10.1038/ejhg.2011.189] [Cited by in Crossref: 38] [Cited by in F6Publishing: 28] [Article Influence: 3.5] [Reference Citation Analysis]
11 Nuñez-Gonzalez L, Carrera N, Garcia-Gonzalez MA. Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians. Int J Mol Sci 2021;22:11414. [PMID: 34768847 DOI: 10.3390/ijms222111414] [Reference Citation Analysis]
12 Lü Q, Zhang Y, Song C, An Z, Wei S, Huang J, Huang L, Tang L, Tong N. A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review. J Endocrinol Invest 2016;39:333-40. [PMID: 26260218 DOI: 10.1007/s40618-015-0371-y] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 2.3] [Reference Citation Analysis]
13 Zhou H, Liang X, Qing Y, Meng B, Zhou J, Huang S, Lu S, Huang Z, Yang H, Ma Y, Luo Z. Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review. BMC Endocr Disord. 2018;18:82. [PMID: 30409157 DOI: 10.1186/s12902-018-0298-3] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
14 Vargas-Poussou R, Dahan K, Kahila D, Venisse A, Riveira-Munoz E, Debaix H, Grisart B, Bridoux F, Unwin R, Moulin B, Haymann JP, Vantyghem MC, Rigothier C, Dussol B, Godin M, Nivet H, Dubourg L, Tack I, Gimenez-Roqueplo AP, Houillier P, Blanchard A, Devuyst O, Jeunemaitre X. Spectrum of mutations in Gitelman syndrome. J Am Soc Nephrol. 2011;22:693-703. [PMID: 21415153 DOI: 10.1681/asn.2010090907] [Cited by in Crossref: 122] [Cited by in F6Publishing: 53] [Article Influence: 11.1] [Reference Citation Analysis]
15 Gug C, Mihaescu A, Mozos I. Two mutations in the thiazide-sensitive NaCl co-transporter gene in a Romanian Gitelman syndrome patient: case report. Ther Clin Risk Manag. 2018;14:149-155. [PMID: 29403282 DOI: 10.2147/tcrm.s150483] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
16 Wang F, Shi C, Cui Y, Li C, Tong A. Mutation profile and treatment of Gitelman syndrome in Chinese patients. Clin Exp Nephrol. 2017;21:293-299. [PMID: 27216017 DOI: 10.1007/s10157-016-1284-6] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 1.7] [Reference Citation Analysis]
17 Basson J, Simino J, Rao DC. Between candidate genes and whole genomes: time for alternative approaches in blood pressure genetics. Curr Hypertens Rep. 2012;14:46-61. [PMID: 22161147 DOI: 10.1007/s11906-011-0241-8] [Cited by in Crossref: 27] [Cited by in F6Publishing: 25] [Article Influence: 2.7] [Reference Citation Analysis]
18 Barbosa EJ, Glad CA, Nilsson AG, Bosaeus N, Nyström HF, Svensson PA, Bengtsson BÅ, Nilsson S, Bosaeus I, Boguszewski CL, Johannsson G. Extracellular water and blood pressure in adults with growth hormone (GH) deficiency: a genotype-phenotype association study. PLoS One 2014;9:e105754. [PMID: 25157616 DOI: 10.1371/journal.pone.0105754] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.6] [Reference Citation Analysis]
19 Gagnon KB, Delpire E. Physiology of SLC12 transporters: lessons from inherited human genetic mutations and genetically engineered mouse knockouts. Am J Physiol Cell Physiol 2013;304:C693-714. [PMID: 23325410 DOI: 10.1152/ajpcell.00350.2012] [Cited by in Crossref: 100] [Cited by in F6Publishing: 86] [Article Influence: 11.1] [Reference Citation Analysis]
20 Knoers NV. Inherited forms of renal hypomagnesemia: an update. Pediatr Nephrol 2009;24:697-705. [PMID: 18818955 DOI: 10.1007/s00467-008-0968-x] [Cited by in Crossref: 37] [Cited by in F6Publishing: 25] [Article Influence: 2.6] [Reference Citation Analysis]