(Q50720109)

18 March 2018

title

Early and pre-symptomatic neuropsychological dysfunction in the PPND family with the N279K tau mutation. (English)

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18 March 2018

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6

Wszolek ZK

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18 March 2018

author name string

Ferman TJ

1

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18 March 2018

McRae CA

2

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18 March 2018

Arvanitakis Z

3

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18 March 2018

Tsuboi Y

4

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18 March 2018

Vo A

5

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18 March 2018

publication date

1 June 2003

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18 March 2018

number of pages

6

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Parkinsonism and Related Disorders

inferred from page(s)

published in

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18 March 2018

volume

9

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18 March 2018

issue

5

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18 March 2018

page(s)

265-270

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18 March 2018

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

cites work

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

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7 January 2021

The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").

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https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900098-6

7 January 2021

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family

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7 January 2021

Phenotypic correlations in FTDP-17.

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7 January 2021

Frontotemporal dementia with novel tau pathology and a Glu342Valtau mutation

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https://api.crossref.org/works/10.1016%2FS1353-8020%2802%2900098-6

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.

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7 January 2021

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

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7 January 2021

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

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7 January 2021

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

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7 January 2021

Frontal lobe function in progressive supranuclear palsy

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7 January 2021

Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy

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7 January 2021

Verbal fluency as a function of a measure of verbal intelligence and in relation to different types of cerebral pathology.

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7 January 2021

Performance on neuropsychological tests related to single photon emission computerised tomography findings in frontotemporal dementia.

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7 January 2021

Dementia and neurodevelopmental predisposition: cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia

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7 January 2021

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

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7 January 2021

10.1016/S1353-8020(02)00098-6

Identifiers

DOI

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18 March 2018

PubMed ID

12781592

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18 March 2018