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Archives of Disease in Childhood
|
January 23, 2008
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1)
R McFarland, G Hudson, R W Taylor, et al.
Neuromuscular Disorders : NMD
|
October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy
M J Barron, P F Chinnery, D Howel, et al.
BMJ Case Reports
|
June 21, 2011
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ (POLG1)
R McFarland, G Hudson, R W Taylor, et al.
International Journal of Obesity (2005)
|
May 16, 2019
Do differences in compositional time use explain ethnic variation in the prevalence of obesity in children? Analyses using 24-hour accelerometry
R W Taylor, J J Haszard, V L Farmer, et al.
Neuropathology and Applied Neurobiology
|
July 6, 2012
Mitochondrial DNA deletions and depletion within paraspinal muscles
G R Campbell, A Reeve, I Ziabreva, et al.
The Journal of Laryngology and Otology
|
September 21, 2001
Cochlear implantation of a patient with a previously undescribed mitochondrial DNA defect
P R Counter, M P Hilton, D Webster, et al.
Heliyon
|
November 21, 2022
Organic matter composition and thermal stability influence greenhouse gases production in subtropical peatland under different vegetation types
G O Akinbi, L W Ngatia, J M Grace, et al.
Diabetologia
|
December 24, 2004
Comparison of high-fat and high-protein diets with a high-carbohydrate diet in insulin-resistant obese women
K A McAuley, C M Hopkins, K J Smith, et al.
American Journal of Medical Genetics
|
July 16, 1999
Nonrandom tissue distribution of mutant mtDNA
P F Chinnery, P J Zwijnenburg, M Walker, et al.
Biochemical and Biophysical Research Communications
|
February 25, 1998
A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis
R W Taylor, P F Chinnery, M J Bates, et al.
Page
of 26
Search research articles
Search
Showing results (201-210 of 254) with videos related to
Sort By:
Page
of 26
Archives of Disease in Childhood
|
January 23, 2008
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1)
R McFarland, G Hudson, R W Taylor, et al.
Neuromuscular Disorders : NMD
|
October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy
M J Barron, P F Chinnery, D Howel, et al.
BMJ Case Reports
|
June 21, 2011
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ (POLG1)
R McFarland, G Hudson, R W Taylor, et al.
International Journal of Obesity (2005)
|
May 16, 2019
Do differences in compositional time use explain ethnic variation in the prevalence of obesity in children? Analyses using 24-hour accelerometry
R W Taylor, J J Haszard, V L Farmer, et al.
Neuropathology and Applied Neurobiology
|
July 6, 2012
Mitochondrial DNA deletions and depletion within paraspinal muscles
G R Campbell, A Reeve, I Ziabreva, et al.
The Journal of Laryngology and Otology
|
September 21, 2001
Cochlear implantation of a patient with a previously undescribed mitochondrial DNA defect
P R Counter, M P Hilton, D Webster, et al.
Heliyon
|
November 21, 2022
Organic matter composition and thermal stability influence greenhouse gases production in subtropical peatland under different vegetation types
G O Akinbi, L W Ngatia, J M Grace, et al.
Diabetologia
|
December 24, 2004
Comparison of high-fat and high-protein diets with a high-carbohydrate diet in insulin-resistant obese women
K A McAuley, C M Hopkins, K J Smith, et al.
American Journal of Medical Genetics
|
July 16, 1999
Nonrandom tissue distribution of mutant mtDNA
P F Chinnery, P J Zwijnenburg, M Walker, et al.
Biochemical and Biophysical Research Communications
|
February 25, 1998
A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis
R W Taylor, P F Chinnery, M J Bates, et al.
Page
of 26