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

Year Number of Results
1971 1
1975 1
1985 1
1987 1
1992 1
1995 2
1997 1
1999 1
2000 1
2001 3
2002 1
2003 5
2004 3
2005 2
2006 11
2007 5
2008 7
2009 4
2010 5
2011 12
2012 8
2013 5
2014 12
2015 11
2016 5
2017 6
2018 7
2019 7
2020 6
2021 0
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Similar articles for PMID: 18003771

118 results
Results by year
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Page 1
CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Konrad M, Hou J, Weber S, Dötsch J, Kari JA, Seeman T, Kuwertz-Bröking E, Peco-Antic A, Tasic V, Dittrich K, Alshaya HO, von Vigier RO, Gallati S, Goodenough DA, Schaller A. Konrad M, et al. J Am Soc Nephrol. 2008 Jan;19(1):171-81. doi: 10.1681/ASN.2007060709. Epub 2007 Nov 14. J Am Soc Nephrol. 2008. PMID: 18003771 Free PMC 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
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.
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.
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
Unusual clinical presentation and possible rescue of a novel claudin-16 mutation.
Müller D, Kausalya PJ, Bockenhauer D, Thumfart J, Meij IC, Dillon MJ, van't Hoff W, Hunziker W. Müller D, et al. J Clin Endocrinol Metab. 2006 Aug;91(8):3076-9. doi: 10.1210/jc.2006-0200. Epub 2006 May 16. J Clin Endocrinol Metab. 2006. PMID: 16705067
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.
Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation.
Ekinci Z, Karabaş L, Konrad M. Ekinci Z, et al. Turk J Pediatr. 2012 Mar-Apr;54(2):168-70. Turk J Pediatr. 2012. PMID: 22734304
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): compound heterozygous mutation in the claudin 16 (CLDN16) gene.
Hampson G, Konrad MA, Scoble J. Hampson G, et al. BMC Nephrol. 2008 Sep 24;9:12. doi: 10.1186/1471-2369-9-12. BMC Nephrol. 2008. PMID: 18816383 Free PMC article.
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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