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Browsing by Author Haas, D.

Full Text	Issue Date	Title	Author(s)
	2011	Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy	Smits, P.; Saada, A.; Wortmann, S.B.; Heister, A.; Brink, M., et al
	2009	Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria.	Haas, D.; Niklowitz, P.; Horster, F.; Baumgartner, E.R.; Prasad, C., et al
	2004	Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiency.	Wolf, N.I.; Haas, D.; Hoffmann, G.F.; Jakobs, C.; Salomons, G.S., et al