Absence of Association between Sickle Trait Hemoglobin and Placental Malaria Outcomes

Heterozygous hemoglobin S (HbAS), or sickle trait, protects children from life-threatening falciparum malaria, potentially by attenuating binding of Plasmodium-infected red blood cells (iRBCs) to extracellular ligands. Such binding is central to the pathogenesis of placental malaria (PM). We hypothe...

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Detaylı Bibliyografya
Yayımlandı:Am J Trop Med Hyg
Asıl Yazarlar: Patel, Jaymin C., Mwapasa, Victor, Kalilani, Linda, ter Kuile, Feiko O., Khairallah, Carole, Thwai, Kyaw L., Meshnick, Steven R., Taylor, Steve M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The American Society of Tropical Medicine and Hygiene 2016
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Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4856594/
https://ncbi.nlm.nih.gov/pubmed/27001763
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4269/ajtmh.15-0672
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