Perceptions of Care and Perceived Discrimination: A Qualitative Assessment of Adults Living with Sickle Cell Disease
Author:
Funder
Yale School of Medicine
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40615-024-02153-3.pdf
Reference41 articles.
1. Hassell KL. Population estimates of sickle cell disease in the U.S. Am J Prev Med. 2010;38(4 Suppl):512–21.
2. Fu Y, Andemariam B, Herman C. Estimating sickle cell disease prevalence by state: a model using US-born and foreign-born state-specific population data. Blood. 2023;142(Supplement 1):3900–3900.
3. Platt OS, et al. Mortality in sickle cell disease – life expectancy and risk factors for early death. N Engl J Med. 1994;330(23):1639–44.
4. Shah N, et al. Treatment patterns and economic burden of sickle-cell disease patients prescribed hydroxyurea: a retrospective claims-based study. Health Qual Life Outcomes. 2019;17(1):155.
5. Steinberg MH, et al. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA. 2003;289(13):1645–51.
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