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Rapid improvement of a complex migrainous episode with sodium valproate in a patient with CADASIL
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited disease of small arteries caused by mutations in the Notch3 gene. Complex migrainous episodes, such as acute confusional migraine, status migrainosus with persisting aura, and “CADASI...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Milan
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253158/ https://www.ncbi.nlm.nih.gov/pubmed/22065121 http://dx.doi.org/10.1007/s10194-011-0400-y |