Cerebral autosomal dominant arteriopathy with subcortical infarcts and

Unlu M et al. Detection of complement factor B in the cerebrospinal fluid of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy disease using two-dimensional gel electrophoresis and mass spectrometry. Neurosci Lett 2000 282 149-152. 

Missense mutations in the Notch3 gene cause CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and lenkoencephalopathy). Notch is a type I integral membrane protein proteolytically processed in its extracellular domain by fnrin and the metalloproteinase knzbanian. The signal transduction cascade... 

Van den Boom R, Lesnik Oberstein SA, van Duinen SG, Bor-nebroek M, Ferrari MD, Haan J, van Buchem MA (2002) Subcortical lacunar lesions an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Radiology 224 791-796... 

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy... 

Jung HH, Bassetti C, Tournier-Lasserve E et al. (1995). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy a clinicopathological... 

Razvi SS M, Davidson R, Bone I et al. (2005). The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland. 

Cerebral ischemic injury is a common cause of dementia in older adults. Combination cases of vascular dementia and Alzheimer disease are also quite frequent. Vascular causes of dementia include subcortical vascular dementia, multi-infarct dementia, ischemic dementia, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), and leuko-araiosis (see the Cerebrovascular Diseases section earlier in this chapter). ... 

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