Raggruppamento Primario: Malattie Neuromuscolari

Filtra

Data

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

Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.

Caregivers’ Expectations on Possible Functional Changes following Disease-Modifying Treatment in Type II and III Spinal Muscular Atrophy: A Comparative Study

Measuring Fatigue and Fatigability in Spinal Muscular Atrophy (SMA): Challenges and Opportunities

Assessing Prevalence and Characteristics of Oro-bulbar Involvement in Children and Adults with SMA Type 2 and 3 Using a Multimodal Approach

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