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Cited by in F6Publishing
For: Gitelman Syndrome Collaborative Study Group. [Expert consensus for the diagnosis and treatment of patients with Gitelman syndrome]. Zhonghua Nei Ke Za Zhi 2017;56:712-6. [PMID: 28870047 DOI: 10.3760/cma.j.issn.0578-1426.2017.09.021] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
Number Citing Articles
1 Guo X, Yu S, Sun J, Mou L. A case of Gitelman syndrome with membranous nephropathy. BMC Nephrol 2022;23:267. [PMID: 35883046 DOI: 10.1186/s12882-022-02875-8] [Reference Citation Analysis]
2 Becue C, Ceuleers B, den Brinker M, Somers I, Ledeganck KJ, Dotremont H, Trouet D. Screening for an Underlying Tubulopathy in Children With Growth Failure, Simply Maths? Front Pediatr 2022;10:902252. [DOI: 10.3389/fped.2022.902252] [Reference Citation Analysis]
3 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]
4 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]
5 Chen Q, Wang X, Min J, Wang L, Mou L. Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome. BMC Nephrol 2021;22:12. [PMID: 33413160 DOI: 10.1186/s12882-020-02211-y] [Reference Citation Analysis]
6 Zeng Y, Li P, Fang S, Wu C, Zhang Y, Lin X, Guan M. Genetic Analysis of SLC12A3 Gene in Chinese Patients with Gitelman Syndrome. Med Sci Monit 2019;25:5942-52. [PMID: 31398183 DOI: 10.12659/MSM.916069] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 2.3] [Reference Citation Analysis]