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MFM - nmd

Diagnostic et histoire naturelle de la dystrophie musculaire de Duchenne

Oct 31, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Diagnostic et histoire naturelle de la dystrophie musculaire de Duchenne Desguerre I, Laugel V. Arch Pediatr. 2015. 22(12 Suppl 1):12S24-30. Duchenne myopathy is today the most frequently encountered progressive muscular dystrophy in...

Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype

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

< Retour aux Publications Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype Servais L, Montus M, Guiner C, Ben Yaou R, Annoussamy M, Moraux A, Hogrel JY, Seferian AM, Zehrouni K, Le Moing AG, Gidaro T, Vanhulle C,...

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...
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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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