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Neuromuscular Disorders : NMD|July 20, 2010
Debio-025 is more effective than prednisone in reducing muscular pathology in mdx miceErin R Wissing, Douglas P Millay, Grégoire Vuagniaux, et al.Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.Neuromuscular Disorders : NMD|July 20, 2010
Using mouse cranial muscles to investigate neuromuscular pathology in vivoL M Murray, T H Gillingwater, S H ParsonNeuromuscular Disorders : NMD|July 15, 2010
Hereditary muscular dystrophies and the heartM C E Hermans, Y M Pinto, I S J Merkies, et al.Neuromuscular Disorders : NMD|June 19, 2010
Impact of tracheostomy on swallowing performance in Duchenne muscular dystrophyNicolas Terzi, Hélène Prigent, Michèle Lejaille, et al.Neuromuscular Disorders : NMD|September 7, 2010
Personalized exon skipping strategies to address clustered non-deletion dystrophin mutationsSarah Forrest, Penny L Meloni, Francesco Muntoni, et al.Neuromuscular Disorders : NMD|September 7, 2010
Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutationTeerin Liewluck, Tracy L Lovell, Anna V Bite, et al.Neuromuscular Disorders : NMD|December 7, 2010
Novel GNE mutations in two phenotypically distinct HIBM2 patientsConrad C Weihl, Sara E Miller, Craig M Zaidman, et al.Neuromuscular Disorders : NMD|November 16, 2010
Charcot-Marie-Tooth 1A patients with low level of impairment have a higher energy cost of walking than healthy individualsFederica Menotti, Francesco Felici, Antonello Damiani, et al.Neuromuscular Disorders : NMD|March 30, 2010
Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian familyAndrea Stober, Angelo Aleo, Valerio Kuhl, et al.Pageof 341