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Springer Publishing Company

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Markers of activated coagulation in patients with factor V Leiden and/or G20210A prothrombin gene mutation

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Homozygous 20210G/A Prothrombin Gene Mutation Associated with Bilateral Iliac Vein Thrombosis: A Case Report

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Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a)

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The G20210A Mutation of the Prothrombin Gene in Patients with Previous First Episodes of Deep-Vein Thrombosis - a critical evaluation of the test and the development of diagnostic criteria

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