Results 21 to 30 of about 3,724 (147)
Neurological and systemic manifestations of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a nationwide study in Korea [PDF]
Abstract Background This study investigated the epidemiological and clinical features of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in South Korea, comparing patients to age‐ and sex‐matched controls.
Jung Y.
europepmc +2 more sources
Is the oxidant/antioxidant status altered in CADASIL patients?
The altered aggregation of proteins in non-native conformation is associated with endoplasmic reticulum derangements, mitochondrial dysfunction and excessive production of reactive oxygen species. Cerebral autosomal dominant arteriopathy with subcortical
Jonica Campolo +10 more
doaj +1 more source
CADASIL Argentine Registry: Study Design and Preliminary Data [PDF]
Abstract Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), the most common hereditary small vessel disease, leads to early‐onset stroke and vascular cognitive impairment (VCI). Despite its importance, data from Latin America remain scarce.
Cristalli C +13 more
europepmc +2 more sources
Background and objective: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited systemic arteriopathy, the classic feature of which is small vessel lesions.
Chen Zhang +6 more
doaj +1 more source
IntroductionData reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited.
Alan P. Pan +8 more
doaj +1 more source
CADASIL Syndrome Presenting as Adjustment Disorder
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), usually referred to as CADASIL, is an inherited autosomal dominant condition that can cause stroke, dementia and other neurological impairments ...
Sevda Bağ, Pelin Özkara, Evrim Erten
doaj +1 more source
Investigating the effects of NOTCH3 Asian‐specific mutant on blood‐brain‐barrier using patient iPSC‐derived cell types [PDF]
Abstract Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), is the genetic form of vascular dementia leading to vascular impairments and cognitive decline. CADASIL is caused by mutations in the NOTCH3 gene which encodes a single‐pass transmembrane receptor. The NOTCH3 mutant (MT) is reported
Lee J, Ng A, Tan E, Zeng L.
europepmc +2 more sources
Background and Purpose: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) mainly affects the cerebral small arteries.
Chen Ling +19 more
doaj +1 more source
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): Three case reports from Serbia [PDF]
Introduction Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary microangiopathy leading to recurrent strokes and vascular dementia in young and middleaged patients.
Zidverc-Trajković Jasna +9 more
doaj +1 more source
Insulin-Independent and Dependent Glucose Transporters in Brain Mural Cells in CADASIL
Typical cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the human NOTCH3 gene.
Mahmod Panahi +15 more
doaj +1 more source

