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Mediciones de la función motora y otros parámetros de resultado clínico en niños ambulatorios con Distrofia Muscular de Duchenne
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Mediciones de la función motora y otros parámetros de resultado clínico en niños ambulatorios con Distrofia Muscular de Duchenne

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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El objetivo de este estudio es presentar las medidas de resultado clínico más confiables y sus correlaciones con el músculo cuantitativo MRI en pacientes ambulantes con distrofia muscular de Duchenne.

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Medicina número 143 distrofia muscular de Duchenne ensayo medida de la función motora seis minutos a pie resonancia magnética cuantitativa degeneración de la grasa muscular
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