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The Use of Functional Scales for Clinical Evaluation of Duchenne Muscular Dystrophy

Sep 30, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications The Use of Functional Scales for Clinical Evaluation of Duchenne Muscular Dystrophy Barra TMF, Baraldi KF Revista Neurociências. 2013. 21(3):420-426. Literature review of scientific articles, books and dissertations published from 2000 to...

Assisted bicycle training delays functional deterioration in boys with duchenne muscular dystrophy: the randomized controlled trial “no use is disuse”.

Sep 29, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Assisted bicycle training delays functional deterioration in boys with duchenne muscular dystrophy: the randomized controlled trial “no use is disuse”. Jansen M, van Alfen N, Geurts AC, de Groot IJ. Neurorehabil Neural Repair....

Registre Français de la maladie de Pompe. Caractérisation d’une cohorte de 126 patients adultes

Sep 28, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Registre Français de la maladie de Pompe. Caractérisation d’une cohorte de 126 patients adultes P. Laforêt, K. Laloui, B. Granger, D. Hamroun, N. Taouagh, JY. Hogrel, D. Orlikowski, F. Bouhour, A. Lacour, E. Salort-Campana, I....

Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients.

Sep 27, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients. Servais L, Deconinck N, Moraux A, Benali M, Canal A, Van Parys F, Vereecke W, Wittevrongel S, Mayer M, Desguerre I, Maincent K, Themar-Noel C,...

Motor Function Measure: validation of a short form (MFM-20) for young children with neuromuscular diseases

Sep 26, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Motor Function Measure: validation of a short form (MFM-20) for young children with neuromuscular diseases Capucine de Lattre, Christine Payan, Carole Vuillerot, Pascal Rippert, Denis de Castro, Carole Bérard, Isabelle Poirot and the...
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  • Effects of nusinersen after one year of treatment in 123 children with SMA type 1 or 2: a French real-life observational study
  • Long-term benefit of enzyme replacement therapy with alglucosidase alfa in adults with Pompe disease: prospective analysis from the French Pompe Registry
  • Muscle MRI: A biomarker of disease severity in Duchenne muscular dystrophy? A systematic review
  • Evaluation of Speed-Accuracy Trade-Off in a Computer Task to Identify Motor Difficulties in Individuals With Duchenne Muscular Dystrophy – A Cross-Sectional Study
  • Timed immersion expiration measures in patients with muscular dystrophies

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