Subject Index

Coagulation Factors and Inhibitors
Fibrinolysis, fibrinogen, fibrin
Haemorrhagic Disorders
Invited
Other
Platelets
Thrombotic Disorders and antithrombotic therapy
Vascular Biology

Haemorrhagic Disorders

Acquired coagulation disorders (including DIC)
Gene therapy
Haemophilia A and B
Haemophilia: therapy
Haemostatic agents
Immunology (including ITP and HIT)
Inherited coagulation disorders
Other haemmorrhagic disorders
Perinatal/pediatric haemostatis
Transfusion and storage
von Willebrand disease
von Willebrand factor

Determination of overall hemostasis potential in different coagulation factors deficient plasma and in plasma samples from patients with hemophilia A and B
Antovic A., Petrini P., Blombäck M., He S.

Early FVIII Exposure and Subsequent Inhibitor Development in Children with Severe Haemophilia A
Chalmers EA, Williams MD, Richards M, Brown SA, Liesner R, Thomas A, Vidler V, Keeling D, Smith D, Hill FGH

Hemophilia B Mice Have Delayed Wound Healing
Meng ZH, Lenkowski A, Hoffman M, Hedner U, Roberts HR, Monroe DM

Prophylaxis with Factor VIII Protects Children with Hemophilia a from Inhibitor Development
Santagostino E, Mancuso ME, Rocino A, Mazzucconi MG, Mancuso G, Tagliaferri A, Messina M, Luciani M, Boeri E, Mannucci PM

Successful Diagnosis in Pregnant Obligate Carriers of Hemophilia a of Fetal Sex Using Conventional Pcr Analysis of Maternal Plasma
Colaizzo D, Tiscia T, Foti L, Vergura P, Sonni P, Cappucci F, Grandone E, Toni D, Margaglione M, Vecchione G, Chinni E, Santacroce R, Tomaiuolo M, Sessa F, Sarno M, Grandone E, Di Minno G, Margaglione M

The Concerted Action on Neutralizing Antibodies in Severe Haemophilia A
(Canal Study): Preliminary Findings

Gouw SC

The Time Courses of Fibrin Formation, Prothrombin Activation and TAFI Activation in Normal and Factor VIII-Deficient Plasma
Foley JH, Kim PY, Yu AYH, Ward VA, Nesheim ME