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MFM - nmd

Improvements in motor tasks through the use of smartphone technology for individuals with Duchenne muscular dystrophy

Nov 22, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Improvements in motor tasks through the use of smartphone technology for individuals with Duchenne muscular dystrophy Capelini CM, da Silva TD, Tonks J, Watson S, Alvarez MPB, de Menezes LDC, Favero FM, Caromano FA, Massetti T, de Mello...

Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study

Nov 21, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study Fatehi F, Salort-Campana E, Le Troter A, Lareau-Trudel E, Bydder M, Fouré A, Guye M, Bendahan D, Attarian S PLoS One....

Patients with Duchenne and Becker muscular dystrophies are not more asymmetrical than healthy controls on timed performance of upper limb tasks

Nov 20, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Patients with Duchenne and Becker muscular dystrophies are not more asymmetrical than healthy controls on timed performance of upper limb tasks Artilheiro MC, Sá CSC, Fávero FM, Caromano FA, Voos MC. Braz J Med Biol Res. 2017. 50(8):...

Reliability and validity analyses of the North Star Ambulatory Assessment in Brazilian Portuguese

Nov 19, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Reliability and validity analyses of the North Star Ambulatory Assessment in Brazilian Portuguese Okama LO, Zampieri LM, Ramos CL, Toledo FO, Alves CRJ, Mattiello-Sverzut AC, Mayhew A, Sobreira CFR Neuromuscul Disord. 2017....

Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III

Nov 18, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III Kölbel H, Hauffa BP, Wudy SA, Bouikidis A, Della Marina A, Schara U PLoS One. 2017. 9;12(3):e0173144. Study of prevalence of hyperleptinemia in a spinal...

Electrical impedance myography (EIM) in individuals with COL6 and LAMA2 congenital muscular dystrophy: a cross-sectional and two-year analysis

Nov 17, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Electrical impedance myography (EIM) in individuals with COL6 and LAMA2 congenital muscular dystrophy: a cross-sectional and two-year analysis Nichols C, Jain MS, Meilleur KG, Wu T, Collins J, Waite MR, Dastgir J, Salman A, Donkervoort S,...
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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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