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Neuromuscular Disorders : NMD|January 16, 2021
Effect of long term enzyme replacement therapy in late onset Pompe disease: A single-centre experienceGeorge K Papadimas, Christoforos Anagnostopoulos, Sophia Xirou, et al.
Neuromuscular Disorders : NMD|January 4, 2022
Idiopathic eosinophilic myositis: a systematic literature reviewCécile Fermon, François-Jérôme Authier, Laure Gallay
Neuromuscular Disorders : NMD|January 4, 2022
Revised upper limb module in type II and III spinal muscular atrophy: 24-month changesGiorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.
Neuromuscular Disorders : NMD|April 19, 2008
Feeding problems and malnutrition in spinal muscular atrophy type IISonia Messina, Marika Pane, Paola De Rose, et al.
Neuromuscular Disorders : NMD|April 24, 2017
Investigation on acute effects of enzyme replacement therapy and influence of clinical severity on physiological variables related to exercise tolerance in patients with late onset Pompe diseaseAnnalisa Sechi, Desy Salvadego, Alessandro Da Ponte, et al.
Neuromuscular Disorders : NMD|April 25, 2017
Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletionsEri Takeshita, Narihiro Minami, Kumiko Minami, et al.
Neuromuscular Disorders : NMD|March 23, 2021
Understanding European patient expectations towards current therapeutic development in spinal muscular atrophyNicole Gusset, Caroline Stalens, Eva Stumpe, et al.
Neuromuscular Disorders : NMD|December 28, 2021
Patient reported quality of life in limb girdle muscular dystrophyLaurel V Kovalchick, Kameron Bates, Jeffrey Statland, et al.
Neuromuscular Disorders : NMD|August 2, 2011
Molecular and clinical study of McArdle's disease in a cohort of 123 European patients. Identification of 20 novel mutationsIrene Vieitez, Susana Teijeira, Jose M Fernandez, et al.
Neuromuscular Disorders : NMD|August 30, 2011
Acetylcholine receptor antibodies in patients with genetic myopathies: clinical and biological significanceRussell J M Lane, Federico Roncaroli, Peter Charles, et al.
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