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Article

Sweet's syndrome in a woman with a prothrombin gene (G20210A) mutation.

International journal of dermatology - 1 Sept 2002

Tursen Umit, Bocekli Ebru, Kaya Tamer Irfan, Dusmez Duygu, Ikizoglu Guliz

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12358831
DOI: 10.1046/j.1365-4362.2002.01608.x

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Related research

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Sweet's syndrome in a woman with a prothrombin gene (G20210A) mutation.PMID 12358831Read ↗

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

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

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.Semantic proximity Read ↗

Superior sagittal sinus thrombosis in a patient heterozygous for the novel 20210 A allele of the prothrombin gene.Semantic proximity Read ↗

Homozygous 20210G/A prothrombin gene mutation associated with bilateral iliac vein thrombosis: a case report.Semantic proximity Read ↗

Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation.Semantic proximity Read ↗

Recurrent ischemic colitis in a young female with the prothrombin G20210A mutation.Semantic proximity Read ↗

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

Heterozygous prothrombin G20210A gene mutation in a patient with livedoid vasculitis.Semantic proximity Read ↗

Cardiology patient pages. Prothrombin 20210 mutation (factor II mutation).Semantic proximity Read ↗

Acroangiodermatitis in a carrier of the thrombophilic 20210A mutation in the prothrombin gene.Semantic proximity Read ↗

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

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