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Neuromuscular Disorders : NMD|August 12, 2018
A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein geneJake Plewa, Abhilasha Surampalli, Marie Wencel, et al.
Neuromuscular Disorders : NMD|August 12, 2018
Respiratory insight to congenital muscular dystrophies and congenital myopathies and its relation to clinical trialBrigitte Fauroux, Alessandro Amaddeo, Susana Quijano-Roy, et al.
Neuromuscular Disorders : NMD|July 16, 2018
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvementLidia Gonzalez-Quereda, Eduard Gallardo, Ana Töpf, et al.
Neuromuscular Disorders : NMD|May 31, 2017
Dramatic elevation in urinary amino terminal titin fragment excretion quantified by immunoassay in Duchenne muscular dystrophy patients and in dystrophin deficient rodentsAlan S Robertson, Mark J Majchrzak, Courtney M Smith, et al.
Neuromuscular Disorders : NMD|June 12, 2017
Skeletal muscle water T2 as a biomarker of disease status and exercise effects in patients with Duchenne muscular dystrophyAmi Mankodi, Noura Azzabou, Thomas Bulea, et al.
Neuromuscular Disorders : NMD|March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutationsFatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
Neuromuscular Disorders : NMD|April 9, 2018
From excitation to intracellular Ca2+ movements in skeletal muscle: Basic aspects and related clinical disordersBruno Allard
Neuromuscular Disorders : NMD|May 15, 2018
Novel valosin-containing protein mutations associated with multisystem proteinopathySejad Al-Tahan, Ebaa Al-Obeidi, Hiroshi Yoshioka, et al.
Neuromuscular Disorders : NMD|August 21, 2016
Factors influencing compliance with non-invasive ventilation at long-term in patients with myotonic dystrophy type 1: A prospective cohortGhilas Boussaïd, Frédéric Lofaso, Dante Brasil Santos, et al.
Neuromuscular Disorders : NMD|September 27, 2016
Dysferlin mutations and mitochondrial dysfunctionAmy E Vincent, Hannah S Rosa, Charlotte L Alston, et al.
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