✦ LIBER ✦

A novel presenilin 1 mutation (L174

✍ Scribed by A. Bertoli Avella; B. Marcheco Teruel; J. Llibre Rodriguez; N. Gomez Viera; I. Borrajero Martinez; E. Severijnen; M. Joosse; C. van Duijn; L. Heredero Baute; P. Heutink

Book ID: 106257025
Publisher: Springer
Year: 2002
Tongue: English
Weight: 343 KB
Volume: 4
Category: Article
ISSN: 1364-6745
DOI: 10.1007/s10048-002-0136-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel presenilin 1 mutation (L282F) in

A novel presenilin 1 mutation (L282F) in familial Alzheimer’s disease

✍ Tsuyoshi Hamaguchi; Akiyoshi Morinaga; Tamao Tsukie; Ryozo Kuwano; Masahito Yama 📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 290 KB

A novel presenilin-1 mutation: Increased

A novel presenilin-1 mutation: Increased β-amyloid and neurofibrillary changes

✍ T. Gómez-Isla; W. Wasco; W. P. Pettingell; S. Gurubhagavatula; S. D. Schmidt; P. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 517 KB

Very early-onset familial Alzheimer's di

Very early-onset familial Alzheimer's disease: a novel presenilin 1 mutation

✍ Jill S. Goldman; Bruce Reed; Rosalie Gearhart; Joel H. Kramer; Bruce L. Miller 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 47 KB 👁 1 views

## Background: Early-onset familial alzheimer's disease (eofad) is linked to mutations in three autosomal dominant genes: ps1, ps2 and app. the clinical presentation and age of onset of mutations is variable. ## Objectives: The aim of this report is to describe a novel ps1 mutation believed to be

Molecular consequences of presenilin-1 m

Molecular consequences of presenilin-1 mutation

✍ Russo, C.; Schettini, G.; Saido, T. C.; Hulette, C.; Lippa, C.; Lannfelt, L.; Gh 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 137 KB

Atypical dementia associated with a nove

Atypical dementia associated with a novel presenilin-2 mutation

✍ Giuliano Binetti; Simona Signorini; Rosanna Squitti; Antonella Alberici; Luisa B 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 240 KB 👁 2 views

A novel presenilin 1 mutation (V261L) as

A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer’s disease and spastic paraparesis

✍ P. E. Jiménez Caballero; C. De Diego Boguna; E. Martin Correa; M. Serviá Candela 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 181 KB