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Biochimica Et Biophysica Acta|March 24, 2009
The inheritance of pathogenic mitochondrial DNA mutationsL M Cree, D C Samuels, P F ChinneryNeuromuscular Disorders : NMD|May 11, 2006
Is selection required for the accumulation of somatic mitochondrial DNA mutations in post-mitotic cells?S E Durham, D C Samuels, P F ChinneryJournal of Internal Medicine|February 5, 2009
Batteries not included: diagnosis and management of mitochondrial diseaseR McFarland, D M TurnbullNeurology|August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystoniaR McFarland, P F Chinnery, E L Blakely, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1985
The comparative efficacy of antiepileptic drugs for partial and tonic-clonic seizuresD Chadwick, D M TurnbullNeurology|January 26, 2005
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicismG Hudson, M Deschauer, K Busse, et al.Clinical Radiology|January 9, 2007
MRI for the demonstration of subclinical muscle involvement in muscular dystrophyS Sookhoo, I Mackinnon, K Bushby, et al.Neuromuscular Disorders : NMD|January 11, 2005
Extraocular muscles have fundamentally distinct properties that make them selectively vulnerable to certain disordersC Y Yu Wai Man, P F Chinnery, P G GriffithsMedical Hypotheses|August 16, 2005
Optic neuropathies--importance of spatial distribution of mitochondria as well as functionC Y Yu Wai Man, P F Chinnery, P G GriffithsQuarterly Journal of Experimental Physiology (Cambridge, England)|April 1, 1984
Mitochondrial oxidative enzyme activity in individual fibre types in hypo- and hyperthyroid rat skeletal musclesM A Johnson, D M TurnbullPageof 27