Popolazione Mix: BAMBINO-ADULTO

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The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy

Ataluren treatment of patients with nonsense mutation dystrophinopathy.

Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy

Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial

Correction to: Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study

Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study

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

Co-morbid tics and stereotypies: a systematic literature review

Quantitative assessment of tip-toe behavior in individuals with autism spectrum disorder and intellectual disability: A cross-sectional study

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

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