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- Discover the MFM Play app
- How to Best Measure Disease Progression in Adult Spinal Muscular Atrophy Patients: A Clinical and Neurophysiological Study
- Rasch analysis to evaluate the motor function measure for patients with facioscapulohumeral muscular dystrophy
- Assessment of the validity and reliability of the 32-item Motor Function Measure in individuals with Type 2 or non-ambulant Type 3 spinal muscular atrophy
- Assessment of respiratory muscles and motor function in children with SMA treated by nusinersen
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