(Q36438039)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

title

Novel TARDBP sequence variant and C9ORF72 repeat expansion in a family with frontotemporal dementia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

main subject

dementia

0 references

frontotemporal dementia

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

5

Bryan J Traynor

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

author name string

Anna-Lotta Kaivorinne

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Virpi Moilanen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Marko Kervinen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Kari Majamaa

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Anne M Remes

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

language of work or name

English

0 references

publication date

1 April 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

Alzheimer Disease and Associated Disorders

11 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

volume

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

page(s)

190-193

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations

11 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

Screening for C9ORF72 repeat expansion in FTLD.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease course.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511614

Screening of the TARDBP gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22892647

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/WAD.0B013E318266FAE5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22892647%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference