Autori: Capasso A

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Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome?

Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey

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

Can the CHOP-INTEND be used as An Outcome Measure in the First Months of Age? Implications for Clinical Trials and Real World Data

Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?

Profile of cognitive abilities in spinal muscular atrophy type II and III: what is the role of motor impairment?

Early treatment of type II SMA slows rate of progression of scoliosis

Patient reported outcome measure for upper limb in Duchenne muscular dystrophy: correlation with PUL2.0

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

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