Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

CADASIL: a monogenic condition causing stroke and subcortical vascular dementia.

Cerebrovascular diseases (Basel, Switzerland) - 1 Jan 2002

Dichgans Martin

Abstract excerpt

Mutations in Notch3 are the cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), an inherited small vessel disease leading to subcortical strokes and vascular dementia. The phenotypic presentation is variable but remarkable for a high freq...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Dementia, Multi-Infarct
Share to Dementia, Vascular
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Proto-Oncogene Proteins

Share to Receptor, Notch3

Share to Receptors, Cell Surface

Share to Receptors, Notch

Share to Stroke

Source

Identifiers

PMID: 11901241
DOI: 10.1159/000049148

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11901241-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CADASIL: a monogenic condition causing stroke and subcortical vascular dementia.PMID 11901241Read ↗

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Semantic proximity Read ↗

CADASIL.Semantic proximity Read ↗

Cadasil.Semantic proximity Read ↗

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum.Semantic proximity Read ↗

Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.Semantic proximity Read ↗

CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.Semantic proximity Read ↗

CADASIL: A NOTCH3-associated cerebral small vessel disease.Semantic proximity Read ↗

CADASIL: hereditary disease of arteries causing brain infarcts and dementiaSemantic proximity Read ↗

CADASIL.Semantic proximity Read ↗

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.Semantic proximity Read ↗

The Pathobiology of Cerebrovascular Lesions in CADASIL Small Vessel DiseaseSemantic proximity Read ↗

Cerebral hemorrhages in CADASIL: report of four cases and a brief review.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.