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Activated monocytes and platelet-monocyte aggregates in patients with sickle cell disease*DOI 10.1046/j.1365-2257.2002.t01-1-00433.x
Red Blood Cell Supports in Severe Clinical Conditions in Sickle Cell DiseasesSemantic proximity
Aberrant monocyte subsets in patients with Behçet's diseaseSemantic proximity
The role of monocytes in thrombotic disordersSemantic proximity
Development of pro-inflammatory phenotype in monocytes after engulfing Hb-activated platelets in hemolytic disorders.Semantic proximity
Cytokines and plasma factors in sickle cell diseaseSemantic proximity
Platelet P-selectin and platelet mass, volume and component in sickle cell disease: relationship to genotype.Semantic proximity
Monocytes complexed to platelets differentiate into functionally deficient dendritic cells.Semantic proximity
Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia.Semantic proximity
In vitro evidence of complement activation in patients with sickle cell diseaseSemantic proximity
The possible association of in vivo leukocyte-platelet heterophilic aggregate formation and the development of diabetic angiopathySemantic proximity
Soluble P-selectin and vascular endothelial growth factor in steady state sickle cell disease: relationship to genotype.Semantic proximity
Neutrophils and monocytes from subjects with the Mediterranean G6PD variant: effect of Plasmodium falciparum hemozoin on G6PD activity, oxidative burst and cytokine production.Semantic proximity
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