Skip to main content
Lower alloimmunization rates in pediatric sickle cell patients on chronic erythrocytapheresis compared to chronic simple transfusions.
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial.
Sample suitability for the detection of minor white cell populations (microchimerism) by polymerase chain reaction.
Circulating red cells usually remain of host origin after bone marrow transplantation for severe combined immunodeficiency.