CADASIL is a hereditary cerebral small vessel disease, caused by a mutation in the NOTCH3 gene, leading to migraine with aura, cerebrovascular accidents and cognitive decline at young to middle adult age. MRI scans of the brain may show lacunar infarcts, white matter lesions and microbleeds. In this thesis MRI scans of the brains are used to investigate the disease course in CADASIL. It is shown that lacunar infarcts, white matter lesions and microbleeds are progressive in CADASIL patients. Vascular risk factors are not associated with rate of progression of these MRI abnormalities. However, the rate of disease progression can be predicted by measuring the amount of MRI abnormalities at baseline. Lacunar infarcts, microbleeds and increased ...
Objective: To assess, by using quantitative MRI metrics, structural and metabolic brain abnormalitie...
BACKGROUND AND PURPOSE: Cerebral autosomal dominant arteriopathy with subcor-tical infarcts and leuk...
PhD ThesisCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)...
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopat...
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalop...
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopat...
OBJECTIVE: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopath...
Mutations in Notch3 are the cause of cerebral autosomal dominant arteriopathy with subcortical infar...
Background: Mutations in the NOTCH3 gene cause CADASIL, a cerebral small vessel disease manifest...
Although there is evidence for correlations between disability and magnetic resonance imaging (MRI) ...
CADASIL is an arteriopathy caused by mutations of the Notch3 gene. White matter hyperintensities (WM...
Introduction Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopa...
International audienceBACKGROUND AND PURPOSE: In cerebral autosomal dominant arteriopathy with subco...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)...
Objective: To assess, by using quantitative MRI metrics, structural and metabolic brain abnormalitie...
BACKGROUND AND PURPOSE: Cerebral autosomal dominant arteriopathy with subcor-tical infarcts and leuk...
PhD ThesisCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)...
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopat...
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalop...
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopat...
OBJECTIVE: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopath...
Mutations in Notch3 are the cause of cerebral autosomal dominant arteriopathy with subcortical infar...
Background: Mutations in the NOTCH3 gene cause CADASIL, a cerebral small vessel disease manifest...
Although there is evidence for correlations between disability and magnetic resonance imaging (MRI) ...
CADASIL is an arteriopathy caused by mutations of the Notch3 gene. White matter hyperintensities (WM...
Introduction Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopa...
International audienceBACKGROUND AND PURPOSE: In cerebral autosomal dominant arteriopathy with subco...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)...
Objective: To assess, by using quantitative MRI metrics, structural and metabolic brain abnormalitie...
BACKGROUND AND PURPOSE: Cerebral autosomal dominant arteriopathy with subcor-tical infarcts and leuk...
PhD ThesisCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy...