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Neuromuscular Disorders : NMD|May 3, 2016
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathyV Guglielmi, A Oosterhof, N C Voermans, et al.
Neuromuscular Disorders : NMD|March 8, 2016
TRPV4 related scapuloperoneal spinal muscular atrophy: Report of an Italian family and review of the literatureF Biasini, S Portaro, A Mazzeo, et al.
Neuromuscular Disorders : NMD|January 6, 2015
Autophagic vacuolar pathology in desminopathiesConrad C Weihl, Stanley Iyadurai, Robert H Baloh, et al.
Neuromuscular Disorders : NMD|September 2, 2014
Skeletal muscle imaging in facioscapulohumeral muscular dystrophy, pattern and asymmetry of individual muscle involvementN H M Rijken, E L van der Kooi, J C M Hendriks, et al.
Neuromuscular Disorders : NMD|June 8, 2013
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a German neuromuscular center populationBurkhard Gess, Anja Schirmacher, Matthias Boentert, et al.
Neuromuscular Disorders : NMD|September 5, 2015
Novel mutations in DNAJB6 gene cause a very severe early-onset limb-girdle muscular dystrophy 1D diseaseJohanna Palmio, Per Harald Jonson, Anni Evilä, et al.
Neuromuscular Disorders : NMD|January 30, 2016
Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiencyZhaoxia Wang, Daojun Hong, Wei Zhang, et al.
Neuromuscular Disorders : NMD|February 1, 2016
How robust is ACTIVLIM for the follow-up of activity limitations in patients with neuromuscular diseases?Charles Sèbiyo Batcho, Peter Y K Van den Bergh, Philip Van Damme, et al.
Neuromuscular Disorders : NMD|January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutationsD Natera-de Benito, M Bestué, J J Vilchez, et al.
Neuromuscular Disorders : NMD|January 27, 2016
Where do we stand in trial readiness for autosomal recessive limb girdle muscular dystrophies?Volker Straub, Marta Bertoli
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