The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain-Reference-Cited by-同舟云学术

The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain

Published:1999-09 Issue:9 Volume:122 Page:1709-1719
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Gómez-Isla Teresa,Growdon Whitfield B.,McNamara Megan J.,Nochlin David,Bird Thomas D.,Arango Juan Carlos,Lopera Francisco,Kosik Kenneth S.,Lantos Peter L.,Cairns Nigel J.,Hyman Bradley T.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/122/9/1709/17873753/1221709.pdf

Reference34 articles.

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2. Chartier-Harlin M, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, et al. Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene. Nature1991; 353: 844–6.

3. Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques PK, Collinge J, et al. Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor. Brain1997; 120: 491–501.

4. Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease [see comments]. Nature1991; 349: 704–9. Comment in: Nature 1991; 349: 633–4, Comment in: Nature 1991; 350: 564.

5. Gómez-Isla T, Hollister R, West H, Mui S, Growdon JH, Petersen RC, et al. Neuronal loss correlates with but exceeds neurofibrillary tangles in Alzheimer's disease. Ann Neurol1997; 41: 17–24.

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