(Q41776157)

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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

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Europe PubMed Central

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

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Europe PubMed Central

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

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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3 March 2020

publication date

31 October 2013

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3 March 2020

Case reports in neurology

1 reference

Europe PubMed Central

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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

1 reference

Europe PubMed Central

PMC publication ID

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

3 March 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

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3 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

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3 March 2020

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