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

Incidence of venous thromboembolism in families with inherited thrombophilia.

Thrombosis and haemostasis - 1 Feb 1999

Simioni P, Sanson B J, Prandoni P, Tormene D, Friederich P W, Girolami B, Gavasso S, Huisman M V, Büller H R, Wouter ten Cate J, Girolami A, Prins M H

Abstract excerpt

The risk of spontaneous or risk-period related venous thromboembolism in family members of symptomatic carriers of antithrombin (AT), protein C (PC) or protein S (PS) defects, as well as of the Factor V Leiden mutation is still undefined. We performed a retrospective cohort study in family members (n = 793) of unselected patients with a documented venous thromboembolism and one of these deficiencies to make an...

Read the complete abstract on PubMed

Topics

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

Share to Postoperative Complications
Share to Contraceptives, Oral, Hormonal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Antithrombins

Share to Pregnancy Complications, Hematologic

Share to Protein C Deficiency

Share to Protein S Deficiency

Share to Puerperal Disorders

Share to Thrombophilia

Source

Identifiers

PMID: 10063991

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Incidence of venous thromboembolism in families with inherited thrombophilia.PMID 10063991Read ↗

Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: a multicenter collaborative family study.Semantic proximity Read ↗

In families with inherited thrombophilia the risk of venous thromboembolism is dependent on the clinical phenotype of the proband.Semantic proximity Read ↗

Prophylaxis and Treatment of Venous Thromboembolism in Individuals with Inherited ThrombophiliaSemantic proximity Read ↗

Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT).Semantic proximity Read ↗

Inherited risk factors for venous thromboembolism.Semantic proximity Read ↗

The risk of arterial thrombosis in carriers of natural coagulation inhibitors: a prospective family cohort study.Semantic proximity Read ↗

The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both.Semantic proximity Read ↗

Thrombotic Risk in Hereditary Antithrombin III, Protein C, or Protein S DeficiencySemantic proximity Read ↗

Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.Semantic proximity Read ↗

Hereditary risk factors for thrombophilia and probability of venous thromboembolism during pregnancy and the puerperium.Semantic proximity Read ↗

Screening for inherited thrombophilia: indications and therapeutic implications.Semantic proximity Read ↗

Inherited risk factors in low-risk venous thromboembolism in patients under 45 years.Semantic proximity Read ↗

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