2009
DOI: 10.1590/s0004-27492009000100020
|View full text |Cite
|
Sign up to set email alerts
|

Surgical correction of strabismus in Lambert-Eaton myasthenic syndrome: case reports

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2010
2010
2020
2020

Publication Types

Select...
2
2

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 12 publications
0
1
0
Order By: Relevance
“…This episode was investigated by a neurologist, and the electromyography revealed a 160% amplitude increment after a train of stimuli delivered at 50 Hz in the left median nerve and, the diagnostic was Lambert-Eaton syndrome, a very rare and acquired autoimmune disorder. After a careful observation period of 9 months, the deviation was stable and a recess-resect procedure was then performed in the right eye [32].…”
Section: Discussionmentioning
confidence: 99%
“…This episode was investigated by a neurologist, and the electromyography revealed a 160% amplitude increment after a train of stimuli delivered at 50 Hz in the left median nerve and, the diagnostic was Lambert-Eaton syndrome, a very rare and acquired autoimmune disorder. After a careful observation period of 9 months, the deviation was stable and a recess-resect procedure was then performed in the right eye [32].…”
Section: Discussionmentioning
confidence: 99%