Les progrès de la recherche et de la prise en charge des maladies neuromusculaires de l’enfance ont prolongé la survie des patients. L’évaluation s’impose donc pour le suivi des patients et aussi en recherche clinique car les premiers essais cliniques tant attendus commencent à paraître. Une métrologie rigoureuse et adaptée est alors indispensable parce qu'il n'est possible ni de se contenter d’une quantification approximative ni d'utiliser des outils non adaptés à des pathologies évolutives. Nous résumons l’état des connaissances sur la métrologie appliquée à l’évaluation fonctionnelle motrice des patients atteints de maladies neuromusculaires et proposons une revue de la littérature sur les outils disponibles avec des analyses précises de...
International audienceOBJECTIVES: To study the responsiveness (sensitivity to change) of the Motor F...
International audienceGiven the progress of research and management in Spinal Muscular Atrophy (SMA)...
Objectives: To monitor treatment effects in patients with congenital myopathies and congenital muscu...
Advances in the research and treatment of childhood neuromuscular diseases have led to longer patien...
Os objetivos do estudo foram: traduzir a escala francesa Medida da Função Motora (MFM) para o portug...
AbstractObjectiveTo develop a classification for neuromuscular disease patients in each of the three...
International audienceObjectivePhysiotherapists are demanding of valid outcome measures to assess th...
To validate a useful version of the Motor Function Measure (MFM) in children with neuromuscular dise...
Background: Functional evaluation instruments for patients with neuromuscular disorders are rare. Th...
Assessment in patients with NMD consists principally of measures of motor impairment since they are ...
Neuromuscular disorders are characterised by progressive muscle weakness, which in time causes funct...
International audienceOBJECTIVES: To study the responsiveness (sensitivity to change) of the Motor F...
International audienceGiven the progress of research and management in Spinal Muscular Atrophy (SMA)...
Objectives: To monitor treatment effects in patients with congenital myopathies and congenital muscu...
Advances in the research and treatment of childhood neuromuscular diseases have led to longer patien...
Os objetivos do estudo foram: traduzir a escala francesa Medida da Função Motora (MFM) para o portug...
AbstractObjectiveTo develop a classification for neuromuscular disease patients in each of the three...
International audienceObjectivePhysiotherapists are demanding of valid outcome measures to assess th...
To validate a useful version of the Motor Function Measure (MFM) in children with neuromuscular dise...
Background: Functional evaluation instruments for patients with neuromuscular disorders are rare. Th...
Assessment in patients with NMD consists principally of measures of motor impairment since they are ...
Neuromuscular disorders are characterised by progressive muscle weakness, which in time causes funct...
International audienceOBJECTIVES: To study the responsiveness (sensitivity to change) of the Motor F...
International audienceGiven the progress of research and management in Spinal Muscular Atrophy (SMA)...
Objectives: To monitor treatment effects in patients with congenital myopathies and congenital muscu...