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Neuromuscular Disorders : NMD|July 16, 2013
Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagyTakashi Kurashige, Tetsuya Takahashi, Yu Yamazaki, et al.
Neuromuscular Disorders : NMD|December 27, 2011
Distal myopathies--new genetic entities expand diagnostic challengeBjarne Udd
Neuromuscular Disorders : NMD|March 20, 2012
Modafinil for excessive daytime sleepiness in myotonic dystrophy type 1--the patients' perspectiveD Hilton-Jones, M Bowler, H Lochmueller, et al.
Neuromuscular Disorders : NMD|December 21, 2011
Multiple exon skipping strategies to by-pass dystrophin mutationsCarl F Adkin, Penelope L Meloni, Susan Fletcher, et al.
Neuromuscular Disorders : NMD|February 24, 2012
Mutation spectrum and phenotypic manifestation in FSHD Greek patientsP Sakellariou, K Kekou, H Fryssira, et al.
Neuromuscular Disorders : NMD|August 2, 2015
GNE myopathy in Roma patients homozygous for the p.I618T founder mutationTeodora Chamova, Velina Guergueltcheva, Mariana Gospodinova, et al.
Neuromuscular Disorders : NMD|January 6, 2015
Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defectYiran Guo, Minal J Menezes, Manoj P Menezes, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Growing up with spinal muscular atrophy with respiratory distress (SMARD1)Mark James Hamilton, Cheryl Longman, Ann O'Hara, et al.
Neuromuscular Disorders : NMD|November 27, 2015
Evaluation of muscle oxygenation by near infrared spectroscopy in patients with facioscapulohumeral muscular dystrophyN Olivier, J Boissière, E Allart, et al.
Neuromuscular Disorders : NMD|August 26, 2014
An analysis of the sensitivity and specificity of MHC-I and MHC-II immunohistochemical staining in muscle biopsies for the diagnosis of inflammatory myopathiesPedro M Rodríguez Cruz, Yue-Bei Luo, James Miller, et al.
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