Cargando…
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...
Autores principales: | Giampaolo, Adele, Abbonizio, Francesca, Arcieri, Romano, Hassan, Hamisa Jane |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373003/ https://www.ncbi.nlm.nih.gov/pubmed/28335488 http://dx.doi.org/10.3390/jcm6030034 |
Ejemplares similares
-
Comparing regional models of congenital bleeding disorders: preliminary steps in the Italian context
por: Nuti, Sabina, et al.
Publicado: (2017) -
Key role of MEK/ERK pathway in sustaining tumorigenicity and in vitro radioresistance of embryonal rhabdomyosarcoma stem-like cell population
por: Ciccarelli, Carmela, et al.
Publicado: (2016) -
First Report of the Italian Registry on Immune-Mediated Congenital Heart Block (Lu.Ne Registry)
por: Fredi, Micaela, et al.
Publicado: (2019) -
Commentary: First Report of the Italian Registry on Immune-Mediated Congenital Heart Block (Lu.Ne Registry)
por: Costedoat-Chalumeau, Nathalie, et al.
Publicado: (2020) -
The Italian registry for patients with Prader–Willi syndrome
por: Salvatore, Marco, et al.
Publicado: (2023)