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Neuromuscular Disorders : NMD|April 19, 2017
Respiratory function in facioscapulohumeral muscular dystrophy 1M Wohlgemuth, C G C Horlings, E L van der Kooi, et al.Neuromuscular Disorders : NMD|April 24, 2017
Beneficial effect of tocilizumab in myasthenia gravis refractory to rituximabDagur Ingi Jonsson, Ritva Pirskanen, Fredrik PiehlNeuromuscular Disorders : NMD|April 24, 2017
Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapyM Auranen, A Paetau, P Piirilä, et al.Neuromuscular Disorders : NMD|July 27, 2019
Longitudinal study of upper extremity reachable workspace in fascioscapulohumeral muscular dystrophyMaya N Hatch, Kiin Kim, Gregorij Kurillo, et al.Neuromuscular Disorders : NMD|January 22, 2008
Hand weakness in Duchenne muscular dystrophy and its relation to physical disabilityFabiana Luisa Mattar, Claudia SobreiraNeuromuscular Disorders : NMD|June 7, 2008
Distal inflammatory myopathy: unusual presentation of polymyositis or new entity?Dalia Dimitri, Odile Dubourg, Thierry Maisonobe, et al.Neuromuscular Disorders : NMD|March 5, 2017
Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvementSara Missaglia, Lorenzo Maggi, Marina Mora, et al.Neuromuscular Disorders : NMD|March 18, 2017
Matching pairs difficulty in children with spinal muscular atrophy type IGraziela Jorge Polido, Alessandra Ferreira Barbosa, Carlos Hitoshi Morimoto, et al.Neuromuscular Disorders : NMD|March 20, 2021
A rare case of monozygotic triplets with Duchenne muscular dystrophyLiang Wang, Jinfu Lin, Fu Xiong, et al.Neuromuscular Disorders : NMD|March 20, 2021
Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletionMarco Spinazzi, Jerome Poupiot, Julien Cassereau, et al.Pageof 340