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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.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.Clinical Cardiology|November 1, 1991
Endomyocardial biopsy in infants and children with cardiomyopathyR Narayan, S Menahem, C W Chow, et al.Systematic Parasitology|January 5, 2000
Haycocknema perplexum n. g., n. sp. (Nematoda: Robertdollfusidae): an intramyofibre parasite in manD M Spratt, I Beveridge, J R Andrews, et al.Annals of Internal Medicine|June 20, 2001
Incidence of malignant disease in biopsy-proven inflammatory myopathy. A population-based cohort studyR Buchbinder, A Forbes, S Hall, et al.Journal of Paediatrics and Child Health|April 12, 2000
Elevated aminotransferase as a presenting finding in a patient with occult muscle diseaseT Begum, M R Oliver, A J Kornberg, et al.The Journal of Rheumatology|May 20, 1999
Incidence of inflammatory myopathies in Victoria, Australia, and evidence of spatial clusteringM Patrick, R Buchbinder, D Jolley, et al.Journal of Pediatric Orthopedics. Part B|July 1, 1997
Muscle abnormalities in idiopathic toe-walkersD M Eastwood, X Dennett, L K Shield, et al.Neurology|December 22, 1999
Benign acute childhood myositis: laboratory and clinical featuresM T Mackay, A J Kornberg, L K Shield, et al.Australian Paediatric Journal|January 1, 1988
Becker and Duchenne muscular dystrophy: a comparative morphological studyX Dennett, L K Shield, L J Clingan, et al.Pageof 54