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The American Journal of Pathology|September 1, 1984
Nature of amyloid deposits in hypernephroma. Immunocytochemical studies in 2 cases associated with amyloid polyneuropathyM C Dalakas, S Fujihara, V Askanas, et al.Lancet (London, England)|December 19, 2001
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositisG Vattemi, W K Engel, J McFerrin, et al.Archives of Neurology|December 1, 1977
Muscle-type phosphorylase activity present in muscle cells cultured from three patients with myophosphorylase deficiencyM C Meienhofer, V Askanas, D Proux-Daegelen, et al.Brain : a Journal of Neurology|July 2, 1998
Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathiesC C Yang, R B Alvarez, W K Engel, et al.Experimental Neurology|March 1, 1992
Glucocorticoid increases acetylcholinesterase and organization of the postsynaptic membrane in innervated cultured human muscleV Askanas, J McFerrin, Y C Park-Matsumoto, et al.Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996
Transfer of beta-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscleV Askanas, J McFerrin, S Baqué, et al.Archives of Neurology|December 1, 1978
Reincarnation in cultured muscle of mitochondrial abnormalities. Two patients with epilepsy and lactic acidosisV Askanas, W K Engel, D E Britton, et al.Neuroreport|October 25, 1993
Prion protein is abnormally accumulated in inclusion-body myositisV Askanas, M Bilak, W K Engel, et al.Journal of the Neurological Sciences|May 1, 1981
Immunocytochemical localization of thymosin-alpha 1 in thymic epithelial cells of normal and myasthenia gravis patients and in thymic culturesM C Dalakas, W K Engel, J E McClure, et al.Annals of the New York Academy of Sciences|January 1, 1981
Identification of human thymic epithelial cells with antibodies to thymosin alpha 1 in myasthenia gravisM C Dalakas, W K Engel, J E McClure, et al.Pageof 12