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Article

Factor V Leiden mutation presenting as repeated massive GI hemorrhages secondary to venous thrombosis.

The American journal of gastroenterology - 1 Dec 1997

Lynch J P, Rosato E F, Kochman M L

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Share to Duodenum
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 9399782

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Related research

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Factor V Leiden mutation presenting as repeated massive GI hemorrhages secondary to venous thrombosis.PMID 9399782Read ↗

Acute mesenteric ischemia caused by venous thrombosis in a patient with Leiden V factor mutation.Semantic proximity Read ↗

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

Mesenteric venous thrombosis in a 40-year-old man with homozygous factor II G20210A mutation.Semantic proximity Read ↗

Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.Semantic proximity Read ↗

Upper gastrointestinal bleeding in a young patient with Budd Chiari syndrome due to a mutation of factor V Leiden: a case report.Semantic proximity Read ↗

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

Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele.Semantic proximity Read ↗

Thrombophilia as a multigenic disorder.Semantic proximity Read ↗

Recurrent Thromboembolism due to Factor V Leiden Mutation: A Case ReportSemantic proximity Read ↗

Mesenteric venous thrombosis revealing both factor II G20212A mutation and hyperhomocysteinemia related to pernicious anemia.Semantic proximity Read ↗

Inherited factor V deficiency associated with a novel heterozygous missense mutation (p.G493R) in a patient with excessive surgical bleeding.Semantic proximity Read ↗

Massive muscle haematoma three months after starting vitamin K antagonist therapy for deep-vein thrombosis in an antithrombin deficient patient: another case of factor IX propeptide mutation.Semantic proximity Read ↗

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