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Spinal Muscular Atrophy Functional Composite Score Revised (SMA-FCR) in Untreated and Nusinersen-Treated Patient Cohorts

Upper limb progression in Duchenne muscular dystrophy: Insights from a 36-month longitudinal study using the PUL 20

Application of the neonatal ‘floppy module’ to older infants: can it be used for differential diagnosis?

Loss of ambulation in SMA III at the time of disease-modifying treatments: an international study

Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24-Month Follow-Up From the Italian Registry

Navigating new motor function trajectories: Consensus recommendations for assessment in the era of newborn screening and early treatment in SMA

Vertebral fractures and muscle function in glucocorticoid-treated individuals with Duchenne muscular dystrophy: a cohort study

Motor function in Rett syndrome: comparing clinical and parental assessments

Early parenting intervention promotes 24-month psychomotor development in preterm children

Exploring relationships between joint hypermobility and neurodevelopment in children (4-13 years) with hereditary connective tissue disorders and developmental coordination disorder

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