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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Cyril Martin1,2, Vincent Pialoux1,2,3, Camille Faes1,2
1Center of Research and Innovation on Sports (CRIS EA647), Team 'Vascular Biology and Red Blood Cell', University of Lyon 1, University of Lyon, Lyon, France.
Supervised physical activity may benefit sickle cell disease (SCD) patients by reducing oxidative stress and inflammation. Regular exercise shows potential to improve blood flow and nitric oxide metabolism in SCD.
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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