Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland (Q33394006)

26 July 2017

title

Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland (English)

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frontotemporal lobar degeneration

26 July 2017

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inferred from title

author name string

Anna-Lotta Kaivorinne

1

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26 July 2017

Johanna Krüger

2

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26 July 2017

Katja Kuivaniemi

3

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26 July 2017

Hannu Tuominen

4

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26 July 2017

Virpi Moilanen

5

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26 July 2017

Kari Majamaa

6

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26 July 2017

Anne M Remes

7

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26 July 2017

publication date

17 December 2008

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26 July 2017

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26 July 2017

volume

8

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26 July 2017

page(s)

48

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

26 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson'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=2625345

Functional correlates of Apolipoprotein E genotype in Frontotemporal Lobar Degeneration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 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=2625345

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

The H2 MAPT haplotype is associated with familial 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=2625345

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in 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=2625345

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

Mutation screening of the MAPT and STH genes in Polish patients with clinically diagnosed 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=2625345

Finnish Disease Heritage I: characteristics, causes, background

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625345

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=2625345

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=2625345

Mutation in the tau gene in familial multiple system tauopathy with presenile 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=2625345

Apolipoprotein-E genotyping in Alzheimer's disease 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=2625345

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

21 June 2018

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21 June 2018

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

The genetic and pathological classification of familial frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Association between the extended tau haplotype and frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Tau haplotype frequency in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Increased risk for frontotemporal dementia through interaction between tau polymorphisms and apolipoprotein E epsilon4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Association between tau H2 haplotype and age at onset in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-48

Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration

21 January 2018

1 reference

12 December 2020

Prevalence of TAU mutations in an Italian clinical series of familial frontotemporal patients

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12 December 2020

The tau H2 haplotype is almost exclusively Caucasian in origin

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12 December 2020

Apolipoprotein E genotyping by one-stage PCR

1 reference

12 December 2020

Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia

1 reference

12 December 2020

Association of the Tau haplotype with Parkinson's disease in the Greek population

1 reference

12 December 2020

APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)

1 reference

12 December 2020

Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia

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12 December 2020

Identifiers

DOI

10.1186/1471-2377-8-48

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Dimensions Publication ID

26 July 2017

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26 July 2017

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