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Annals of Neurology|January 31, 2003
Consequences of a novel caveolin-3 mutation in a large German familyDirk Fischer, Anja Schroers, Ingmar Blümcke, et al.
Muscle & Nerve|March 5, 2015
Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophyUlrike Bonati, Maurice Schmid, Patricia Hafner, et al.
Neuromuscular Disorders : NMD|April 2, 2014
Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA geneUlrike Bonati, Nina Bechtel, Karl Heinimann, et al.
Journal of Child Neurology|August 7, 2019
Association Between Health-Related Quality of Life and Motor Function in Ambulant and Nonambulant Duchenne Muscular Dystrophy PatientsVanya Gocheva, Simone Schmidt, Anna-Lena Orsini, et al.
Plos One|January 26, 2017
Feasibility of Using Microsoft Kinect to Assess Upper Limb Movement in Type III Spinal Muscular Atrophy PatientsXing Chen, Juliane Siebourg-Polster, Detlef Wolf, et al.
Journal of Neurology|July 3, 2017
Quantifying fat replacement of muscle by quantitative MRI in muscular dystrophyJedrzej Burakiewicz, Christopher D J Sinclair, Dirk Fischer, et al.
Journal of Visualized Experiments : Jove|March 20, 2018
An Objective and Child-friendly Assessment of Arm Function by Using a 3-D SensorXing Chen, Detlef Wolf, Juliane Siebourg-Polster, et al.
European Journal of Pediatrics|April 8, 2014
Neurofibromatosis type 1 (NF1) with an unusually severe phenotype due to digeny for NF1 and ryanodine receptor 1 associated myopathyFlorence Martin, Veronika Kana, Andrea Capone Mori, et al.
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