(Q35075257)

6 August 2017

title

Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy (English)

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6 August 2017

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10

John Q Trojanowski

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6 August 2017

5

Leo F McCluskey

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6 August 2017

Felix Geser

1

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6 August 2017

Beth Stein

2

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6 August 2017

Michael Partain

3

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6 August 2017

Lauren B Elman

4

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6 August 2017

Sharon X Xie

6

1 reference

6 August 2017

Vivianna M Van Deerlin

7

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6 August 2017

Linda K Kwong

8

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6 August 2017

Virginia M-Y Lee

9

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6 August 2017

language of work or name

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12 January 2011

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6 August 2017

published in

Acta Neuropathologica

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6 August 2017

volume

121

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6 August 2017

issue

4

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6 August 2017

page(s)

509-517

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-011-0797-z

6 August 2017

exact match

0 references

cites work

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Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy

8 July 2018

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Synergistic Interactions between Abeta, tau, and alpha-synuclein: acceleration of neuropathology and cognitive decline

8 July 2018

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Study of 962 patients indicates progressive muscular atrophy is a form of ALS.

8 July 2018

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Survival profiles of patients with frontotemporal dementia and motor neuron disease

8 July 2018

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Clinical and pathological continuum of multisystem TDP-43 proteinopathies

8 July 2018

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Amyotrophic lateral sclerosis-plus syndrome with TAR DNA-binding protein-43 pathology

8 July 2018

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

8 July 2018

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Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease

8 July 2018

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

8 July 2018

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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

8 July 2018

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

8 July 2018

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

8 July 2018

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Frontotemporal dementia: clinicopathological correlations

8 July 2018

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Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium

8 July 2018

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Sporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy exists: additional autopsy case with a clinical course of 19 years

8 July 2018

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Survival in frontotemporal dementia

8 July 2018

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Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS

8 July 2018

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Staging of the intracerebral inclusion body pathology associated with idiopathic Parkinson's disease (preclinical and clinical stages).

8 July 2018

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El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

8 July 2018

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8 July 2018

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Effect of topographical distribution of α-synuclein pathology on TDP-43 accumulation in Lewy body disease.

8 July 2018

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Amyotrophic lateral sclerosis: dash-like accumulation of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord

27 September 2018

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Selective occurrence of TDP-43-immunoreactive inclusions in the lower motor neurons in Machado-Joseph disease.

27 September 2018

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A long-term prospective study of the natural course of sporadic adult-onset lower motor neuron syndromes.

27 September 2018

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Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125638

Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis

27 September 2018

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El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

27 September 2018

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TDP-43 in differential diagnosis of motor neuron disorders

27 September 2018

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Crossref

https://api.crossref.org/works/10.1007%2FS00401-011-0797-Z

FRONTOTEMPORAL LOBAR DEGENERATION WITH UPPER MOTOR NEURON DISEASE/ PRIMARY LATERAL SCLEROSIS

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00401-011-0797-Z

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00401-011-0797-Z

The natural history of primary lateral sclerosis

21 January 2018

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12 December 2020

TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions

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12 December 2020

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

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12 December 2020

Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia

1 reference

12 December 2020

10.1007/S00401-011-0797-Z

Identifiers

DOI

1 reference

6 August 2017

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6 August 2017

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