From Informed Consent through Database Lock: An Interactive Clinical Trial Conducted Using the Internet von Eilenberg, Kristin L., Hoover, Amy M., Rutherford, Michael L., Melfi, Catherine A., Segal, Scott

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Characterizing medical decision‐making in sickle cell disease during childhood: Qualitative perspectives of caregivers von Blakey, Ariel O., Amaro, Christina M., Eilenberg, Jenna Sandler, Brochier, Annelise, Kavanagh, Patricia L., Garg, Arvin, Drainoni, Mari‐Lynn, Long, Kristin

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Bidirectional processes linking social determinants of health and pediatric sickle cell anemia management: A qualitative study von Long, Kristin A., Blakey, Ariel O., Amaro, Christina M., Eilenberg, Jenna S., Brochier, Annelise, Garg, Arvin, Drainoni, Mari‐Lynn, Pashankar, Farzana, Esrick, Erica B., Kavanagh, Patricia L.

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Effects of Experienced Discrimination in Pediatric Sickle Cell Disease: Caregiver and Provider Perspectives von Blakey, Ariel O., Lavarin, Claudine, Brochier, Annelise, Amaro, Christina M., Eilenberg, Jenna Sandler, Kavanagh, Patricia L., Garg, Arvin, Drainoni, Mari-Lynn, Long, Kristin A.

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