(Q44461414)

3 December 2017

Factor V Leiden and prothrombin gene G20210A mutations in ocular Behçet disease (English)

1 reference

3 December 2017

0 references

1 reference

Halil Gürhan Karabulut

object named as

Halil Gürhan Karabulut

3

0 references

author name string

Figen Batioğlu

1

1 reference

PubMed ID

12780409

3 December 2017

Leyla S Atmaca

2

1 reference

PubMed ID

12780409

3 December 2017

Derya Beyza Sayin

4

1 reference

3 December 2017

1 June 2003

1 reference

3 December 2017

1 reference

3 December 2017

81

1 reference

3 December 2017

3

1 reference

3 December 2017

283-285

1 reference

Prothrombin gene 20210 G-A mutation in the Turkish population.

3 December 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Peripheral retinal neovascularization (Eales disease) associated with the factor V Leiden mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Peripheral retinal neovascularization and retinal vascular occlusion associated with activated protein C resistance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

World distribution of factor V Leiden

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Retinal arterial occlusion in a child with factor V Leiden and thermolabile methylene tetrahydrofolate reductase mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Factor V Leiden mutation is associated with ocular involvement in Behçet disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Antibodies to endothelial cells in patients with Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Coagulation factor V gene mutation increases the risk of venous thrombosis in behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Prothrombin gene 20210 G-A mutation in Turkish patients with thrombosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Factor V Q 506 mutation in children with thrombosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Factor V Leiden and prothrombin 20210 A mutations in patients with central and branch retinal vein occlusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Activated protein C resistance in young adults with central retinal vein occlusion

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Association of factor V Leiden and prothrombin gene mutation with Behçet's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00068.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1600-0420.2003.00068.X

1 reference

3 December 2017

1 reference

PubMed ID

12780409