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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 mutations
S 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 population
J 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 study
L 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 dehydrogenase
M 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 chain
N 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 muscle
K M Clark, L A Bindoff, R N Lightowlers, et al.
Annals of Neurology
|
August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutations
P 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 oxidation
R 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 diet
F A Wijburg, P G Barth, L A Bindoff, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 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 mutations
S 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 population
J 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 study
L 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 dehydrogenase
M 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 chain
N 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 muscle
K M Clark, L A Bindoff, R N Lightowlers, et al.
Annals of Neurology
|
August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutations
P 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 oxidation
R 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 diet
F A Wijburg, P G Barth, L A Bindoff, et al.
Page
of 6