(Q38401876)

2 September 2017

title

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations (English)

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2 September 2017

main subject

frontotemporal dementia

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based on heuristic

inferred from title

author

Stuart Pickering-Brown

10

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2 September 2017

Jennifer C Thompson

4

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Julie Snowden

object named as

Julie S Snowden

1

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David Neary

8

object named as

David Neary

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2 September 2017

Jennifer Adams

2

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2 September 2017

Jennifer Harris

3

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2 September 2017

Sara Rollinson

5

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2 September 2017

Anna Richardson

6

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2 September 2017

Matthew Jones

7

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2 September 2017

David M Mann

9

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2 September 2017

publication date

16 October 2015

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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

2 September 2017

published in

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2 September 2017

volume

16

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2 September 2017

issue

7-8

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2 September 2017

page(s)

497-505

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Neuropathological background of phenotypical variability in frontotemporal dementia

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1074700

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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

21 January 2018

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Quantitative classification of primary progressive aphasia at early and mild impairment stages

21 January 2018

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

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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

21 January 2018

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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

21 January 2018

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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

21 January 2018

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Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

21 January 2018

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

21 January 2018

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Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

21 January 2018

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Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia

21 January 2018

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A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

21 January 2018

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Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

21 January 2018

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Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

21 January 2018

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Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

21 January 2018

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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

21 January 2018

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Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

21 January 2018

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Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

21 January 2018

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21 January 2018

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Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

21 January 2018

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21 January 2018

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21 January 2018

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Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation

21 January 2018

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Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations

21 January 2018

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Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

21 January 2018

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Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

21 January 2018

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Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases

21 January 2018

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Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech

21 January 2018

1 reference

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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1074700

Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1074700

10.3109/21678421.2015.1074700

21 January 2018

Identifiers

DOI

1 reference

2 September 2017

1 reference