Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. (Q38435579)

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8 December 2019

title

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene (English)

1 reference

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8 December 2019

main subject

frontotemporal dementia

1 reference

based on heuristic

inferred from title

author

Stuart Pickering-Brown

1

1 reference

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8 December 2019

David Allsop

13

1 reference

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8 December 2019

author name string

A M T Richardson

2

1 reference

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8 December 2019

J S Snowden

3

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8 December 2019

A M McDonagh

4

1 reference

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8 December 2019

A Burns

5

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8 December 2019

W Braude

6

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8 December 2019

M Baker

7

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8 December 2019

W-K Liu

8

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8 December 2019

S-H Yen

9

1 reference

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8 December 2019

J Hardy

10

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8 December 2019

M Hutton

11

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8 December 2019

Y Davies

12

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8 December 2019

D Craufurd

14

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8 December 2019

D Neary

15

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8 December 2019

D M A Mann

16

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8 December 2019

language of work or name

English

0 references

publication date

1 April 2002

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8 December 2019

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8 December 2019

volume

125

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8 December 2019

issue

Pt 4

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8 December 2019

page(s)

732-751

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Frontal lobe degeneration of non-Alzheimer type. I. Neuropathology

8 December 2019

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

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

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Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon4 frequency, but no tau gene mutations

21 January 2018

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A distinct familial presenile dementia with a novel missense mutation in the tau gene

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The apolipoprotein E epsilon4 allele frequency is normal in fronto-temporal dementia, but correlates with age at onset of disease

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21 January 2018

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