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For: Kurtz I. Molecular pathogenesis of Bartter's and Gitelman's syndromes. Kidney Int. 1998;54:1396-1410. [PMID: 9767561 DOI: 10.1046/j.1523-1755.1998.00124.x] [Cited by in Crossref: 64] [Cited by in F6Publishing: 47] [Article Influence: 2.7] [Reference Citation Analysis]
Number Citing Articles
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9 Riveira-Munoz E, Chang Q, Godefroid N, Hoenderop JG, Bindels RJ, Dahan K, Devuyst O; Belgian Network for Study of Gitelman Syndrome. Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome. J Am Soc Nephrol. 2007;18:1271-1283. [PMID: 17329572 DOI: 10.1681/asn.2006101095] [Cited by in Crossref: 100] [Cited by in F6Publishing: 38] [Article Influence: 6.7] [Reference Citation Analysis]
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17 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]
18 Sabath E, Meade P, Berkman J, de los Heros P, Moreno E, Bobadilla NA, Vázquez N, Ellison DH, Gamba G. Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease. Am J Physiol Renal Physiol 2004;287:F195-203. [PMID: 15068971 DOI: 10.1152/ajprenal.00044.2004] [Cited by in Crossref: 63] [Cited by in F6Publishing: 50] [Article Influence: 3.5] [Reference Citation Analysis]
19 Hanna RM, Ahdoot RS, Kalantar-zadeh K, Ghobry L, Kurtz I. Calcium Transport in the Kidney and Disease Processes. Front Endocrinol 2022;12:762130. [DOI: 10.3389/fendo.2021.762130] [Reference Citation Analysis]
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21 Lin SH, Yu IS, Jiang ST, Lin SW, Chu P, Chen A, Sytwu HK, Sohara E, Uchida S, Sasaki S, Yang SS. Impaired phosphorylation of Na(+)-K(+)-2Cl(-) cotransporter by oxidative stress-responsive kinase-1 deficiency manifests hypotension and Bartter-like syndrome. Proc Natl Acad Sci U S A 2011;108:17538-43. [PMID: 21972418 DOI: 10.1073/pnas.1107452108] [Cited by in Crossref: 90] [Cited by in F6Publishing: 85] [Article Influence: 8.2] [Reference Citation Analysis]
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24 Meade P, Hoover RS, Plata C, Vázquez N, Bobadilla NA, Gamba G, Hebert SC. cAMP-dependent activation of the renal-specific Na + -K + -2Cl cotransporter is mediated by regulation of cotransporter trafficking. American Journal of Physiology-Renal Physiology 2003;284:F1145-54. [DOI: 10.1152/ajprenal.00421.2002] [Cited by in Crossref: 44] [Cited by in F6Publishing: 44] [Article Influence: 2.3] [Reference Citation Analysis]
25 Zhou H, Ren Y, Lu C, Li Y, Tian H, Chen T, Piccinni G. Thyroid Function in 35 Patients with Gitelman Syndrome. BioMed Research International 2020;2020:1-6. [DOI: 10.1155/2020/7963898] [Reference Citation Analysis]
26 Robitaille P, Merouani A, He N, Pei Y. Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness. Eur J Pediatr. 2011;170:1209-1211. [PMID: 21479528 DOI: 10.1007/s00431-011-1464-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
27 Fujimura J, Nozu K, Yamamura T, Minamikawa S, Nakanishi K, Horinouchi T, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Miyako K, Nozu Y, Morisada N, Nagase H, Ninchoji T, Kaito H, Iijima K. Clinical and Genetic Characteristics in Patients With Gitelman Syndrome. Kidney Int Rep. 2018;4:119-125. [PMID: 30596175 DOI: 10.1016/j.ekir.2018.09.015] [Cited by in Crossref: 14] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
28 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]
29 Sampathkumar K, Muralidharan U, Kannan A, Ramakrishnan M, Ajeshkumar R. Childhood Bartter's syndrome: An Indian case series. Indian J Nephrol 2010;20:207-10. [PMID: 21206684 DOI: 10.4103/0971-4065.73455] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
30 Gross P. Gitelman syndrome: when will it turn into Gitelman disease? Pediatr Nephrol 2003;18:613-6. [PMID: 12728368 DOI: 10.1007/s00467-003-1171-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
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33 Lin S, Cheng N, Hsu Y, Halperin ML. Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter. American Journal of Kidney Diseases 2004;43:304-12. [DOI: 10.1053/j.ajkd.2003.10.018] [Cited by in Crossref: 77] [Cited by in F6Publishing: 57] [Article Influence: 4.3] [Reference Citation Analysis]
34 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]
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36 Galla JH. Metabolic Alkalosis. JASN 2000;11:369-75. [DOI: 10.1681/asn.v112369] [Cited by in Crossref: 37] [Cited by in F6Publishing: 23] [Article Influence: 1.7] [Reference Citation Analysis]
37 Meyer M, Berrios M, Lo C. Transient Antenatal Bartter's Syndrome: A Case Report. Front Pediatr 2018;6:51. [PMID: 29594084 DOI: 10.3389/fped.2018.00051] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
38 Sardani Y, Qin K, Haas M, Aronson AJ, Rosenfield RL. Bartter syndrome complicated by immune complex nephropathy. Case report and literature review. Pediatr Nephrol 2003;18:913-8. [PMID: 12836094 DOI: 10.1007/s00467-003-1194-1] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
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40 Gamba G, Bobadilla NA. Molecular Physiology of the Renal Na+-Cl− and Na+-K+-2Cl− Cotransporters. In: Lauf PK, Adragna NC, editors. Cell Volume and Signaling. Springer US; 2005. pp. 55-65. [DOI: 10.1007/0-387-23752-6_5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
41 Bettinelli A, Tosetto C, Colussi G, Tommasini G, Edefonti A, Bianchetti MG. Electrocardiogram with prolonged QT interval in Gitelman disease. Kidney International 2002;62:580-4. [DOI: 10.1046/j.1523-1755.2002.00467.x] [Cited by in Crossref: 57] [Cited by in F6Publishing: 44] [Article Influence: 2.9] [Reference Citation Analysis]
42 de Haan J, Geers T, Berghout A. Gitelman syndrome in pregnancy. International Journal of Gynecology & Obstetrics 2008;103:69-71. [DOI: 10.1016/j.ijgo.2008.05.007] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 1.4] [Reference Citation Analysis]
43 Walch A, Duke M, Auty T, Wong A. Profound Hypokalaemia Resulting in Maternal Cardiac Arrest: A Catastrophic Complication of Hyperemesis Gravidarum? Case Rep Obstet Gynecol 2018;2018:4687587. [PMID: 30151287 DOI: 10.1155/2018/4687587] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
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45 Bianchetti MG, Edefonti A, Bettinelli A. The biochemical diagnosis of Gitelman disease and the definition of "hypocalciuria". Pediatr Nephrol 2003;18:409-11. [PMID: 12793424 DOI: 10.1007/s00467-003-1084-6] [Cited by in Crossref: 15] [Cited by in F6Publishing: 8] [Article Influence: 0.8] [Reference Citation Analysis]
46 Takahashi N, Chernavvsky DR, Gomez RA, Igarashi P, Gitelman HJ, Smithies O. Uncompensated polyuria in a mouse model of Bartter's syndrome. Proc Natl Acad Sci U S A 2000;97:5434-9. [PMID: 10779555 DOI: 10.1073/pnas.090091297] [Cited by in Crossref: 192] [Cited by in F6Publishing: 170] [Article Influence: 8.7] [Reference Citation Analysis]
47 Li J, Hu S, Nie Y, Wang R, Tan M, Li H, Zhu S. A novel compound heterozygous KCNJ1 gene mutation presenting as late-onset Bartter syndrome: Case report. Medicine (Baltimore) 2019;98:e16738. [PMID: 31441846 DOI: 10.1097/MD.0000000000016738] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
48 Seyberth HW. An improved terminology and classification of Bartter-like syndromes. Nat Clin Pract Nephrol. 2008;4:560-567. [PMID: 18695706 DOI: 10.1038/ncpneph0912] [Cited by in Crossref: 75] [Cited by in F6Publishing: 60] [Article Influence: 5.4] [Reference Citation Analysis]
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50 Chen YC, Yang WC, Yang AH, Lin SH, Li HY, Lin CC. Primary Sjögren's syndrome associated with Gitelman's syndrome presenting with muscular paralysis. Am J Kidney Dis 2003;42:586-90. [PMID: 12955689 DOI: 10.1016/s0272-6386(03)00792-3] [Cited by in Crossref: 15] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
51 de Arriba G, Sánchez-heras M, Basterrechea MA. Gitelman syndrome during pregnancy: a therapeutic challenge. Arch Gynecol Obstet 2009;280:807-9. [DOI: 10.1007/s00404-009-0994-3] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 1.8] [Reference Citation Analysis]
52 Herrero-Morín JD, Rodríguez J, Coto E, Gil-Peña H, Alvarez V, Espinosa L, Loris C, Gil-Calvo M, Santos F. Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life. Nephrol Dial Transplant 2011;26:151-5. [PMID: 20571093 DOI: 10.1093/ndt/gfq352] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
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55 Ellison DH. Divalent cation transport by the distal nephron: insights from Bartter's and Gitelman's syndromes. Am J Physiol Renal Physiol 2000;279:F616-25. [PMID: 10997911 DOI: 10.1152/ajprenal.2000.279.4.F616] [Cited by in Crossref: 73] [Cited by in F6Publishing: 22] [Article Influence: 3.3] [Reference Citation Analysis]
56 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]
57 Takemori S, Tanigaki S, Nozu K, Yoshihashi H, Uchiumi Y, Sakaguchi K, Tsushima K, Kitamura A, Kobayashi C, Matsuhima M, Tajima A, Nagano C, Kobayashi Y. Prenatal diagnosis of MAGED2 gene mutation causing transient antenatal Bartter syndrome. Eur J Med Genet 2021;64:104308. [PMID: 34400373 DOI: 10.1016/j.ejmg.2021.104308] [Reference Citation Analysis]
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