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

Year Number of Results
1985 1
1992 2
1995 1
1998 1
1999 1
2000 4
2001 5
2002 2
2003 6
2004 4
2005 2
2006 6
2008 11
2009 8
2010 4
2011 5
2012 5
2013 5
2014 2
2015 4
2016 4
2017 4
2018 2
2019 2
2020 1
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Similar Articles for PMID: 12949294

79 results
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The neonatal variant of Bartter syndrome and deafness: preservation of renal function.
Shalev H, Ohali M, Kachko L, Landau D. Shalev H, et al. Pediatrics. 2003 Sep;112(3 Pt 1):628-33. doi: 10.1542/peds.112.3.628. Pediatrics. 2003. PMID: 12949294
Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.
Jeck N, Reinalter SC, Henne T, Marg W, Mallmann R, Pasel K, Vollmer M, Klaus G, Leonhardt A, Seyberth HW, Konrad M. Jeck N, et al. Pediatrics. 2001 Jul;108(1):E5. doi: 10.1542/peds.108.1.e5. Pediatrics. 2001. PMID: 11433084
Type IV Bartter syndrome: report of two new cases.
Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F. Zaffanello M, et al. Pediatr Nephrol. 2006 Jun;21(6):766-70. doi: 10.1007/s00467-006-0090-x. Epub 2006 Apr 1. Pediatr Nephrol. 2006. PMID: 16583241
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
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.
Birkenhäger R, Otto E, Schürmann MJ, Vollmer M, Ruf EM, Maier-Lutz I, Beekmann F, Fekete A, Omran H, Feldmann D, Milford DV, Jeck N, Konrad M, Landau D, Knoers NV, Antignac C, Sudbrak R, Kispert A, Hildebrandt F. Birkenhäger R, et al. Nat Genet. 2001 Nov;29(3):310-4. doi: 10.1038/ng752. Nat Genet. 2001. PMID: 11687798
A case of antenatal Bartter syndrome with sensorineural deafness.
Lee HS, Cheong HI, Ki CS. Lee HS, et al. J Pediatr Endocrinol Metab. 2010 Oct;23(10):1077-81. doi: 10.1515/jpem.2010.170. J Pediatr Endocrinol Metab. 2010. PMID: 21158220
Atypical Bartter syndrome with sensorineural deafness with G47R mutation of the beta-subunit for ClC-Ka and ClC-Kb chloride channels, barttin.
Miyamura N, Matsumoto K, Taguchi T, Tokunaga H, Nishikawa T, Nishida K, Toyonaga T, Sakakida M, Araki E. Miyamura N, et al. J Clin Endocrinol Metab. 2003 Feb;88(2):781-6. doi: 10.1210/jc.2002-021398. J Clin Endocrinol Metab. 2003. PMID: 12574213
Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.
Wang HH, Feng Y, Li HB, Wu H, Mei LY, Wang XW, Jiang L, He CF. Wang HH, et al. Int J Pediatr Otorhinolaryngol. 2017 Jan;92:17-20. doi: 10.1016/j.ijporl.2016.10.028. Epub 2016 Oct 26. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28012523
Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families.
García-Nieto V, Flores C, Luis-Yanes MI, Gallego E, Villar J, Claverie-Martín F. García-Nieto V, et al. Pediatr Nephrol. 2006 May;21(5):643-8. doi: 10.1007/s00467-006-0062-1. Epub 2006 Mar 29. Pediatr Nephrol. 2006. PMID: 16572343
[Bartter syndrome and it's neonatal type].
Jankauskiene A, Jakutovic M. Jankauskiene A, et al. Medicina (Kaunas). 2003;39 Suppl 1:88-93. Medicina (Kaunas). 2003. PMID: 12761427 Free article. Review. Lithuanian.
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