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Browsing by Author Spronsen, F.J. van

Full Text	Issue Date	Title	Author(s)
	2011	NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease	Hoefs, S.J.G.; Spronsen, F.J. van; Lenssen, E.W.H.; Nijtmans, L.G.J.; Rodenburg, R.J.T., et al
	2011	The 48-hour tetrahydrobiopterin loading test in patients with phenylketonuria: evaluation of protocol and influence of baseline phenylalanine concentration.	Anjema, K.; Venema, G.; Hofstede, F.C.; Carbasius Weber, E.C.; Bosch, A.M., et al
	2011	Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern	Mohamed, M.; Guillard, M.; Wortmann, S.B.; Cirak, S.; Marklova, E., et al
	2009	Het juiste medicijn voor cerebrotendineuze xanthomatose	Verrips, A.; Wevers, R.A.; Spronsen, F.J. van; Sikkens, H.
	2008	Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.	Janssen, A.J.; Schuelke, M.; Smeitink, J.A.M.; Trijbels, F.J.; Sengers, R.C., et al
	1995	Information processing in patients with early and continuously-treated phenylketonuria	Stemerdink, B.A.; Meere, J.J. van der; Molen, M.W. van der; Kalverboer, A.F.; Hendrikx, M.M.T., et al