Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Jul;85(7):532-5.
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

Charlotte F J van Tuijn, Eduard J van Beers, John-John B Schnog, Bart J Biemond

Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease

Charlotte F J van Tuijn et al. Am J Hematol. 2010 Jul.
No abstract available

PubMed Disclaimer

References

    1. Schnog JJ,Lard LR,Rojer RA, et al. New concepts in assessing sickle cell disease severity. Am J Hematol 1998; 58: 61–66. - PubMed
    1. Serjeant GR. The emerging understanding of sickle cell disease. Br J Haematol 2001; 112: 3–18. - PubMed
    1. 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
    1. Anie KA. Psychological complications in sickle cell disease. Br J Haematol 2005; 129: 723–729. - PubMed
    1. Palermo TM,Riley CA,Mitchell BA. Daily functioning and quality of life in children with sickle cell disease pain: Relationship with family and neighborhood socioeconomic distress. J Pain 2008; 9: 833–840. - PMC - PubMed

Publication types