Similar articles for PMID: 15875219

Year	Number of Results
1997	4
1998	3
1999	2
2000	4
2001	3
2002	2
2003	7
2004	8
2005	8
2006	8
2007	4
2008	6
2009	7
2010	8
2011	7
2012	3
2013	8
2014	10
2015	6
2016	12
2017	10
2018	7
2019	11
2020	12
2021	6
2022	6
2023	4
2024	0

1

A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.

Rodríguez-Soriano J, Vallo A, Pérez de Nanclares G, Bilbao JR, Castaño L. Rodríguez-Soriano J, et al. Pediatr Nephrol. 2005 Jul;20(7):891-6. doi: 10.1007/s00467-005-1867-z. Epub 2005 May 5. Pediatr Nephrol. 2005. PMID: 15875219

2

A Spanish founder mutation in the chloride channel gene, CLCNKB, as a cause of atypical Bartter syndrome in adult age.

Gorgojo JJ, Donnay S, Jeck N, Konrad M. Gorgojo JJ, et al. Horm Res. 2006;65(2):62-8. doi: 10.1159/000090601. Epub 2006 Jan 2. Horm Res. 2006. PMID: 16391491

3

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.

Zelikovic I, Szargel R, Hawash A, Labay V, Hatib I, Cohen N, Nakhoul F. Zelikovic I, et al. Kidney Int. 2003 Jan;63(1):24-32. doi: 10.1046/j.1523-1755.2003.00730.x. Kidney Int. 2003. PMID: 12472765 Free article.

4

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Konrad M, Vollmer M, Lemmink HH, VAN DEN Heuvel LPWJ, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NVAM, Seyberth HW, Feldmann D, Hildebrandt F. Konrad M, et al. J Am Soc Nephrol. 2000 Aug;11(8):1449-1459. doi: 10.1681/ASN.V1181449. J Am Soc Nephrol. 2000. PMID: 10906158

5

ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.

Andrini O, Keck M, Briones R, Lourdel S, Vargas-Poussou R, Teulon J. Andrini O, et al. Am J Physiol Renal Physiol. 2015 Jun 15;308(12):F1324-34. doi: 10.1152/ajprenal.00004.2015. Epub 2015 Mar 25. Am J Physiol Renal Physiol. 2015. PMID: 25810436 Free article. Review.

6

Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome.

Bettinelli A, Borsa N, Syrén ML, Mattiello C, Coviello D, Edefonti A, Giani M, Travi M, Tedeschi S. Bettinelli A, et al. Pediatr Res. 2005 Dec;58(6):1269-73. doi: 10.1203/01.pdr.0000185267.95466.41. Pediatr Res. 2005. PMID: 16306206

7

Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.

Cheng CJ, Lo YF, Chen JC, Huang CL, Lin SH. Cheng CJ, et al. J Physiol. 2017 Aug 15;595(16):5573-5586. doi: 10.1113/JP274344. Epub 2017 Jun 27. J Physiol. 2017. PMID: 28555925 Free PMC article.

8

Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm.

García Castaño A, Pérez de Nanclares G, Madariaga L, Aguirre M, Madrid A, Nadal I, Navarro M, Lucas E, Fijo J, Espino M, Espitaletta Z, Castaño L, Ariceta G; RenalTube Group. García Castaño A, et al. PLoS One. 2013 Sep 18;8(9):e74673. doi: 10.1371/journal.pone.0074673. eCollection 2013. PLoS One. 2013. PMID: 24058621 Free PMC article.

9

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.

Jeck N, Konrad M, Peters M, Weber S, Bonzel KE, Seyberth HW. Jeck N, et al. Pediatr Res. 2000 Dec;48(6):754-8. doi: 10.1203/00006450-200012000-00009. Pediatr Res. 2000. PMID: 11102542

10

Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome.

Yu Y, Xu C, Pan X, Ren H, Wang W, Meng X, Huang F, Chen N. Yu Y, et al. Clin Genet. 2010 Feb;77(2):155-62. doi: 10.1111/j.1399-0004.2009.01288.x. Epub 2009 Oct 6. Clin Genet. 2010. PMID: 19807735

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