8 research outputs found

    New data from the Italian National Register of Congenital Coagulopathies, 2016 Annual Survey

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    In Italy, the National Register of Congenital Coagulopathies (NRCC) collects epidemiological and therapeutic data from patients affected by haemophilia A (HA), haemophilia B (HB), von Willebrand's disease (vWD) and other rare coagulation disorders. Here we present data from the 2016 annual survey

    Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

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    Immunosuppression for acquired hemophilia A: Results from the European Acquired Haemophilia Registry (EACH2)

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    Management of bleeding in acquired hemophilia A: Results from the European Acquired Haemophilia (EACH2) registry

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