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MFM - nmd

Functional outcome measures for infantile Charcot-Marie-Tooth disease: a systematic review

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

< Retour aux Publications Functional outcome measures for infantile Charcot-Marie-Tooth disease: a systematic review Mandarakas MR, Rose KJ, Sanmaneechai O, Menezes MP, Refshauge KM, Burns JJ Peripher Nerv Syst. 2018. 23(2), 99-107. Systematic review of the outcome...

Timed function tests, motor function measure, and quantitative thigh muscle MRI in ambulant children with Duchenne muscular dystrophy: A cross-sectional analysis

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

< Retour aux Publications Timed function tests, motor function measure, and quantitative thigh muscle MRI in ambulant children with Duchenne muscular dystrophy: A cross-sectional analysis Schmidt S, Hafner P, Klein A, Rubino-Nacht D, Gocheva V, Schroeder J,...

Corticosteroids in Duchenne muscular dystrophy: impact on the motor function measure sensitivity to change and implications for clinical trials

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

< Retour aux Publications Corticosteroids in Duchenne muscular dystrophy: impact on the motor function measure sensitivity to change and implications for clinical trials Schreiber A, Brochard S, Rippert P, Fontaine-Carbonnel S, Payan C, Poirot I, Hamroun D,...

Quantitative muscle MRI to follow up late onset Pompe patients: a prospective study

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

<Back to Publications Quantitative muscle MRI to follow up late onset Pompe patients: a prospective study Figueroa-Bonaparte S, Llauger J, Segovia S, Belmonte I, Pedrosa I, Montiel E, Montesinos P, Sánchez-González J, Alonso-Jiménez A, Gallardo E, Illa I,...

Turkish version of the Motor Function Measure Scale (MFM-32) forneuromuscular diseases: a cross-cultural adaptation, reliability, and validity study

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

< Retour aux Publications Turkish version of the Motor Function Measure Scale (MFM-32) forneuromuscular diseases: a cross-cultural adaptation, reliability, and validity study Inal HS, Tarakçi E, Tarakçi D, Aksoy G, Mergen Kiliç S, Beser H, Beser Ç, Özdinçler AR,...

Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa

Nov 25, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa Decostre V, Laforêt P, De Antonio M, Kachetel K, Canal A, Ollivier G, Nadaj-Pakleza A, Petit FM, Wahbi K, Fayssoil A, Eymard B, Behin A,...
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Recent Posts

  • How to Best Measure Disease Progression in Adult Spinal Muscular Atrophy Patients: A Clinical and Neurophysiological Study
  • Rasch analysis to evaluate the motor function measure for patients with facioscapulohumeral muscular dystrophy
  • Assessment of the validity and reliability of the 32-item Motor Function Measure in individuals with Type 2 or non-ambulant Type 3 spinal muscular atrophy
  • Assessment of respiratory muscles and motor function in children with SMA treated by nusinersen
  • Association Between Health-Related Quality of Life and Motor Function in Ambulant and Nonambulant Duchenne Muscular Dystrophy Patients

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