Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8683654 | Epilepsy & Behavior | 2018 | 6 Pages |
Abstract
Juvenile myoclonic epilepsy is often regarded as a benign epileptic syndrome, but in this setting, half of the individuals with JME have refractory epilepsy with only about a quarter of those seizure-free in the previous year. Despite some advances in the understanding of this syndrome, there is still much to do before we can offer all the best outcomes.
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Authors
Gonçalo Cação, Joana Parra, Shahidul Mannan, Sanjay M. Sisodiya, Josemir W. Sander,