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Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
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Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy

Article DOI: 10.3791/58784-v • 09:18 min • January 12th, 2019
January 12th, 2019 •
1,2, 1,2, 1,3, 1,4,5, 1, 1, 6, 7, 1,2, 1,2,3
1Division of Pediatric Neurology, University Children's Hospital Basel (UKBB), University of Basel, 2Department of Neurology, University Hospital Basel, University of Basel, 3Division of Neurology, University Clinic of Medicine, Cantonal Hospital Baselland, Bruderholz, 4Division of Pediatric Neurology, CHUV, 5Division of Neuropaediatrics, Inselspital, University Children's Hospital Bern, 6Department of Radiology, Division of Radiological Physics, University Hospital Basel, University of Basel, 7Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, L'Escale, Service de Médecine Physique et de Réadaptation Pédiatrique

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Summary
Automatic Translation

The aim of this study is to present the most reliable clinical outcome measures and their correlations with quantitative muscle MRI in ambulant patients with Duchenne muscular dystrophy.

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Measurements Motor Function Clinical Outcome Parameters Ambulant Children Duchenne Muscular Dystrophy Treatment Response Clinical Decline Clinical Trials Patient Compliance Ambulatory Patients Nonambulatory Patients Physiotherapist University Children's Hospital Basal Clinical Assessment Tasks Lying Down Head Position Knee Position Foot Position Upper Limb Position
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