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Neuromuscular Disorders : NMD|August 29, 2006
Severe phenotype in infantile facioscapulohumeral muscular dystrophyLars Klinge, Michelle Eagle, Irene D Haggerty, et al.
Neuromuscular Disorders : NMD|August 29, 2006
Severe fascioscapulohumeral muscular dystrophy presenting with Coats' disease and mental retardationLaurence A Bindoff, Nanette Mjellem, Kristian Sommerfelt, et al.
Neuromuscular Disorders : NMD|September 6, 2006
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)L Corrado, S D'Alfonso, L Bergamaschi, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegiaAngela Magariello, Maria Muglia, Alessandra Patitucci, et al.
Neuromuscular Disorders : NMD|April 25, 2006
Chronic inflammatory demyelinating polyneuropathyGérard Said
Neuromuscular Disorders : NMD|August 22, 2006
Raised troponin T in inclusion body myositis is common and serum levels are persistent over timeC Lindberg, L Klintberg, A Oldfors
Neuromuscular Disorders : NMD|August 22, 2006
Fetal arthrogryposis and maternal serum antibodiesPaola Dalton, Linda Clover, Robert Wallerstein, et al.
Neuromuscular Disorders : NMD|December 7, 2007
Heart transplantation in a child with LGMD2I presenting as isolated dilated cardiomyopathyAdele D'Amico, Stefania Petrini, Francesco Parisi, et al.
Neuromuscular Disorders : NMD|December 7, 2007
Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisalMerrilee Needham, Amanda Hooper, Ian James, et al.
Neuromuscular Disorders : NMD|December 7, 2007
Danon disease: a novel Lamp-2 gene mutation in a family with four affected membersT Tuñón, D Guerrero, A Urchaga, et al.
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