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Eye (London, England)|March 8, 2014
Treatment strategies for inherited optic neuropathies: past, present and futureP Yu-Wai-Man, M Votruba, A T Moore, et al.Journal of Medical Genetics|November 13, 2008
Inherited mitochondrial optic neuropathiesP Yu-Wai-Man, P G Griffiths, G Hudson, et al.American Journal of Human Genetics|April 17, 1999
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathyK M Clark, R W Taylor, M A Johnson, 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.European Journal of Biochemistry|March 15, 1994
Redox control of beta-oxidation in rat liver mitochondriaS Eaton, D M Turnbull, K BartlettAnalytical Biochemistry|February 15, 1993
A rapid fluorometric method for the determination of carnitine palmitoyltransferaseJ Schäfer, D M Turnbull, H ReichmannNeurology|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.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.Pageof 27