Rab, Minke A.E.; van Oirschot, Brigitte A.; Bos, Jennifer; Merkx, Tesy H.; van Wesel, Annet C.W.; Abdulmalik, Osheiza; Safo, Martin K.; Versluijs, Birgitta A.; Houwing, Maite E.; Cnossen, Marjon H.; Riedl, Jurgen; Schutgens, Roger E.G.; Pasterkamp, Gerard; Bartels, Marije; van Beers, Eduard J.; van Wijk, Richard
(John Wiley & Sons Inc., 2019-05-01)
In sickle cell disease (SCD), sickle hemoglobin (HbS) polymerizes upon deoxygenation, resulting in sickling of red blood cells (RBCs). These sickled RBCs have strongly reduced deformability, leading to vaso-occlusive crises ...