Vollständige Reversibilität einer beginnenden Kumarin-Nekrose unter fibrinolytischer Therapie nach Thrombose bei partiellem (heterozygotem) Protein-C-Mangel
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-71682-9_76.pdf
Reference43 articles.
1. Bertina RM, Broekmans AW, van der Linden IK, Mertens K (1982) Protein C deficiency in a dutch family with thrombotic disease. Thromb Haemostas 48: 1
2. Branson HE, Marble R, Katz J, Griffin JH (1983) Inherited protein C deficiency and coumarin- responsive chronic relapsing purpura fulminans in a newborn infant. Lancet 11: 1165
3. Broekmans AW, Bertina RM, Loeliger EA, Hofmann V, Klingemann H-G (1983) Protein C and the development of skin necrosis during anticoagulant therapy. Thromb Haemostas 49: 251
4. Broekmans AW, Veitkamp JJ, Bertina RM (1983) Congenital protein C deficiency and venous thromboembolism: A study of three dutch families. New Engl J Med 309: 340
5. Comp PC, Esmon CT (1981) Generation of fibrinolytic activity by infusion of activated protein C into dogs. J. Clin Invest 68: 1221
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