(Q43008443)

12 November 2017

Factor V Leiden mutation does not correlate with retinal vascular occlusion in white patients with Behçet's disease (English)

1 reference

retinal vascular occlusion

12 November 2017

0 references

1 reference

1 reference

3

1 reference

12 November 2017

Chen Y

1

1 reference

12 November 2017

Stanford MR

2

1 reference

12 November 2017

Vaughan RW

4

1 reference

12 November 2017

Kondeatis E

5

1 reference

12 November 2017

Fortune F

6

1 reference

12 November 2017

language of work or name

English

0 references

publication date

1 August 2003

1 reference

British Journal of Ophthalmology

12 November 2017

1 reference

12 November 2017

87

1 reference

12 November 2017

8

1 reference

12 November 2017

1048-1049

1 reference

Global survey of genetic variation in CCR5, RANTES, and MIP-1alpha: impact on the epidemiology of the HIV-1 pandemic.

12 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1771783

Resistance to activated protein C as a basis for venous thrombosis.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1771783

Vascular involvement in Behçet's disease: relation with thrombophilic factors, coagulation activation, and thrombomodulin

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1771783

The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1771783

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

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1771783

Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1771783

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

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12881356

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Factor V Leiden mutation in patients with Behçet's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12881356

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/BJO.87.8.1048

1 reference

12 November 2017

1 reference

12 November 2017

1 reference