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Muscle & Nerve|December 6, 2020
Knowledge and perceptions of the COVID-19 pandemic among patients with myasthenia gravisYingkai Li, C Douglas Emmett, Marjan Cobbaert, et al.Muscle & Nerve|July 4, 2019
Validation of the triple timed up-and-go test in Lambert-Eaton myastheniaShruti M Raja, Donald B Sanders, Vern C Juel, et al.Muscle & Nerve|May 26, 2017
Reliability of the triple-timed up-and-go testDonald B Sanders, Jeffrey T Guptill, Kathy L Aleš, et al.Muscle & Nerve|March 21, 2013
A randomized, double-blind, placebo-controlled phase II study of eculizumab in patients with refractory generalized myasthenia gravisJames F Howard, Richard J Barohn, Gary R Cutter, et al.Muscle & Nerve|December 28, 2017
3,4-diaminopyridine base effectively treats the weakness of Lambert-Eaton myastheniaDonald B Sanders, Vern C Juel, Yadollah Harati, et al.Experimental Neurology|September 23, 1998
Mitochondria in sporadic amyotrophic lateral sclerosisR H Swerdlow, J K Parks, D S Cassarino, et al.Muscle & Nerve|December 9, 2020
Reduced plasmablast frequency is associated with seronegative myasthenia gravisJeffrey T Guptill, Richard Barfield, Cliburn Chan, et al.Muscle & Nerve|May 26, 2016
International clinimetric evaluation of the MG-QOL15, resulting in slight revision and subsequent validation of the MG-QOL15rTed M Burns, Reza Sadjadi, Kimiaki Utsugisawa, et al.Journal for Immunotherapy of Cancer|July 20, 2021
Consensus disease definitions for neurologic immune-related adverse events of immune checkpoint inhibitorsAmanda C Guidon, Leeann B Burton, Bart K Chwalisz, et al.JAMA Neurology|November 23, 2020
Effect of Ezogabine on Cortical and Spinal Motor Neuron Excitability in Amyotrophic Lateral Sclerosis: A Randomized Clinical TrialBrian J Wainger, Eric A Macklin, Steve Vucic, et al.Pageof 12