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Neutrophils, platelets, and inflammatory pathways at the nexus of sickle cell disease pathophysiology
Sickle cell disease (SCD) is a severe genetic blood disorder characterized by hemolytic anemia, episodic vaso-occlusion, and progressive organ damage. Current management of the disease remains symptomatic or preventative. Specific treatment targeting major complications such as vaso-occlusion is sti...
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| Yayımlandı: | Blood |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society of Hematology
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4760086/ https://ncbi.nlm.nih.gov/pubmed/26758915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-09-618538 |
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