A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy (Q48325349)

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scientific article published on 22 February 2014

Language	Label	Description	Also known as
English	A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy	scientific article published on 22 February 2014

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Parkinson's disease

1 reference

based on heuristic

inferred from title

parkinsonian syndrome

1 reference

based on heuristic

inferred from title

Matthew J. Farrer

11

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Carles Vilariño-Güell

5

object named as

Carles Vilarino-Guell

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

author name string

Eiichi Araki

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Yoshio Tsuboi

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Justus Daechsel

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Austen Milnerwood

4

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Naoki Fujii

6

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Takayasu Mishima

7

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Takayuki Oka

8

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Hideo Hara

9

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Jiro Fukae

10

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

language of work or name

0 references

publication date

22 February 2014

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

29

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

9

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

1201-1204

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)--a literature review

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

DCTN1 mutations in Perry syndrome

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Elucidating the genetics and pathology of Perry syndrome

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Neurodegeneration involving putative respiratory neurons in Perry syndrome

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Pallidonigral TDP-43 pathology in Perry syndrome

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Autonomic failures in Perry syndrome with DCTN1 mutation

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Mutant dynactin in motor neuron disease.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Distal spinal and bulbar muscular atrophy caused by dynactin mutation.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Key interaction modes of dynamic +TIP networks

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Clinical and pathological continuum of multisystem TDP-43 proteinopathies

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25833

21 January 2018

Identifiers

10.1002/MDS.25833

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/24676999

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