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Resorce #1
Thomas, V. J., and L. M. Taylor. "The psychosocial experience of people with sickle cell disease and its impact on quality of life: Qualitative findings from focus groups." British journal of health psychology 7.3 (2002): 345-363. -
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Resource Timeline
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Resource #2
Palermo, Tonya Mizell, et al. "Parental report of health-related quality of life in children with sickle cell disease." Journal of behavioral medicine 25.3 (2002): 269-283. -
Resource #3
Smith, Wally R., et al. "Daily assessment of pain in adults with sickle cell disease." Annals of internal medicine 148.2 (2008): 94-101. -
Resource #4
Panepinto, Julie A., and Melanie Bonner. "Health‐related quality of life in sickle cell disease: Past, present, and future." Pediatric blood & cancer 59.2 (2012): 377-385. -
Resource #5
DeBaun, Michael R., and Joseph Telfair. "Transition and sickle cell disease." Pediatrics 130.5 (2012): 926-935. -
Resource #6
McCavit, Timothy L., et al. "National trends in incidence rates of hospitalization for stroke in children with sickle cell disease." Pediatric blood & cancer 60.5 (2013): 823-827.