Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department

Sickle cell disease (SCD ORPHA232; OMIM 603903) is a rare hereditary red cell disorder, which global distribution is changed in the last decade due to immigration-fluxes from endemic areas to Western-countries. One of the main clinical manifestations of SCD are the acute painful vaso-occlusive crisi...

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Detalhes bibliográficos
Publicado no:Orphanet J Rare Dis
Main Authors: Forni, Gian Luca, Finco, Gabriele, Graziadei, Giovanna, Balocco, Manuela, Rigano, Paolo, Perrotta, Silverio, Olivieri, Oliviero, Cappellini, Maria Domenica, De Franceschi, Lucia
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Letter to the Editor
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4230640/
https://ncbi.nlm.nih.gov/pubmed/24957117
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-9-91
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