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Thromb Haemost 1999; 81(05): 846-847
DOI: 10.1055/s-0037-1614581
Letters to the Editor
Schattauer GmbH

Can Low Level of von Willebrand Factor Decrease the Risk of Thrombosis in Families with Antithrombin or Protein C Deficiency?

Maria M. Jelenska
1   From the Department of Vascular Surgery and Transplantology, Warsaw University Medical School, Poland
,
Malgorzata Palester-Chlebowczyk
1   From the Department of Vascular Surgery and Transplantology, Warsaw University Medical School, Poland
,
Tadeusz R. Grochowiecki
1   From the Department of Vascular Surgery and Transplantology, Warsaw University Medical School, Poland
,
Stanislaw Zajac
1   From the Department of Vascular Surgery and Transplantology, Warsaw University Medical School, Poland
› Author Affiliations
Further Information

Publication History

Received 17 October 1998

Accepted after resubmission 18 January 1999

Publication Date:
09 December 2017 (online)

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  • References

  • 1 Rosendaal FR. Risk factors for venous thrombosis: prevalence, risk, and interaction.. Seminars in Hematol 1997; 34: 171-87.
    PubMedSearch in Google Scholar
  • 2 Seligsohn U, Zivelin A. Thrombophilia as a multigenic disorder.. Thromb Haemostas 1997; 78: 297-301.
    PubMedSearch in Google Scholar
  • 3 Rosendaal FR. Thrombosis in the young: epidemiology and risk factors. A focus on venous thrombosis.. Thromb Haemost 1997; 78: 1-6.
    Thieme ConnectPubMedSearch in Google Scholar
  • 4 Nichols WC, Amano K, Cacheris PM, Figueiredo MS, Michaelides K, Schwaab S, Hoyer L, Kaufman RJ, Ginsburg D. Moderation of haemophilia A phenotype by the factor V R506Q mutation.. Blood 1996; 88:: 1183-7.
    PubMedSearch in Google Scholar
  • 5 Van’t Veer C, Golden NJ, Kalafatis M, Simioni P, Bertina RM, Mann KG. An in vitro analysis of the combination of haemophilia A and factor V Leiden.. Blood 1997; 90: 3067-72.
    CrossrefPubMedSearch in Google Scholar
  • 6 Wolf M, Boyer-Neumann C, Molho-Sabatier P, Neumann C, Meyer D, Larrieu MJ. Familial variant of antithrombin III (AT III Bligny, 47Arg to His) associated with protein C deficiency.. Thromb Haemost 1990; 63: 215-20.
    Thieme ConnectPubMedSearch in Google Scholar
  • 7 Girolami A, Cappellato MG, Vicarioto MA, Casonato S, Marafioti F. Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento).. Blut 1986; 52: 29-33.
    CrossrefPubMedSearch in Google Scholar
  • 8 Sadler E, Gralnick HR. Commentary: a new classification for von Willebrand disease.. Blood 1994; 84: 676-9.
    PubMedSearch in Google Scholar