Thinking beyond sickling to better understand pain in sickle cell disease

Author:

Darbari Deepika S.1,Ballas Samir K.2,Clauw Daniel J.3

Affiliation:

1. Division of Hematology; Department of Pediatrics; Center for Cancer and Blood Disorders; Children's National Medical Center; George Washington University; Washington DC USA

2. Department of Medicine; Cardeza Foundation; Jefferson Medical College; Thomas Jefferson University; Philadelphia PA USA

3. Departments of Anesthesia, Medicine and Psychiatry; University of Michigan Medical School; Ann Arbor MI USA

Publisher

Wiley

Subject

Hematology,General Medicine

Reference76 articles.

1. Pathogenesis and treatment of sickle cell disease;Bunn;N Engl J Med,1997

2. Steiner CA Miller JL Sickle Cell Disease Patients in U.S. Hospitals, 2004: Statistical Brief #21 2006

3. Mortality in sickle cell disease. Life expectancy and risk factors for early death;Platt;N Engl J Med,1994

4. Severe painful vaso-occlusive crises and mortality in a contemporary adult sickle cell anemia cohort study;Darbari;PLoS ONE,2013

5. Daily assessment of pain in adults with sickle cell disease;Smith;Ann Intern Med,2008

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