Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation (Q33554860)

28 July 2017

title

Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation (English)

1 reference

Ricardo Francisco Allegri

28 July 2017

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8

object named as

Ricardo F Allegri

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Peter Henry St George-Hyslop

28 July 2017

Gustavo Sevlever

7

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object named as

Peter St George-Hyslop

5

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author name string

Miguel A Riudavets

1

1 reference

28 July 2017

Leonardo Bartoloni

2

1 reference

28 July 2017

Juan C Troncoso

3

1 reference

28 July 2017

Olga Pletnikova

4

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28 July 2017

Marcelo Schultz

6

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28 July 2017

publication date

25 April 2013

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28 July 2017

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28 July 2017

volume

23

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28 July 2017

issue

5

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28 July 2017

page(s)

595-600

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Neuronal to oligodendroglial alpha-synuclein redistribution in a double transgenic model of multiple system atrophy

28 July 2017

cites work

1 reference

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21 June 2018

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Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation

21 June 2018

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21 June 2018

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Forebrain degeneration and ventricle enlargement caused by double knockout of Alzheimer's presenilin-1 and presenilin-2

21 June 2018

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Degradative organelles containing mislocalized alpha-and beta-synuclein proliferate in presenilin-1 null neurons

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14

21 June 2018

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21 June 2018

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A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notch.

21 June 2018

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A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques

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21 January 2018

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Pick bodies in a family with presenilin-1 Alzheimer's disease

21 January 2018

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Presenilin mutations associated with fronto-temporal dementia

21 January 2018

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Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family

21 January 2018

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Aβ deposition is associated with enhanced cortical α-synuclein lesions in Lewy body diseases

21 January 2018

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PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier

21 January 2018

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Differentiating the frontal variant of Alzheimer's disease

21 January 2018

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Time course of glucose metabolism in relation to cognitive performance and postmortem neuropathology in Met146Val PSEN1 mutation carriers

21 January 2018

1 reference

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Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23489366

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Immunocytochemical and ultrastructural studies of neuronal and oligodendroglial cytoplasmic inclusions in multiple system atrophy. 2. Oligodendroglial cytoplasmic inclusions

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23489366

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/BPA.12051

1 reference

28 July 2017

1 reference

28 July 2017

1 reference