Perceptions of US adolescents and adults with sickle cell disease on their quality of care

Authors

Julie Kanter, University of Alabama, Birmingham
Robert Gibson, Medical College of Georgia
Raymona H. Lawrence, Georgia Southern University
Matthew P. Smeltzer, University of Memphis
Norma L. Pugh, RTI International
Jeffrey Glassberg, Mount Sinai School of Medicine
Rita V. Masese, Duke University School of Nursing
Allison A. King, Washington University School of Medicine in St. Louis
Cecelia Calhoun, Washington University School of Medicine in St. Louis
Jane S. Hankins, St. Jude Children’s Research Hospital
Marsha Treadwell, University of California, San Francisco

Journal

JAMA Network Open

Publication Date

5-1-2020

Volume

3

Issue

5

First Page

e206016

Document Type

Open Access Publication

DOI

10.1001/jamanetworkopen.2020.6016

Rights and Permissions

Kanter J, Gibson R, Lawrence RH, et al. Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care. JAMA Netw Open. 2020;3(5):e206016. doi:10.1001/jamanetworkopen.2020.6016. This is an open access article distributed under the terms of the CC-BY License. © 2020 Kanter J et al. JAMA Network Open.

Recommended Citation

Kanter, Julie; Gibson, Robert; Lawrence, Raymona H.; Smeltzer, Matthew P.; Pugh, Norma L.; Glassberg, Jeffrey; Masese, Rita V.; King, Allison A.; Calhoun, Cecelia; Hankins, Jane S.; and Treadwell, Marsha, "Perceptions of US adolescents and adults with sickle cell disease on their quality of care." JAMA Network Open. 3, 5. e206016 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/9263