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)

From Wikidata

Jump to navigation Jump to search

scientific article published on 11 January 2008

Language	Label	Description	Also known as
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

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

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)

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

0 references

frontotemporal lobar degeneration

1 reference

based on heuristic

inferred from title

Stuart Pickering-Brown

1

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

object named as

Julie S Snowden

8

0 references

7

object named as

David Neary

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

author name string

Sara Rollinson

2

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Daniel Du Plessis

3

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Karen E Morrison

4

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Anoop Varma

5

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Anna M T Richardson

6

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

David M A Mann

9

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

language of work or name

0 references

publication date

11 January 2008

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

131

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Pt 3

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

721-731

1 reference

Europe PubMed Central

PubMed publication ID

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.

1 reference

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

21 January 2018

Clinicopathologic correlation in PGRN mutations

1 reference

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

21 January 2018

Frontotemporal dementia: clinicopathological correlations

1 reference

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

1 reference

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

21 January 2018

Characteristics of frontotemporal dementia patients with a Progranulin mutation

1 reference

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

PubMed publication ID

2 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38392876&oldid=1757343148"