Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia
- 1 October 1995
- journal article
- case report
- Published by Wiley in American Journal of Hematology
- Vol. 50 (2) , 140-143
- https://doi.org/10.1002/ajh.2830500211
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Pharmacological modification of hemoglobin F expression in sickle cell anemia: An update on hydroxyurea studiesCellular and Molecular Life Sciences, 1993
- High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell diseaseThe Journal of Pediatrics, 1991
- Treatment of Sickle Cell Anemia with Hydroxyurea and ErythropoietinNew England Journal of Medicine, 1990
- Levels of Fetal Hemoglobin Necessary for Treatment of Sickle Cell DiseaseNew England Journal of Medicine, 1988
- Recurrent cerebral ischemia during hypertransfusion therapy in sickle cell anemiaThe Journal of Pediatrics, 1983
- Efficacy of transfusion therapy for one to two years in patients with sickle cell disease and cerebrovascular accidentsThe Journal of Pediatrics, 1980
- 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