Hydroxyurea for Children with Sickle Cell Disease
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference72 articles.
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1. The implementation of automated red blood cell exchange (erythrocytapheresis) as a treatment modality in sickle cell disease patients: Single center experience;Transfusion and Apheresis Science;2023-08
2. Effect of Hydroxyurea Therapy on Growth Parameters in Older Children (6-15 Year-Old) with Sickle Cell Disease: Low Dose Versus High Dose;Hemoglobin;2023-07-04
3. A PHARMacist led Initiative for the Management of Hydroxyurea Therapy in Pediatric Sickle Cell Anemia patients attending a Multidisciplinary Tertiary Hemoglobinopathy Clinic: A retrospective cohort study ( PHARMIT‐SCA );JACCP: JOURNAL OF THE AMERICAN COLLEGE OF CLINICAL PHARMACY;2021-09-13
4. Effects of hydroxyurea on brain function in children with sickle cell anemia;Pediatric Blood & Cancer;2021-07-31
5. Tolerability and age‐dependent toxicokinetics following perinatal hydroxyurea treatment in Sprague Dawley rats;Journal of Applied Toxicology;2020-11-25
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