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Neuromuscular Disorders : NMD|May 11, 2015
Clinical, neuropathological and radiological evidence for a rare complication of rituximab therapyE G Healy, R Phadke, M Kidd, et al.
Neuromuscular Disorders : NMD|May 11, 2015
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathyN Kraeva, L Heytens, H Jungbluth, et al.
Neuromuscular Disorders : NMD|May 11, 2015
SIL1-related Marinesco-Sjoegren syndrome (MSS) with associated motor neuronopathy and bradykinetic movement disorderSusan Byrne, Nomazulu Dlamini, Daniel Lumsden, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenonD Annane, M Fiorelli, B Mazoyer, et al.
Neuromuscular Disorders : NMD|September 6, 2025
Risdiplam and nusinersen in spinal muscular atrophy: a descriptive real-world study on motor function outcomes in northwestern IranMohammad Barzegar, Bita Poorshiri, Khatereh Rezazadeh, et al.
Neuromuscular Disorders : NMD|August 14, 2016
Identification of a novel splice site HSPG2 mutation and prenatal diagnosis in Schwartz Jampel Syndrome type 1 using whole exome sequencingAneek Das Bhowmik, Ashwin Dalal, Divya Matta, et al.
Neuromuscular Disorders : NMD|June 23, 2015
Quantitative muscle MRI: A powerful surrogate outcome measure in Duchenne muscular dystrophyUlrike Bonati, Patricia Hafner, Sabine Schädelin, et al.
Neuromuscular Disorders : NMD|November 5, 1997
Changes of laminin beta 2 chain expression in congenital muscular dystrophyR D Cohn, R Herrmann, U M Wewer, et al.
Neuromuscular Disorders : NMD|November 5, 1997
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'J C Rubio, M A Martín, J Bautista, et al.
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