(Q35501862)

English

A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP).

scientific article published on February 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP). (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

frontotemporal lobar degeneration

1 reference

based on heuristic

inferred from title

3

object named as

N J Cairns

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

author name string

R A Armstrong

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

D Carter

2

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Europe PubMed Central

PubMed publication ID

8 August 2017

language of work or name

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publication date

1 February 2012

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Europe PubMed Central

PubMed publication ID

8 August 2017

Neuropathology and Applied Neurobiology

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Europe PubMed Central

PubMed publication ID

8 August 2017

38

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Europe PubMed Central

PubMed publication ID

8 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

25-38

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

1 reference

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12 July 2018

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

1 reference

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12 July 2018

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

1 reference

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What determines the molecular composition of abnormal protein aggregates in neurodegenerative disease?

1 reference

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12 July 2018

TAR DNA-binding protein 43 immunohistochemistry reveals extensive neuritic pathology in FTLD-U: a midwest-southwest consortium for FTLD study

1 reference

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12 July 2018

The genetics of frontotemporal lobar degeneration

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12 July 2018

Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update

1 reference

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12 July 2018

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

1 reference

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12 July 2018

Frontotemporal lobar degeneration: clinical and pathological relationships

1 reference

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12 July 2018

Clinicopathologic correlation in PGRN mutations

1 reference

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12 July 2018

TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry

1 reference

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12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Quantifying the pathology of neurodegenerative disorders: quantitative measurements, sampling strategies and data analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Frontotemporal lobar degeneration--tau as a pied piper?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Tau-positive glial inclusions in progressive supranuclear palsy, corticobasal degeneration and Pick's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Subcortical neurofibrillary tangles, neuropil threads, and argentophilic glial inclusions in corticobasal degeneration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Statistical methods for assessing agreement between two methods of clinical measurement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Appearance of paired nucleated, Tau-positive glia in patients with progressive supranuclear palsy brain tissue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

12 July 2018

Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study

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https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Frontotemporal lobar degeneration without lobar atrophy.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

TDP-43 pathology in familial British dementia.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Morphological differences of intraneuronal ubiquitin-positive inclusions in the dentate gyrus and parahippocampal gyrus of motor neuron disease with dementia.

1 reference

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21 January 2018

Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Correlations between the morphology of diffuse and primitive beta-amyloid (A beta) deposits and the frequency of associated cells in Down's syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Ballooned neurones in the limbic lobe are associated with Alzheimer type pathology and lack diagnostic specificity.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Spatial correlations between the vacuolation, prion protein deposits, and surviving neurons in the cerebral cortex in sporadic Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt-Jakob disease (vCJD).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

Quantification of pathological lesions in the frontal and temporal lobe of ten patients diagnosed with Pick's disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

[Argyrophilic grain disease (AgD), a frequent and largely underestimated cause of dementia in old patients]

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

26 September 2018

Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206199

26 September 2018

Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2011.01188.X

21 January 2018

A quantitative study of the pathological lesions in the neocortex and hippocampus of twelve patients with corticobasal degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/21696412

12 December 2020

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Thorn-shaped astrocytes: possibly secondarily induced tau-positive glial fibrillary tangles

1 reference

https://pubmed.ncbi.nlm.nih.gov/21696412

12 December 2020

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Ubiquitin-positive inclusions and progression of pathology in frontotemporal dementia and motor neurone disease identifies a group with mainly early pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/21696412

12 December 2020

based on heuristic

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Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21696412

12 December 2020

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Identifiers

10.1111/J.1365-2990.2011.01188.X

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

ResearchGate publication ID

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