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Neuromuscular Disorders : NMD|July 14, 2010
Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectinKatharine Forrest, Jemima E Mellerio, Stephanie Robb, et al.Neuromuscular Disorders : NMD|July 17, 2010
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophyElena Mazzone, Diego Martinelli, Angela Berardinelli, et al.Neuromuscular Disorders : NMD|January 4, 2011
Transient restoration of succinate dehydrogenase activity after rhabdomyolysis in iron-sulphur cluster deficiency myopathyGittan Kollberg, Atle Melberg, Elisabeth Holme, et al.Neuromuscular Disorders : NMD|January 4, 2011
Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophyJuan Parra, Rebeca Martínez-Hernández, Eva Also-Rallo, et al.Neuromuscular Disorders : NMD|January 4, 2011
Recombinant expression of the AChR-alpha1 subunit for the detection of conformation-dependent epitopes in Myasthenia GravisKathryn H Ching, Peter D Burbelo, Richard M Kimball, et al.Neuromuscular Disorders : NMD|February 1, 2011
Muscle satellite cells from GRMD dystrophic dogs are not phenotypically distinguishable from wild type satellite cells in ex vivo cultureZachary Berg, Lucas R Beffa, Daniel P Cook, et al.Neuromuscular Disorders : NMD|March 1, 2011
Myonuclear breakdown in sporadic inclusion body myositis is accompanied by DNA double strand breaksMakoto Nishii, Satoshi Nakano, Seika Nakamura, et al.Neuromuscular Disorders : NMD|May 10, 2011
Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe diseaseDavid Orlikowski, Nadine Pellegrini, Hélène Prigent, et al.Neuromuscular Disorders : NMD|July 28, 2019
Clinical spectrum and gene mutations in a Chinese cohort with anoctaminopathyShuang Cai, Mingshi Gao, Jianying Xi, et al.Pageof 340