References
- Middeldorp S. Pregnancy failure and heritable thrombophilia. Semin Hematol 2007;44:93–97.
- Kempf Haber M, Klimek M. Thrombophilia in pregnancy and its influence on venous thromboembolism and recurrent miscarriages. Przegl Lek 2005;62:164–168.
- Buchholz T, Thaler CJ. Inherited thrombophilia: impact on human reproduction. Am J Reprod Immunol 2003;49:1–13.
- Behjati R, Modarressi MH, Jeddi-Tehrani M, Dokoohaki P, Ghasemi J, Zarnani AH, et al Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion. Ann Hematol 2006;85:268–271.
- Glueck CJ, Wang P, Goldenberg N, Sieve L. Pregnancy loss, polycystic ovary syndrome, thrombophilia, hypofibrinolysis, enoxaparin, metformin. Clin Appl Thromb Hemost 2004;10:323–334.
- Balta G, Altay C, Gurgey A. PAI-1 gene 4G/5G genotype: a risk factor for thrombosis in vessels of internal organs. Am J Hematol 2002;71:89–93.
- Coulam CB, Wallis D, Weinstein J, DasGupta DS, Jeyendran RS. Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis. Am J Reprod Immunol 2008;60:426–431.
- Wiwanitkit V. Angiotensin-converting enzyme gene polymorphism: I and D alleles from some different countries. Clin Appl Thromb Hemost 2004;10:179–182.
- Bereczky Z, Katona E, Muszbek L. Fibrin stabilization (Factor XIII), fibrin structure and thrombosis. Pathophysiol Haemost Thromb 2003/2004;33:430–437.
- Kohler HP. Role of blood coagulation factor XIII in vascular diseases. Swiss Med Wkly 2001;131:31–34.
- Gohil R, Peck G, Sharma P. The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls. Thromb Haemost 2009;102:360–370.