Autori: Bruno C

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Data

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

Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?

Respiratory Needs in Patients with Type 1 Spinal Muscular Atrophy Treated with Nusinersen

Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world data

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

Nusinersen in type 1 SMA infants, children and young adults: Preliminary results on motor function

An observational study of functional abilities in infants, children, and adults with type 1 SMA

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

Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational Study

The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys

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