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Neuromuscular Disorders : NMD|May 3, 2016
Myasthenia gravis with muscle specific kinase antibodies mimicking amyotrophic lateral sclerosisMaartje G Huijbers, Erik H Niks, Rinse Klooster, et al.
Neuromuscular Disorders : NMD|October 26, 2017
Lower limb muscle magnetic resonance imaging in myotonic dystrophy type 1 correlates with the six-minute walk test and CTG repeatsDonghwi Park, Sang-Hoon Lee, Jin-Hong Shin, et al.
Neuromuscular Disorders : NMD|June 25, 2018
Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutationTeodora Chamova, Stoyan Bichev, Tihomir Todorov, et al.
Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.
Neuromuscular Disorders : NMD|September 4, 2018
Characteristic findings of skeletal muscle MRI in caveolinopathiesKumiko Ishiguro, Takahiro Nakayama, Masaru Yoshioka, et al.
Neuromuscular Disorders : NMD|June 19, 2018
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance (SLONM-MGUS): An alternative treatment using cyclophosphamide-thalidomide-dexamethasone (CTD) regimenTheerawat Kumutpongpanich, Weerapat Owattanapanich, Jantima Tanboon, et al.
Neuromuscular Disorders : NMD|June 19, 2018
A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pairSonja Strang-Karlsson, Katherine Johnson, Ana Töpf, et al.
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Neuromuscular Disorders : NMD|September 16, 2019
Membrane recruitment of nNOSµ in microdystrophin gene transfer to enhance durabilityJessica F Boehler, Valeria Ricotti, J Patrick Gonzalez, et al.
Neuromuscular Disorders : NMD|August 19, 2019
Normative data and percentile curves for the three-minute walk test and timed function tests in healthy Caucasian boys from 2.5 up to 6 years oldJasmine Hoskens, Nathalie Goemans, Hilde Feys, et al.
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