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Neuromuscular Disorders : NMD|March 1, 2003
Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient miceToshikuni Sasaoka, Michihiro Imamura, Kenji Araishi, et al.Neuromuscular Disorders : NMD|March 1, 2003
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain geneSylvie Besse, Valérie Allamand, Jean-Thomas Vilquin, et al.Neuromuscular Disorders : NMD|March 1, 2003
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutationsMarinos C Dalakas, Ayush Dagvadorj, Bertrand Goudeau, et al.Neuromuscular Disorders : NMD|May 18, 2004
Pneumothorax associated with long-term non-invasive positive pressure ventilation in Duchenne muscular dystrophyAndrea Vianello, Giovanna Arcaro, Federico Gallan, et al.Neuromuscular Disorders : NMD|May 18, 2004
Distinct phenotypes of congenital acetylcholine receptor deficiencyG Burke, J Cossins, S Maxwell, et al.Neuromuscular Disorders : NMD|May 18, 2004
A case of childhood Pompe disease demonstrating phenotypic variability of p.Asp645AsnMarian A Kroos, Janbernd Kirschner, Frank N Gellerich, et al.Neuromuscular Disorders : NMD|September 8, 2004
Mutations in Czech LGMD2A patients revealed by analysis of calpain3 mRNA and their phenotypic outcomeTána Chrobáková, Markéta Hermanová, Iva Kroupová, et al.Neuromuscular Disorders : NMD|September 1, 2004
Therapeutic efforts in Duchenne muscular dystrophy; the need for a common language between basic scientists and cliniciansVictor DubowitzNeuromuscular Disorders : NMD|September 1, 2004
Prednisolone decreases cellular adhesion molecules required for inflammatory cell infiltration in dystrophin-deficient skeletal muscleMichelle Wehling-Henricks, James J Lee, James G TidballNeuromuscular Disorders : NMD|September 1, 2022
Correlations of disease severity outcome measures in inclusion body myositisNamita A Goyal, Steven A Greenberg, Jonathan Cauchi, et al.Pageof 341