Sickle Cell Trait

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  Subject Areas on Research

  • Absence of Association Between Sickle Trait Hemoglobin and Placental Malaria Outcomes. 
  • Beta-lactam antibiotic-induced pseudoporphyria. 
  • Cerebral infarction in sickle cell trait. 
  • D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study. 
  • Efficacy of chloroquine on Plasmodium falciparum transmitted at Amani, eastern Usambara Mountains, north-east Tanzania: an area where malaria has recently become endemic. 
  • Glycosylated hemoglobin levels in a benign form of sickle cell anemia in Saudi Arabia. 
  • Impact of red blood cell variants on childhood malaria in Mali: a prospective cohort study. 
  • Impaired cytoadherence of Plasmodium falciparum-infected erythrocytes containing sickle hemoglobin. 
  • Implementation of the NCAA Sickle Cell Trait Screening Policy: A Survey of Athletic Staff and Student-athletes. 
  • New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease. 
  • Pathological effects of sickle cell anemia on the pulp. 
  • Perspectives and Practices of Athletic Trainers and Team Physicians Implementing the 2010 NCAA Sickle Cell Trait Screening Policy. 
  • Quantification of macular ischaemia in sickle cell retinopathy. 
  • RNA repair as a novel approach to genetic therapy. 
  • Rhabdomyolysis and hemolysis associated with sickle cell trait and glucose-6-phosphate dehydrogenase deficiency. 
  • The clinical manifestations of cerebral malaria among Nigerian children with the sickle cell trait. 
  • Third trimester and early postpartum period of pregnancy have the greatest risk for ACS in women with SCD. 
  • Transient open-angle glaucoma associated with sickle cell trait: report of 4 cases. 
  • Use of the tourniquet during surgery in patients with sickle cell hemoglobinopathies. 
  • VCL-ALK renal cell carcinoma in children with sickle-cell trait: the eighth sickle-cell nephropathy? 
  • Vitreous hemorrhage associated with sickle-cell trait and sickle-cell hemoglobin-C disease.