Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations (Q38392876)

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scientific article published on 11 January 2008

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English	Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations	scientific article published on 11 January 2008

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scholarly article

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Europe PubMed Central

2 September 2017

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

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Europe PubMed Central

2 September 2017

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frontotemporal lobar degeneration

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based on heuristic

inferred from title

Stuart Pickering-Brown

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Europe PubMed Central

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object named as

Julie S Snowden

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object named as

David Neary

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Europe PubMed Central

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author name string

Sara Rollinson

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Europe PubMed Central

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Daniel Du Plessis

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Europe PubMed Central

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Karen E Morrison

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Europe PubMed Central

2 September 2017

Anoop Varma

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Europe PubMed Central

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Anna M T Richardson

6

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Europe PubMed Central

2 September 2017

David M A Mann

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Europe PubMed Central

2 September 2017

language of work or name

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publication date

11 January 2008

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Europe PubMed Central

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Europe PubMed Central

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131

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Europe PubMed Central

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Pt 3

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Europe PubMed Central

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721-731

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Europe PubMed Central

2 September 2017

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Different variants of frontotemporal dementia: a neuropathological and immunohistochemical study.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Inheritance of frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Clinicopathologic correlation in PGRN mutations

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Frontotemporal dementia: clinicopathological correlations

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Clinicopathological correlates in frontotemporal dementia

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Characteristics of frontotemporal dementia patients with a Progranulin mutation

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Neuropathologic, biochemical, and molecular characterization of the frontotemporal dementias

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Progranulin and frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

The complex aetiology of frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Mutations in progranulin explain atypical phenotypes with variants in MAPT.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

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/10.1093%2FBRAIN%2FAWM331

21 January 2018

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

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/10.1093%2FBRAIN%2FAWM331

21 January 2018

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Frontotemporal lobar degeneration: clinical and pathological relationships

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Progressive anomia with preserved oral spelling and automatic speech.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

17q-linked frontotemporal dementia-amyotrophic lateral sclerosis without tau mutations with tau and alpha-synuclein inclusions.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM331

21 January 2018

Identifiers

10.1093/BRAIN/AWM331

1 reference

Europe PubMed Central

2 September 2017

1 reference

Europe PubMed Central

2 September 2017

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