Prevention of secondary stroke and resolution of transfusional iron overload in children with sickle cell anemia using hydroxyurea and phlebotomy
- 30 September 2004
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 145 (3) , 346-352
- https://doi.org/10.1016/j.jpeds.2004.04.058
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial strokeThe Journal of Pediatrics, 2002
- Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusionsThe Journal of Pediatrics, 1995
- Stroke in a cohort of patients with homozygous sickle cell diseaseThe Journal of Pediatrics, 1992
- Cerebral infarction in sickle cell anemiaNeurology, 1988
- Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell diseaseBlood, 1984
- The natural history of stroke in sickle cell diseaseThe American Journal of Medicine, 1978
- Transfusion therapy for cerebrovascular abnormalities in sickle cell diseaseThe Journal of Pediatrics, 1976
- A prophylactic transfusion program for children with sickle cell anemia complicated by CNS infarctionAmerican Journal of Hematology, 1976
- Occlusion of Large Cerebral Vessels in Sickle-Cell AnemiaNew England Journal of Medicine, 1972
- The involvement of the nervous system in sickle-cell anemiaThe Journal of Pediatrics, 1940