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@ARTICLE{Schreiber:140967,
author = {Schreiber, S. and Willisch-Neumann, A. and Schreiber, F.
and Assmann, A. and Scheumann, V. and Perosa, V. and Jandke,
S. and Mawrin, C. and Carare, R. O. and Werring, D. J.},
title = {{I}nvited {R}eview: {T}he spectrum of age-related small
vessel diseases: potential overlap and interactions of
amyloid and nonamyloid vasculopathies.},
journal = {Neuropathology $\&$ applied neurobiology},
volume = {46},
number = {3},
issn = {0305-1846},
address = {Oxford [u.a.]},
publisher = {Wiley-Blackwell},
reportid = {DZNE-2020-07289},
pages = {219-239},
year = {2019},
abstract = {Deep perforator arteriopathy (DPA) and cerebral amyloid
angiopathy (CAA) are the commonest known cerebral small
vessel diseases (CSVD), which cause ischaemic stroke,
intracebral haemorrhage (ICH) and vascular cognitive
impairment (VCI). While thus far mainly considered as
separate entities, we here propose that DPA and CAA share
similarities, overlap and interact, so that 'pure' DPA or
CAA are extremes along a continuum of age-related small
vessel pathologies. We suggest blood-brain barrier (BBB)
breakdown, endothelial damage and impaired perivascular
β-amyloid (Aβ) drainage are hallmark common mechanisms
connecting DPA and CAA. We also suggest a need for new
biomarkers (e.g. high-resolution imaging) to deepen
understanding of the complex relationships between DPA and
CAA.},
subtyp = {Review Article},
keywords = {Aging: pathology / Amyloid beta-Peptides: metabolism /
Animals / Cerebral Small Vessel Diseases: pathology / Female
/ Humans / Male},
cin = {U Clinical Researchers - Magdeburg / AG Düzel},
ddc = {610},
cid = {I:(DE-2719)7000000 / I:(DE-2719)5000006},
pnm = {342 - Disease Mechanisms and Model Systems (POF3-342) / 344
- Clinical and Health Care Research (POF3-344)},
pid = {G:(DE-HGF)POF3-342 / G:(DE-HGF)POF3-344},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:31386773},
doi = {10.1111/nan.12576},
url = {https://pub.dzne.de/record/140967},
}