Show simple item record

dc.contributor.authorWalter Otieno, Benson BA Estambale, Michael M Odera, Joash R Aluoch, José A Stoute
dc.date.accessioned2020-11-18T06:00:14Z
dc.date.available2020-11-18T06:00:14Z
dc.date.issued2013
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/2806
dc.description.abstractMalaria infection leads to the formation of circulating immune complexes CICs which have been implicated in the pathogenesis of complicated malaria which includes severe malarial anemia. Children with sickle cell trait HbAS are less predisposed to getting severe manifestations of malaria. We carried out a study to determine the competence of the red blood cells RBCs of children with HbAS to bind immune complexes ICs and compared this with normal hemoglobin HbAA. Descriptors:en_US
dc.publisherARMY MEDICAL RESEARCH UNIT-KENYA APO NEW YORK 09675en_US
dc.subject*IMMUNITY *PLASMODIUM FALCIPARUM ANEMIAS ASSAYING CHILDREN DEOXYGENATION ERYTHROCYTES KENYA MALARIA PATHOGENESIS RECEPTOR SITES(PHYSIOLOGY) SICKLE CELLSen_US
dc.titleRed blood cell immune complex binding capacity in children with sickle cell trait (HbAS) living in P. falciparum malaria holoendemic region of Western Kenyaen_US
dc.typeArticleen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record