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Article

Recurrent thrombembolic risk in patients with multiple thrombophilic disorders.

Romanian journal of internal medicine = Revue roumaine de medecine interne - 1 Jan 2008

Agoşton-Coldea Lucia, Rusu L D, Bobar Camelia, Rusu M L, Mocan Teodora, Procopciuc Lucia Maria

Abstract excerpt

Genetic mutations of the coagulation factors II and V (G20210A and G1691A - factor V Leiden)--as well as the one for methylene tetrahydrofolat reductase's (MTHFT) gene C677T are diseases with dominant autosomal transmission characterized by thromboembolic events leading to deep vein thrombosis and/or pulmonary embolism. The authors show the clinical observation of 2 cases of recurrent deep venous thrombosis...

Read the complete abstract on PubMed

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Share to Anticoagulants
Share to Factor V

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Polymorphism, Single Nucleotide

Share to Protein S Deficiency

Share to Prothrombin

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Share to Venous Thrombosis

Source

Identifiers

PMID: 19366087

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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