Problems of chronic transfusion in sickle cell disease
- 1 January 1991
- journal article
- case report
- Published by Wiley in Journal of Clinical Apheresis
- Vol. 6 (4) , 234-240
- https://doi.org/10.1002/jca.2920060413
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Alloimmunization in Sickle Cell Anemia and Transfusion of Racially Unmatched BloodNew England Journal of Medicine, 1990
- Hematologic Responses of Patients with Sickle Cell Disease to Treatment with HydroxyureaNew England Journal of Medicine, 1990
- A prospective study of the incidence of delayed haemolytic transfusion reactions following peri‐operative blood transfusionBritish Journal of Haematology, 1988
- Microcomputer application of Bayesean probability testing for the identification of bacteriaInternational Journal of Bio-Medical Computing, 1988
- Experience with donors matched for minor blood group antigens in patients with sickle cell anemia who are receiving chronic transfusion therapyTransfusion, 1987
- Broadening the base of a rare donor program by targeting minority populationsTransfusion, 1986
- The incidence of development of irregular red cell antibodies in patients with sickle cell anemiaTransfusion, 1986
- Excessive binding of natural anti-alpha-galactosyl immunoglobin G to sickle erythrocytes may contribute to extravascular cell destruction.Journal of Clinical Investigation, 1986
- Posttransfusion Crises in Sickle Cell AnemiaSouthern Medical Journal, 1985
- Delayed hemolytic transfusion reactions. Evidence for complement activation involving allogeneic and autologous red cellsTransfusion, 1984