Complement in Sickle Cell Disease: Are We Ready for Prime Time?

Sickle cell disease (SCD) is a widely spread inherited hemoglobinopathy that includes a group of congenital hemolytic anemias, all characterized by the predominance of sickle hemoglobin (HbS). Its features are anemia, predisposal to bacterial infections and complications such as vaso-occlusive crisi...

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Detalles Bibliográficos
Autores principales: Varelas, Christos, Tampaki, Athina, Sakellari, Ioanna, Anagnostopoulos, Αchilles, Gavriilaki, Eleni, Vlachaki, Efthymia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001680/
https://www.ncbi.nlm.nih.gov/pubmed/33790681
http://dx.doi.org/10.2147/JBM.S287301

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001680/
https://www.ncbi.nlm.nih.gov/pubmed/33790681
http://dx.doi.org/10.2147/JBM.S287301

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