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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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Detalles Bibliográficos
Autores principales: Tsironis, Theocharis, Catania, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275166/
https://www.ncbi.nlm.nih.gov/pubmed/30555945
http://dx.doi.org/10.1016/j.ensci.2018.11.024