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Browsing by Author Wilcken, B.

Full Text	Issue Date	Title	Author(s)
	2010	3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy.	Wortmann, S.B.; Kremer, H.P.H.; Graham, A.; Willemsen, M.H.; Loupatty, F.J., et al
	2010	Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.	Willemsen, M.A.A.P.; Verbeek, M.M.; Kamsteeg, E.J.; Rijk-van Andel, J.F. de; Aeby, A., et al
	2007	Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion.	Vyletal, P.; Sokolova, J.; Cooper, D.N.; Kraus, J.P.; Krawczak, M., et al
	2006	Abnormal glycosylation with hypersialylated O-glycans in patients with Sialuria.	Wopereis, S.; Hamid, U.M. Abd; Critchley, A.; Royle, L.; Dwek, R.A., et al