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For: Jiang L, Chen C, Yuan T, Qin Y, Hu M, Li X, Xing X, Lee X, Nie M, Chen L. Clinical severity of Gitelman syndrome determined by serum magnesium. Am J Nephrol 2014;39:357-66. [PMID: 24776766 DOI: 10.1159/000360773] [Cited by in Crossref: 24] [Cited by in F6Publishing: 22] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Urwin S, Willows J, Sayer JA. The challenges of diagnosis and management of Gitelman syndrome. Clin Endocrinol 2020;92:3-10. [DOI: 10.1111/cen.14104] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
2 van der Merwe PD, Rensburg MA, Haylett WL, Bardien S, Davids MR. Gitelman syndrome in a South African family presenting with hypokalaemia and unusual food cravings. BMC Nephrol. 2017;18:38. [PMID: 28125972 DOI: 10.1186/s12882-017-0455-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
3 Li C, Zhou X, Han W, Jiang X, Liu J, Fang L, Wang H, Guan Q, Gao L, Zhao J, Xu J, Xu C. Identification of two novel mutations in SLC12A3 gene in two Chinese pedigrees with Gitelman syndrome and review of literature. Clin Endocrinol (Oxf) 2015;83:985-93. [PMID: 25990047 DOI: 10.1111/cen.12820] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
4 Zha B, Zheng P, Liu J, Huang X. Coexistence of Graves' Disease in a 14-year-old young girl with Gitelman Syndrome. Clin Endocrinol (Oxf) 2015;83:995-7. [PMID: 25892104 DOI: 10.1111/cen.12800] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
5 Yu RZ, Chen MS. Gitelman syndrome caused by a rare homozygous mutation in the SLC12A3 gene: A case report. World J Clin Cases 2020; 8(18): 4252-4258 [PMID: 33024786 DOI: 10.12998/wjcc.v8.i18.4252] [Cited by in CrossRef: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Yang M, Zhao L, Gao P, Zhu X, Han Y, Chen X, Li L, Xiao Y, Wei L, Li C, Xiao L, Yuan S, Liu F, Dong LQ, Kanwar YS, Sun L. DsbA-L ameliorates high glucose induced tubular damage through maintaining MAM integrity. EBioMedicine 2019;43:607-19. [PMID: 31060900 DOI: 10.1016/j.ebiom.2019.04.044] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 4.3] [Reference Citation Analysis]
7 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]
8 Dong B, Chen Y, Liu X, Wang Y, Wang F, Zhao Y, Sun X, Zhao W. Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes. BMC Nephrol 2020;21:328. [PMID: 32758178 DOI: 10.1186/s12882-020-01996-2] [Reference Citation Analysis]
9 Tian D, Shi X, Zhao Y, Peng X, Zou L, Xu L, Ma Y, Wen Y, Faulhaber-Walter R, Chen L. The effect of A1 adenosine receptor in diabetic megalin loss with caspase-1/IL18 signaling. Diabetes Metab Syndr Obes 2019;12:1583-96. [PMID: 31695457 DOI: 10.2147/DMSO.S215531] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
10 Wolyniec W, Jakubowska SK, Nagel M, Wolyniec Z, Obolonczyk L, Swiatkowska-stodulska R, Sworczak K, Renke M. A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene. Nefrología 2016;36:304-9. [DOI: 10.1016/j.nefro.2015.04.006] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Peng X, Zhao B, Zhang L, Jiang L, Yuan T, Wang Y, Wang H, Ma J, Li N, Zheng K, Nie M, Li X, Xing X, Chen L. Hydrochlorothiazide Test as a Tool in the Diagnosis of Gitelman Syndrome in Chinese Patients. Front Endocrinol (Lausanne). 2018;9:559. [PMID: 30319542 DOI: 10.3389/fendo.2018.00559] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
12 Jiang L, Peng X, Ma J, Yuan T, Qin Y, Wang O, Wang H, Wang Y, Chen G, Yue C, Li C, Nie M, Xing X, Li X, Lee X, Chen L. NORMOMAGNESEMIC GITELMAN SYNDROME PATIENTS EXHIBIT A STRONGER REACTION TO THIAZIDE THAN HYPOMAGNESEMIC PATIENTS. Endocr Pract 2015;21:1017-25. [PMID: 26121437 DOI: 10.4158/EP14432.OR] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
13 Yuan T, Jiang L, Chen C, Peng X, Nie M, Li X, Xing X, Li X, Chen L. Glucose tolerance and insulin responsiveness in Gitelman syndrome patients. Endocr Connect. 2017;6:243-252. [PMID: 28432081 DOI: 10.1530/ec-17-0014] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
14 Chotard E, Blanchard A, Ostertag A, Latourte A, Gailly G, Frochot V, Lioté F, Bousson V, Richette P, Bardin T, Vargas-Poussou R, Ea HK. Calcium Pyrophosphate Crystal Deposition in a Cohort of 57 Patients with Gitelman Syndrome. Rheumatology (Oxford) 2021:keab578. [PMID: 34508565 DOI: 10.1093/rheumatology/keab578] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Roumeliotou S, Theohari A, Tsamoulis D, Vafeidou K, Siountri I, Siomou E. Persistent mild hypokalemia in an otherwise healthy 6-year-old girl: Answers. Pediatr Nephrol 2022. [PMID: 35118535 DOI: 10.1007/s00467-022-05458-9] [Reference Citation Analysis]
16 Shahzad MA, Mukhtar M, Ahmed A, Ullah W, Saeed R, Hamid M. Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review. Case Rep Med 2019;2019:4204907. [PMID: 30867665 DOI: 10.1155/2019/4204907] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
17 Tang W, Huang X, Liu Y, Lv Q, Li T, Song Y, Zhang X, Chen X, Shi Y. A novel homozygous mutation (p.N958K) of SLC12A3 in Gitelman syndrome is associated with endoplasmic reticulum stress. J Endocrinol Invest 2021;44:471-80. [PMID: 32642858 DOI: 10.1007/s40618-020-01329-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Li X, Chen R, Chen M. Clinical Characteristics and Gene Mutation Analysis of the Chinese Han Population with Gitelman Syndrome: 3 Case Reports and a Literature Review. Case Rep Med 2020;2020:6263721. [PMID: 33163079 DOI: 10.1155/2020/6263721] [Reference Citation Analysis]
19 Xia MF, Bian H, Liu H, Wu HJ, Zhang ZG, Lu ZQ, Gao X. Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review. Clin Case Rep. 2017;5:578-586. [PMID: 28469853 DOI: 10.1002/ccr3.874] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
20 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]
21 Chen X, Han Y, Gao P, Yang M, Xiao L, Xiong X, Zhao H, Tang C, Chen G, Zhu X, Yuan S, Liu F, Dong LQ, Liu F, Kanwar YS, Sun L. Disulfide-bond A oxidoreductase-like protein protects against ectopic fat deposition and lipid-related kidney damage in diabetic nephropathy. Kidney Int 2019;95:880-95. [PMID: 30791996 DOI: 10.1016/j.kint.2018.10.038] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 5.3] [Reference Citation Analysis]
22 Valinsky WC, Touyz RM, Shrier A. Aldosterone and Ion Channels. Vitam Horm 2019;109:105-31. [PMID: 30678852 DOI: 10.1016/bs.vh.2018.10.004] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
23 Peng X, Jiang L, Chen C, Qin Y, Yuan T, Wang O, Xing X, Li X, Nie M, Chen L. Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome. PLoS One. 2017;12:e0180811. [PMID: 28700713 DOI: 10.1371/journal.pone.0180811] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]