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The American Journal of Bioethics Volume 13, 2013 - Issue 4
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Not Your Typical Frequent Flyer: Overcoming Mythology in Caring for Sickle Cell Disease Patients

Dowin H. Boatright Denver Health Medical Center
&
Jean Abbott University of Colorado School of Medicine
Pages 18-20 | Published online: 20 Mar 2013

Citations (3)

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Read on this site (1)

Melissa Creary & Arri Eisen. (2013) Acknowledging Levels of Racism in the Definition of “Difficult”. The American Journal of Bioethics 13:4, pages 16-18.
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Articles from other publishers (2)

Angie Mae Rodday, Kimberly S Esham, Nicole Savidge & Susan K Parsons. (2020) Patterns of healthcare utilization among patients with sickle cell disease hospitalized with pain crises. eJHaem 1:2, pages 438-447.
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Shan-Estelle Brown, Daniel F. Weisberg, Gabriela Balf-Soran & William H. Sledge. (2015) Sickle Cell Disease Patients With and Without Extremely High Hospital Use: Pain, Opioids, and Coping. Journal of Pain and Symptom Management 49:3, pages 539-547.
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