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Article

Dutch hereditary cerebral amyloid angiopathy: structural lesions and apolipoprotein E genotype.

Annals of neurology - 1 May 1997

Bornebroek M, Haan J, Van Duinen S G, Maat-Schieman M L, Van Buchem M A, Bakker E, Van Broeckhoven C, Roos R A

Abstract excerpt

Hereditary cerebral hemorrhage with amyloidosis-Dutch type is caused by a mutation at codon 693 of the beta amyloid precursor protein gene. The disease is clinically characterized by strokes and dementia. In addition to cerebral plaques, cerebral amyloid angiopathy is the pathological hallmark. We investigated the correlation between radiological (white matter hyperintensities and focal lesions on magnetic...

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Identifiers

PMID: 9153536
DOI: 10.1002/ana.410410523

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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