(Q42907079)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20842367%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features (English)

1 reference

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13 February 2020

0 references

2

1 reference

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13 February 2020

Fabio Moda

3

1 reference

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13 February 2020

Mario Botta

4

1 reference

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13 February 2020

Marcella Catania

7

1 reference

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13 February 2020

Mario Salmona

12

1 reference

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13 February 2020

Giuseppe Di Fede

13

1 reference

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13 February 2020

Fabrizio Tagliavini

14

1 reference

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13 February 2020

Giorgio Giaccone

1

1 reference

ORCID Public Data File 2021

Veronica Redaelli

9

object named as

Veronica Redaelli

1 reference

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13 February 2020

8

Maria Luisa Moro

1 reference

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13 February 2020

5

Giulia Mazzoleni

1 reference

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13 February 2020

6

Andrea Uggetti

1 reference

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13 February 2020

author name string

Alberto Spagnoli

10

1 reference

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13 February 2020

Roberta Simona Rossi

11

1 reference

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13 February 2020

publication date

15 September 2010

1 reference

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13 February 2020

published in

Acta Neuropathologica

1 reference

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13 February 2020

volume

120

1 reference

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13 February 2020

issue

6

1 reference

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13 February 2020

page(s)

803-812

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https://scigraph.springernature.com/pub.10.1007/s00401-010-0747-1

13 February 2020

exact match

0 references

cites work

Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0747-1

Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0747-1

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0747-1

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0747-1

Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0747-1

Phases of A beta-deposition in the human brain and its relevance for the development of AD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0747-1