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English
LRRK2 screening in a Canadian Parkinson's disease cohort
scientific article published on 01 August 2007
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
title
LRRK2 screening in a Canadian Parkinson's disease cohort
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
main subject
Parkinson's disease
1 reference
based on heuristic
inferred from title
author name string
D A Grimes
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
L Racacho
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
F Han
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
M Panisset
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
D E Bulman
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
publication date
1 August 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
published in
Canadian Journal of Neurological Sciences
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
volume
34
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
page(s)
336-338
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
cites work
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LRRK2 in Parkinson's disease: protein domains and functional insights
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parkinson's disease: a test of the multifactorial etiologic hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
G2019S LRRK2 mutation in French and North African families with Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LRRK2 mutations in Parkinson disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100006788
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S0317167100006788
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
PubMed publication ID
17803033
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17803033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
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