W Ruitenbeek - JoVE Visualize

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Neurology|February 5, 1999

Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiencyM E Rubio-Gozalbo, J A Smeitink, W Ruitenbeek, et al.

Journal of Neuroscience Methods|January 1, 1997

Use of gene targeting for compromising energy homeostasis in neuro-muscular tissues: the role of sarcomeric mitochondrial creatine kinaseK Steeghs, A Heerschap, A de Haan, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndromeD D de Vries, C J Buzing, W Ruitenbeek, et al.

Pediatric Research|May 1, 1996

Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathyM Huizing, W Ruitenbeek, F P Thinnes, et al.

Neuropediatrics|June 1, 1992

Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic dietF A Wijburg, P G Barth, L A Bindoff, et al.

European Journal of Pediatrics|December 1, 1990

Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathiesG C Korenke, H A Bentlage, W Ruitenbeek, et al.

Clinical Neurology and Neurosurgery|January 1, 1987

Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literatureP M van Erven, J P Cillessen, E M Eekhoff, et al.

Human Mutation|January 1, 1996

Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.

Acta Neurologica Scandinavica|July 1, 1985

Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liverP M Van Erven, F J Gabreëls, W Ruitenbeek, et al.

Nature Genetics|August 1, 1992

Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessJ M van den Ouweland, H H Lemkes, W Ruitenbeek, et al.

Pageof 11

Showing results (91-100 of 108) with videos related to

Sort By:

Pageof 11

Neurology|February 5, 1999

Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiencyM E Rubio-Gozalbo, J A Smeitink, W Ruitenbeek, et al.

Journal of Neuroscience Methods|January 1, 1997

Use of gene targeting for compromising energy homeostasis in neuro-muscular tissues: the role of sarcomeric mitochondrial creatine kinaseK Steeghs, A Heerschap, A de Haan, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndromeD D de Vries, C J Buzing, W Ruitenbeek, et al.

Pediatric Research|May 1, 1996

Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathyM Huizing, W Ruitenbeek, F P Thinnes, et al.

Neuropediatrics|June 1, 1992

Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic dietF A Wijburg, P G Barth, L A Bindoff, et al.

European Journal of Pediatrics|December 1, 1990

Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathiesG C Korenke, H A Bentlage, W Ruitenbeek, et al.

Clinical Neurology and Neurosurgery|January 1, 1987

Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literatureP M van Erven, J P Cillessen, E M Eekhoff, et al.

Human Mutation|January 1, 1996

Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.

Acta Neurologica Scandinavica|July 1, 1985

Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liverP M Van Erven, F J Gabreëls, W Ruitenbeek, et al.

Nature Genetics|August 1, 1992

Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessJ M van den Ouweland, H H Lemkes, W Ruitenbeek, et al.

Pageof 11