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Neuromuscular Disorders : NMD|March 3, 2020
Clinical and electrophysiological evaluation of myasthenic features in an alpha-dystroglycanopathy cohort (FKRP-predominant)Paloma Gonzalez-Perez, Cheryl Smith, Wendy L Sebetka, et al.
Neuromuscular Disorders : NMD|January 21, 2014
Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophyMarika Pane, Elena S Mazzone, Lavinia Fanelli, et al.
Neuromuscular Disorders : NMD|November 13, 2012
Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementiaAnne-Kathrin Peyer, Jochen Kinter, Jürgen Hench, et al.
Neuromuscular Disorders : NMD|November 13, 2012
Childhood chronic inflammatory demyelinating polyradiculoneuropathy: combined analysis of a large cohort and eleven published seriesHugh J McMillan, Peter B Kang, H Royden Jones, et al.
Neuromuscular Disorders : NMD|November 13, 2012
Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota HutteriteTeerin Liewluck, Jennifer A Tracy, Eric J Sorenson, et al.
Neuromuscular Disorders : NMD|March 1, 2015
Conserved expression of truncated telethonin in a patient with limb-girdle muscular dystrophy 2GRita Barresi, Charlotte Morris, Judith Hudson, et al.
Neuromuscular Disorders : NMD|March 16, 2015
A normal life without muscle dystrophinM Zatz, N M Vieira, E Zucconi, et al.
Neuromuscular Disorders : NMD|March 10, 2015
Treatment of myasthenia gravis with dropped head: a report of 2 cases and review of the literatureMichihiro Tamai, Takao Hashimoto, Takashi Isobe, et al.
Neuromuscular Disorders : NMD|March 10, 2015
Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1)C A Sewry, J L Holton, D J Dick, et al.
Neuromuscular Disorders : NMD|March 10, 2015
A novel large deletion in the RYR1 gene in a Belgian family with late-onset and recessive core myopathyGauthier Remiche, Hazim Kadhim, Marc Abramowicz, et al.
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