(Q45856768)

English

The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels

scientific article published in January 1999

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

0 references

0 references

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

author name string

Chantarangkul V

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

Taioli E

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

Santos JH

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

Tagliabue L

5

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

publication date

1 January 1999

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

Thrombosis Research

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

93

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

1-8

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperhomocysteinemia: a risk factor for arterial and venous thrombotic disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'-untranslated region of the prothrombin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

A prothrombin gene mutation is significantly associated with venous thrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Validated questionnaire for the identification of previous personal or familial venous thromboembolism

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Re: "Validated questionnaire for the identification of previous personal or familial venous thromboembolism"

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Interrelation of hyperhomocyst(e)inemia, factor V Leiden, and risk of future venous thromboembolism

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900136-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(98)00136-4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/10065893

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q45856768&oldid=2086723635"