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Neuromuscular Disorders : NMD|October 29, 2021
Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findingsFangzhi Frank Jia, Alexander P Drew, Garth Alexander Nicholson, et al.
Neuromuscular Disorders : NMD|March 26, 2022
Evaluation of real-life outcome data of patients with spinal muscular atrophy treated with nusinersen in SwitzerlandAnne Tscherter, Christina T Rüsch, Dominique Baumann, et al.
Neuromuscular Disorders : NMD|March 27, 2022
Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cyclesK J Suetterlin, R Männikkö, E Matthews, et al.
Neuromuscular Disorders : NMD|September 19, 2018
Personalized gene and cell therapy for Duchenne Muscular DystrophyFlorian Barthélémy, Nicolas Wein
Neuromuscular Disorders : NMD|October 13, 2019
'Amish Nemaline Myopathy' in 2 Italian siblings harbouring a novel homozygous mutation in Troponin-I geneAdele D'Amico, Fabiana Fattori, Chiara Fiorillo, et al.
Neuromuscular Disorders : NMD|July 6, 2019
European regulators' views on a wearable-derived performance measurement of ambulation for Duchenne muscular dystrophy regulatory trialsMarion Haberkamp, Jane Moseley, Dimitrios Athanasiou, et al.
Neuromuscular Disorders : NMD|April 4, 2018
Critical period of neuromuscular development: Importance for a new treatment of SMAGerta Vrbová, Urszula Sławińska
Neuromuscular Disorders : NMD|April 10, 2023
A pathogenic CTBP1 variant featuring HADDTS with dystrophic myopathologyHazim Kadhim, Eliane El-Howayek, Sandra Coppens, et al.
Neuromuscular Disorders : NMD|April 23, 2023
Broad spectrum of phenotype and genotype in Korean α-dystroglycan related muscular dystrophy presenting to a tertiary pediatric neuromuscular centerYoung Jun Ko, Anna Cho, Woo Joong Kim, et al.
Neuromuscular Disorders : NMD|March 30, 2023
How a paternal uniparental isodisomy of chromosome 17 leads to autosomal recessive limb-girdle muscular dystrophy R3Camille Verebi, Roseline Caumes, Sandra Chantot-Bastaraud, et al.
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