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Hamostaseologie 2002; 22(02): 55-56
DOI: 10.1055/s-0037-1619541
DOI: 10.1055/s-0037-1619541
In memoriam I. Witt
Fibrinolyse bei Dysfibrinogenämien
Further Information
Publication History
Publication Date:
27 December 2017 (online)
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Literatur
- 1 Rupp C, Beck EA. Congenital dysfibrinogenemia. In: Beck EA, Furlan M. (Hrsg). Variants of human fibrinogen. Bern, Stuttgart, Toronto: Hans Huber; 1984: 65-130.
- 2 Samama M, Conard J, Soria J. Congential dysfibrinogenemia and thrombosis. Fibrinolysis 1988; 2 (Suppl. 02) 18-23.
- 3 Matsuda M. Molecular abnormalities of fibrinogen. Thromb Haemost 1989; 62: SA-11.
- 4 Koopman J, Haverkate F, Lord S, Caekebeke-Peelinck K, Brommer E, Briet E. A six base deletion in the γchain gene of dysfibrinogen Vlissingen, coding for Asn 319 and Asp 320, resulting in defective interaction with Ca2+ . Thromb Haemost 1989; 62: A470.
- 5 Yonekawa O, Vermond A, Nieuwenhuizen W. Localisation of a new site in fibrin, involved in acceleration of t-PA mediated activation of plasminogen. Thromb Haemost 1989; 62: A194.
- 6 Holm B, Godal HC. Quantitation of the three normally occurring plasma fibrinogens in health and during socalled “acute phase” by SDS electrophoresis of fibrin obtained from EDTA-plasma. Thromb Res 1984; 35: 279-90.
- 7 Witt I. Lysis resistance of fibrin clots under postoperative acute phase conditions. Haemostasis 1986; 16 (Suppl. 05) 37.
- 8 Witt I, Schöndorf TH, Franz K, Weber U. Veränderungen der Fibrinolyse nach Hüftgelenkseingriffen und ihre Bedeutung als Risikofaktoren für postoperative Thrombosen. In: Weber U, Schöndorf TH. (Hrsg). Aktuelle Probleme in der Orthopädie und Traumatologie. Stuttgart, New York: Thieme; 1988: 32-7.