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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Francis G O'Connor1, M Alaric Franzos, Nathaniel S Nye
1Department of Military and Emergency Medicine, Consortium for Health and Military Performance, Uniformed Services University of the Health Sciences, Bethesda, MD.
Sickle cell trait (SCT) can cause exertional collapse (ECAST), even sudden death. A 2019 summit addressed SCT policies, ECAST management, education, and research to improve safety for military personnel.
08:23Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
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