Please use this identifier to cite or link to this item: http://dspace.hmtu.edu.vn/handle/DHKTYTHD_123/406
Title: Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies
Authors: Manwani, Deepa
Frenette, Paul S.
Issue Date: 2013
Publisher: American Society of Hematology
Abstract: Recurrent and unpredictable episodes of vaso-occlusion are the hallmark of sickle cell disease. Symptomatic management and prevention of these events using the fetal hemoglobin–reactivating agent hydroxyurea are currently the mainstay of treatment. Discoveries over the past 2 decades have highlighted the important contributions of various cellular and soluble participants in the vaso-occlusive cascade. The role of these elements and the opportunities for therapeutic intervention are summarized in this review.
URI: http://220.231.117.85:8000/handle/DHKTYTHD_123/406
Appears in CollectionsHuyết học = Hematology

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