Sickle cell disease and adolescents’ perspectives on self-care management resources

Author:

Clayton-Jones Dora L.ORCID,Hamilton Jill B.,Haglund Kristin,Ong Lee Za,Kennedy Kalen C.,Pena Sylvia,Stamper Latoya,Jenerette CorettaORCID

Publisher

Elsevier BV

Reference55 articles.

1. National Center on Birth Defects and Developmental Disabilities. Data & statistics on sickle cell disease. Centers for Disease Control and Prevention. Reviewed May 2, 2022. 〈https://www.cdc.gov/ncbddd/sicklecell/data.html〉. Accessed March 13, 2023.

2. Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management [published correction appears in Scientific World Journal;Ballas;Sci World J,2013

3. The number of people with sickle-cell disease in the United States: national and state estimates;Brousseau;Am J Hematol,2010

4. Transition from child-centered to adult health-care systems for adolescents with chronic conditions. A position paper of the Society for Adolescent Medicine;Blum;J Adolesc Health,1993

5. National Alliance to Advance Adolescent Health. Six core elements of health care transition. Got® Transition. 〈https://www.gottransition.org/six-core-elements〉 Accessed 13 March 2023.

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