(Q38493216)

English

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

scientific article published on 20 March 2011

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Europe PubMed Central

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3 September 2017

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene (English)

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Europe PubMed Central

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3 September 2017

frontotemporal dementia

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based on heuristic

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Stuart Pickering-Brown

13

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3 September 2017

Andrew Robinson

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Andrew Robinson

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Timothy Griffiths

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Timothy D Griffiths

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Julie S Snowden

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Parastoo Momeni

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Parastoo Momeni

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3 September 2017

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David Neary

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3 September 2017

author name string

Quan Hu

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3 September 2017

Sara Rollinson

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3 September 2017

Nicola Halliwell

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Yvonne S Davidson

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3 September 2017

Atik Baborie

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Evelyn Jaros

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Robert H Perry

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Anna Richardson

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David M A Mann

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3 September 2017

publication date

20 March 2011

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3 September 2017

Acta Neuropathologica

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122

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99-110

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3 September 2017

An overview on Primary Progressive Aphasia and its variants

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Behaviour in frontotemporal dementia, Alzheimer's disease and vascular dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Investigation of the single case in neuropsychology: confidence limits on the abnormality of test scores and test score differences

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Efficiency and power in genetic association studies

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Cognition and anatomy in three variants of primary progressive aphasia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Caudate atrophy on MRI is a characteristic feature of FTLD-FUS

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Prominent phenotypic variability associated with mutations in Progranulin

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

The neuropathology and clinical phenotype of FTD with progranulin mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

The clinical spectrum of stereotypies in frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

FUS pathology in basophilic inclusion body disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Frontal lobe dementia and motor neuron disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

A study of stereotypic behaviours in Alzheimer's disease and frontal and temporal variant frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Sensitivity of current criteria for the diagnosis of behavioral variant frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Distinct behavioural profiles in frontotemporal dementia and semantic dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Frontotemporal lobar degeneration: clinical and pathological relationships

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

A comparison of bayesian methods for haplotype reconstruction from population genotype data

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Non-Picks frontotemporal dementia imitating schizophrenia in a 22-year-old man.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

Genetic contribution of FUS to frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

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%2FS00401-011-0816-0

21 January 2018

Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0816-0

21 January 2018

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10.1007/S00401-011-0816-0

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Europe PubMed Central

PubMed publication ID

3 September 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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