Novel TARDBP mutations in Nordic ALS patients (Q44606466)

4 December 2017

title

Novel TARDBP mutations in Nordic ALS patients (English)

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amyotrophic lateral sclerosis

4 December 2017

main subject

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4 December 2017

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4 December 2017

Peter M Andersen

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4 December 2017

Huei-Hsin Chiang

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4 December 2017

Ole Gredal

series ordinal

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4 December 2017

Peter B Christensen

series ordinal

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4 December 2017

publication date

29 March 2012

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Journal of Human Genetics

4 December 2017

published in

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4 December 2017

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4 December 2017

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4 December 2017

page(s)

316-319

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Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group

4 December 2017

cites work

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The role of hypothermia in the management of severe brain injury: a meta-analysis

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Cognitive impairment in amyotrophic lateral sclerosis

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Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.

21 January 2018

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https://api.crossref.org/works/10.1038%2FJHG.2012.24

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

TDP-43 A315T mutation in familial motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

TDP-43 mutation in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease course.

21 January 2018

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https://api.crossref.org/works/10.1038%2FJHG.2012.24

TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

Amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

inferred from DOI database lookup

7 January 2021

based on heuristic

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.24

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/JHG.2012.24

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Dimensions Publication ID

4 December 2017

1016611180

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