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Lookup NU author(s): Professor Raj KalariaORCiD
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Progress in molecular genetics has enabled the dissection of several autosomal dominantly inherited forms of cerebrovascular disorders. Mutations in diverse genes might induce pathological changes in intracranial vessels, resulting in cerebral haemorrhages and ischaemic strokes. Such pathologies, however, might also result from systemic vascular disease caused by mutations or polymorphisms in genes that regulate cardiovascular physiology, blood coagulation, lipid metabolism and metabolic functions. Interestingly, several mutations that directly affect CNS vasculature involve genes that control inter- or intracellular signalling functions. Although highly variable phenotypes make it difficult to pinpoint the genotypes, genetic characterization of cerebrovascular disorders is valuable for understanding the pathogenesis and management of sporadic disease.
Author(s): Kalaria RN
Publication type: Review
Publication status: Published
Journal: Trends in Neurosciences
Year: 2001
Volume: 24
Issue: 7
Pages: 392-400
ISSN (print): 0166-2236
ISSN (electronic): 1878-108X
URL: http://dx.doi.org/10.1016/S0166-2236(00)01836-1
DOI: 10.1016/S0166-2236(00)01836-1
PubMed id: 11410270