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Patrick F. Chinnery

Showing results (101-110 of 370) with videos related to

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Intensive Care Medicine|March 13, 2010
Fall in circulating mononuclear cell mitochondrial DNA content in human sepsisAngela Pyle, David J Burn, Charlotte Gordon, et al.
Biochimica Et Biophysica Acta|July 9, 2004
Abnormal cardiac energetics in patients carrying the A3243G mtDNA mutation measured in vivo using phosphorus MR spectroscopyRaffaele Lodi, Bheeshma Rajagopalan, Andrew M Blamire, et al.
American Journal of Human Genetics|August 5, 2008
Pathogenic mitochondrial DNA mutations are common in the general populationHannah R Elliott, David C Samuels, James A Eden, et al.
Neuromuscular Disorders : NMD|October 26, 2002
The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathyJoanna L Elson, David C Samuels, Margaret A Johnson, et al.
Journal of Neurology|February 19, 2009
Vertigo and vestibular abnormalities in spinocerebellar ataxia type 6Patrick Yu-Wai-Man, Grainne Gorman, David E Bateman, et al.
Annals of Clinical and Translational Neurology|September 23, 2016
A multiple sclerosis-like disorder in patients with OPA1 mutationsPatrick Yu-Wai-Man, Achillefs Spyropoulos, Holly J Duncan, et al.
Mitochondrion|August 12, 2018
Assessing mitochondrial heteroplasmy using next generation sequencing: A note of cautionMauro Santibanez-Koref, Helen Griffin, Douglass M Turnbull, et al.
Brain : a Journal of Neurology|September 22, 2009
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic populationFiona L M Norwood, Chris Harling, Patrick F Chinnery, et al.
Annals of Neurology|September 5, 2002
Normokalemic periodic paralysis revisited: does it exist?Patrick F Chinnery, Timothy J Walls, Michael G Hanna, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Subclinical semitendinosus and obturator externus involvement defines an autosomal dominant myopathy with early respiratory failureDaniel Birchall, Maja von der Hagen, David Bates, et al.
Pageof 37

Showing results (101-110 of 370) with videos related to

Sort By:
Pageof 37
Intensive Care Medicine|March 13, 2010
Fall in circulating mononuclear cell mitochondrial DNA content in human sepsisAngela Pyle, David J Burn, Charlotte Gordon, et al.
Biochimica Et Biophysica Acta|July 9, 2004
Abnormal cardiac energetics in patients carrying the A3243G mtDNA mutation measured in vivo using phosphorus MR spectroscopyRaffaele Lodi, Bheeshma Rajagopalan, Andrew M Blamire, et al.
American Journal of Human Genetics|August 5, 2008
Pathogenic mitochondrial DNA mutations are common in the general populationHannah R Elliott, David C Samuels, James A Eden, et al.
Neuromuscular Disorders : NMD|October 26, 2002
The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathyJoanna L Elson, David C Samuels, Margaret A Johnson, et al.
Journal of Neurology|February 19, 2009
Vertigo and vestibular abnormalities in spinocerebellar ataxia type 6Patrick Yu-Wai-Man, Grainne Gorman, David E Bateman, et al.
Annals of Clinical and Translational Neurology|September 23, 2016
A multiple sclerosis-like disorder in patients with OPA1 mutationsPatrick Yu-Wai-Man, Achillefs Spyropoulos, Holly J Duncan, et al.
Mitochondrion|August 12, 2018
Assessing mitochondrial heteroplasmy using next generation sequencing: A note of cautionMauro Santibanez-Koref, Helen Griffin, Douglass M Turnbull, et al.
Brain : a Journal of Neurology|September 22, 2009
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic populationFiona L M Norwood, Chris Harling, Patrick F Chinnery, et al.
Annals of Neurology|September 5, 2002
Normokalemic periodic paralysis revisited: does it exist?Patrick F Chinnery, Timothy J Walls, Michael G Hanna, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Subclinical semitendinosus and obturator externus involvement defines an autosomal dominant myopathy with early respiratory failureDaniel Birchall, Maja von der Hagen, David Bates, et al.
Pageof 37