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For: Tago N, Kokubo Y, Inamoto N, Naraba H, Tomoike H, Iwai N. A high prevalence of Gitelman's syndrome mutations in Japanese. Hypertens Res 2004;27:327-31. [PMID: 15198479 DOI: 10.1291/hypres.27.327] [Cited by in Crossref: 33] [Cited by in F6Publishing: 22] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Qin YZ, Liu YM, Wang Y, You C, Li LN, Zhou XY, Lv WM, Hong SH, Xiao LX. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review. World J Clin Cases 2022; 10(21): 7483-7494 [DOI: 10.12998/wjcc.v10.i21.7483] [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 Kondo A, Nagano C, Ishiko S, Omori T, Aoto Y, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagai S, Okada E, Shima Y, Nakanishi K, Ninchoji T, Kaito H, Takeda H, Nagase H, Morisada N, Iijima K, Nozu K. Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases. Sci Rep 2021;11:16099. [PMID: 34373523 DOI: 10.1038/s41598-021-95521-6] [Reference Citation Analysis]
4 Ergani SY, Orgul G, Tolunay HE, Arici M, Yucel A, Uygur D. Gitelman Syndrome in Pregnancy: A Clinical Challenge. Z Geburtshilfe Neonatol 2021. [PMID: 34126642 DOI: 10.1055/a-1498-2940] [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 L, Huang K, Wang S, Fu H, Wang J, Shen H, Lu Z, Chen J, Bao Y, Feng C, Dong G, Mao J. Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome. Front Pediatr 2021;9:544925. [PMID: 33996672 DOI: 10.3389/fped.2021.544925] [Reference Citation Analysis]
7 Mori T, Chiga M, Fujimaru T, Kawamoto R, Mandai S, Nanamatsu A, Nomura N, Ando F, Susa K, Sohara E, Rai T, Uchida S. Phenotypic differences of mutation-negative cases in Gitelman syndrome clinically diagnosed in adulthood. Hum Mutat 2021;42:300-9. [PMID: 33348466 DOI: 10.1002/humu.24159] [Reference Citation Analysis]
8 Chinen T, Saeki E, Mori T, Sohara E, Uchida S, Akimoto T. A case of Gitelman syndrome: our experience with a patient treated in clinical practice on a local island. J Rural Med 2019;14:258-62. [PMID: 31788154 DOI: 10.2185/jrm.3014] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
9 Blanchard A, Vallet M, Dubourg L, Hureaux M, Allard J, Haymann JP, de la Faille R, Arnoux A, Dinut A, Bergerot D, Becker PH, Courand PY, Baron S, Houillier P, Tack I, Devuyst O, Jeunemaitre X, Azizi M, Vargas-Poussou R. Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study. J Am Soc Nephrol 2019;30:1534-45. [PMID: 31285285 DOI: 10.1681/ASN.2019010031] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
10 Wu WF, Pan M. The outcome of two pregnancies in a patient with Gitelman syndrome: case report and review of the literature. J Matern Fetal Neonatal Med 2020;33:4171-3. [PMID: 30922139 DOI: 10.1080/14767058.2019.1598359] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
11 Zhong F, Ying H, Jia W, Zhou X, Zhang H, Guan Q, Xu J, Fang L, Zhao J, Xu C. Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome. J Endocrinol Invest 2019;42:653-65. [PMID: 30413979 DOI: 10.1007/s40618-018-0966-1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
12 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]
13 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]
14 Chen Y, Zhang Z, Lin X, Pan Q, Zheng F, Li H. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree. BMC Med Genet. 2018;19:17. [PMID: 29378538 DOI: 10.1186/s12881-018-0527-7] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
15 Zhang Y, Zhang F, Chen D, Lü Q, Tang L, Yang C, Lei M, Tong N. A novel homozygous mutation in the solute carrier family 12 member 3 gene in a Chinese family with Gitelman syndrome. Braz J Med Biol Res 2016;49:e5261. [PMID: 27783806 DOI: 10.1590/1414-431X20165261] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
16 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]
17 Wang L, Dong C, Xi YG, Su X. Thiazide-sensitive Na+-Cl- cotransporter: genetic polymorphisms and human diseases. Acta Biochim Biophys Sin (Shanghai) 2015;47:325-34. [PMID: 25841442 DOI: 10.1093/abbs/gmv020] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
18 Makino S, Tajima T, Shinozuka J, Ikumi A, Awaguni H, Tanaka S, Maruyama R, Imashuku S. Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642H/R642W Mutation in the SLC12A3 Gene. Case Rep Pediatr. 2014;2014:279389. [PMID: 25140267 DOI: 10.1155/2014/279389] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
19 Kageyama K, Terui K, Shoji M, Tsutaya S, Matsuda E, Sakihara S, Nigawara T, Moriyama T, Yasujima M, Suda T. Diagnosis of a case of Gitelman’s syndrome based on renal clearance studies and gene analysis of a novel mutation of the thiazide-sensitive Na-Cl cotransporter. J Endocrinol Invest 2005;28:822-6. [DOI: 10.1007/bf03347574] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
20 Fava C, Fava C, Montagnana M, Fava C, Montagnana M, Rosberg L, Burri P, Jönsson A, Wanby P, Wahrenberg H, Hulthén UL, Aurell M, Guidi GC, Melander O. Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes: Short Communication. DNA Sequence 2009;18:395-9. [DOI: 10.1080/10425170701400456] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
21 Roser M, Eibl N, Eisenhaber B, Seringer J, Nagel M, Nagorka S, Luft FC, Frei U, Gollasch M. Gitelman syndrome. Hypertension 2009;53:893-7. [PMID: 19349556 DOI: 10.1161/HYPERTENSIONAHA.108.127993] [Cited by in Crossref: 14] [Cited by in F6Publishing: 5] [Article Influence: 1.1] [Reference Citation Analysis]
22 Qin L, Shao L, Ren H, Wang W, Pan X, Zhang W, Wang Z, Shen P, Chen N. Identification of five novel variants in the thiazide-sensitive NaCl co-transporter gene in Chinese patients with Gitelman syndrome. Nephrology (Carlton) 2009;14:52-8. [PMID: 19207868 DOI: 10.1111/j.1440-1797.2008.01042.x] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 1.0] [Reference Citation Analysis]
23 Hsu Y, Yang S, Chu N, Sytwu H, Cheng C, Lin S. Heterozygous mutations of the sodium chloride cotransporter in Chinese children: prevalence and association with blood pressure. Nephrology Dialysis Transplantation 2008;24:1170-5. [DOI: 10.1093/ndt/gfn619] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 1.0] [Reference Citation Analysis]
24 Riveira-Munoz E, Devuyst O, Belge H, Jeck N, Strompf L, Vargas-Poussou R, Jeunemaître X, Blanchard A, Knoers NV, Konrad M, Dahan K. Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome. Nephrol Dial Transplant 2008;23:3120-5. [PMID: 18469313 DOI: 10.1093/ndt/gfn229] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 1.0] [Reference Citation Analysis]
25 Aoi N, Nakayama T, Tahira Y, Haketa A, Yabuki M, Sekiyama T, Nakane C, Mano H, Kawachi H, Sato N, Soma M, Matsumoto K. Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome. Endocrine 2007;31:149-53. [PMID: 17873326 DOI: 10.1007/s12020-007-0024-9] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis]
26 Iwai N, Kajimoto K, Kokubo Y, Tomoike H. Extensive Genetic Analysis of 10 Candidate Genes for Hypertension in Japanese. Hypertension 2006;48:901-7. [DOI: 10.1161/01.hyp.0000242485.23148.bb] [Cited by in Crossref: 19] [Cited by in F6Publishing: 9] [Article Influence: 1.2] [Reference Citation Analysis]
27 Reboul M, Higueret L, Biteau N, Iron A. Rapid and accurate detection of the CFTR gene mutation 1811+1.6kbA>G by real-time fluorescence resonance energy transfer PCR. Molecular and Cellular Probes 2005;19:358-62. [DOI: 10.1016/j.mcp.2005.06.010] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]