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Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.

Thrombosis and haemostasis - 1 Oct 1999

Oner A F, Arslan S, Caksen H, Ceylan A

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PMID: 10544935

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Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.PMID 10544935Read ↗

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.Semantic proximity Read ↗

Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.Semantic proximity Read ↗

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

[Budd-Chiari Syndrome in a patient with essential thrombocytopenia carrier of the prothrombin gene mutation G2021A].Semantic proximity Read ↗

Prothrombin gene mutation in Budd-Chiari syndrome-The first case report from India.Semantic proximity Read ↗

Multiple thrombophilic factors in a patient with Budd-Chiari syndrome.Semantic proximity Read ↗

Homozygous factor V Leiden mutation in a child with Budd-Chiari syndrome.Semantic proximity Read ↗

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

Eclampsia in a woman homozygous for the prothrombin G20210A mutation.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 ↗

Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis.Semantic proximity Read ↗

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

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