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.
Abbonizio, F., Hassan, H.J., Riccioni, R., Santagostino, E., Arcieri, R., Giampaolo, A., et al. (2020). New data from the Italian National Register of Congenital Coagulopathies, 2016 Annual Survey. BLOOD TRANSFUSION, 18(1), 58-66 [10.2450/2019.0211-18].
New data from the Italian National Register of Congenital Coagulopathies, 2016 Annual Survey
Sergio, Siragusa
2020-01-01
Abstract
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.
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