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| | 1 - 10 of 103 journal articles in the PubMed database | Email to a friend | | |
| Hampson G, Konrad MA, Scoble J
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): compound heterozygous mutation in the claudin 16 (CLDN16) gene. [JOURNAL ARTICLE]
BMC Nephrol 2008 Sep 24; 9(1):12.
Abstract | Full Citation | Find Related Articles | | Tajima T, Nakae J, Fujieda K
Two heterozygous mutations of CLDN16 in a Japanese patient with FHHNC. [Case Reports, Journal Article]
Pediatr Nephrol 2003 Dec; 18(12):1280-2.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kang JH, Choi HJ, Cho HY, et al.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations. [Case Reports, Journal Article]
Pediatr Nephrol 2005 Oct; 20(10):1490-3.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Peru H, Akin F, Elmas S, et al.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: report of three Turkish siblings. [JOURNAL ARTICLE]
Pediatr Nephrol 2008 Feb 6.
Abstract | Full Citation | Find Related Articles | | Müller D, Kausalya PJ, Bockenhauer D, et al.
Unusual clinical presentation and possible rescue of a novel Claudin-16 mutation. [JOURNAL ARTICLE]
J Clin Endocrinol Metab 2006 May 16.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Müller D, Kausalya PJ, Meij IC, et al.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail. [Journal Article]
Hum Mol Genet 2006 Apr 1; 15(7):1049-58.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Weber S, Schneider L, Peters M, et al.
Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. [Journal Article]
J Am Soc Nephrol 2001 Sep; 12(9):1872-81.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Staiger K, Staiger H, Haas C, et al.
Hypomagnesemia and nephrocalcinosis in a patient with two heterozygous mutations in the CLDN16 gene. [JOURNAL ARTICLE]
J Nephrol 2007 January - February 2007; 20(1):107-110.
Abstract | Full Citation | Find Related Articles | | Tasic V, Dervisov D, Koceva S, et al.
Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study. [Case Reports, Journal Article]
Pediatr Nephrol 2005 Jul; 20(7):1003-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
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