(Q30483458)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author name string

Shira G Ziegler

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Michael J Eblan

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Kathleen S Hruska

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Barbara K Stubblefield

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Ozlem Goker-Alpan

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Mary E LaMarca

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Ellen Sidransky

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

publication date

25 April 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

29 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

91

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

195-200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

Genetics of Parkinson's disease and parkinsonism

29 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

A common LRRK2 mutation in idiopathic Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Parkinsonism among Gaucher disease carriers

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Glucocerebrosidase mutations in subjects with parkinsonism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

20 June 2018

Genetics of parkinsonism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Occurrence of Parkinson's syndrome in type I Gaucher disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Glucocerebrosidase mutations are an important risk factor for Lewy body disorders.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Case-control study of the parkin gene in early-onset Parkinson disease.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Parkin implicated in sporadic Parkinson's disease

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Analysis of the glucocerebrosidase gene in Parkinson's disease

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

Neuropathology provides clues to the pathophysiology of Gaucher disease.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950300

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

26 November 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

The glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

Glucocerebrosidase mutation T369M appears to be another polymorphism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

Mutation analysis of Gaucher disease patients in Taiwan: High prevalence of the RecNciI and L444P mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

Glucocerebrosidase mutations are also found in subjects with early-onset parkinsonism from Venezuela

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

Absence of G209A and G88C mutations in the alpha-synuclein gene of Parkinson's disease in a Chinese population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

The α-Synuclein Gene and Parkinson Disease in a Chinese Population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.03.004

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YMGME.2007.03.004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462935%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference