Neuropathic pain in patients with sickle cell disease
Author:
Affiliation:
1. Section of Pediatric Hematology/Oncology; Milwaukee Wisconsin
2. Medical College of Wisconsin; Milwaukee Wisconsin
3. Children's Research Institute of the Children's Hospital of Wisconsin; Milwaukee Wisconsin
Funder
National Institutes of Health National Heart, Lung, and Blood Institute
Midwest Athletes Against Childhood Cancer and Blood Diseases Fund
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.24838/fullpdf
Reference35 articles.
1. Mortality in sickle cell disease. Life expectancy and risk factors for early death;Platt;N Engl J Med,1994
2. Daily assessment of pain in adults with sickle cell disease;Smith;Ann Intern Med,2008
3. Pain in children and adolescents with sickle cell disease: A descriptive study;Walco;J Pediatr Psychol,1990
4. Patient-reported outcomes: Descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease;Wilkie;J Natl Med Assoc,2010
5. Assessment of sickle cell pain in children and young adults using the adolescent pediatric pain tool;Franck;J Pain Symptom Manage,2002
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