Autori: Coratti G*

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A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable?

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

Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey

Long term follow-up of scoliosis progression in type II SMA patients

Language Development in Preschool Duchenne Muscular Dystrophy Boys

Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy

Assessing floppy infants: a new module

Predictive models in SMA II natural history trajectories using machine learning: A proof of concept study

Neurological assessment of newborns with spinal muscular atrophy identified through neonatal screening

Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patients

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