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MFM - nmd

Reliability and validity of Trunk Control Test in patients with neuromuscular diseases

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

< Retour aux Publications Reliability and validity of Trunk Control Test in patients with neuromuscular diseases Parlak Demir Y, Yildirim SA. Physiother Theory Pract. 2015. 31(1):39-44. Determination of the reliability and validity of the Trunk Control Test (TCT)...

Instruments for the evaluation of motor abilities for children with severe multiple disabilities: A systematic review of the literature

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

< Retour aux Publications Instruments for the evaluation of motor abilities for children with severe multiple disabilities: A systematic review of the literature Mensch SM, Rameckers EA, Echteld MA, Evenhuis HM. Res Dev Disabil. 2015. 47:185-98. Based on a...

Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years

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

< Retour aux Publications Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years Werlauff U, Petri, H, Witting N, Vissing J. Journal of Neuromuscular Diseases. 2015. 2(2):167-174. Eighty-four patients with...

Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophy

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

< Retour aux Publications Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophy Bonati U, Schmid M, Hafner P, Haas T, Bieri O, Gloor M, Fischmann A, Fischer D. Muscle Nerve. 2015. 51(6):918-21. The aim of this study was to...

Muscle Quantitative MR Imaging and Clustering Analysis in Patients with Facioscapulohumeral Muscular Dystrophy Type 1

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

< Retour aux Publications Muscle Quantitative MR Imaging and Clustering Analysis in Patients with Facioscapulohumeral Muscular Dystrophy Type 1 Lareau-Trudel E, Le Troter A, Ghattas B, Pouget J, Attarian S, Bendahan D, Salort-Campana E. PLoS One. 2015....

Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies

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

< Retour aux Publications Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies Meilleur KG, Jain MS, Hynan LS, Shieh CY, Kim E, Waite M, McGuire M, Fiorini C, Glanzman AM, Main M,...
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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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