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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.Journal of the Neurological Sciences|December 1, 1988
Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficienciesE Byrne, I Trounce, X Dennett, et al.Australian and New Zealand Journal of Medicine|December 1, 1991
Biochemical and molecular investigation of mitochondrial disease: an illustrative case showing the value of a multifaceted approachE Byrne, B Jean-Francois, D Thyagarajan, et al.Journal of the Neurological Sciences|March 1, 1991
Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletionsI Trounce, E Byrne, S Marzuki, et al.Clinical and Experimental Neurology|January 1, 1993
Motor nerve biopsy: feasibility and safetyP Gates, E Byrne, P McKelvie, 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 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|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.International Journal of Cardiology|October 1, 1990
Haemochromatosis presenting as severe cardiac failure in a young adolescentS Menahem, A P Salmon, X DennettPageof 54