๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Frequently asked questions by hospitalists managing pain in adults with sickle cell disease

โœ 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

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Treatment of pain in adults with sickle
โœ Samir K. Ballas ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 598 KB

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

Urinary cysteinyl leukotriene E4 is asso
โœ Joshua J. Field; James Krings; Nicole L. White; Yan Yan; Morey A. Blinder; Rober ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 102 KB ๐Ÿ‘ 2 views

Leukotriene E(4) (LTE(4)) levels are associated with rate of pain episodes in children with sickle cell disease (SCD). Because complications of SCD manifest differently in adults than children, we examined a cohort of adults with SCD to determine the relationship between baseline LTE(4) and SCD-rela