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Non-convulsive status epilepticus causing focal neurological deficits in CADASIL
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary small vessel disease caused by mutations of the Notch3 gene. Clinical manifestations include migraine with or without aura, psychiatric disorders, recurrent ischaemic strokes and cogn...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3029129/ https://ncbi.nlm.nih.gov/pubmed/21686667 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.08.2008.0713 |
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