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Prothrombin 20210A mutation: a mild risk factor for venous thromboembolism but not for arterial thrombotic disease and pregnancy-related complications in a family study.
Bank I, Libourel EJ, Middeldorp S, Van Pampus EC, Koopman MM, Hamulyák K, Prins MH, Van Der Meer J, Büller HR. Bank I, et al. Among authors: van der meer j, van pampus ec. Arch Intern Med. 2004 Sep 27;164(17):1932-7. doi: 10.1001/archinte.164.17.1932. Arch Intern Med. 2004. PMID: 15451770
Increased risk for fetal loss in carriers of the factor V Leiden mutation.
Meinardi JR, Middeldorp S, de Kam PJ, Koopman MM, van Pampus EC, Hamulyák K, Prins MH, Büller HR, van der Meer J. Meinardi JR, et al. Among authors: van der meer j, van pampus ec. Ann Intern Med. 1999 May 4;130(9):736-9. doi: 10.7326/0003-4819-130-9-199905040-00013. Ann Intern Med. 1999. PMID: 10357692
Risk of venous thromboembolism in carriers of factor V Leiden with a concomitant inherited thrombophilic defect: a retrospective analysis.
Meinardi JR, Middeldorp S, de Kam PJ, Koopman MM, van Pampus EC, Hamulyák K, Prins MH, Büller HR, van der Meer J. Meinardi JR, et al. Among authors: van der meer j, van pampus ec. Blood Coagul Fibrinolysis. 2001 Dec;12(8):713-20. doi: 10.1097/00001721-200112000-00014. Blood Coagul Fibrinolysis. 2001. PMID: 11734673
Co-segregation of thrombophilic disorders in factor V Leiden carriers; the contributions of factor VIII, factor XI, thrombin activatable fibrinolysis inhibitor and lipoprotein(a) to the absolute risk of venous thromboembolism.
Libourel EJ, Bank I, Meinardi JR, Baljé -Volkers CP, Hamulyak K, Middeldorp S, Koopman MM, van Pampus EC, Prins MH, Büller HR, van der Meer J. Libourel EJ, et al. Among authors: van der meer j, van pampus ec. Haematologica. 2002 Oct;87(10):1068-73. Haematologica. 2002. PMID: 12368162
46 results