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Journal of Bioenergetics and Biomembranes|April 1, 1997
Treatment of mitochondrial diseaseR W Taylor, P F Chinnery, K M Clark, et al.
Neurology|June 28, 2006
Mitochondrial disease in adults: a scale to monitor progression and treatmentA M Schaefer, C Phoenix, J L Elson, et al.
Eye (London, England)|May 28, 2005
Assessment of visual function in chronic progressive external ophthalmoplegiaC Y Yu Wai Man, T Smith, P F Chinnery, et al.
Gene Therapy|January 19, 2000
Peptide nucleic acid delivery to human mitochondriaP F Chinnery, R W Taylor, K Diekert, et al.
American Journal of Human Genetics|February 7, 2003
The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree ratesNeil Howell, Christy Bogolin Smejkal, D A Mackey, et al.
American Journal of Human Genetics|January 3, 2001
Point mutations of the mtDNA control region in normal and neurodegenerative human brainsP F Chinnery, G A Taylor, N Howell, et al.
American Journal of Human Genetics|December 15, 2000
Analysis of European mtDNAs for recombinationJ L Elson, R M Andrews, P F Chinnery, et al.
The British Journal of Ophthalmology|March 21, 2006
The role of mitochondrial haplogroups in primary open angle glaucomaR Andrews, T Ressiniotis, D M Turnbull, et al.
American Journal of Human Genetics|January 9, 2003
The epidemiology of Leber hereditary optic neuropathy in the North East of EnglandP Yu-Wai-Man, P G Griffiths, D T Brown, et al.
Brain : a Journal of Neurology|December 28, 1999
The spectrum of hearing loss due to mitochondrial DNA defectsP F Chinnery, C Elliott, G R Green, et al.
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