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Journal of Bioenergetics and Biomembranes|April 1, 1996
Importance of mitochondrial transmembrane processes in human mitochondriopathiesM Huizing, V DePinto, W Ruitenbeek, et al.
Cell|August 27, 1993
Skeletal muscles of mice deficient in muscle creatine kinase lack burst activityJ van Deursen, A Heerschap, F Oerlemans, et al.
Electrophoresis|April 1, 1996
Electrophoretic separation of multiprotein complexes from blood platelets and cell lines: technique for the analysis of diseases with defects in oxidative phosphorylationH Schägger, H Bentlage, W Ruitenbeek, et al.
Annals of Neurology|September 1, 1993
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndromeD D de Vries, B G van Engelen, F J Gabreëls, et al.
Neuropediatrics|April 29, 1998
Systemic infantile complex I deficiency with fatal outcome in two brothersM E Rubio-Gozalbo, W Ruitenbeek, U Wendel, et al.
Archives of Neurology|March 1, 1991
Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitineP L Bernsen, F J Gabreëls, W Ruitenbeek, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Klinische Padiatrie|September 1, 1988
[Encephalomyelopathy, cardiomyopathy, cataract and changes in the retinal pigment epithelium resulting from a cytochrome c oxidase deficiency]L Sieverding, A A Schmaltz, J Apitz, et al.
European Journal of Pediatrics|March 1, 1993
Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathiesJ M Trijbels, H R Scholte, W Ruitenbeek, et al.
Neurology|June 1, 1992
No evidence for reduced thrombocyte cytochrome oxidase activity in Alzheimer's diseaseA J Van Zuylen, G J Bosman, W Ruitenbeek, et al.
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