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Article

G20210A prothrombin mutation and critical limb ischaemia in patients with peripheral arterial disease.

European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery - 1 Jul 2009

Sartori M, Favaretto E, Legnani C, Cini M, Conti E, Pili C, Palareti G

Abstract excerpt

OBJECTIVES: To assess the possible association between inherited thrombophilic alterations and the severity of peripheral arterial disease (PAD). DESIGN: A case-control study. METHODS: We evaluated the presence of G20210A prothrombin (FII) and R506Q FV Leiden mutations, antithrombin, protein C and S deficiencies in 176 patients with PAD at Fontaine's stage II and in 106 patients with critical limb ischaemia...

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Identifiers

PMID: 19356951
DOI: 10.1016/j.ejvs.2009.02.014

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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