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Journal of Neuroimmunology|June 17, 1998
The expression of co-stimulatory and accessory molecules on cultured human muscle cells is not dependent on stimulus by pro-inflammatory cytokines: relevance for the pathogenesis of inflammatory myopathyP Bernasconi, P Confalonieri, F Andreetta, et al.Italian Journal of Neurological Sciences|October 1, 1980
Friedreich's ataxia. I. Clinical, neurophysiological and in vivo biochemical studiesA D'Angelo, S Di Donato, G Crenna, et al.Neurology|October 27, 1997
Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 geneC Gellera, D Pareyson, B Castellotti, et al.Neurology|July 1, 1986
Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductaseS Di Donato, F E Frerman, M Rimoldi, et al.Acta Neuropathologica|October 1, 1996
Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriersC Di Blasi, L Morandi, R Barresi, et al.Archives of Gerontology and Geriatrics. Supplement|June 23, 2004
Aging and vestibular system: specific tests and role of melatonin in cognitive involvementD Alpini, A Cesarani, F Fraschini, et al.Clinical Neuropathology|January 1, 1985
Centronuclear myopathy with unusual mitochondrial abnormalitiesN Canal, G C Comi, M Comola, et al.Human Mutation|October 26, 1999
Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenitaR Brugnoni, S Galantini, P Confalonieri, et al.Brain : a Journal of Neurology|April 5, 2001
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skippingC Di Blasi, Y He, L Morandi, et al.Italian Journal of Neurological Sciences|December 1, 1982
Functional evaluation of Duchenne muscular dystrophy: proposal for a protocolF Cornelio, F Dworzak, L Morandi, et al.Pageof 16