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English
Two additional homozygous patients for the 20210 prothrombin polymorphism with no venous thrombosis
scientific article published on 01 December 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
title
Two additional homozygous patients for the 20210 prothrombin polymorphism with no venous thrombosis
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
main subject
thrombosis
1 reference
based on heuristic
inferred from title
homozygosity
1 reference
based on heuristic
inferred from title
author
Paolo Simioni
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
author name string
A Girolami
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
D Tormene
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
L Scarano
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
publication date
1 December 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
published in
Thrombosis Research
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
volume
96
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
page(s)
415-417
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
cites work
Asymptomatic homozygous nt 20210 G to A prothrombin polymorphism in two blood donors belonging to two different kindreds
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
It is not sure yet whether the nt 20210 G to A prothrombin polymorphism represents a cause of familial venous thrombophilia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A prothrombin gene mutation is significantly associated with venous thrombosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A patient homozygous for a mutation in the prothrombin gene 3'-untranslated region associated with massive thrombosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical studies and thrombin generation in patients homozygous or heterozygous for the G20210A mutation in the prothrombin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Emphasis on congenital conditions predisposing to thrombosis should not make us disregard the importance of acquired factors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900131-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0049-3848(99)00131-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
PubMed publication ID
10605957
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10605957
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10605957%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
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