(Q34557808)

English

The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease

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scholarly article

1 reference

Europe PubMed Central

3 August 2017

The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease (English)

1 reference

Europe PubMed Central

3 August 2017

8

object named as

Kari Skullerud

1 reference

Europe PubMed Central

3 August 2017

10

object named as

Nigel J Cairns

1 reference

Europe PubMed Central

3 August 2017

Charles Duyckaerts

5

object named as

Charles Duyckaerts

1 reference

Europe PubMed Central

3 August 2017

3

object named as

Eileen H Bigio

1 reference

Europe PubMed Central

3 August 2017

author name string

Richard A Armstrong

1

1 reference

Europe PubMed Central

3 August 2017

Marla Gearing

2

1 reference

Europe PubMed Central

3 August 2017

Felix F Cruz-Sanchez

4

1 reference

Europe PubMed Central

3 August 2017

Ian R A Mackenzie

6

1 reference

Europe PubMed Central

3 August 2017

Robert H Perry

7

1 reference

Europe PubMed Central

3 August 2017

Hedeaki Yokoo

9

1 reference

Europe PubMed Central

3 August 2017

publication date

1 October 2010

1 reference

Europe PubMed Central

3 August 2017

Acta Neuropathologica

1 reference

Europe PubMed Central

3 August 2017

121

1 reference

Europe PubMed Central

3 August 2017

2

1 reference

Europe PubMed Central

3 August 2017

219-228

1 reference

Europe PubMed Central

3 August 2017

https://scigraph.springernature.com/pub.10.1007/s00401-010-0753-3

0 references

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=3035044

7 July 2018

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

FUS pathology in basophilic inclusion body disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Recent advances in the genetics of amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Delocalization of the multifunctional RNA splicing factor TLS/FUS in hippocampal neurones: exclusion from the nucleus and accumulation in dendritic granules and spine heads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Neurofilament inclusion body disease: a new proteinopathy?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 July 2018

Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 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=3035044

7 July 2018

Roles of head and tail domains in alpha-internexin's self-assembly and coassembly with the neurofilament triplet proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

7 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=3035044

7 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=3035044

7 July 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/10.1007%2FS00401-010-0753-3

21 January 2018

Topography of alpha-internexin-positive neuronal aggregates in 10 patients with neuronal intermediate filament inclusion disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

21 January 2018

Spatial patterns of the pathological changes in neuronal intermediate filament inclusion disease (NIFID): an alpha-internexin immunohistochemical study.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

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/10.1007%2FS00401-010-0753-3

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/10.1007%2FS00401-010-0753-3

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/10.1007%2FS00401-010-0753-3

21 January 2018

Staging disease severity in pathologically confirmed cases of frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

21 January 2018

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

21 January 2018

Temporal lobe pathology of human patients with neurofilament inclusion disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

21 January 2018

Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: a comparative clinicopathological study

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0753-3

21 January 2018

Laminar degeneration of the frontal and temporal cortex in neuronal intermediate filament inclusion disease (NIFID): a study original using alpha-internexin immunohistochemistry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

27 October 2018

Overexpression of alpha-internexin causes abnormal neurofilamentous accumulations and motor coordination deficits in transgenic mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035044

27 October 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/20886222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of neuronal inclusions in "dementia with neurofilament inclusions"

1 reference

https://pubmed.ncbi.nlm.nih.gov/20886222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20886222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathological changes in ten cases of neuronal intermediate filament inclusion disease (NIFID): a study using alpha-internexin immunohistochemistry and principal components analysis (PCA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20886222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00401-010-0753-3

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

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