(Q33255969)

24 July 2017

title

Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease (English)

1 reference

24 July 2017

0 references

frontotemporal dementia

1 reference

Stefanie L Butland

2

0 references

Scott J. Neal

object named as

Scott J Neal

7

0 references

Howard Feldman

object named as

Howard Feldman

5

0 references

Blair R Leavitt

9

object named as

Blair R Leavitt

1 reference

24 July 2017

Ian R Mackenzie

1

1 reference

24 July 2017

Rebecca S Devon

3

1 reference

24 July 2017

Emily Dwosh

4

1 reference

24 July 2017

Caroline Lindholm

6

1 reference

24 July 2017

B F Francis Ouellette

8

1 reference

24 July 2017

publication date

31 August 2006

1 reference

24 July 2017

1 reference

24 July 2017

volume

6

1 reference

24 July 2017

page(s)

32

1 reference

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

24 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Update on the neuropathological diagnosis of frontotemporal dementias

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Pathology of CAG repeat diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Phenotypic correlations in FTDP-17.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Molecular genetic characterisation of frontotemporal dementia on chromosome 3

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1570137

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

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

Neutrophil apoptosis and dysfunction in uremia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-32

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16945149

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16945149

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16945149

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2377-6-32

1 reference

Dimensions Publication ID

24 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-6-32

9 September 2019

1 reference

24 July 2017

1 reference