Dutch hereditary cerebral amyloid angiopathy: Structural lesions and apolipoprotein E genotype
β Scribed by Dr M. Bornebroek; J. Haan; S. G. Van Duinen; M. L. C. Maat-Schieman; M. A. Van Buchem; E. Bakker; C. Van Broeckhoven; R. A. C. Roos
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 468 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0364-5134
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electroencephalography (to demonstrate burst suppression), and we occasionally repeat computed tomographic scanning (to demonstrate cerebral edema or multiple cerebral infarcts) to assist in our assessment. Moreover, we often consider naloxone or flumazenil to reverse possible confounding drugs such
## Abstract The amyloid Ξ²βprotein is a 39β42 amino acid peptide that is deposited in senile plaques and in cerebral vessel walls in individuals with Alzheimer's disease, Down's syndrome, hereditary cerebral hemorrhage with amyloidosisβDutch type (HCHW AβD), and, to a much lesser extent, normal agin