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P F Chinnery

Showing results (101-110 of 152) with videos related to

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Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.
Parkinsonism & Related Disorders|August 9, 2011
Long-term improvement under deferiprone in a case of neurodegeneration with brain iron accumulationA Kwiatkowski, G Ryckewaert, P Jissendi Tchofo, 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.
Journal of Neuropathology and Experimental Neurology|July 20, 2000
Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorderD A Cottrell, P G Ince, E L Blakely, et al.
Heart (British Cardiac Society)|March 27, 1999
Diagnostic utility of metabolic exercise testing in a patient with cardiovascular diseaseP M Elliott, M G Hanna, S A Ward, et al.
American Journal of Medical Genetics|July 16, 1999
Nonrandom tissue distribution of mutant mtDNAP 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 sclerosisR W Taylor, P F Chinnery, M J Bates, et al.
Journal of Medical Genetics|July 8, 2009
OPA1 increases the risk of normal but not high tension glaucomaP Yu-Wai-Man, J D Stewart, G Hudson, et al.
Journal of Neurology|April 4, 2007
Analysis of spectrum and frequencies of mutations in McArdle disease. Identification of 13 novel mutationsM Deschauer, A Morgenroth, P R Joshi, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic populationJ E Newkirk, R W Taylor, N Howell, et al.
Pageof 16

Showing results (101-110 of 152) with videos related to

Sort By:
Pageof 16
Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.
Parkinsonism & Related Disorders|August 9, 2011
Long-term improvement under deferiprone in a case of neurodegeneration with brain iron accumulationA Kwiatkowski, G Ryckewaert, P Jissendi Tchofo, 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.
Journal of Neuropathology and Experimental Neurology|July 20, 2000
Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorderD A Cottrell, P G Ince, E L Blakely, et al.
Heart (British Cardiac Society)|March 27, 1999
Diagnostic utility of metabolic exercise testing in a patient with cardiovascular diseaseP M Elliott, M G Hanna, S A Ward, et al.
American Journal of Medical Genetics|July 16, 1999
Nonrandom tissue distribution of mutant mtDNAP 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 sclerosisR W Taylor, P F Chinnery, M J Bates, et al.
Journal of Medical Genetics|July 8, 2009
OPA1 increases the risk of normal but not high tension glaucomaP Yu-Wai-Man, J D Stewart, G Hudson, et al.
Journal of Neurology|April 4, 2007
Analysis of spectrum and frequencies of mutations in McArdle disease. Identification of 13 novel mutationsM Deschauer, A Morgenroth, P R Joshi, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic populationJ E Newkirk, R W Taylor, N Howell, et al.
Pageof 16