Autori: Ricci M

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

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

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

Nusinersen efficacy data for 24-month in type 2 and 3 spinal muscular atrophy

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