(Q67218833)

English

Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations

scientific article published on 01 July 2008

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scholarly article

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Europe PubMed Central

PubMed ID

18645174

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

title

Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

main subject

Corticobasal syndrome

1 reference

based on heuristic

inferred from title

primary progressive aphasia

1 reference

2

1 reference

stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

Kristoffer Haugarvoll

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

author name string

Owen A Ross

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

publication date

1 July 2008

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stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

1 reference

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

volume

71

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stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

issue

4

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stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

page(s)

303; author reply 303-4

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Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

retrieved

11 January 2020

Identifiers

DOI

10.1212/01.WNL.0000320511.30222.DD

1 reference

stated in

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

1 reference

Europe PubMed Central

PubMed ID

18645174

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18645174%20AND%20SRC:MED&resulttype=core&format=json

(Q67218833)

Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations

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