Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation. (Q42735789)

From Wikidata

Jump to navigation Jump to search

scientific article published on December 2007

edit

Language	Label	Description	Also known as
English	Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation.	scientific article published on December 2007

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

case report

0 references

title

Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

main subject

Alzheimer's disease

0 references

author

Mathieu Anheim

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

Christine Tranchant

series ordinal

6

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

author name string

D Hannequin

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

C Boulay

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

C Martin

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

D Campion

series ordinal

5

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

language of work or name

English

0 references

publication date

1 December 2007

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

published in

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

volume

78

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

issue

12

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

page(s)

1414-1415

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

cites work

Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Abeta 42 production

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

Early-onset Alzheimer's disease in 2 large Belgian families

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

27 May 2018

Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

16 August 2018

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

16 August 2018

Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

16 August 2018

Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

16 August 2018

The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2095586

retrieved

16 August 2018

Identifiers

DOI

10.1136/JNNP.2007.123026

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

PMC publication ID

2095586

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

PubMed publication ID

18024701

1 reference

stated in

Europe PubMed Central

PMC publication ID

2095586

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18024701%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 December 2019

ResearchGate publication ID

5821933

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42735789&oldid=1578692511"