These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
260 related articles for article (PubMed ID: 28685938)
21. Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome. Aoi N; Nakayama T; Tahira Y; Haketa A; Yabuki M; Sekiyama T; Nakane C; Mano H; Kawachi H; Sato N; Soma M; Matsumoto K Endocrine; 2007 Apr; 31(2):149-53. PubMed ID: 17873326 [TBL] [Abstract][Full Text] [Related]
22. Novel mutation in the SLC12A3 gene in a Sri Lankan family with Gitelman syndrome & coexistent diabetes: a case report. Subasinghe CJ; Sirisena ND; Herath C; Berge KE; Leren TP; Bulugahapitiya U; Dissanayake VHW BMC Nephrol; 2017 Apr; 18(1):140. PubMed ID: 28446151 [TBL] [Abstract][Full Text] [Related]
23. Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family. Yagi H; Yahata K; Usui T; Hasegawa C; Seta K; Sugawara A Intern Med; 2011; 50(11):1211-4. PubMed ID: 21628937 [TBL] [Abstract][Full Text] [Related]
24. Eplerenone improved hypokalemia in a patient with Gitelman's syndrome. Ito Y; Yoshida M; Nakayama M; Tsutaya S; Ogawa K; Maeda H; Miyata M; Oiso Y Intern Med; 2012; 51(1):83-6. PubMed ID: 22214629 [TBL] [Abstract][Full Text] [Related]
25. A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene. Wolyniec W; Jakubowska SK; Nagel M; Wolyniec Z; Obolonczyk L; Swiatkowska-Stodulska R; Sworczak K; Renke M Nefrologia; 2016; 36(3):304-9. PubMed ID: 26306968 [TBL] [Abstract][Full Text] [Related]
26. [Acquired Gitelman syndrome associated with Sjögren's syndrome and scleroderma]. Hinschberger O; Martzolff L; Ioannou G; Baumann D; Jaeger F; Kieffer P Rev Med Interne; 2011 Aug; 32(8):e96-8. PubMed ID: 20888090 [TBL] [Abstract][Full Text] [Related]
27. 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; 13(5):330-338. PubMed ID: 38308744 [TBL] [Abstract][Full Text] [Related]
28. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Blanchard A; Bockenhauer D; Bolignano D; Calò LA; Cosyns E; Devuyst O; Ellison DH; Karet Frankl FE; Knoers NV; Konrad M; Lin SH; Vargas-Poussou R Kidney Int; 2017 Jan; 91(1):24-33. PubMed ID: 28003083 [TBL] [Abstract][Full Text] [Related]
29. 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(1):275. PubMed ID: 30340552 [TBL] [Abstract][Full Text] [Related]
31. Arg913Gln variation of SLC12A3 gene is associated with diabetic nephropathy in type 2 diabetes and Gitelman syndrome: a systematic review. De la Cruz-Cano E; Jiménez-González CDC; Morales-García V; Pineda-Pérez C; Tejas-Juárez JG; Rendón-Gandarilla FJ; Jiménez-Morales S; Díaz-Gandarilla JA BMC Nephrol; 2019 Oct; 20(1):393. PubMed ID: 31660880 [TBL] [Abstract][Full Text] [Related]
32. Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome. Lo YF; Nozu K; Iijima K; Morishita T; Huang CC; Yang SS; Sytwu HK; Fang YW; Tseng MH; Lin SH Clin J Am Soc Nephrol; 2011 Mar; 6(3):630-9. PubMed ID: 21051746 [TBL] [Abstract][Full Text] [Related]
33. Gitelman syndrome with normocalciuria - a case report. Flisiński M; Skalska E; Mączyńska B; Butt-Hussaim N; Sobczyńska-Tomaszewska A; Haus O; Manitius J BMC Nephrol; 2022 May; 23(1):170. PubMed ID: 35509038 [TBL] [Abstract][Full Text] [Related]
34. Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene. Conticini E; Negro A; Magnani L; Ugolini R; Atienza-Mateo B; Frediani B; Salvarani C Reumatismo; 2020 Apr; 72(1):67-70. PubMed ID: 32292023 [TBL] [Abstract][Full Text] [Related]
35. Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review. Xu J; He J; Xu S; Wang R; Peng N; Zhang M BMC Nephrol; 2023 May; 24(1):123. PubMed ID: 37131142 [TBL] [Abstract][Full Text] [Related]
36. [Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia]. Ryšavá R; Reiterová J; Urbanová M; Štekrová J; Lněnička P; Tesař V Vnitr Lek; 2016; 62 Suppl 6():78-83. PubMed ID: 28124936 [TBL] [Abstract][Full Text] [Related]
37. Gitelman's syndrome: report of one case. Chan CF; Mu SC; Lau BH; Chang CJ; Lin SH Acta Paediatr Taiwan; 2008; 49(1):31-4. PubMed ID: 18581727 [TBL] [Abstract][Full Text] [Related]
38. Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes. Fava C; Montagnana M; Rosberg L; Burri P; Jönsson A; Wanby P; Wahrenberg H; Hulthén UL; Aurell M; Guidi GC; Melander O DNA Seq; 2007 Oct; 18(5):395-9. PubMed ID: 17654016 [TBL] [Abstract][Full Text] [Related]
39. Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review. Zhou H; Liang X; Qing Y; Meng B; Zhou J; Huang S; Lu S; Huang Z; Yang H; Ma Y; Luo Z BMC Endocr Disord; 2018 Nov; 18(1):82. PubMed ID: 30409157 [TBL] [Abstract][Full Text] [Related]
40. A novel initial codon mutation of the thiazide-sensitive Na-Cl cotransporter gene in a Japanese patient with Gitelman's syndrome. Aoki K; Tajima T; Yabushita Y; Nakamura A; Nezu U; Takahashi M; Kimura M; Terauchi Y Endocr J; 2008 Jul; 55(3):557-60. PubMed ID: 18520105 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]