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Transforming Transition from Pediatric to Adult Care in Sickle Cell Disease: Leveraging Technology to Enhance Patient Education and Engagement
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Protocolizing Uncertainty: Pain Management in Sickle Cell Disease
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Sickle Cell Disease and Food Addiction as Potential Contributors to the Racial Disparity in Cognitive and Behavioral Deficits in Young and Middle-Aged Black Americans
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The Role of Heme and Heme Degradation in the Severity of Acute
Chest Syndrome in Children with Sickle Cell Disease
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An Identity Crisis for Sickle Cell Disease in Brazil
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Alloimmunization and Age of Death among Deceased Sickle Cell Disease Patients
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