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L A Bindoff

Showing results (41-50 of 58) with videos related to

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European Journal of Neurology|April 24, 2016
ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?O Hikmat, C Tzoulis, P M Knappskog, et al.
Neurology|April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutationsS Winterthun, G Ferrari, L He, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic populationJ E Newkirk, R W Taylor, N Howell, et al.
Journal of the Neurological Sciences|March 1, 1991
Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular studyL A Bindoff, C Desnuelle, M A Birch-Machin, et al.
The Journal of Biological Chemistry|June 5, 1992
The sequence of the flavoprotein subunit of bovine heart succinate dehydrogenaseM A Birch-Machin, L Farnsworth, B A Ackrell, et al.
Biochemical and Biophysical Research Communications|April 28, 1989
Tissue specific defect of complex I of the mitochondrial respiratory chainN J Watmough, M A Birch-Machin, L A Bindoff, et al.
Nature Genetics|July 1, 1997
Reversal of a mitochondrial DNA defect in human skeletal muscleK M Clark, L A Bindoff, R N Lightowlers, et al.
Annals of Neurology|August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutationsP F Chinnery, M A Johnson, T M Wardell, et al.
The Journal of Biological Chemistry|December 5, 1991
Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidationR S Kler, S Jackson, K Bartlett, 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.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
European Journal of Neurology|April 24, 2016
ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?O Hikmat, C Tzoulis, P M Knappskog, et al.
Neurology|April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutationsS Winterthun, G Ferrari, L He, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic populationJ E Newkirk, R W Taylor, N Howell, et al.
Journal of the Neurological Sciences|March 1, 1991
Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular studyL A Bindoff, C Desnuelle, M A Birch-Machin, et al.
The Journal of Biological Chemistry|June 5, 1992
The sequence of the flavoprotein subunit of bovine heart succinate dehydrogenaseM A Birch-Machin, L Farnsworth, B A Ackrell, et al.
Biochemical and Biophysical Research Communications|April 28, 1989
Tissue specific defect of complex I of the mitochondrial respiratory chainN J Watmough, M A Birch-Machin, L A Bindoff, et al.
Nature Genetics|July 1, 1997
Reversal of a mitochondrial DNA defect in human skeletal muscleK M Clark, L A Bindoff, R N Lightowlers, et al.
Annals of Neurology|August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutationsP F Chinnery, M A Johnson, T M Wardell, et al.
The Journal of Biological Chemistry|December 5, 1991
Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidationR S Kler, S Jackson, K Bartlett, 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.
Pageof 6