The role of rehabilitation in the management of late-onset Pompe disease: a narrative review
Metabolic impairments in patients with myotonic dystrophy type 2
Immune-mediated necrotizing myopathy due to statins exposure
Novel desmoplakin mutations in familial Carvajal syndrome
Heart Transplantation in a patient with Myotonic Dystrophy Type 1 and end-stage dilated cardiomyopathy: a short term follow-up
Therapeutic approach with Ataluren in Duchenne symptomatic carriers with nonsense mutations in dystrophin gene. Results of a 9-month follow-up in a case report.
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