Hydroxycarbamide decreases the free alpha‐hemoglobin pool in red blood cells of adult patients with sickle cell anemia
Open Access
- 28 July 2020
- journal article
- letter
- Published by Wiley in American Journal of Hematology
- Vol. 95 (11) , E302-E305
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Sickle cell diseaseNature Reviews Disease Primers, 2018
- A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapyAmerican Journal of Hematology, 2017
- Elevated soluble α‐hemoglobin pool in sickle cell anemiaAmerican Journal of Hematology, 2017
- Red blood cells free α‐haemoglobin pool: a biomarker to monitor the β‐thalassemia intermedia variability. The ALPHAPOOL studyBritish Journal of Haematology, 2017
- Current Management of Sickle Cell AnemiaCold Spring Harbor Perspectives in Medicine, 2013
- Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysisBlood, 2012
- Genetic modifiers of sickle cell diseaseAmerican Journal of Hematology, 2012
- Decreased sickle red blood cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylationBlood, 2010
- How I use hydroxyurea to treat young patients with sickle cell anemiaBlood, 2010
- Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations.Proceedings of the National Academy of Sciences, 1993