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Browsing by Author Scholte, H.R.

Full Text	Issue Date	Title	Author(s)
	2007	A simplified and reliable assay for complex I in human blood lymphocytes.	Wit, L.E. de; Spruijt, L.; Schoonderwoerd, G.C.; Coo, I.F.M. de; Smeets, H.J.M., et al
	2005	Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation.	Jacobs, L.J.; Coo, I.F.M. de; Nijland, J.G.; Galjaard, R.J.; Los, F.J., et al
	1996	Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiency.	Bakker, H.; Bogert, C. van den; Drewes, J.G.; Barth, P.G.; Scholte, H.R., et al
	1995	Isolated mitochondria from frozen muscle have limited value in diagnostics	Scholte, H.R.; Trijbels, J.M.F.
	1995	Deficiëntie van de adenine-nucleotide-translocator in spierweefsel: een mitochondriale ziekte, behandeld met vitamine E	Bakker, H.D.; Bogert, C. van den; Scholte, H.R.; Jeneson, J.A.L.; Ruitenbeek, W., et al