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Treating Lennox–Gastaut syndrome in epileptic pediatric patients with third-generation rufinamide
Lennox–Gastaut syndrome (LGS) is a rare but debilitating pediatric epileptic encephalopathy characterized by multiple intractable seizure types. Treatment of LGS is challenging because of the small number of antiepileptic drugs (AEDs) which are effective for this syndrome, as well as the need for po...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Dove Medical Press
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951747/ https://www.ncbi.nlm.nih.gov/pubmed/20957124 http://dx.doi.org/10.2147/NDT.S6465 |