Raggruppamento Primario: Malattie Neuromuscolari

Filtra

Data

Intrathecal administration of nusinersen in adult and adolescent patients with spinal muscular atrophy and scoliosis: Transforaminal versus conventional approach

Longitudinal natural history in young boys with Duchenne muscular dystrophy

Performance of Upper Limb module for Duchenne muscular dystrophy

Development of an academic disease registry for spinal muscular atrophy

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

Long-term progression in type II spinal muscular atrophy: A retrospective observational study

Revised upper limb module for spinal muscular atrophy: 12?month changes

Ambulatory function in spinal muscular atrophy: Age-related patterns of progression

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

Torna in alto