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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 1997
Are mitochondrial DNA deletions causative in chronic progressive external ophthalmoplegia patients?M J Jean-Francois, S Collins, N Kotsimbos, et al.Human Genetics|November 1, 1992
Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathyP Lertrit, A S Noer, E Byrne, et al.Journal of the Neurological Sciences|March 1, 1991
Mitochondrial encephalomyopathies: a correlation between neuropathological findings and defects in mitochondrial DNAP A McKelvie, J B Morley, E Byrne, et al.Clinical and Experimental Neurology|January 1, 1993
Motor nerve biopsy: feasibility and safetyP Gates, E Byrne, P McKelvie, et al.Acta Neurologica Scandinavica|January 1, 1993
Significance of mitochondrial DNA deletions in myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.Annals of Neurology|November 1, 1991
Mitochondrial DNA sequence analysis in congenital myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.Human Genetics|December 1, 1991
Normal variants of human mitochondrial DNA and translation products: the building of a reference data baseS Marzuki, A S Noer, P Lertrit, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 22, 2008
Proximal myotonic myopathy: a report of a kindredP Nestor, X Dennett, B DayAmerican Journal of Human Genetics|October 1, 1991
A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndromeA S Noer, H Sudoyo, P Lertrit, et al.Pageof 59