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Neurology|February 13, 2002
Three lipoprotein receptors and cholesterol in inclusion-body myositis muscleM Jaworska-Wilczynska, G M Wilczynski, W K Engel, et al.Journal of Neurocytology|August 1, 1987
De novo neuromuscular junction formation on human muscle fibres cultured in monolayer and innervated by foetal rat spinal cord: ultrastructural and ultrastructural--cytochemical studiesV Askanas, H Kwan, R B Alvarez, et al.Neuromuscular Disorders : NMD|October 29, 2000
Mitochondrial DNA variants in inclusion body myositisC C Kok, A Boyt, S Gaudieri, et al.Neurology|January 1, 1985
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free dietV Askanas, W K Engel, H H Kwan, et al.Proceedings of the National Academy of Sciences of the United States of America|March 29, 2001
Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replicationY Wang, Y Michikawa, C Mallidis, et al.Archives of Neurology|October 1, 1979
X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue culturesV Askanas, W K Engel, N B Reddy, et al.Pageof 12