Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort. (Q48161565)

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24 February 2020

title

Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort (English)

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24 February 2020

1 reference

Caroline H Williams-Gray

5

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24 February 2020

Raquel Duran

7

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24 February 2020

Roger A. Barker

10

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24 February 2020

author name string

Sophie E Winder-Rhodes

1

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24 February 2020

Jonathan R Evans

2

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24 February 2020

Maria Ban

3

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24 February 2020

Sarah L Mason

4

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24 February 2020

Tom Foltynie

6

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24 February 2020

Niccolo E Mencacci

8

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24 February 2020

Stephen J Sawcer

9

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24 February 2020

language of work or name

English

0 references

publication date

1 February 2013

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24 February 2020

number of pages

8

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based on heuristic

inferred from page(s)

published in

Brain

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24 February 2020

volume

136

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24 February 2020

issue

Pt 2

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24 February 2020

page(s)

392-399

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Structure of the Parkin in-between-ring domain provides insights for E3-ligase dysfunction in autosomal recessive Parkinson's disease

24 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Hematologically important mutations: Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

GBA-associated PD presents with nonmotor characteristics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

The natural history of treated Parkinson's disease in an incident, community based cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Differential phenotype in Parkinson's disease patients with severe versus mild GBA mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Movement Disorder Society Task Force report on the Hoehn and Yahr staging scale: status and recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Parkinsonism among Gaucher disease carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

The enigma of the E326K mutation in acid β-glucocerebrosidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Occurrence of Parkinson's syndrome in type I Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Gaucher disease with parkinsonian manifestations: does glucocerebrosidase deficiency contribute to a vulnerability to parkinsonism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Exploring the link between glucocerebrosidase mutations and parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

Neuropathology provides clues to the pathophysiology of Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

The heterogeneity of Parkinson's disease: clinical and prognostic implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS318

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWS318

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23413260%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

1 reference

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