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Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiencyH Porschke, W Kress, H Reichmann, et al.
Journal of Neurology|March 1, 1994
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophyR Gold, W Kress, T Bettecken, et al.
Journal of Neuropathology and Experimental Neurology|November 15, 2001
Effects of oncostatin M on human cerebral endothelial cells and expression in inflammatory brain lesionsK Ruprecht, T Kuhlmann, F Seif, et al.
Neurology|April 30, 2010
Cardiotoxicity and other adverse events associated with mitoxantrone treatment for MSE Kingwell, M Koch, B Leung, et al.
Journal of Neuroscience Research|August 27, 1999
Expression of the beta-trace protein in human pachymeninx as revealed by in situ hybridization and immunocytochemistryB Blödorn, W Brück, H Tumani, et al.
Der Orthopade|May 15, 2012
[Nerve lesions after minimally invasive total hip arthroplasty]B M Holzapfel, F Heinen, D E Holzapfel, et al.
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