Clinical trials in sickle cell disease: Adopting the combination chemotherapy paradigm
Open Access
- 27 August 2007
- journal article
- editorial
- Published by Wiley in American Journal of Hematology
- Vol. 83 (1) , 1-3
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypesBlood Reviews, 2007
- Protective effect of arginine on oxidative stress in transgenic sickle mouse modelsFree Radical Biology and Medicine, 2006
- Robust Vascular Protective Effect of Hydroxamic Acid Derivatives in a Sickle Mouse Model of InflammationMicrocirculation, 2006
- Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF‐β/BMP pathwayBritish Journal of Haematology, 2006
- Unraveling the hemolytic subphenotype of sickle cell diseaseBlood, 2005
- Pulmonary Hypertension as a Risk Factor for Death in Patients with Sickle Cell DiseaseNew England Journal of Medicine, 2004
- Heparin inhibits the flow adhesion of sickle red blood cells to P-selectinBlood, 2002
- Hydroxyurea and Sickle Cell Anemia Clinical Utility of a Myelosuppressive “Switching” AgentMedicine, 1996
- Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell AnemiaNew England Journal of Medicine, 1995
- Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.Journal of Clinical Investigation, 1984