A rapid, simple method for evaluation of functional asplenia in sickle cell disease
β Scribed by J.T. Casper; G.E. Rodey; L.G. Thatcher
- Book ID
- 118538306
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 118 KB
- Volume
- 84
- Category
- Article
- ISSN
- 1097-6833
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The treatment of various complications of sickle cell disease has included red cell exchange in the past, and the development of automated pheresis equipment has greatly simplified such exchanges. Traditionally, the patient's red cells have been exchanged while their plasma was returned to them. Rec
Patients with sickle cell disease (SCD) form immune alloantibodies more frequently than other transfused populations because red cells (RBCs) from white donors (with a higher incidence of certain Rh, Duffy, Kell, and Kidd blood group antigens) are transfused to black patients often lacking these ant