Autori: Baranello G

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Data

The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophy

Evaluation of body composition as a potential biomarker in spinal muscular atrophy

Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients

Longitudinal natural history in young boys with Duchenne muscular dystrophy

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Outcome measures for children with movement disorders

Two single cases treated by a new pseudoelastic upper-limb orthosis for secondary dystonia of the young

Spontaneous Breathing Pattern as Respiratory Functional Outcome in Children with Spinal Muscular Atrophy (SMA)

Sleep disorders in spinal muscular atrophy

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