(Q48263968)

10 February 2018

title

Frontotemporal dementia and Parkinsonism linked to chromosome 17 with the N279K tau mutation. (English)

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10 February 2018

Frontotemporal dementia and parkinsonism linked to chromosome 17

main subject

0 references

Parkinson's disease

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based on heuristic

inferred from title

frontotemporal dementia

1 reference

based on heuristic

inferred from title

parkinsonian syndrome

1 reference

5

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10 February 2018

Ryan J Uitti

series ordinal

3

object named as

Ryan J Uitti

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10 February 2018

6

Zbigniew K Wszolek

1 reference

10 February 2018

Jerzy Slowinski

1

1 reference

10 February 2018

Jake Dominik

series ordinal

2

1 reference

10 February 2018

Zeshan Ahmed

series ordinal

4

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10 February 2018

publication date

1 February 2007

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10 February 2018

published in

Neuropathology

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10 February 2018

volume

27

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10 February 2018

issue

1

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10 February 2018

page(s)

73-80

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10 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

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/10.1111%2FJ.1440-1789.2006.00742.X

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

A Case of Dementia Parkinsonism Resembling Progressive Supranuclear Palsy Due to Mutation in the Tau Protein Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Selective neurofibrillary degeneration of the hippocampal CA2 sector is associated with four-repeat tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Phenotypic correlations in FTDP-17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Clinical neurophysiologic findings in patients with rapidly progressive familial parkinsonism and dementia with pallido-ponto-nigral degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Update on the neuropathological diagnosis of frontotemporal dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

The Effect of tau genotype on clinical features in FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00742.X

10.1111/J.1440-1789.2006.00742.X

21 January 2018

Identifiers

DOI

1 reference

10 February 2018

release_dybfc43hnbatdfgebmv32za7zu

Fatcat ID

0 references

PubMed ID

17319286

1 reference

10 February 2018