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Article

Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele.

Thrombosis and haemostasis - 1 Sept 1998

De Stefano V, Chiusolo P, Paciaroni K, Teofili L, La Barbera E O, Casorelli I, Leone G

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PMID: 9759637

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Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele.PMID 9759637Read ↗

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

Chronic thromboembolic pulmonary hypertension in a patient heterozygous for both factor V Leiden and G20210 prothrombin mutation.Semantic proximity Read ↗

[Portal and mesenteric vein thrombosis in a patient with a mutation of the 20210 gen of the prothrombin].Semantic proximity Read ↗

Portal, splenic and mesenteric vein thrombosis in a patient with factor V Leiden mutation and antithrombin III deficiency.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 ↗

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The prothrombin 20210 G to A variation and thrombosis.Semantic proximity Read ↗

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