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Clinical and Experimental Neurology|January 1, 1992
Hereditary sensory radicular neuropathy: defective neurogenic inflammationR A Westerman, A Block, A Nunn, et al.
Journal of the Neurological Sciences|July 1, 1985
Oxygen electrode studies with human skeletal muscle mitochondria in vitro. A re-appraisalE Byrne, I Trounce
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1994
Single fibre EMG studies in chronic fatigue syndrome: a reappraisalL Roberts, E Byrne
Biological Signals and Receptors|May 15, 2001
Mitochondrial function and alzheimer's diseaseJ Ojaimi, E Byrne
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1987
Chronic fatigue and myalgia syndrome: mitochondrial and glycolytic studies in skeletal muscleE Byrne, I Trounce
The Medical Journal of Australia|April 19, 1980
Giant cell arteritis. A five-year review of biopsy-proven cases in a teaching hospitalB Dare, E Byrne
Journal of Child Neurology|October 31, 1998
Congenital muscular dystrophy, white-matter abnormalities, and neuronal migration disorders: the expanding conceptM T Mackay, A J Kornberg, L Shield, et al.
The Journal of Pediatrics|March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemiaM L Freckmann, D R Thorburn, D M Kirby, et al.
Plant Signaling & Behavior|March 31, 2011
Involvement of ribosomal protein RPL27a in meristem activity and organ developmentDóra Szakonyi, Mary E Byrne
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