(Q49029987)

English

Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies.

scientific article published on 21 July 2011

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scholarly article

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Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21773886

Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies. (English)

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21773886

frontotemporal dementia

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based on heuristic

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motor neuron disease

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based on heuristic

inferred from title

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based on heuristic

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Laura Silveira Moriyama

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Laura Silveira-Moriyama

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Andrew John Lees

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Andrew J Lees

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Adamantios Mamais

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Adamantios Mamais

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http://europepmc.org/abstract/MED/21773886

Tammaryn Lashley

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Tammaryn Lashley

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http://europepmc.org/abstract/MED/21773886

Rina Bandopadhyay

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Rina Bandopadhyay

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http://europepmc.org/abstract/MED/21773886

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Zeshan Ahmed

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Rohan de Silva

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http://europepmc.org/abstract/MED/21773886

Karen M Doherty

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Karen M Doherty

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http://europepmc.org/abstract/MED/21773886

Geshanthi Hondhamuni

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Geshanthi Hondhamuni

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Selina Wray

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Jia Newcombe

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http://europepmc.org/abstract/MED/21773886

S.S. O'Sullivan

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Sean S O'Sullivan

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Janice L Holton

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http://europepmc.org/abstract/MED/21773886

author name string

Stephen Wroe

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http://europepmc.org/abstract/MED/21773886

Tamas Revesz

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http://europepmc.org/abstract/MED/21773886

publication date

21 July 2011

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17 February 2018

http://europepmc.org/abstract/MED/21773886

Acta Neuropathologica

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http://europepmc.org/abstract/MED/21773886

122

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4

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415-428

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https://scigraph.springernature.com/pub.10.1007/s00401-011-0857-4

0 references

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Pathological glial tau accumulations in neurodegenerative disease: review and case report

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Neuropathology of variants of progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Progressive supranuclear palsy: pathology and genetics

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Constant neurofibrillary changes in the neocortex in progressive supranuclear palsy. Basic differences with Alzheimer's disease and aging

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Argyrophilic thread-like structure in corticobasal degeneration and supranuclear palsy.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Atypical progressive supranuclear palsy with corticospinal tract degeneration.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

The neuropathology of FTD associated With ALS.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

A clinical and neuropathological study of an unusual case of sporadic tauopathy. A variant of corticobasal degeneration?

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Neuropathology of parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam: an update

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

A novel leukoencephalopathy associated with tau deposits primarily in white matter glia.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

What is primary lateral sclerosis?

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Corticobasal degeneration: widespread argentophilic threads and glia in addition to neurofibrillary tangles. Similarities of cytoskeletal abnormalities in corticobasal degeneration and progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal degeneration?

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0857-4

21 January 2018

Identifiers

10.1007/S00401-011-0857-4

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21773886

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0 references

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21773886

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