(Q38190017)

30 August 2017

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title

VPS35 Parkinson's disease phenotype resembles the sporadic disease (English)

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30 August 2017

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1 reference

4

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30 August 2017

7

Werner Poewe

1 reference

30 August 2017

Walter Struhal

1

1 reference

30 August 2017

Stefan Presslauer

2

1 reference

30 August 2017

Sabine Spielberger

3

1 reference

30 August 2017

Eduard Auff

5

1 reference

30 August 2017

Thomas Bruecke

6

1 reference

30 August 2017

Gerhard Ransmayr

8

1 reference

30 August 2017

Austrian VPS-35 Investigators Team

9

1 reference

30 August 2017

publication date

21 February 2014

1 reference

Journal of Neural Transmission

30 August 2017

published in

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30 August 2017

volume

121

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30 August 2017

issue

7

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30 August 2017

page(s)

755-759

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VPS35 mutation in Japanese patients with typical Parkinson's disease.

30 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

The FAB: a Frontal Assessment Battery at bedside.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

Stress, depression and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

Frequency of the D620N mutation in VPS35 in Parkinson disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

A systematic review of prevalence studies of depression in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

Screening for VPS35 mutations in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

VPS35 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-014-1179-1

Identification of VPS35 mutations replicated in French families with Parkinson disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24557499

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00702-014-1179-1

1 reference

30 August 2017

1 reference