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MFM - nmd

Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy

Sep 12, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy Fischmann A, Gloor M, Fasler S, Haas T, Rodoni Wetzel R, Bieri O, Wetzel S, Heinimann K, Scheffler K, Fischer D. J...

Impaired Mandibular Function in Spinal Muscular Atrophy Type II: Need for Early Recognition

Sep 11, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Impaired Mandibular Function in Spinal Muscular Atrophy Type II: Need for Early Recognition van Bruggen HW, van den Engel-Hoek L, van der Pol WL, de Wijer A, de Groot IJ, Steenks MH. J Child Neurol. Nov 2011. 26: 1392 – 1396. The aim...

Idebenone for the treatment of Duchenne muscular dystrophy (Protocol)

Sep 10, 2019 | Articles dans les revues scientifiques, Publications

< Retour aux Publications Idebenone for the treatment of Duchenne muscular dystrophy (Protocol) Geng J, Dong J, Jiang K, Shen L, Wu T, Ni H, Shi LL, Wang G, Wu H. The Cochrane Library 2011. Description of a protocol aiming at assessing efficacy of ibedenone on...

High-frequency, low-intensity vibrations increase bone mass and muscle strength in upper limbs, improving autonomy in disabled children

Sep 9, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications High-frequency, low-intensity vibrations increase bone mass and muscle strength in upper limbs, improving autonomy in disabled children Reyes ML, Hernandez M, Holmgren LJ, Sanhueza E, Escobar RG. J Bone Miner Res, 2011. 26(8): 1759-66. The...

Motor Function Measure Scale (MFM): New Instrument for Follow-Up Brazilian Patients with Neuromuscular Disease

Sep 8, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Motor Function Measure Scale (MFM): New Instrument for Follow-Up Brazilian Patients with Neuromuscular Disease Iwabe C, Nucci A, Pfeilsticker BHM, Magna LA. Muscular Dystrophy ed.Croacia : Intech. 2012. 303-320. Book chapter presenting the...

Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease

Sep 7, 2019 | Articles dans les revues scientifiques, Publications

<Back to Publications Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease Orlikowski D, Pellegrini N, Prigent H, Laforêt P, Carlier R, Carlier P, Eymard B, Lofaso F, Annane D. Neuromuscul Disord....
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Recent Posts

  • How to Best Measure Disease Progression in Adult Spinal Muscular Atrophy Patients: A Clinical and Neurophysiological Study
  • 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

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