Similar articles

• An unequal burden: poor patient-provider communication and sickle cell disease.

  Haywood C Jr, Bediako S, Lanzkron S, Diener-West M, Strouse J, Haythornthwaite J, Onojobi G, Beach MC; IMPORT Investigators. Haywood C Jr, et al. Patient Educ Couns. 2014 Aug;96(2):159-64. doi: 10.1016/j.pec.2014.05.013. Epub 2014 May 23. Patient Educ Couns. 2014. PMID: 24935607 Free PMC article.
• A patient's perspective on sickle cell disease treatment.

  Dames-Fincher G. Dames-Fincher G. J Natl Med Assoc. 1992 Sep;84(9):739, 741. J Natl Med Assoc. 1992. PMID: 1404470 Free PMC article. No abstract available.
• The role of family: perceptions of children with sickle cell.

  Lee EJ, Phoenix D, Jackson BS, Brown W. Lee EJ, et al. J Natl Black Nurses Assoc. 1999 Fall-Winter;10(2):37-45. J Natl Black Nurses Assoc. 1999. PMID: 10732595
• African-American families with chronically ill children: oversights and insights.

  Sterling YM, Peterson J, Weekes DP. Sterling YM, et al. J Pediatr Nurs. 1997 Oct;12(5):292-300. doi: 10.1016/S0882-5963(97)80047-4. J Pediatr Nurs. 1997. PMID: 9330505 Review.
• Depression and anxiety in patients with sickle cell disease: conceptual and methodological considerations.

  Molock SD, Belgrave FZ. Molock SD, et al. J Health Soc Policy. 1994;5(3-4):39-53. doi: 10.1300/J045v05n03_04. J Health Soc Policy. 1994. PMID: 10138762 Review.