Association between haemophilia and inherited thrombophilia: a single centre survey

I.R. Walker, J. Teitel, M.-C. Poon, B. Ritchie, J. Akabutu, G. D. Sinclair, M. Pai, J. W. Y. Wu, S. Reddy, C. Carter, G. Growe, D. Lillicrap, M. Lam, M. A. Blajchman, D.H. Lee, Effect of the Factor V Leiden Mutation on the Clinical Expression of Severe Hemophilia A Thrombosis and Haemostasis. ,vol. 83, pp. 387- 391 ,(2000) , 10.1055/S-0037-1613824

VALDER R. ARRUDA, JOYCE M. ANNICHINO-BIZZACCHI, SANDRA V. ANTUNES, FERNANDO F. COSTA, Association of severe haemophilia A and factor V Leiden: report of three cases. Haemophilia. ,vol. 2, pp. 51- 53 ,(1996) , 10.1111/J.1365-2516.1996.TB00011.X

A. TAGLIAFERRI, C. DI PERNA, M. FRANCHINI, G. F. RIVOLTA, C. PATTACINI, Hemophilia severity score system: validation from an Italian Regional Hemophilia Reference Center. Journal of Thrombosis and Haemostasis. ,vol. 7, pp. 720- 722 ,(2009) , 10.1111/J.1538-7836.2009.03288.X

Massimo Franchini, Martina Montagnana, Giovanni Targher, Dino Veneri, Marco Zaffanello, Gian Salvagno, Franco Manzato, Giuseppe Lippi, Interpatient phenotypic inconsistency in severe congenital hemophilia: a systematic review of the role of inherited thrombophilia. Seminars in Thrombosis and Hemostasis. ,vol. 35, pp. 307- 312 ,(2009) , 10.1055/S-0029-1222609

K. Kurnik, W. Kreuz, S. Horneff, C. During, R. Schobess, C. Bidlingmaier, C. E. Ettingshausen, A. Krumpel, N. Bogdanova, U. Nowak-Gottl, Effects of the factor V G1691A mutation and the factor II G20210A variant on the clinical expression of severe hemophilia A in children – results of a multicenter study Haematologica. ,vol. 92, pp. 982- 985 ,(2007) , 10.3324/HAEMATOL.11161

S. Halimeh, C. Escuriola Ettingshausen, K. Kurnik, R. Schobess, C. Wermes, H. Pollmann, W. D. Kreuz, U. Nowak-Göttl, Symptomatic Onset of severe Hemophilia A in Childhood is dependent on the Presence of Prothrombotic Risk Factors 31st Hemophilia Symposium Hamburg 2000. ,vol. 85, pp. 77- 80 ,(2002) , 10.1007/978-3-642-59383-3_9