The expanding role of genetics in the lewy body diseases: the glucocerebrosidase gene. (Q42585265)

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27 January 2020

editorial

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title

The expanding role of genetics in the lewy body diseases: the glucocerebrosidase gene (English)

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27 January 2020

1

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27 January 2020

Steven T. DeKosky

series ordinal

3

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27 January 2020

author name string

Oscar L Lopez

series ordinal

2

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publication date

1 May 2009

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27 January 2020

published in

Archives of Neurology

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27 January 2020

volume

66

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27 January 2020

issue

5

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27 January 2020

page(s)

555-556

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Association of glucocerebrosidase mutations with dementia with lewy bodies

27 January 2020

cites work

1 reference

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Mutations for Gaucher disease confer high susceptibility to Parkinson disease

28 May 2018

1 reference

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The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations

28 May 2018

1 reference

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Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2763140

Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA).

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2763140

Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2763140

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2763140

Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese

28 May 2018

1 reference

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Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease

28 May 2018

1 reference

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Gaucher disease and the synucleinopathies

28 May 2018

1 reference

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Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype

28 May 2018

1 reference

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Lewy bodies in Alzheimer's disease: a neuropathological review of 145 cases using alpha-synuclein immunohistochemistry.

28 May 2018

1 reference

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Occurrence of Parkinson's syndrome in type I Gaucher disease

28 May 2018

1 reference

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

28 May 2018

1 reference

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Parkinson's syndrome preceding clinical manifestation of Gaucher's disease

16 August 2018

1 reference

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Analysis of the glucocerebrosidase gene in Parkinson's disease

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2763140

Lysosomal hydrolases in cerebrospinal fluid from subjects with Parkinson's disease

1 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19433653

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19433653

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1001/ARCHNEUROL.2009.61

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19433653%20AND%20SRC:MED&resulttype=core&format=json

release_lnaqzd3ktnd7ve3lgtwyid6fuy

27 January 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/lnaqzd3ktnd7ve3lgtwyid6fuy

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19433653%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

PubMed publication ID

19433653

1 reference