Results 111 to 120 of about 10,883 (231)
Molecular Chaperone BRICHOS Inhibits CADASIL-Mutated NOTCH3 Aggregation In Vitro [PDF]
Daniel V. Oliveira +5 more
openalex +1 more source
Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) mainly manifests with cognitive impairment.
Jingjing Su +10 more
doaj +1 more source
Detection of the founder effect in Finnish CADASIL families [PDF]
Kati Mykkänen +10 more
openalex +1 more source
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene. Clinical manifestations of CADASIL include lacunar infarcts, transient ischemic attacks, dementia, migraine ...
Mohamed Amine Mnaili, MD
doaj +1 more source
CSF Biomarkers Profile in CADASIL—A Model of Pure Vascular Dementia: Usefulness in Differential Diagnosis in the Dementia Disorder [PDF]
Patrizia Formichi +5 more
openalex +1 more source
Strategies for early detection and therapy in mouse models of Alzheimer’s disease and CADASIL
Anna Pfeffer
openalex +2 more sources
CADASIL in the Differential Diagnosis of Atypical Parkinsonism. Case Report
openalex +1 more source
Hilde van den Brink +16 more
openalex +1 more source
Silent brain infarcts and leukoaraiosis in young patients with first-ever ischemic stroke [PDF]
We investigated the features of and risk factors for magnetic resonance imaging(MRI)-defined SBIs and leukoaraiosis in 1008 consecutive adults aged 15-49 years with first-ever ischemic stroke.We analyzed the radiologic features of SBIs and leukoaraiosis ...
Kurkinen, Minna
core
Therapeutic antibody targeting of Notch3 signaling prevents mural cell loss in CADASIL [PDF]
Arturo Israel Machuca‐Parra +10 more
openalex +1 more source

