Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1985 1
1987 1
1988 1
1992 1
1993 1
1994 2
1995 1
1996 1
1997 6
1998 6
1999 4
2000 6
2001 7
2002 2
2003 10
2004 3
2005 5
2006 6
2007 4
2008 6
2009 5
2010 5
2011 5
2012 7
2013 8
2014 11
2015 9
2016 14
2017 15
2018 13
2019 16
2020 22
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 28381550

181 results
Results by year
Filters applied: . Clear all
Page 1
Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
Seys E, Andrini O, Keck M, Mansour-Hendili L, Courand PY, Simian C, Deschenes G, Kwon T, Bertholet-Thomas A, Bobrie G, Borde JS, Bourdat-Michel G, Decramer S, Cailliez M, Krug P, Cozette P, Delbet JD, Dubourg L, Chaveau D, Fila M, Jourde-Chiche N, Knebelmann B, Lavocat MP, Lemoine S, Djeddi D, Llanas B, Louillet F, Merieau E, Mileva M, Mota-Vieira L, Mousson C, Nobili F, Novo R, Roussey-Kesler G, Vrillon I, Walsh SB, Teulon J, Blanchard A, Vargas-Poussou R. Seys E, et al. J Am Soc Nephrol. 2017 Aug;28(8):2540-2552. doi: 10.1681/ASN.2016101057. Epub 2017 Apr 5. J Am Soc Nephrol. 2017. PMID: 28381550 Free PMC article.
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Brochard K, Boyer O, Blanchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaître X, Vargas-Poussou R. Brochard K, et al. Nephrol Dial Transplant. 2009 May;24(5):1455-64. doi: 10.1093/ndt/gfn689. Epub 2008 Dec 18. Nephrol Dial Transplant. 2009. PMID: 19096086
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.
Konrad M, Vollmer M, Lemmink HH, van den Heuvel LP, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NV, Seyberth HW, Feldmann D, Hildebrandt F. Konrad M, et al. J Am Soc Nephrol. 2000 Aug;11(8):1449-59. J Am Soc Nephrol. 2000. PMID: 10906158 Free article.
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.
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.
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.
García Castaño A, Pérez de Nanclares G, Madariaga L, Aguirre M, Madrid Á, Chocrón S, Nadal I, Navarro M, Lucas E, Fijo J, Espino M, Espitaletta Z, García Nieto V, Barajas de Frutos D, Loza R, Pintos G, Castaño L; RenalTube Group, Ariceta G. García Castaño A, et al. PLoS One. 2017 Mar 13;12(3):e0173581. doi: 10.1371/journal.pone.0173581. eCollection 2017. PLoS One. 2017. PMID: 28288174 Free PMC article.
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.
A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report.
Zhu B, Jiang H, Cao M, Zhao X, Jiang H. Zhu B, et al. BMC Med Genet. 2019 Aug 13;20(1):137. doi: 10.1186/s12881-019-0869-9. BMC Med Genet. 2019. PMID: 31409296 Free PMC article.
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 Free article.
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.
181 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback