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