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Thrombosis Research|February 15, 1993
Supranormal antithrombin III levels induced by concentrate administration are ineffective in quenching thrombin generation in acute promyelocytic leukemiaF Rodeghiero, G Castaman, L Gugliotta, et al.
British Journal of Haematology|January 1, 1993
Type I von Willebrand disease, subtype 'platelet low': decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cellsA B Federici, P G de Groot, M Moia, et al.
The New England Journal of Medicine|October 6, 2000
Mutations in coagulation factors in women with unexplained late fetal lossI Martinelli, E Taioli, I Cetin, et al.
Blood|September 1, 1984
Studies of the pathophysiology of acquired von Willebrand's disease in seven patients with lymphoproliferative disorders or benign monoclonal gammopathiesP M Mannucci, R Lombardi, R Bader, et al.
Journal of Thrombosis and Haemostasis : JTH|January 10, 2008
The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210AI Martinelli, T Battaglioli, V De Stefano, et al.
British Journal of Haematology|May 31, 2001
The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutationV De Stefano, I Martinelli, P M Mannucci, et al.
The New England Journal of Medicine|September 9, 1999
The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutationV De Stefano, I Martinelli, P M Mannucci, et al.
Blood|February 9, 2000
Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretionS Duga, R Asselta, E Santagostino, et al.
Thrombosis and Haemostasis|December 15, 1986
An enzyme immunoassay (ELISA) for the quantitation of human factor VIIC Boyer, M Wolf, C Rothschild, et al.
Thrombosis and Haemostasis|August 26, 2000
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiencyF Peyvandi, P V Jenkins, P M Mannucci, et al.
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