Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family. (Q41776157)

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scientific article published on 31 October 2013

Language	Label	Description	Also known as
English	Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family.	scientific article published on 31 October 2013

Statements

scholarly article

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3 March 2020

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Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family (English)

1 reference

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3 March 2020

frontotemporal dementia

1 reference

based on heuristic

inferred from title

4

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3 March 2020

author name string

Agnès Jacquin

1

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3 March 2020

Olivier Rouaud

2

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3 March 2020

Pierre Soichot

3

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3 March 2020

Inna Dygai-Cochet

5

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3 March 2020

Marie Sarazin

6

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3 March 2020

Tania Stojkovic

7

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3 March 2020

Martine Lemesle-Martin

8

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3 March 2020

Maurice Giroud

9

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3 March 2020

Thibault Moreau

10

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publication date

31 October 2013

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3 March 2020

Case reports in neurology

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3 March 2020

5

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3 March 2020

3

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3 March 2020

187-194

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3 March 2020

Structural brain imaging in frontotemporal dementia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

6 June 2018

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

6 June 2018

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

6 June 2018

TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

6 June 2018

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

6 June 2018

Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: recurrence of the VCP R155H mutation in an Italian family and implications for genetic counselling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

Direct voxel-based comparison between grey matter hypometabolism and atrophy in Alzheimer's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

Valosin-containing protein gene mutations: clinical and neuropathologic features.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

Mutant valosin-containing protein causes a novel type of frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

18 August 2018

Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3843933

2 December 2018

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24348398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1159/000356481

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Europe PubMed Central

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3 March 2020

1 reference

Europe PubMed Central

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3 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24348398%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

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