Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease
- PMID: 20575034
- PMCID: PMC7159444
- DOI: 10.1002/ajh.21731
Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease
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References
-
- Schnog JJ,Lard LR,Rojer RA, et al. New concepts in assessing sickle cell disease severity. Am J Hematol 1998; 58: 61–66. - PubMed
-
- Serjeant GR. The emerging understanding of sickle cell disease. Br J Haematol 2001; 112: 3–18. - PubMed
-
- Levenson JL,McClish DK,Dahman BA, et al. Depression and anxiety in adults with sickle cell disease: The PiSCES project. Psychosom Med 2008; 70: 192–196. - PubMed
-
- Anie KA. Psychological complications in sickle cell disease. Br J Haematol 2005; 129: 723–729. - PubMed
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