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Factor V Leiden mutation

Known as: Factor V Leiden, factor leiden mutation v, leiden mutation factor v 
An abnormality that refers to mutation of factor V Leiden, which is a variant of human factor V. It results in thrombophilia, deep vein thrombosis… 
National Institutes of Health

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F5 geneHereditary Diseasesfactor V Leiden

Papers overview

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2006
2006
Role of the factor V Leiden mutation in septic peritonitis assessed in factor V Leiden transgenic mice*
Objective:The factor V Leiden (FVL) mutation (Arg506Glu) results in the production of an FV protein that when activated is… 
2006
2006
Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation
The impact of the G20210A prothrombin mutation, factor V Leiden and 677T mutation of methylene tetrahydrofalate reductase (MTHFR… 
2005
2005
Factor V Leiden mutation: a contributory factor for cerebral palsy?
Fifty‐seven children with cerebral palsy (CP) and imaging evidence of vascular thrombosis (study group) and 167 children with CP… 
Review
2001
Review
2001
Cerebrovascular Disorders in Children With the Factor V Leiden Mutation
Since 1995, at least 128 children with a cerebrovascular disorder, cerebral palsy, or both and the factor V Leiden mutation have… 
Review
2001
Review
2001
Factor V Leiden mutation: potential thrombogenic role in renal vein, dialysis graft and transplant vascular thrombosis
Factor V is an important blood coagulation factor, the procoagulatory activity of which is inhibited by activated protein C. The… 
Highly Cited
1998
Highly Cited
1998
Factor V Leiden mutation in patients with Behçet's disease.
OBJECTIVE To determine the relation between factor V Leiden and Behçet's disease (BD), which is described as chronic relapsing… 
Highly Cited
1998
Highly Cited
1998
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahidrofolate reductase among patients with sickle cell disease in Brazil
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homozygosity for transition 677C… 
1998
1998
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil.
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homozygosity for transition 677C… 
Highly Cited
1996
Highly Cited
1996
Large-scale screening for factor V Leiden mutation in a north-eastern German population.
Preliminary epidemiological data showed a high but varying prevalence of factor V Leiden mutation in various European populations… 
1995
1995
The Factor V Leiden Mutation which Predisposes to Thrombosis Is Not Common in Patients with Antiphospholipid Syndrome
Summary Antiphospholipid syndrome is associated with venous, arterial, and placental thrombosis, possibly through autoantibody… 
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