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Thromb Haemost 2003; 90(05): 963-964
DOI: 10.1055/s-0037-1613499
DOI: 10.1055/s-0037-1613499
Letters to the Editor
Deep vein thrombosis after orthopedic surgery in a patient with type 1 von Willebrand disease and mutations in the MTHFR and beta-fibrinogen genes
Weitere Informationen
Publikationsverlauf
Received
15. Juni 2003
Accepted after resubmission
08. Juli 2003
Publikationsdatum:
06. Dezember 2017 (online)
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References
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- 3 Kasper CK. Postoperative thrombosis in hemophilia B. Ν Engl J Med 1973; 289: 160.
- 4 Goodnough LT, Saito H, Ratnoff OD. Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases. Med-icine (Baltimore) 1983; 62: 248-55.
- 5 Casares PZ, Gillet DS, Verity DH. et al. Bilateral simultaneous central retinal vein occlusion (crvo) caused by Waldenstrom's macroglobulinemia with acquired von Willebrand's disease. Br J Haematol 2002; 118: 344-7.
- 6 Bowen D, Dasani H, Yung B. et al A deep venous thrombosis and pulmonary embolism in a patient with type III von Willebrand's disease, protein C and antithrombin III deficiency. Br J Haematol 1992; 81: 446-7.
- 7 Keijzer MB, den Heijer M, Blom HJ. et al Interaction between hyperhomocysteinemia, mutated methylenetetrahyfrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis. Thromb Haemost 2002; 88: 723-8.
- 8 Harrington DJ, Malefora A, Schmeleva V. et al Genetic variations observed in arterial and venous thromboembolism-relevance for therapy, risk prevention and prognosis. Clin Chem Lab Med 2003; 41: 496-500.