(Q38384506)

English

Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy

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scholarly article

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy (English)

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

Frontotemporal dementia and parkinsonism linked to chromosome 17

0 references

frontotemporal dementia

1 reference

based on heuristic

inferred from title

parkinsonian syndrome

1 reference

based on heuristic

inferred from title

Zbigniew K Wszolek

7

object named as

Z K Wszolek

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

David S Knopman

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object named as

D S Knopman

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

Ronald C. Petersen

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object named as

R C Petersen

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

Dennis W. Dickson

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object named as

D W Dickson

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

author name string

P Tacik

1

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

M Sanchez-Contreras

2

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

M DeTure

3

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

M E Murray

4

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

R Rademakers

5

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

O A Ross

6

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

J E Parisi

8

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

publication date

8 March 2017

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

Neuropathology and Applied Neurobiology

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

43

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Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

3

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

200-214

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

Globular Glial Tauopathy Presenting as Semantic Variant Primary Progressive Aphasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Temporal Variant Frontotemporal Dementia is Associated with Globular Glial Tauopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

A novel tau mutation, p.K317N, causes globular glial tauopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Globular Glial Mixed Four Repeat Tau and TDP-43 Proteinopathy with Motor Neuron Disease and Frontotemporal Dementia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Globular glial tauopathies (GGT): consensus recommendations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy brain bank

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Tau pathology in a family with dementia and a P301L mutation in tau.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Apolipoprotein E affects the rate of Alzheimer disease expression: beta-amyloid burden is a secondary consequence dependent on APOE genotype and duration of disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Structure and novel exons of the human tau gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

23 June 2018

Apolipoprotein E allelotype is associated with neuropathological findings in Alzheimer's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Glial and neuronal tau pathology in tauopathies: characterization of disease-specific phenotypes and tau pathology progression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Tau gene mutations and their effects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5386812

31 August 2018

Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12367

21 January 2018

A family with a tau P301L mutation presenting with parkinsonism

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12367

21 January 2018

A case of frontotemporal dementia with tau P301L mutation in the Far East

1 reference

https://pubmed.ncbi.nlm.nih.gov/27859539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/27859539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/27859539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments

1 reference

https://pubmed.ncbi.nlm.nih.gov/27859539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial frontotemporal dementia with a P301L tau mutation in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/27859539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/NAN.12367

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

1 reference

Europe PubMed Central

22 May 2018

http://europepmc.org/abstract/PMC/5386812

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