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dc.contributor.advisor
dc.contributor.authorNzila, AM
dc.contributor.authorKokwaro, G
dc.contributor.authorWinstanley, PA
dc.contributor.authorMarsh, K
dc.contributor.authorWard, SA
dc.date.accessioned2013-06-10T12:36:12Z
dc.date.available2013-06-10T12:36:12Z
dc.date.issued2004
dc.identifier.citationTrends Parasitol. 2004 Mar;20(3):109-12en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/16676416
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/30815
dc.description.abstractPlasmodium falciparum parasites resistant to the combination sulfadoxine-pyrimethamine are spreading in Africa, particularly in East Africa. This is a matter of concern because there are no other affordable drugs available. This article provides the evidence indicating that sulfadoxine-pyrimethamine resistance can be reversed in vitro and discusses how this information might be exploited to extend the therapeutic lifetime of sulfadoxine-pyrimethamine in vivoen
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.titleTherapeutic potential of folate uptake inhibition in Plasmodium falciparumen
dc.typeArticleen
local.publisherCollege of Humanities Sciencesen


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