Autori: Dosi C

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Communicative development inventory in type 1 and presymptomatic infants with spinal muscular atrophy: a cohort study

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

Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in na‹ve patients with spinal muscular atrophy and following switch from other therapies

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?

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

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