The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia

Author:

Jacquemin M.12,Vanlinthout I.2,Van Horenbeeck I.2,Debasse M.2,Toelen J.2,Schoeters J.2,Lavend'homme R.1,Freson K.1,Peerlinck K.13

Affiliation:

1. Center for Molecular and Vascular Biology; University of Leuven; Leuven Belgium

2. Laboratorium Geneeskunde; UZ Leuven; Leuven Belgium

3. Vascular Medicine and Haemostasis; UZ Leuven; Leuven Belgium

Funder

Excellentie Financiering KU Leuven

Programma Financiering KU Leuven

Fund for Scientific Research-Flanders

Research Council of the University of Leuven

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Reference24 articles.

1. Gerinnungsphysiologische Schnellmethode zur Bestimmung des Fibrinogens;Clauss;Acta Haematol,1957

2. Laboratory diagnosis of dysfibrinogenemia;Cunningham;Arch Pathol Lab Med,2002

3. Congenital fibrinogen disorders: an update;Moerloose;Semin Thromb Hemost,2013

4. Evaluation of a fully automated centrifugal analyzer for performance of hemostasis tests;Chantarangkul;Clin Chem,1987

5. Method for the determination of functional (clottable) fibrinogen by the new family of ACL coagulometers;Rossi;Thromb Res,1988

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