Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Diagnosis and management offactor V Leiden

31 Oct 2016

Abstract excerpt

INTRODUCTION: The discovery of the factor V Leiden (FVL) missense mutation (Arg506Gln) causing factor V resistance to the anticoagulant action of activated protein C was a landmark that allowed a better understanding of the basis of inherited thrombotic risk. FVL mutation is currently the most common known hereditary defect predisposing to venous thrombosis. Areas covered: Novel data-driven FVL diagnosis and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Atrial Fibrillation Management and Outcomes
Share to Blood Coagulation and Thrombosis Mechanisms
Share to Venous Thromboembolism Diagnosis and Management

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 27797270
DOI: 10.1080/17474086.2016.1249364

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 25 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Diagnosis and management offactor V LeidenPMID 27797270Read ↗

Activated protein C resistance and factor V Leiden: a review.Semantic proximity Read ↗

Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders.Semantic proximity Read ↗

Management of inherited thrombophilia: guide for genetics professionals.Semantic proximity Read ↗

Update on selected inherited venous thrombotic disorders.Semantic proximity Read ↗

Testing for inherited thrombophilia and consequences for antithrombotic prophylaxis in patients with venous thromboembolism and their relativesSemantic proximity Read ↗

Management of antithrombin deficiency: an update for cliniciansSemantic proximity Read ↗

Factor V Leiden thrombophilia.Semantic proximity Read ↗

Genetic Testing for Thrombophilia-Related Genes: Observations of Testing Patterns for Factor V Leiden (G1691A) and Prothrombin Gene “Mutation” (G20210A)Semantic proximity Read ↗

Factor V Leiden: an overview.Semantic proximity Read ↗

Inherited Thrombophilia: Implications for Prevention and Treatment of Venous ThromboembolismSemantic proximity Read ↗

Clinical, Laboratory, and Molecular Aspects of Factor V DeficiencySemantic proximity Read ↗

Inherited and acquired factor V deficiency.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.