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Browsing by Author Devuyst, O.

Full Text	Issue Date	Title	Author(s)
	2011	Clinical utility gene card for: Gitelman syndrome	Knoers, N.V.A.M.; Devuyst, O.; Kamsteeg, E.J.
	2011	CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia	Stuiver, M.; Lainez, S.; Will, C., et al
	2009	EUNEFRON, the European Network for the Study of Orphan Nephropathies.	Devuyst, O.; Meij, I.; Jeunemaitre, X., et al
	2008	Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome.	Riveira-Munoz, E.; Devuyst, O.; Belge, H., et al
	2007	Gitelman's syndrome: towards genotype-phenotype correlations?	Riveira-Munoz, E.; Chang, Q.; Bindels, R.J.M., et al
	2011	The 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
	2006	Introduction: special issue on aquaporins.	Chaumont, F.; Deen, P.M.T.; Delporte, C., et al
	2007	Renal expression of parvalbumin is critical for NaCl handling and response to diuretics.	Belge, H.; Gailly, P.; Schwaller, B., et al
	2007	Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.	Riveira-Munoz, E.; Chang, Q.; Godefroid, N., et al