The treatment of an adult patient with sickle cell disease whose clinical course is characterized by frequent painful crises creates a number of logistic problems in a tertiary care city hospital. Because such patients usually have no objective signs of painful crises, they are often considered to b
โฆ LIBER โฆ
Frequently asked questions by hospitalists managing pain in adults with sickle cell disease
โ Scribed by Wally R. Smith; Lanetta B. Jordan; Kathryn L. Hassell
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 102 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1553-5592
- DOI
- 10.1002/jhm.933
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