(Q36962892)

17 August 2017

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene (English)

1 reference

frontotemporal lobar degeneration

17 August 2017

1 reference

inferred from title

author

Stuart Pickering-Brown

10

1 reference

17 August 2017

Jonathan D Rohrer

1

0 references

Jason D. Warren

Jason D Warren

2

0 references

Nick C. Fox

Nick C Fox

12

0 references

Martin Rossor

Martin N Rossor

15

0 references

John Anthony Hardy

11

John Hardy

1 reference

17 August 2017

13

John Collinge

1 reference

17 August 2017

4

Simon Mead

1 reference

17 August 2017

3

Rohani Omar

1 reference

17 August 2017

9

Safa Al-Sarraj

1 reference

17 August 2017

7

Janice Holton

1 reference

17 August 2017

Jonathan Beck

5

1 reference

17 August 2017

Tamas Revesz

6

1 reference

17 August 2017

John M Stevens

8

1 reference

17 August 2017

Elizabeth K Warrington

14

1 reference

17 August 2017

1 April 2008

1 reference

17 August 2017

Archives of Neurology

1 reference

17 August 2017

65

1 reference

17 August 2017

4

1 reference

17 August 2017

506-513

1 reference

Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Clinical features of frontotemporal dementia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Behavioral disorders in the frontal and temporal variants of frontotemporal dementia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Nothing to say, something to sing: primary progressive dynamic aphasia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Clinical and pathological overlap between frontotemporal dementia, primary progressive aphasia and corticobasal degeneration: the Pick complex.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Testing for nominal dysphasia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Arithmetic skills in patients with unilateral cerebral lesions.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

A modified card sorting test sensitive to frontal lobe defects

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Measuring dysgraphia: a graded-difficulty spelling test.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Perisylvian language networks of the human brain.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Pathologic heterogeneity in clinically diagnosed corticobasal degeneration.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

Familial aggregation in frontotemporal dementia.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

The Effect of tau genotype on clinical features in FTDP-17

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2578869

4 December 2018

Frontotemporal dementia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413474

12 December 2020

inferred from PubMed ID database lookup

Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413474

12 December 2020

inferred from PubMed ID database lookup

Progranulin mutations in Dutch familial frontotemporal lobar degeneration

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413474

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1001/ARCHNEUR.65.4.506

1 reference

17 August 2017

1 reference

17 August 2017

1 reference