Autori: Zanin R*

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Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016

Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study

Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?

Type I spinal muscular atrophy patients treated with nusinersen: 4-year follow-up of motor, respiratory and bulbar function

Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment

Functional outcome measures in young, steroid-naive boys with Duchenne muscular dystrophy

Evaluation of body composition as a potential biomarker in spinal muscular atrophy

Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients

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

Two single cases treated by a new pseudoelastic upper-limb orthosis for secondary dystonia of the young

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