Italian Registry of Congenital Bleeding Disorders

Italian Registry of Congenital Bleeding Disorders

In Italy, the surveillance of people with bleeding disorders is based on the National Registry of Congenital Coagulopathies (NRCC) managed by the Italian National Institute of Health (Istituto Superiore di Sanità). The NRCC collects epidemiological and therapeutic data from the 54 Hemophilia Treatme...

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Bibliographic Details
Main Authors: Adele Giampaolo, Francesca Abbonizio, Romano Arcieri, Hamisa Jane Hassan
Format: Article
Language:English
Published: MDPI AG 2017-03-01
Series:Journal of Clinical Medicine
Subjects:
registry
bleeding disorders
Hemophilia A
Hemophilia B
rare diseases
clotting factors
Online Access:http://www.mdpi.com/2077-0383/6/3/0034

Internet

http://www.mdpi.com/2077-0383/6/3/0034

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