Advances in molecular genetics and pathology of cerebrovascular disorders
- 1 July 2001
- journal article
- review article
- Published by Elsevier in Trends in Neurosciences
- Vol. 24 (7) , 392-400
- https://doi.org/10.1016/s0166-2236(00)01836-1
Abstract
No abstract availableKeywords
This publication has 70 references indexed in Scilit:
- Prominent Cerebral Amyloid Angiopathy in Transgenic Mice Overexpressing the London Mutant of Human APP in NeuronsThe American Journal of Pathology, 2000
- Apolipoprotein E facilitates neuritic and cerebrovascular plaque formation in an Alzheimer's disease modelAnnals of Neurology, 2000
- Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3v EGF-like repeat domainsEuropean Journal of Human Genetics, 2000
- Behavioral Disturbances without Amyloid Deposits in Mice Overexpressing Human Amyloid Precursor Protein with Flemish (A692G) or Dutch (E693Q) MutationNeurobiology of Disease, 2000
- Amyloid‐β Protein Angiopathies Masquerading as Alzheimer's Disease?aAnnals of the New York Academy of Sciences, 1997
- The apolipoprotein E gene in Binswanger's disease and vascular dementiaClinical Genetics, 1996
- Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaNature, 1996
- The Molecular Pathology of Hereditary Cystatin C Amyloid Angiopathy Causing Brain HemorrhageBrain Pathology, 1996
- Mutation in gelsolin gene in Finnish hereditary amyloidosis.The Journal of Experimental Medicine, 1990
- CHRONIC FAMILIAL VASCULAR ENCEPHALOPATHYThe Lancet, 1977