Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is the most common monogenic disorder of the cerebral …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL), a hereditary cerebral small vessel disease caused by …

Personalized medical care focuses on prediction of disease risk and response to
medications. To build the risk models, access to both large-scale genomic resources and …

Cysteine-altering missense variants (NOTCH3 cys) in one of the 34 epidermal growth-factor-
like repeat (EGFr) domains of the NOTCH3 protein are the cause of NOTCH3-associated …

The recent discovery that the prevalence of cysteine mutations in the NOTCH3 gene
responsible for CADASIL was more than 100 times higher in the general population than …

Introduction Cerebral autosomal‐dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is a relatively common cerebral small vessel disease …

Background and Purpose: Cerebral autosomal dominant arteriopathy with subcortical
infarcts and leukoencephalopathy (CADASIL) is a monogenic cerebral small vessel disease …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is a cerebral small vessel disease caused by mutations in …

Objectives Intracerebral hemorrhage (ICH) and cerebral microbleeds (CMB) in cerebral
autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy are …

Background: Young stroke incidence has increased worldwide with lifestyle changes.
Etiology and risk factors for both ischemic and hemorrhagic stroke in young Asians remain …