(Q33849069)

29 July 2017

1 reference

title

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (English)

1 reference

Hereditary inclusion body myopathy

29 July 2017

main subject

frontotemporal dementia

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author

Maria Rita Passos-Bueno

5

object named as

M R Passos-Bueno

1 reference

29 July 2017

R D Fanganiello

1

1 reference

29 July 2017

V E Kimonis

2

1 reference

29 July 2017

C C Côrte

3

1 reference

29 July 2017

R Nitrini

4

1 reference

29 July 2017

language of work or name

English

0 references

publication date

11 March 2011

1 reference

Brazilian Journal of Medical and Biological Research

29 July 2017

published in

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29 July 2017

volume

44

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29 July 2017

issue

4

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29 July 2017

page(s)

374-380

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Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

A study of the Lund-Manchester research criteria for frontotemporal dementia: clinical and single-photon emission CT correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

Pathological consequences of VCP mutations on human striated muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

Atrophy patterns in histologic vs clinical groupings of frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0100-879X2011007500028

10.1590/S0100-879X2011007500028

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference