Neuroimaging features in C9orf72 and TARDBP double mutation with FTD phenotype (Q48595957)

13 February 2018

http://europepmc.org/abstract/MED/25138285

title

Neuroimaging features in C9orf72 and TARDBP double mutation with FTD phenotype (English)

1 reference

13 February 2018

http://europepmc.org/abstract/MED/25138285

0 references

5

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4 June 2020

Silvia Morbelli

8

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4 June 2020

Flavio Nobili

10

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4 June 2020

author name string

Paola Origone

1

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4 June 2020

Jennifer Accardo

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25138285%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Simonetta Verdiani

3

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4 June 2020

Merit Lamp

4

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4 June 2020

Emilia Bellone

6

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4 June 2020

Agnese Picco

7

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4 June 2020

Paola Mandich

9

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4 June 2020

publication date

20 August 2014

1 reference

13 February 2018

http://europepmc.org/abstract/MED/25138285

published in

Neurocase

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25138285%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

volume

21

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4 June 2020

issue

4

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4 June 2020

page(s)

529-534

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The GGGGCC repeat expansion in C9ORF72 in a case with discordant clinical and FDG-PET findings: PET trumps syndrome

4 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Screening for C9ORF72 repeat expansion in FTLD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Novel TARDBP sequence variant and C9ORF72 repeat expansion in a family with frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Brain ¹⁸F-FDG and ¹¹C-PiB PET findings in two siblings with FTD/ALS associated with the C9ORF72 repeat expansion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Observation of static pictures of dynamic actions enhances the activity of movement-related brain areas

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

The major symptom dimensions of obsessive-compulsive disorder are mediated by partially distinct neural systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

EANM procedure guidelines for PET brain imaging using [18F]FDG, version 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Recent advances in the imaging of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057

Frontal asymmetry in behavioral variant frontotemporal dementia: clinicoimaging and pathogenetic correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13554794.2014.951057