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Pathology|October 1, 1988
Amniotic fluid embolism: fatal case confirmed at autopsy five weeks after deliveryH D Attwood, W J DelpradoClinical 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.Internal Medicine Journal|August 2, 2001
Quadriceps muscle wasting persists 5 months after total hip arthroplasty for osteoarthritis of the hip: a pilot studyK Reardon, M Galea, X Dennett, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 22, 2008
McArdle's disease resembling an inflammatory myopathyT O'Brien, S Collins, X Dennett, et al.Neurology|September 1, 1987
Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation productE Byrne, S Marzuki, N Sattayasai, 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.Biochimica Et Biophysica Acta|November 21, 1991
Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNAS Collins, C Rudduck, S Marzuki, et al.Pageof 6