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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 2
1998 2
2000 2
2002 1
2003 2
2004 3
2005 4
2006 5
2007 10
2008 12
2009 8
2010 12
2011 20
2012 12
2013 7
2014 4
2015 8
2016 17
2017 11
2018 8
2019 10
2020 8
2021 0
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Similar articles for PMID: 21415153

142 results
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Page 1
Spectrum of mutations in Gitelman syndrome.
Vargas-Poussou R, Dahan K, Kahila D, Venisse A, Riveira-Munoz E, Debaix H, Grisart B, Bridoux F, Unwin R, Moulin B, Haymann JP, Vantyghem MC, Rigothier C, Dussol B, Godin M, Nivet H, Dubourg L, Tack I, Gimenez-Roqueplo AP, Houillier P, Blanchard A, Devuyst O, Jeunemaitre X. Vargas-Poussou R, et al. J Am Soc Nephrol. 2011 Apr;22(4):693-703. doi: 10.1681/ASN.2010090907. Epub 2011 Mar 17. J Am Soc Nephrol. 2011. PMID: 21415153 Free PMC article.
Gitelman's syndrome: a pathophysiological and clinical update.
Nakhoul F, Nakhoul N, Dorman E, Berger L, Skorecki K, Magen D. Nakhoul F, et al. Endocrine. 2012 Feb;41(1):53-7. doi: 10.1007/s12020-011-9556-0. Epub 2011 Nov 15. Endocrine. 2012. PMID: 22169961 Review.
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. Lo YF, et al. Clin J Am Soc Nephrol. 2011 Mar;6(3):630-9. doi: 10.2215/CJN.06730810. Epub 2010 Nov 4. Clin J Am Soc Nephrol. 2011. PMID: 21051746 Free PMC article.
Genotype, phenotype, and follow-up in Taiwanese patients with salt-losing tubulopathy associated with SLC12A3 mutation.
Tseng MH, Yang SS, Hsu YJ, Fang YW, Wu CJ, Tsai JD, Hwang DY, Lin SH. Tseng MH, et al. J Clin Endocrinol Metab. 2012 Aug;97(8):E1478-82. doi: 10.1210/jc.2012-1707. Epub 2012 Jun 7. J Clin Endocrinol Metab. 2012. PMID: 22679066
Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome.
Riveira-Munoz E, Devuyst O, Belge H, Jeck N, Strompf L, Vargas-Poussou R, Jeunemaître X, Blanchard A, Knoers NV, Konrad M, Dahan K. Riveira-Munoz E, et al. Nephrol Dial Transplant. 2008 Oct;23(10):3120-5. doi: 10.1093/ndt/gfn229. Epub 2008 May 9. Nephrol Dial Transplant. 2008. PMID: 18469313
Novel SLC12A3 mutations in Chinese patients with Gitelman's syndrome.
Shao L, Ren H, Wang W, Zhang W, Feng X, Li X, Chen N. Shao L, et al. Nephron Physiol. 2008;108(3):p29-36. doi: 10.1159/000117815. Epub 2008 Feb 21. Nephron Physiol. 2008. PMID: 18287808
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome.
Lee JW, Lee J, Heo NJ, Cheong HI, Han JS. Lee JW, et al. J Korean Med Sci. 2016 Jan;31(1):47-54. doi: 10.3346/jkms.2016.31.1.47. Epub 2015 Dec 24. J Korean Med Sci. 2016. PMID: 26770037 Free PMC article.
Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome.
Balavoine AS, Bataille P, Vanhille P, Azar R, Noël C, Asseman P, Soudan B, Wémeau JL, Vantyghem MC. Balavoine AS, et al. Eur J Endocrinol. 2011 Oct;165(4):665-73. doi: 10.1530/EJE-11-0224. Epub 2011 Jul 13. Eur J Endocrinol. 2011. PMID: 21753071
Gitelman's syndrome: towards genotype-phenotype correlations?
Riveira-Munoz E, Chang Q, Bindels RJ, Devuyst O. Riveira-Munoz E, et al. Pediatr Nephrol. 2007 Mar;22(3):326-32. doi: 10.1007/s00467-006-0321-1. Epub 2006 Oct 24. Pediatr Nephrol. 2007. PMID: 17061123 Review.
A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome patients.
Tavira B, Gómez J, Santos F, Gil H, Alvarez V, Coto E. Tavira B, et al. J Hum Genet. 2014 Jul;59(7):376-80. doi: 10.1038/jhg.2014.37. Epub 2014 May 15. J Hum Genet. 2014. PMID: 24830959
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