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MFM - nmd

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,...

Adding quantitative muscle MRI to the FSHD clinical trial toolbox

Nov 24, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Adding quantitative muscle MRI to the FSHD clinical trial toolbox Mul K, Vincenten SCC, Voermans NC, Lemmers RJLF, van der Vliet PJ, van der Maarel SM, Padberg GW, Horlings CGC, van Engelen BGM Neurology. 2017....
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Recent Posts

  • 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
  • Validity and Reliability of the 32-Item Motor Function Measure in 2- to 5-Year-Olds with Neuromuscular Disorders and 2- to 25-Year-Olds with Spinal Muscular Atrophy

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