Autori: Vita G

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Data

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

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

Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophy

Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study

24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy

North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy.

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