Autori: Coratti G*

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Data

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

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

Gain and loss of abilities in type II SMA: A 12-month natural history study

Age and baseline values predict 12 and 24-month functional changes in type 2 SMA

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