(Q38435579)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

main subject

frontotemporal dementia

1 reference

based on heuristic

inferred from title

author

Stuart Pickering-Brown

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

David Allsop

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

author name string

A M T Richardson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

J S Snowden

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

A M McDonagh

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

A Burns

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

W Braude

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M Baker

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

W-K Liu

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

S-H Yen

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

J Hardy

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M Hutton

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Y Davies

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

D Craufurd

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

D Neary

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

D M A Mann

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

language of work or name

English

0 references

publication date

1 April 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

volume

125

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

issue

Pt 4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

page(s)

732-751

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11912108%20AND%20SRC:MED&resulttype=core&format=json

Frontal lobe degeneration of non-Alzheimer type. I. Neuropathology.

8 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

A family with autosomal dominant, non-Alzheimer's presenile dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon4 frequency, but no tau gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Tau gene mutation in familial progressive subcortical gliosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Semantic dementia. Progressive fluent aphasia with temporal lobe atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

A distinct familial presenile dementia with a novel missense mutation in the tau gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Design fluency: the invention of nonsense drawings after focal cortical lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Familial progressive subcortical gliosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

The topographic distribution of brain atrophy in frontal lobe dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Amyloid beta protein deposition in patients with frontotemporal lobar degeneration: relationship to age and apolipoprotein E genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Testing for nominal dysphasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

The apolipoprotein E epsilon4 allele frequency is normal in fronto-temporal dementia, but correlates with age at onset of disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Dementia of frontal lobe type

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

A modified card sorting test sensitive to frontal lobe defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Apolipoprotein E epsilon4 allele has no effect on age at onset or duration of disease in cases of frontotemporal dementia with pick- or microvacuolar-type histology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Phenotypic correlations in FTDP-17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Tau gene mutation K257T causes a tauopathy similar to Pick's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

The neuropathology of chromosome 17-linked dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

Clinical neurophysiologic findings in patients with rapidly progressive familial parkinsonism and dementia with pallido-ponto-nigral degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWF069