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Archives of Neurology|December 19, 2006
Multifocal motor neuropathy with conduction block: slow but not benignDale J Lange, Louis H Weimer, Werner Trojaborg, et al.Journal of Clinical Neuromuscular Disease|August 28, 2012
Facial onset sensorimotor neuronopathy syndrome: a case seriesDobrin Dobrev, Richard J Barohn, Neil E Anderson, et al.Journal of Visualized Experiments : Jove|February 25, 2020
Use of Capillary Electrophoresis Immunoassay to Search for Potential Biomarkers of Amyotrophic Lateral Sclerosis in Human PlateletsJessica M Sage, LaSharice Hall, April McVey, et al.Physical Therapy|July 16, 2016
Activity for Diabetic Polyneuropathy (ADAPT): Study Design and Protocol for a 2-Site Randomized Controlled TrialPatricia M Kluding, J Robinson Singleton, Mamatha Pasnoor, et al.Muscle & Nerve|September 25, 2003
Late-onset distal muscular dystrophy affecting the posterior calvesJonathan S Katz, Thomas A Rando, Richard J Barohn, et al.JAMA Neurology|February 27, 2013
Incidence of amyotrophic lateral sclerosis among American Indians and Alaska nativesPaul H Gordon, Jason M Mehal, Robert C Holman, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|December 31, 2010
Senataxin mutations and amyotrophic lateral sclerosisMichio Hirano, Catarina M Quinzii, Hiroshi Mitsumoto, et al.Muscle & Nerve|December 17, 2011
Consensus treatment recommendations for late-onset Pompe diseaseEdward J Cupler, Kenneth I Berger, Robert T Leshner, et al.Archives of Neurology|September 17, 2003
Challenges in the identification of cobalamin-deficiency polyneuropathyDavid S Saperstein, Gil I Wolfe, Gary S Gronseth, et al.Neurologic Clinics|July 20, 2014
Pompe disease: literature review and case seriesMajed Dasouki, Omar Jawdat, Osama Almadhoun, et al.Pageof 19