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Neuromuscular Disorders : NMD|November 2, 2019
Large in-frame 5' deletions in DMD associated with mild Duchenne muscular dystrophy: Two case reports and a review of the literatureElizabeth M Gibbs, Florian Barthélémy, Emilie D Douine, et al.Neuromuscular Disorders : NMD|July 9, 2021
Characteristics of Guillain-Barré syndrome in a Lebanese tertiary care centerHelen Ismail, Elia Malek, Lea Saroufim, et al.Neuromuscular Disorders : NMD|July 10, 2021
Cerebral involvement and related aspects in myotonic dystrophy type 2Stojan Peric, Vidosava Rakocevic-Stojanovic, Giovanni MeolaNeuromuscular Disorders : NMD|July 2, 2021
New subtype of PCH1C caused by novel EXOSC8 variants in a 16-year-old Spanish patientMaría Elena Rodríguez-García, Francisco Javier Cotrina-Vinagre, Marcello Bellusci, et al.Neuromuscular Disorders : NMD|July 25, 2021
Fatigue, physical activity and associated factors in 779 patients with myasthenia gravisLinda Kahr Andersen, Mette Aadahl, John VissingNeuromuscular Disorders : NMD|January 2, 2021
Cardiovascular disease in non-classic Pompe disease: A systematic reviewH A van Kooten, C H A Roelen, E Brusse, et al.Neuromuscular Disorders : NMD|January 2, 2021
Genetic neuropathies presenting with CIDP-like features in childhoodMiguel A Fernandez-Garcia, Georg M Stettner, Maria Kinali, et al.Neuromuscular Disorders : NMD|July 27, 2021
Intrafamilial phenotypic heterogeneity related to a new DMD splice site variantAntônio Rodrigues Coimbra Neto, Samara Camaçari de Carvalho, Tauana Bernardes Leoni, et al.Neuromuscular Disorders : NMD|April 16, 2013
A Portuguese case of Fukuyama congenital muscular dystrophy caused by a multi-exonic duplication in the fukutin geneC Costa, J Oliveira, A Gonçalves, et al.Neuromuscular Disorders : NMD|April 18, 2013
Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1Keivan Basiri, Katsiaryna Belaya, Wei Wei Liu, et al.Pageof 341