W. Ruitenbeek

A 4–base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

I.F.M. de Coo, W.O. Renier, W. Ruitenbeek et al. · Annals of Neurology · 1999 · 129 citations

Mitochondrial Respiratory Chain, Neurodegenerative Diseases, Mendelian Disorder +14

A 4-base pair deletion in the mitochondrial cytochromeb gene associated with parkinsonism/MELAS overlap syndrome

I.F.M. de Coo, W.O. Renier, W. Ruitenbeek et al. · Annals of Neurology · 1999 · 128 citations · Full text

Mitophagy, Mitochondrial Cytochromeb Gene, Genetics +21

Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency

R. C. A. Sengers, J. M. F. Trijbels, J. A. J. M. Bakkeren et al. · European Journal of Pediatrics · 1984 · 65 citations

Developmental Biology, Biochemistry, Cytochromes B +7

Clinical heterogeneity in respiratory chain complex III deficiency in childhood

J. Mourmans, U. Wendel, Herman Bentlage et al. · Journal of the Neurological Sciences · 1997 · 62 citations

Asthma, Pediatric Epidemiology, Respiratory Diseases +9

A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency

R. C. A. Sengers, Johan Fischer, J. M. F. Trijbels et al. · European Journal of Pediatrics · 1983 · 49 citations

Mitochondrial Myopathy, Defective Respiratory Chain, Mitochondrial Function +7