Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation. (Q42951159)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

0 references

L Lannfelt

1

1 reference

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26 October 2019

K Axelman

series ordinal

2

1 reference

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26 October 2019

L Lilius

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

H Basun

series ordinal

4

1 reference

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26 October 2019

language of work or name

English

0 references

publication date

1 January 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

26 October 2019

number of pages

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

56

1 reference

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26 October 2019

issue

1

1 reference

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26 October 2019

page(s)

332-335

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

26 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Lack of association between apolipoprotein E allele epsilon 4 and sporadic Alzheimer's disease.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Amyloid precursor protein mutation causes Alzheimer's disease in a Swedish family

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801312

Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in Sweden

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7825596

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene fails to identify new mutations in Swedish Alzheimer's disease patients

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7825596

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825596%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

PubMed publication ID

7825596

1 reference