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The Medical Journal of Australia|August 21, 1976
Smoking, transient ischaemic attacks and stroke: A temporal associationK Grainger, F MastagliaJournal of the Neurological Sciences|July 1, 1993
Phenotypic expression of mtDNA heteroplasmy in the skeletal muscle of patients with oculomyopathy: defect in mitochondrial protein synthesisH Sudoyo, S Marzuki, E Byrne, et al.Journal of the Neurological Sciences|March 1, 1992
Molecular genetics of Leber's hereditary optic neuropathy: study of a six-generation family from Western AustraliaH Sudoyo, S Marzuki, F Mastaglia, et al.Cardiovascular Surgery (London, England)|March 12, 1999
Asymptomatic carotid artery stenosis associated with peripheral vascular disease: a prospective studyA K House, R Bell, J House, et al.Tissue Antigens|October 22, 2004
Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3P Price, L Santoso, F Mastaglia, 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.Neuromuscular Disorders : NMD|October 29, 2000
Mitochondrial DNA variants in inclusion body myositisC C Kok, A Boyt, S Gaudieri, et al.The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|October 14, 2003
Clustering of tuberculosis among senegalese immigrants in ItalyA Matteelli, A Gori, G Pinsi, et al.Brain : a Journal of Neurology|June 14, 2003
A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesionsI M P Gommans, M Davis, K Saar, et al.Neurology|June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson diseaseY J Li, M A Hauser, W K Scott, et al.Pageof 2