(Q36047031)

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Spatial patterns of TDP-43 neuronal cytoplasmic inclusions (NCI) in fifteen cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP).

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Spatial patterns of TDP-43 neuronal cytoplasmic inclusions (NCI) in fifteen cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP). (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

frontotemporal lobar degeneration

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based on heuristic

inferred from title

2

object named as

Nigel J Cairns

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Europe PubMed Central

PMC publication ID

11 August 2017

author name string

Richard A Armstrong

1

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Europe PubMed Central

PMC publication ID

11 August 2017

publication date

7 June 2011

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Europe PubMed Central

PMC publication ID

11 August 2017

Neurological Sciences

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Europe PubMed Central

PMC publication ID

11 August 2017

32

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

653-659

1 reference

Europe PubMed Central

PMC publication ID

11 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

1 reference

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2 October 2017

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

1 reference

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2 October 2017

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

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Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathies

1 reference

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2 October 2017

The genetics of frontotemporal lobar degeneration

1 reference

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2 October 2017

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

1 reference

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2 October 2017

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

1 reference

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

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

1 reference

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

1 reference

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Methods of studying the planar distribution of objects in histological sections of brain tissue

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The cytoskeleton in neurodegenerative diseases

1 reference

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

1 reference

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Structural diversity and functional implications of the eukaryotic TDP gene family

1 reference

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Are pathological lesions in neurodegenerative disorders the cause or the effect of the degeneration?

1 reference

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What does the study of the spatial patterns of pathological lesions tell us about the pathogenesis of neurodegenerative disorders?

1 reference

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2 October 2017

From genetics to pathology: tau and alpha-synuclein assemblies in neurodegenerative diseases

1 reference

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The role of cortical connectivity in Alzheimer's disease pathogenesis: a review and model system.

1 reference

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Staging of Alzheimer-related cortical destruction

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2 October 2017

Clustering of cerebral cortical lesions in patients with corticobasal degeneration

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Clustering of Pick bodies in patients with Pick's disease

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Analysis of spatial patterns in histological sections of brain tissue.

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Clustering of ipsilateral cortico-cortical projection neurons to area 7 in the rhesus monkey

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Absence of heterogeneous nuclear ribonucleoproteins and survival motor neuron protein in TDP-43 positive inclusions in frontotemporal lobar degeneration

1 reference

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21 January 2018

Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies

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21 January 2018

TDP-43 is deposited in the Guam parkinsonism-dementia complex brains.

1 reference

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21 January 2018

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions

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

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

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Dementia with Lewy bodies: clustering of Lewy bodies in human patients.

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

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21 January 2018

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

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

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Is the clustering of neurofibrillary tangles in Alzheimer's patients related to the cells of origin of specific cortico-cortical projections?

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Alzheimer pathology disorganizes cortico-cortical circuitry: direct evidence from a transgenic animal model.

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TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions

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Frontotemporal dementia: evidence for impairment of ascending serotoninergic but not noradrenergic innervation. Immunocytochemical and quantitative study using a graph method

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

1 reference

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Spatial patterns of alpha-synuclein positive glial cytoplasmic inclusions in multiple system atrophy

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/21647631

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inferred from PubMed ID database lookup

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

1 reference

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Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10072-011-0639-8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

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