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*

*Corresponding author for this work

Research output: Contribution to journalLetterAcademicpeer-review

Original languageEnglish
Pages (from-to)532-535
Number of pages4
JournalAmerican Journal of Hematology
Volume85
Issue number7
DOIs
Publication statusPublished - Jul 2010
Externally publishedYes

Keywords

  • HEALTH SURVEY
  • SEVERITY
  • ANEMIA
  • SF-36

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