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Australian and New Zealand Journal of Medicine|April 1, 1994
Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathiesM J Jean-Francois, P Lertrit, S F Berkovic, et al.International Journal of Cardiology|October 1, 1990
Haemochromatosis presenting as severe cardiac failure in a young adolescentS Menahem, A P Salmon, X DennettBrain : 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.Human Molecular Genetics|November 1, 1994
Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunctionP Lertrit, R M Kapsa, M J Jean-Francois, et al.Journal of Inherited Metabolic Disease|January 1, 1994
A novel mtDNA deletion in an infant with Pearson syndromeR Kapsa, G N Thompson, D R Thorburn, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|September 1, 2004
Intermittent claudication -- atypical presentation, diagnosis and treatmentI Taylor, X Dennett, K Nicholls, et al.Biochemical and Biophysical Research Communications|January 16, 1989
Anti-mitochondrial autoantibodies of primary biliary cirrhosis as a novel probe in the study of the biosynthetic regulation of the yeast 2-oxo acid dehydrogenase complexesH Sudoyo, S MarzukiJournal of the Neurological Sciences|February 12, 1997
Developmental genetics of deleted mtDNA in mitochondrial oculomyopathyS Marzuki, S F Berkovic, A Saifuddin Noer, et al.Clinical Cardiology|November 1, 1991
Endomyocardial biopsy in infants and children with cardiomyopathyR Narayan, S Menahem, C W Chow, et al.Biochimica Et Biophysica Acta|March 26, 1986
Are all mitochondrial translation products synthesized on membrane-bound ribosomes?S Marzuki, A R HibbsPageof 59