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P F Chinnery

Showing results (51-60 of 152) with videos related to

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American Journal of Human Genetics|February 17, 2001
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with ageJ L Elson, D C Samuels, D M Turnbull, et al.
Journal of the Association for Research in Otolaryngology : JARO|September 12, 2001
Psychophysical evaluation of cochlear hair cell damage due to the A3243G mitochondrial DNA mutationT D Griffiths, S Blakemore, C Elliott, et al.
Human Reproduction (Oxford, England)|October 21, 2000
Transmission of the human mitochondrial genomeN Howell, P F Chinnery, S S Ghosh, et al.
Neurology|August 25, 2004
Infantile hereditary spastic paraparesis due to codominant mutations in the spastin geneP F Chinnery, S M Keers, M J Holden, et al.
Journal of Medical Genetics|May 16, 2002
Spinocerebellar ataxia and the A3243G and A8344G mtDNA mutationsP F Chinnery, D T Brown, K Archibald, et al.
Mitochondrion|August 27, 2005
Pitfalls in restriction fragment length polymorphism analysis of Leber's hereditary optic neuropathy patientsF Carrara, P F Chinnery, P Yu-Wai-Man, et al.
Neurology|August 10, 2005
Mitochondrial DNA copy number threshold in mtDNA depletion myopathyS E Durham, E Bonilla, D C Samuels, et al.
Eye (London, England)|March 8, 2011
Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutationsP Yu-Wai-Man, M Bailie, A Atawan, et al.
Neuromuscular Disorders : NMD|March 27, 1999
Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reportsK M Bushby, C Pollitt, M A Johnson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1997
Management of parkinsonism and psychotic depression in a case of acute intermittent porphyriaP F Chinnery, N E Cartlidge, D J Burn, et al.
Pageof 16

Showing results (51-60 of 152) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|February 17, 2001
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with ageJ L Elson, D C Samuels, D M Turnbull, et al.
Journal of the Association for Research in Otolaryngology : JARO|September 12, 2001
Psychophysical evaluation of cochlear hair cell damage due to the A3243G mitochondrial DNA mutationT D Griffiths, S Blakemore, C Elliott, et al.
Human Reproduction (Oxford, England)|October 21, 2000
Transmission of the human mitochondrial genomeN Howell, P F Chinnery, S S Ghosh, et al.
Neurology|August 25, 2004
Infantile hereditary spastic paraparesis due to codominant mutations in the spastin geneP F Chinnery, S M Keers, M J Holden, et al.
Journal of Medical Genetics|May 16, 2002
Spinocerebellar ataxia and the A3243G and A8344G mtDNA mutationsP F Chinnery, D T Brown, K Archibald, et al.
Mitochondrion|August 27, 2005
Pitfalls in restriction fragment length polymorphism analysis of Leber's hereditary optic neuropathy patientsF Carrara, P F Chinnery, P Yu-Wai-Man, et al.
Neurology|August 10, 2005
Mitochondrial DNA copy number threshold in mtDNA depletion myopathyS E Durham, E Bonilla, D C Samuels, et al.
Eye (London, England)|March 8, 2011
Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutationsP Yu-Wai-Man, M Bailie, A Atawan, et al.
Neuromuscular Disorders : NMD|March 27, 1999
Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reportsK M Bushby, C Pollitt, M A Johnson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1997
Management of parkinsonism and psychotic depression in a case of acute intermittent porphyriaP F Chinnery, N E Cartlidge, D J Burn, et al.
Pageof 16