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Browsing by Author Laak, H. ter

Full Text	Issue Date	Title	Author(s)
	2008	Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency.	Contopoulos-Ioannidis, D.; Evangeliou, A.; Laak, H. ter; Vries, B. de; Pfundt, R.P., et al
	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	Dystrophic muscle changes with giant lysosomes and vitamin E deficiency : A case report	Laak, H. ter; Gabreëls, F.J.M.; Rotteveel, J.