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...

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Detalles Bibliográficos
Autores principales: Martikainen, Mika H., Roine, Susanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2011
Materias:
Brief Report
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

Internet

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

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