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Autori: Mayhew A

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A critical review of functional assessment tools for upper limbs in Duchenne muscular dystrophy

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Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3

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Determining minimal clinically important differences in the Hammersmith Functional Motor Scale Expanded for untreated spinal muscular atrophy patients: An international study

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2-Year Change in Revised Hammersmith Scale Scores in a Large Cohort of Untreated Paediatric Type 2 and 3 SMA Participants

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Clinical Variability in Spinal Muscular Atrophy Type III

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Age and baseline values predict 12 and 24-month functional changes in type 2 SMA

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A critical review of patient and parent caregiver oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in spinal muscular atrophy

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Revised upper limb module for spinal muscular atrophy: 12-month changes

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Quantitative Evaluation of Lower Extremity Joint Contractures in Spinal Muscular Atrophy: Implications for Motor Function

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Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

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