Autori: Civitello M

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Data

2-Year Change in Revised Hammersmith Scale Scores in a Large Cohort of Untreated Paediatric Type 2 and 3 SMA Participants

Functional outcome measures in young, steroid-na‹ve boys with Duchenne muscular dystrophy

Revised upper limb module in type II and III spinal muscular atrophy: 24-month changes

Different trajectories in upper limb and gross motor function in spinal muscular atrophy

Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersen

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

Clinical Variability in Spinal Muscular Atrophy Type III

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

A critical review of patient and parent caregiver oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in spinal muscular atrophy

Development of an academic disease registry for spinal muscular atrophy

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