Raggruppamento Primario: Malattie Neuromuscolari

Filtra

Data

Nusinersen in pediatric and adult patients with type III spinal muscular atrophy

North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up

Early Gross Motor Milestones in Duchenne Muscular Dystrophy

Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New Module

Point-of-care lung and diaphragm ultrasound in a patient with spinal muscular atrophy with respiratory distress type 1

Type I SMA “new natural history”: long-term data in nusinersen-treated patients

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

The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure

Respiratory Trajectories in Type 2 and 3 Spinal Muscular Atrophy in the iSMAC Cohort Study

Clinical Variability in Spinal Muscular Atrophy Type III

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