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R W TAYLOR

Showing results (231-240 of 254) with videos related to

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Lancet (London, England)|July 4, 2006
Transmission of mitochondrial DNA disorders: possibilities for the futureD T Brown, M Herbert, V K Lamb, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutationM Deschauer, P F Chinnery, A M Schaefer, et al.
Neurology|April 28, 2004
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) geneR W Taylor, A M Schaefer, M T McDonnell, et al.
Pediatric Obesity|December 23, 2017
Improving rates of overweight, obesity and extreme obesity in New Zealand 4-year-old children in 2010-2016N Shackleton, B J Milne, R Audas, et al.
Neuropediatrics|July 2, 2009
A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosisE W Y Tam, A Feigenbaum, J B L Addis, et al.
Diabetes Care|November 1, 1995
Insulin and proinsulin secretion in subjects with abnormal glucose tolerance and a mitochondrial tRNA(Leu(UUR)) mutationM Walker, R W Taylor, M W Stewart, et al.
Journal of Inherited Metabolic Disease|December 16, 2006
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathyA A M Morris, R E Appleton, B Power, et al.
Annals of Neurology|February 1, 1996
Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxiaR W Taylor, M A Birch-Machin, J Schaefer, et al.
Neurology|July 26, 2000
Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodiesP F Chinnery, G A Taylor, N Howell, et al.
Neuromuscular Disorders : NMD|February 26, 2013
Initial development and validation of a mitochondrial disease quality of life scaleJ L Elson, M Cadogan, S Apabhai, et al.
Pageof 26

Showing results (231-240 of 254) with videos related to

Sort By:
Pageof 26
Lancet (London, England)|July 4, 2006
Transmission of mitochondrial DNA disorders: possibilities for the futureD T Brown, M Herbert, V K Lamb, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutationM Deschauer, P F Chinnery, A M Schaefer, et al.
Neurology|April 28, 2004
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) geneR W Taylor, A M Schaefer, M T McDonnell, et al.
Pediatric Obesity|December 23, 2017
Improving rates of overweight, obesity and extreme obesity in New Zealand 4-year-old children in 2010-2016N Shackleton, B J Milne, R Audas, et al.
Neuropediatrics|July 2, 2009
A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosisE W Y Tam, A Feigenbaum, J B L Addis, et al.
Diabetes Care|November 1, 1995
Insulin and proinsulin secretion in subjects with abnormal glucose tolerance and a mitochondrial tRNA(Leu(UUR)) mutationM Walker, R W Taylor, M W Stewart, et al.
Journal of Inherited Metabolic Disease|December 16, 2006
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathyA A M Morris, R E Appleton, B Power, et al.
Annals of Neurology|February 1, 1996
Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxiaR W Taylor, M A Birch-Machin, J Schaefer, et al.
Neurology|July 26, 2000
Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodiesP F Chinnery, G A Taylor, N Howell, et al.
Neuromuscular Disorders : NMD|February 26, 2013
Initial development and validation of a mitochondrial disease quality of life scaleJ L Elson, M Cadogan, S Apabhai, et al.
Pageof 26