𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Familial prion disease with alzheimer disease-like tau pathology and clinical phenotype

✍ Scribed by Suman Jayadev; David Nochlin; Parvoneh Poorkaj; Ellen J. Steinbart; James A. Mastrianni; Thomas J. Montine; Bernardino Ghetti; Gerard D. Schellenberg; Thomas D. Bird; James B. Leverenz


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
934 KB
Volume
69
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Decreased drebrin mRNA expression in Alz
✍ Carl Julien; Cyntia Tremblay; Farid Bendjelloul; Alix Phivilay; Marie-AndrΓ©e Cou πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 497 KB

## Abstract To investigate the mRNA expression of the dendritic spine protein drebrin in Alzheimer's disease (AD), we performed post‐mortem in situ hybridization studies in brain sections from 20 AD patients and 21 controls. AD diagnosis was confirmed by decreased drebrin protein and increased AΞ²~4

The clinical phenotype of familial and s
✍ Clive Holmes; Simon Lovestone πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 52 KB πŸ‘ 1 views

## Abstract ## Background Familial factors are clearly associated with an increased risk of developing late onset Alzheimer's disease (LOAD). However, there is emerging evidence to suggest that familial factors may also influence clinical phenotype. To date, most studies have focussed on familial

A South African mixed ancestry family wi
✍ Soraya Bardien; Fatima Abrahams; Himla Soodyall; Lize van der Merwe; Jacquie Gre πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 209 KB

## Abstract Huntington disease‐like 2 (HDL2) is a neurodegenerative disorder caused by an expansion of a CTG repeat in the junctophilin‐3 gene (__JPH3__). A limited number of HDL2 families have been reported, all of apparently Black African ancestry. We report on a South African family that present