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MFM - nmd

Broadening The Imaging Phenotype of Dysferlinopathy at Different Disease Stages

Nov 4, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Broadening The Imaging Phenotype of Dysferlinopathy at Different Disease Stages Díaz J, Woudt L, Suazo L, Garrido C, Caviedes P, Cardenas AM, Castiglioni C, Bevilacqua JA. Muscle Nerve. 2016. 54(2):203-10. The study aimed at describes MRI...

Myotonic dystrophy type 1: frequency of ophthalmologic findings

Nov 3, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Myotonic dystrophy type 1: frequency of ophthalmologic findings Ikeda KS, Iwabe-Marchese C, França MC Jr, Nucci A, Carvalho KM. Arq Neuropsiquiatr. 2016. 74(3):183-8. The purpose of the study was to evaluate the frequency of ophthalmologic...

Toward an objective measure of functional disability in dysferlinopathy

Nov 2, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Toward an objective measure of functional disability in dysferlinopathy Woudt L, Di Capua GA, Krahn M, Castiglioni C, Hughes R, Campero M, Trangulao A, González-Hormazábal P, Godoy-Herrera R, Lévy N, Urtizberea JA, Jara L, Bevilacqua JA....

Computer task performance by subjects with Duchenne muscular dystrophy

Nov 1, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Computer task performance by subjects with Duchenne muscular dystrophy Malheiros SR, da Silva TD, Favero FM, de Abreu LC, Fregni F, Ribeiro DC, de Mello Monteiro CB. Neuropsychiatr Dis Treat. 2015. 30;12:41-8. The study aimed at verifying...

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,...
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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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