Loading...
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...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Publishing Group
2009
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3028380/ https://ncbi.nlm.nih.gov/pubmed/21686761 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.07.2008.0529 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|