Reversible spontaneous EMG activity during myasthenic crisis: Two case reports

Background: Myasthenia Gravis (MG) is an antibody-mediated autoimmune neuromuscular disorder, clinically presenting with fatigable variable muscle weakness. Typical electrodiagnostic findings are a decremental response to repetitive nerve stimulation with post-exercise facilitation, and motor unit i...

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Bibliographic Details
Main Authors: Theocharis Tsironis, Santiago Catania
Format: Article
Language:English
Published: Elsevier 2019-03-01
Series:eNeurologicalSci
Online Access:http://www.sciencedirect.com/science/article/pii/S240565021830056X