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Cited by 294

The DOI matches its Crossref record; 166 of the 166 references it cites were found in a registry or an index.

Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

Open access
Revesz, Tamas, Holton, Janice L., Lashley, Tammaryn, Plant, Gordon, Frangione, Blas, Rostagno, Agueda, Ghiso, Jorge·2009·Acta Neuropathologica

Abstract

In cerebral amyloid angiopathy (CAA), amyloid fibrils deposit in walls of arteries, arterioles and less frequently in veins and capillaries of the central nervous system, often resulting in secondary degenerative vascular changes. Although the amyloid-β peptide is by far the commonest amyloid subunit implicated in sporadic and rarely in hereditary forms of CAA, a number of other proteins may also be involved in rare familial diseases in which CAA is also a characteristic morphological feature. These latter proteins include the ABri and ADan subunits in familial British dementia and familial Danish dementia, respectively, which are also known under the umbrella term BRI2 gene-related dementias, variant cystatin C in hereditary cerebral haemorrhage with amyloidosis of Icelandic-type, variant transthyretins in meningo-vascular amyloidosis, disease-associated prion protein (PrPSc) in hereditary prion disease with premature stop codon mutations and mutated gelsolin (AGel) in familial amyloidosis of Finnish type. In this review, the characteristic morphological features of the different CAAs is described and the implication of the biochemical, genetic and transgenic animal data for the pathogenesis of CAA is discussed.

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Research works printed but not linked: 3

  1. Hersh LB (2003) Peptidases, proteases and amyloid beta-peptide catabolism. Curr Pharm Des 9:449–454. doi: 10.2174/1381612033391676 · doi:10.2174/1381612033391676
  2. Maury CP (1991) Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin. J Clin Invest 87:1195–1199. doi: 10.1172/JCI115118 · doi:10.1172/jci115118
  3. Tomidokoro Y, Rostagno A, Greenberg SM, Frangione B, Rebeck WG, Ghiso J (2004) Biochemical analysis of A beta amyloid deposits in the Iowa variant of Alzheimer’s disease. Neurobiol Aging 25:S38. doi: 10.1016/S0197-4580(04)80125-8 · doi:10.1016/s0197-4580(04)80125-8

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Metadata

Authors
Revesz, T., Holton, J. L., Lashley, T., Plant, G., Frangione, B., Rostagno, A., & Ghiso, J.
Venue
Acta Neuropathologica
Published
2009-02-19
Volume
118
Issue
1
Pages
115-130
ISSN
  • 0001-6322 (ISSN-L)
  • 1432-0533
OpenAlex
W2081598046
Cited by
294
References
166
FWCI
12.38
Type
journal article
Language
en
Open access
green
Licence
www.springer.com/tdm (tdm)

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CoChat. (2026). Citation check: Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies. https://app.cochat.ai/papers/10.1007/s00401-009-0501-8
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Revesz, T., Holton, J. L., Lashley, T., Plant, G., Frangione, B., Rostagno, A., & Ghiso, J. (2009). Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies. Acta Neuropathologica. https://doi.org/10.1007/s00401-009-0501-8

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