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

[Clinical and neuroimaging findings in a family with CADASIL associated to C475T mutation].

Revista de neurologia - 1 Jan 2000

Sempere A P, Pérez-Tur J, García-Barragán N, Sellés J, Medrano V, Mola S

Abstract excerpt

INTRODUCTION: The term CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) refers to an autosomal dominant hereditary arteriopathy of the brain that is characterised by headache, recurring strokes and progressive cognitive deterioration. We report...

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 NOTCH3 gene
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Proto-Oncogene Proteins

Share to Receptor, Notch3

Share to Receptors, Cell Surface

Share to Receptors, Notch

Source

Identifiers

PMID: 14730489

Genes

NOTCH3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14730489-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Clinical and neuroimaging findings in a family with CADASIL associated to C475T mutation].PMID 14730489Read ↗

Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.Semantic proximity Read ↗

[A study of subcortical infarcts and leukoencephalopathy (CADASIL) in a family with autosomal cerebral dominant arteriopathy].Semantic proximity Read ↗

[Two case reports of cerebral autosomal dominant arteriophaty with subcortical infarctions and leukoencephalopathy (CADASIL)].Semantic proximity Read ↗

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

[The clinical and genetic studies in a family of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].Semantic proximity Read ↗

[CADASIL with clinical manifestations of baldness, lumbago and Parkinson's symptoms].Semantic proximity Read ↗

CADASIL.Semantic proximity Read ↗

Clinical, familial, and neuroimaging features of CADASIL-like patients.Semantic proximity Read ↗

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

A CADASIL case with normal skin biopsy and without mutations in exons 3 and 4 of the Notch3 gene.Semantic proximity Read ↗

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

[Clinical, radiological, histopathological and genetic findings in a Danish "CADASIL" family].Semantic proximity Read ↗

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