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Neuromuscular Disorders : NMD|September 5, 2020
How to capture activities of daily living in myotonic dystrophy type 2?Federica Montagnese, Emanuele Rastelli, Kristina Stahl, et al.
Neuromuscular Disorders : NMD|September 7, 2020
Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutationThomas Claeys, Veerle Goosens, Valérie Racé, et al.
Neuromuscular Disorders : NMD|December 27, 2022
Clinical characteristics of dysphagic inclusion body myositisKenichiro Taira, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Neuromuscular Disorders : NMD|December 29, 2022
The effects of facioscapulohumeral dystrophy and dynamic arm support on upper extremity muscle coordination in functional tasksJ M N Essers, K Meijer, A A Peters, et al.
Neuromuscular Disorders : NMD|January 18, 2023
A young female case of asymptomatic immune-mediated necrotizing myopathy: a potential diagnostic option of antibody testing for rhabdomyolysisRyo Sasaki, Taijun Yunoki, Yumiko Nakano, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
Neuromuscular Disorders : NMD|June 2, 2021
A cryptic intronic LAMA2 insertion in a boy with mild congenital muscular dystrophy type 1ASabine Specht, Jennifer Duff, Richard Charlton, et al.
Neuromuscular Disorders : NMD|July 2, 2021
Reliability and validity of the FSHD-composite outcome measure in childhood facioscapulohumeral dystrophyK de Valle, F Dobson, I Woodcock, et al.
Neuromuscular Disorders : NMD|July 2, 2021
Accuracy of patient-reported data for an online patient registry of autoimmune myasthenia gravis and Lambert-Eaton myasthenic syndromeAnnabel M Ruiter, Ellen Strijbos, Robert H P de Meel, et al.
Neuromuscular Disorders : NMD|June 8, 2021
Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersenGiorgia Coratti, Marika Pane, Simona Lucibello, et al.
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