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

Year Number of Results
1954 1
1967 1
1968 1
1969 1
1975 1
1977 2
1978 1
1979 4
1980 2
1985 2
1986 3
1987 2
1988 1
1990 1
1991 1
1992 2
1993 2
1994 3
1995 3
1996 1
1997 2
1998 4
1999 5
2000 10
2001 8
2002 3
2003 6
2004 7
2005 6
2006 12
2007 9
2008 15
2009 11
2010 5
2011 19
2012 11
2013 6
2014 13
2015 16
2016 10
2017 11
2018 10
2019 8
2020 7
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Similar Articles for PMID: 11518780

222 results
Results by year
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Page 1
Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Weber S, Schneider L, Peters M, Misselwitz J, Rönnefarth G, Böswald M, Bonzel KE, Seeman T, Suláková T, Kuwertz-Bröking E, Gregoric A, Palcoux JB, Tasic V, Manz F, Schärer K, Seyberth HW, Konrad M. Weber S, et al. J Am Soc Nephrol. 2001 Sep;12(9):1872-81. J Am Soc Nephrol. 2001. PMID: 11518780 Free article.
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene.
Weber S, Hoffmann K, Jeck N, Saar K, Boeswald M, Kuwertz-Broeking E, Meij II, Knoers NV, Cochat P, Suláková T, Bonzel KE, Soergel M, Manz F, Schaerer K, Seyberth HW, Reis A, Konrad M. Weber S, et al. Eur J Hum Genet. 2000 Jun;8(6):414-22. doi: 10.1038/sj.ejhg.5200475. Eur J Hum Genet. 2000. PMID: 10878661 Free article.
Nephrocalcinosis in siblings--familial hypomagnesemia, hypercalciuria with nephrocalcinosis (FHHNC syndrome).
Prabahar MR, Manorajan R, Fernando ME, Venkatraman R, Balaraman V, Jayakumar M. Prabahar MR, et al. J Assoc Physicians India. 2006 Jun;54:497-500. J Assoc Physicians India. 2006. PMID: 16909703
A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.
Sanjad SA, Hariri A, Habbal ZM, Lifton RP. Sanjad SA, et al. Pediatr Nephrol. 2007 Apr;22(4):503-8. doi: 10.1007/s00467-006-0354-5. Epub 2006 Nov 23. Pediatr Nephrol. 2007. PMID: 17123117
Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.
Wolf MT, Dötsch J, Konrad M, Böswald M, Rascher W. Wolf MT, et al. Pediatr Nephrol. 2002 Aug;17(8):602-8. doi: 10.1007/s00467-002-0884-4. Epub 2002 Jun 11. Pediatr Nephrol. 2002. PMID: 12185465
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in 2 sisters.
Al-Elq AH. Al-Elq AH. Saudi Med J. 2008 Mar;29(3):447-51. Saudi Med J. 2008. PMID: 18327378
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.
Hypomagnesemia and nephrocalcinosis in a patient with two heterozygous mutations in the CLDN16 gene.
Staiger K, Staiger H, Haas C, Thamer C, Risler T, Machicao F, Häring HU. Staiger K, et al. J Nephrol. 2007 Jan-Feb;20(1):107-10. J Nephrol. 2007. PMID: 17347984
A novel mutation of the claudin 16 gene in familial hypomagnesemia with hypercalciuria and nephrocalcinosis mimicking rickets.
Kasapkara CS, Tumer L, Okur I, Hasanoglu A. Kasapkara CS, et al. Genet Couns. 2011;22(2):187-92. Genet Couns. 2011. PMID: 21848011
The role of tight junctions in paracellular ion transport in the renal tubule: lessons learned from a rare inherited tubular disorder.
Haisch L, Almeida JR, Abreu da Silva PR, Schlingmann KP, Konrad M. Haisch L, et al. Am J Kidney Dis. 2011 Feb;57(2):320-30. doi: 10.1053/j.ajkd.2010.08.038. Epub 2010 Dec 24. Am J Kidney Dis. 2011. PMID: 21186073
222 results
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