Autori: Fanelli L*

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Data

Long-term progression in type II spinal muscular atrophy: A retrospective observational study

Ambulatory function in spinal muscular atrophy: Age-related patterns of progression

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

Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy

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

Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy

6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction

Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy

Sleep disorders in spinal muscular atrophy

Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular Dystrophy

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