Autori: Cicala G

Filtra

Data

Identification and treatment of neurodevelopmental and mental disorders in boys and adults with Duchenne muscular dystrophy: a cohort study

Myostatin Levels in SMA Following Disease-Modifying Treatments: A Multi-Center Study

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

Neurological assessment tool for screening infants during the first year after birth: The Brief-Hammersmith Infant Neurological Examination

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

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

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