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

Leg ulcers revealing familial thrombophilia: prothrombin G20210A gene mutation and plasminogen activator inhibitor type 1 (PAI-1) polymorphism.

European journal of dermatology : EJD - 1 Jan 2000

Calistru Ana Maria, Cruz Maria João, Baudrier Teresa, Gonçalves Luciana, Azevedo Filomena

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to DNA
Share to DNA Mutational Analysis
Share to Mutation
Share to Plasminogen Activator Inhibitor 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Genetic

Share to Prothrombin

Share to Thrombophilia

Share to Young Adult

Source

Identifiers

PMID: 21515439
DOI: 10.1684/ejd.2011.1287

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Leg ulcers revealing familial thrombophilia: prothrombin G20210A gene mutation and plasminogen activator inhibitor type 1 (PAI-1) polymorphism.PMID 21515439Read ↗

Leg ulcers associated with factor V Leiden and prothrombin G20210A and methyltetrahydrofolate reductase mutations: successful treatment with warfarin.Semantic proximity Read ↗

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.Semantic proximity Read ↗

Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: a case report.Semantic proximity Read ↗

Factors V Leiden and the prothrombin gene mutation: two common genetic defects associated with thrombosis.Semantic proximity Read ↗

Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.Semantic proximity Read ↗

Recurrent leg ulcers and arterial thrombosis in a 33-year-old homozygous variant of antithrombin.Semantic proximity Read ↗

[Heterozygous prothrombin gene mutation G20210A and associated diseases].Semantic proximity Read ↗

Homozygous 20210G/A prothrombin gene mutation associated with bilateral iliac vein thrombosis: a case report.Semantic proximity Read ↗

Livedoid vasculopathy associated with plasminogen activator inhibitor-1 promoter homozygosity (4G/4G) and prothrombin G20210A heterozygosity: response to t-PA therapy.Semantic proximity Read ↗

Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant.Semantic proximity Read ↗

Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis.Semantic proximity Read ↗

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