References
- Haverkate F, Samama M. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen. Thromb Haemost 1995;73:151–61.
- Soria J, Soria C, Caen P. A new type of congenital dysfibrinogenaemia with defective fibrin lysis – Dusard syndrome: possible relation to thrombosis. Br J Haematol 1983;53:575–86.
- de Moerloose P, Boehlen F, Neerman-Arbez M. Fibrinogen and the risk of thrombosis. Semin Thromb Hemost 2010;36:7–17.
- Koopman J, Haverkate F, Grimbergen J, Lord ST, Mosesson MW, DiOrio JP, Siebenlist KS, Legrand C, Soria J, Soria C. Molecular basis for fibrinogen Dusart (A alpha 554 Arg → Cys) and its association with abnormal fibrin polymerization and thrombophilia. J Clin Invest 1993;91:1637–43.
- Tarumi T, Martincic D, Thomas A, Janco R, Hudson M, Baxter P, Gailani D. Familial thrombophilia associated with fibrinogen Paris V: Dusart syndrome. Blood 2000;96: 1191–3.
- Wada Y, Lord ST. A correlation between thrombotic disease and a specific fibrinogen abnormality (A alpha 554 Arg → Cys) in two unrelated kindred, Dusart and Chapel Hill III. Blood 1994;84:3709–14.
- Carrell N, Gabriel DA, Blatt PM, Carr ME, McDonach J. Hereditary dysfibrinogenemia in a patient with thrombotic disease. Blood 1983;62:439–47.
- Meyer M, Kutcher G, Binneweies T, Barthels M, Eberl W, Loreth RM, Maak B, Matzdorff A, Rauch R, Syrbe G. Mutation spectrum in fibrinogen genes: melocular analysis in 11 German families with dysfibrinogenemia [abstract]. Thromb Haemost 1999:601.
- Hayes T. Dysfibrinogenemia and thrombosis. Arch Pathol Lab Med 2002;126:1387–90.
- Mosesson MW, Siebenlist KR, Meh DA. The structure and biological features of fibrinogen and fibrin. Ann NY Acad Sci 2001;936:11–30.
- Cunningham MT, Brandt JT, Laposata M, Olson JD. Laboratory diagnosis of dysfibrinogenemia. Arch Pathol Lab Med 2002;126:499–505.
- Sjøland JA, Sidelmann JJ, Brabrand M, Pedersen RS, Pedersen JH, Esbensen K, Standeven KF, Ariens RA, Gram J. Fibrin clot structure in patients with end-stage renal disease. Thromb Haemost 2007;98:339–45.
- Acharya SS, Dimichele DM. Rare inherited disorders of fibrinogen. Haemophilia 2008;14:1151–8.
- Collet JP, Woodhead JL, Soria J, Soria C, Mirshahi M, Caen JP, Weisel JW. Fibrinogen Dusart: electron microscopy of molecules, fibers and clots, and viscoelastic properties of clots. Biophys J 1996;70:500–10.
- Lijnen HR, Soria J, Soria C, Collen D, Caen JP. Dysfibrinogenemia (fibrinogen Dusard) associated with impaired fibrin-enhanced plasminogen activation. Thromb Haemost 1984;51:108–9.
- Shapiro SE, Phillips E, Manning RA, Morse CV, Murden SL, Laffan MA, Mumford AD. Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia. Br J Haematol 2013;160: 220–7.