(Q50975064)

English

TARDBP mutation p.Ile383Val associated with semantic dementia and complex proteinopathy.

scientific article published in February 2014

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scholarly article

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

TARDBP mutation p.Ile383Val associated with semantic dementia and complex proteinopathy. (English)

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

0 references

semantic dementia

1 reference

based on heuristic

inferred from title

Raquel Sanchez-Valle

object named as

R Sanchez-Valle

5

0 references

author name string

E Gelpi

1

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

J van der Zee

2

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

A Turon Estrada

3

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

C Van Broeckhoven

4

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

publication date

1 February 2014

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

Neuropathology and Applied Neurobiology

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

40

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

2

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

225-230

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

A harmonized classification system for FTLD-TDP pathology

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

Staging of brain pathology related to sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

novoSNP, a novel computational tool for sequence variation discovery

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

Locus-specific mutation databases for neurodegenerative brain diseases

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

Rethinking ALS: the FUS about TDP-43.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FNAN.12063

21 January 2018

Identifiers

10.1111/NAN.12063

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/23692129

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