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Browsing by Author Devuyst, O.

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Full TextIssue DateTitleAuthor(s)
2012The ERA-EDTA Working Group on inherited kidney disorders.Devuyst, O.; Antignac, C.; Bindels, R.J.M., et al
2009EUNEFRON, the European Network for the Study of Orphan Nephropathies.Devuyst, O.; Meij, I.; Jeunemaitre, X., et al
2008Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome.Riveira-Munoz, E.; Devuyst, O.; Belge, H., et al
2007Gitelman's syndrome: towards genotype-phenotype correlations?Riveira-Munoz, E.; Chang, Q.; Bindels, R.J.M., et al
2011The inositol Inpp5k 5-phosphatase affects osmoregulation through the vasopressin-aquaporin 2 pathway in the collecting system.Pernot, E.; Terryn, S.; Cheong, S.C., et al
2006Introduction: special issue on aquaporins.Chaumont, F.; Deen, P.M.T.; Delporte, C., et al
2007Renal expression of parvalbumin is critical for NaCl handling and response to diuretics.Belge, H.; Gailly, P.; Schwaller, B., et al
2007Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.Riveira-Munoz, E.; Chang, Q.; Godefroid, N., et al
Showing results 3 to 10 of 10

 

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