(Q47970486)

English

A new F-box protein 7 gene mutation causing typical Parkinson's disease

scientific article published on 23 May 2015

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

A new F-box protein 7 gene mutation causing typical Parkinson's disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Parkinson's disease

1 reference

based on heuristic

inferred from title

Nihan Erginel-Unaltuna

11

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

13

object named as

Suzanne Lesage

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

author name string

Ebba Lohmann

1

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Anne-Sophie Coquel

2

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Aurélie Honoré

3

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Hakan Gurvit

4

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Hasmet Hanagasi

5

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Murat Emre

6

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Anne L Leutenegger

7

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Valérie Drouet

8

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Mourad Sahbatou

9

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Gamze Guven

10

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Jean-Francois Deleuze

12

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Alexis Brice

14

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

language of work or name

0 references

publication date

23 May 2015

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

30

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

8

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

1130-1133

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Smoking-responsive juvenile-onset Parkinsonism.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

A new Turkish family with homozygous FBXO7 truncating mutation and juvenile atypical parkinsonism.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a family.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

A critical evaluation of the ubiquitin-proteasome system in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

FBXO7 immunoreactivity in α-synuclein-containing inclusions in Parkinson disease and multiple system atrophy

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Classification of white matter lesions on magnetic resonance imaging in elderly persons

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

The association between cognitive function and white matter lesion location in older adults: a systematic review.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Cortical thinning associated with mild cognitive impairment in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

White matter lesions and depression: a systematic review and meta-analysis

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Prodromal features for Parkinson's disease--baseline data from the TREND study.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

The Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagy

1 reference

https://api.crossref.org/works/10.1002%2FMDS.26266

21 January 2018

Identifiers

10.1002/MDS.26266

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/26010069

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q47970486&oldid=2178495835"