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P F Chinnery

Showing results (121-130 of 152) with videos related to

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Annals of Neurology|August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutationsP F Chinnery, M A Johnson, T M Wardell, 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.
Lancet (London, England)|July 4, 2006
Transmission of mitochondrial DNA disorders: possibilities for the futureD T Brown, M Herbert, V K Lamb, et al.
Neurology|July 11, 2007
Primary spinal cord neurodegeneration in Leber hereditary optic neuropathyE Jaros, D J Mahad, G Hudson, et al.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, et al.
Annals of Neurology|April 20, 2001
A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic lociP F Chinnery, M A Johnson, T J Walls, et al.
Lancet (London, England)|November 8, 2005
Role of the mitochondrial DNA 16184-16193 poly-C tract in type 2 diabetesP F Chinnery, H R Elliott, S Patel, et al.
European Journal of Ophthalmology|March 6, 2008
Is there alteration in aortic stiffness in Leber hereditary optic neuropathy?A Nemes, I F M De Coo, L Spruijt, et al.
Neurology|July 13, 2006
Clinical features of hereditary spastic paraplegia due to spastin mutationC J McDermott, C E Burness, J Kirby, et al.
Journal of Medical Genetics|December 7, 2007
Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutationK Craig, H R Elliott, S M Keers, et al.
Pageof 16

Showing results (121-130 of 152) with videos related to

Sort By:
Pageof 16
Annals of Neurology|August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutationsP F Chinnery, M A Johnson, T M Wardell, 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.
Lancet (London, England)|July 4, 2006
Transmission of mitochondrial DNA disorders: possibilities for the futureD T Brown, M Herbert, V K Lamb, et al.
Neurology|July 11, 2007
Primary spinal cord neurodegeneration in Leber hereditary optic neuropathyE Jaros, D J Mahad, G Hudson, et al.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, et al.
Annals of Neurology|April 20, 2001
A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic lociP F Chinnery, M A Johnson, T J Walls, et al.
Lancet (London, England)|November 8, 2005
Role of the mitochondrial DNA 16184-16193 poly-C tract in type 2 diabetesP F Chinnery, H R Elliott, S Patel, et al.
European Journal of Ophthalmology|March 6, 2008
Is there alteration in aortic stiffness in Leber hereditary optic neuropathy?A Nemes, I F M De Coo, L Spruijt, et al.
Neurology|July 13, 2006
Clinical features of hereditary spastic paraplegia due to spastin mutationC J McDermott, C E Burness, J Kirby, et al.
Journal of Medical Genetics|December 7, 2007
Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutationK Craig, H R Elliott, S M Keers, et al.
Pageof 16