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Neurology|August 26, 1998
Pilot study of myoblast transfer in the treatment of Becker muscular dystrophyA M Neumeyer, D Cros, D McKenna-Yasek, et al.Electromyography and Clinical Neurophysiology|October 11, 2003
EMG analysis of the upper and lower fascicles of the orbicularis oris muscle in deaf individualsS C Regalo, M Vitti, J E Hallak, et al.Neurology|July 17, 1999
Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15F Martínez Murillo, H Kobayashi, E Pegoraro, et al.American Journal of Human Genetics|June 1, 1994
Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in femalesE Pegoraro, R N Schimke, K Arahata, et al.European Journal of Neurology|June 26, 2024
Neurofilament light chain and profilin-1 dynamics in 30 spinal muscular atrophy type 3 patients treated with nusinersenG Musso, L Bello, G Capece, et al.European Journal of Neurology|January 12, 2012
CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosisA Bruson, F Sambataro, G Querin, et al.Journal of Neurology|March 12, 2010
Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2Vincenzo Romeo, E Pegoraro, C Ferrati, et al.Journal of Neurology|July 2, 2010
Right hemisphere dysfunction and emotional processing in ALS: an fMRI studyA Palmieri, M Naccarato, S Abrahams, et al.Neurology|April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiencyC Lamperti, A Naini, M Hirano, et al.European Journal of Neurology|May 5, 2016
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotypeC Bertolin, G Querin, E Da Re, et al.Pageof 8