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P F Chinnery

Showing results (61-70 of 152) with videos related to

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AJNR. American Journal of Neuroradiology|April 14, 2012
Progressive brain iron accumulation in neuroferritinopathy measured by the thalamic T2* relaxation rateA McNeill, G Gorman, A Khan, et al.
Neurology|October 27, 1997
CSF antigliadin antibodies and the Ramsay Hunt syndromeP F Chinnery, P J Reading, D Milne, et al.
Neurology|March 17, 2012
The minimum prevalence of CADASIL in northeast EnglandS K Narayan, G Gorman, R N Kalaria, et al.
Neurology|October 27, 1997
A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegiaP F Chinnery, M A Johnson, R W Taylor, et al.
Annals of Neurology|March 1, 1997
A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysisP F Chinnery, M A Johnson, R W Taylor, et al.
American Journal of Human Genetics|January 3, 2001
Random genetic drift determines the level of mutant mtDNA in human primary oocytesD T Brown, D C Samuels, E M Michael, et al.
American Journal of Human Genetics|June 4, 2016
The Epidemiology of Leber Hereditary Optic Neuropathy in the North East of EnglandP Yu-Wai-Man, P G Griffiths, N Howell, et al.
Journal of Bioenergetics and Biomembranes|April 1, 1997
Treatment of mitochondrial diseaseR W Taylor, P F Chinnery, K M Clark, et al.
Annals of Neurology|March 15, 2000
Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivoP F Chinnery, D J Taylor, D T Brown, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1997
Fulminant encephalopathy due to the catastrophic primary antiphospholipid syndromeP F Chinnery, P J Shaw, P G Ince, et al.
Pageof 16

Showing results (61-70 of 152) with videos related to

Sort By:
Pageof 16
AJNR. American Journal of Neuroradiology|April 14, 2012
Progressive brain iron accumulation in neuroferritinopathy measured by the thalamic T2* relaxation rateA McNeill, G Gorman, A Khan, et al.
Neurology|October 27, 1997
CSF antigliadin antibodies and the Ramsay Hunt syndromeP F Chinnery, P J Reading, D Milne, et al.
Neurology|March 17, 2012
The minimum prevalence of CADASIL in northeast EnglandS K Narayan, G Gorman, R N Kalaria, et al.
Neurology|October 27, 1997
A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegiaP F Chinnery, M A Johnson, R W Taylor, et al.
Annals of Neurology|March 1, 1997
A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysisP F Chinnery, M A Johnson, R W Taylor, et al.
American Journal of Human Genetics|January 3, 2001
Random genetic drift determines the level of mutant mtDNA in human primary oocytesD T Brown, D C Samuels, E M Michael, et al.
American Journal of Human Genetics|June 4, 2016
The Epidemiology of Leber Hereditary Optic Neuropathy in the North East of EnglandP Yu-Wai-Man, P G Griffiths, N Howell, et al.
Journal of Bioenergetics and Biomembranes|April 1, 1997
Treatment of mitochondrial diseaseR W Taylor, P F Chinnery, K M Clark, et al.
Annals of Neurology|March 15, 2000
Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivoP F Chinnery, D J Taylor, D T Brown, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1997
Fulminant encephalopathy due to the catastrophic primary antiphospholipid syndromeP F Chinnery, P J Shaw, P G Ince, et al.
Pageof 16