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MFM - nmd

Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy

Nov 16, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy Bendixen RM, Butrum J, Jain MS, Parks R, Hodsdon B, Nichols C, Hsia M, Nelson L, Keller KC, McGuire M, Elliott JS, Linton MM, Arveson...

Reliability of home-based, motor function measure in hereditary neuromuscular diseases

Nov 15, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Reliability of home-based, motor function measure in hereditary neuromuscular diseases Ruiz-Cortes X, Ortiz-Corredor F, Mendoza-Pulido C J Int Med Res. 2017. 45(1):261-271. The goal of the study was to compare the reliability of the MFM...

Longitudinal Functional and NMR Assessment of Upper Limbs in Duchenne Muscular Dystrophy

Nov 14, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Longitudinal Functional and NMR Assessment of Upper Limbs in Duchenne Muscular Dystrophy Hogrel JY, Wary C, Moraux A, Azzabou N, Decostre V, Ollivier G, Canal A, Lilien C, Ledoux I, Annoussamy M, Reguiba N, Gidaro T, Le Moing AG, Cardas R,...

Treatment with L-citrulline in patients with post-polio syndrome: study protocol for a single-center, randomised, placebo-controlled, double-blind trial

Nov 14, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Treatment with L-citrulline in patients with post-polio syndrome: study protocol for a single-center, randomised, placebo-controlled, double-blind trial Schmidt S, Gocheva V, Zumbrunn T, Rubino-Nacht D, Bonati U, Fischer D, Hafner...

Postrehabilitation Functional Improvements in Patients With Inflammatory Myopathies: The Results of a Randomized Controlled Trial

Nov 14, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Postrehabilitation Functional Improvements in Patients With Inflammatory Myopathies: The Results of a Randomized Controlled Trial Tiffreau V, Rannou F, Kopciuch F, Hachulla E, Mouthon L, Thoumie P, Sibilia J, Drumez E, Thevenon A Arch Phys...
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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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