New data from the Italian National Register of Congenital Coagulopathies, 2016 Annual Survey
- Autori: Abbonizio, Francesca; Hassan, Hamisa J; Riccioni, Roberta; Santagostino, Elena; Arcieri, Romano; Giampaolo, Adele; on behalf of the Italian Association of Haemophilia Centres ; Sergio, Siragusa
- Anno di pubblicazione: 2020
- Tipologia: Articolo in rivista
- OA Link: http://hdl.handle.net/10447/510173
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.