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

Year Number of Results
1982 1
1992 1
1994 1
1995 2
1997 2
1999 2
2000 2
2001 3
2002 1
2003 4
2004 1
2005 2
2006 10
2007 4
2008 7
2009 6
2010 8
2011 14
2012 7
2013 7
2014 11
2015 6
2016 7
2017 7
2018 7
2019 7
2020 3
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Similar Articles for PMID: 21030577

114 results
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Page 1
Renal, ocular, and neuromuscular involvements in patients with CLDN19 mutations.
Faguer S, Chauveau D, Cintas P, Tack I, Cointault O, Rostaing L, Vargas-Poussou R, Ribes D. Faguer S, et al. Clin J Am Soc Nephrol. 2011 Feb;6(2):355-60. doi: 10.2215/CJN.02870310. Epub 2010 Oct 28. Clin J Am Soc Nephrol. 2011. PMID: 21030577 Free PMC article.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.
Godron A, Harambat J, Boccio V, Mensire A, May A, Rigothier C, Couzi L, Barrou B, Godin M, Chauveau D, Faguer S, Vallet M, Cochat P, Eckart P, Guest G, Guigonis V, Houillier P, Blanchard A, Jeunemaitre X, Vargas-Poussou R. Godron A, et al. Clin J Am Soc Nephrol. 2012 May;7(5):801-9. doi: 10.2215/CJN.12841211. Epub 2012 Mar 15. Clin J Am Soc Nephrol. 2012. PMID: 22422540 Free PMC article.
Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Claverie-Martín F, García-Nieto V, Loris C, Ariceta G, Nadal I, Espinosa L, Fernández-Maseda Á, Antón-Gamero M, Avila A, Madrid Á, González-Acosta H, Córdoba-Lanus E, Santos F, Gil-Calvo M, Espino M, García-Martinez E, Sanchez A, Muley R; RenalTube Group. Claverie-Martín F, et al. PLoS One. 2013;8(1):e53151. doi: 10.1371/journal.pone.0053151. Epub 2013 Jan 3. PLoS One. 2013. PMID: 23301036 Free PMC article.
Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease.
Naeem M, Hussain S, Akhtar N. Naeem M, et al. Am J Nephrol. 2011;34(3):241-8. doi: 10.1159/000330854. Epub 2011 Jul 26. Am J Nephrol. 2011. PMID: 21791920 Free article.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): report of three cases with a novel mutation in CLDN19 gene.
Al-Shibli A, Konrad M, Altay W, Al Masri O, Al-Gazali L, Al Attrach I. Al-Shibli A, et al. Saudi J Kidney Dis Transpl. 2013 Mar;24(2):338-44. doi: 10.4103/1319-2442.109601. Saudi J Kidney Dis Transpl. 2013. PMID: 23538362 Free article.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
Al-Haggar M, Bakr A, Tajima T, Fujieda K, Hammad A, Soliman O, Darwish A, Al-Said A, Yahia S, Abdel-Hady D. Al-Haggar M, et al. Clin Exp Nephrol. 2009 Aug;13(4):288-294. doi: 10.1007/s10157-008-0126-6. Epub 2009 Jan 24. Clin Exp Nephrol. 2009. PMID: 19165416
Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report.
Yamaguti PM, dos Santos PA, Leal BS, Santana VB, Mazzeu JF, Acevedo AC, Neves Fde A. Yamaguti PM, et al. BMC Nephrol. 2015 Jul 2;16:92. doi: 10.1186/s12882-015-0079-4. BMC Nephrol. 2015. PMID: 26136118 Free PMC article.
First report of a novel missense CLDN19 mutations causing familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a Chinese family.
Yuan T, Pang Q, Xing X, Wang X, Li Y, Li J, Wu X, Li M, Wang O, Jiang Y, Dong J, Xia W. Yuan T, et al. Calcif Tissue Int. 2015 Apr;96(4):265-73. doi: 10.1007/s00223-014-9951-7. Epub 2015 Jan 4. Calcif Tissue Int. 2015. PMID: 25555744
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry.
Arteaga ME, Hunziker W, Teo AS, Hillmer AM, Mutchinick OM. Arteaga ME, et al. Ren Fail. 2015 Feb;37(1):180-3. doi: 10.3109/0886022X.2014.977141. Epub 2014 Nov 4. Ren Fail. 2015. PMID: 25366522
Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Martin-Nuñez E, Cordoba-Lanus E, Gonzalez-Acosta H, Oliet A, Izquierdo E, Claverie-Martin F. Martin-Nuñez E, et al. World J Pediatr. 2015 Aug;11(3):272-5. doi: 10.1007/s12519-014-0528-3. Epub 2014 Nov 20. World J Pediatr. 2015. PMID: 25410674
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