(Q57982310)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12473404%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

title

A family with a tau P301L mutation presenting with parkinsonism (English)

1 reference

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15 December 2019

1 reference

parkinsonian syndrome

1 reference

10

1 reference

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15 December 2019

5

Katrina Gwinn-Hardy

1 reference

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15 December 2019

author name string

Ruth H Walker

1

1 reference

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15 December 2019

Jill Wiener

3

1 reference

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15 December 2019

Ronald Hobler

4

1 reference

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15 December 2019

Amanda Adam

6

1 reference

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15 December 2019

Jennifer DeWolfe

7

1 reference

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15 December 2019

Rebecca Gibbs

8

1 reference

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15 December 2019

Matt Baker

9

1 reference

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15 December 2019

Mike Hutton

11

1 reference

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15 December 2019

Joseph Friedman

2

1 reference

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15 December 2019

John Hardy

12

1 reference

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15 December 2019

publication date

1 December 2002

1 reference

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15 December 2019

number of pages

3

1 reference

Parkinsonism and Related Disorders

inferred from page(s)

published in

1 reference

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15 December 2019

volume

9

1 reference

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15 December 2019

issue

2

1 reference

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15 December 2019

page(s)

121-123

1 reference

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

15 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

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://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Familial frontotemporal dementia with a P301L tau mutation in Japan

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Complete genomic screen in Parkinson disease: evidence for multiple genes.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900003-2

7 January 2021

10.1016/S1353-8020(02)00003-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12473404%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference