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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.Blood|September 1, 1979
The hemostatic imbalance of plasma-exchange transfusionM A Flaum, R A Cuneo, F R Appelbaum, et al.Neurology|December 1, 1977
Morphologic and immunologic studies in experimental autoimmune myasthenia gravis and myasthenia gravisJ L Trotter, S P Ringel, J D Cook, et al.Archives of Neurology|January 1, 1978
The effect of pharmacologic acetylcholine receptor on fibrillation and myotonia in rat skeletal muscleR A Brumback, T E Bertorini, W K Engel, et al.Neurology|December 1, 1980
Substance P in human cerebrospinal fluid: reductions in peripheral neuropathy and autonomic dysfunctionJ G Nutt, E A Mrox, S E Leeman, 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.Neurology|July 30, 2010
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaJ Yan, H-X Deng, N Siddique, et al.Pageof 19