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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.Acta Neuropathologica|January 1, 1991
Functional respiratory chain studies in mitochondrial cytopathies. Support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndromeE Byrne, I Trounce, S Marzuki, et al.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.Neurology|August 26, 1998
Incoordination in pianists with overuse syndromeH J Fry, M Hallett, T Mastroianni, et al.American Journal of Human Genetics|September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex IP Lertrit, A S Noer, M J Jean-Francois, et al.Brain : a Journal of Neurology|June 1, 1986
Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levelsE Byrne, X Dennett, B Crotty, et al.Neurology|February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathyM M Ryan, B Ilkovski, C D Strickland, et al.Pageof 6