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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy

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Differences in quality of life between pediatric sickle cell patients who used hydroxyurea and those who did not

Emmanuel Nwenyi, Joan Leafman, Kathleen Mathieson

    International Journal of Health Care Quality Assurance
    |August 14, 2014
    PubMed
    Abstract

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