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Journal of the Neurological Sciences|June 1, 1994
Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutationD de Vries, I de Wijs, W Ruitenbeek, et al.
Journal of Neurology|May 1, 1987
Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brainP M van Erven, F J Gabreëls, W Ruitenbeek, et al.
Neuropediatrics|February 1, 1986
Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome)P M van Erven, W Ruitenbeek, F J Gabreëls, et al.
Developmental Medicine and Child Neurology|February 1, 1989
Hypokinesia and rigidity as clinical manifestations of mitochondrial encephalomyopathy: report of three casesP M van Erven, W O Renier, F J Gabreëls, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1987
Neuromuscular investigations in retinitis pigmentosaL A Bastiaensen, W Ruitenbeek, A M Stadhouders, et al.
European Journal of Pediatrics|October 1, 1989
Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathyH Hurvitz, O N Elpeleg, V Barash, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1988
A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscleP M Van Erven, F J Gabreëls, W Ruitenbeek, et al.
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