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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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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BMJ Publishing Group
2009
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| 主題: | |
| 在線閱讀: | 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 |
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