𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Presenilin-I polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type

✍ Scribed by M. Bornebroek; J. Haan; H. Backhovens; P. Deutz; M. A. Van Buchem; M. van den Broeck; E. Bakker; R. A. C. Roos; C. Van Broeckhoven

Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
336 KB
Volume
42
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Cerebral vascular accumulation of Dutch-
Cerebral vascular accumulation of Dutch-type Aβ42, but not wild-type Aβ42, in hereditary cerebral hemorrhage with amyloidosis, Dutch type
✍ Kazuchika Nishitsuji; Takami Tomiyama; Kenichi Ishibashi; Fuyuki Kametani; Kazuh 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 284 KB

## Abstract Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA‐D), is an autosomal dominant disorder caused by the Dutch mutation (E693Q) in the β‐amyloid precursor protein. This mutation produces an aberrant amyloid β (Aβ) species (AβE22Q) and causes severe meningocortical vascular

Alzheimer's disease and hereditary cereb
Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis–dutch type share a decrease in cerebrospinal fluid levels of amyloid β-protein precursor
✍ Dr. William E. van Nostrand; Steven L. Wagner; Joost Haan; Egbert Bakker; Raymun 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 419 KB 👁 1 views

## Abstract The amyloid β‐protein is a 39‐42 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 amyloidosis–Dutch type (HCHW A‐D), and, to a much lesser extent, normal agin