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Antiepileptic drugs for the treatment of infants with severe myoclonic epilepsy
BACKGROUND: This is an updated version of the original Cochrane review published in 2015, Issue 10. Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, refractory form of epilepsy, for which stiripentol (STP) has been recently licensed as add‐on therapy. OBJECTIVES...
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| Publicado no: | Cochrane Database Syst Rev |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Ltd
2017
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6481545/ https://ncbi.nlm.nih.gov/pubmed/28521067 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD010483.pub4 |
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