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Arabic version of the patient education materials assessment tool (PEMAT): translation and validation.
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Determinants of retention in care of newborns diagnosed with sickle cell disease in Liberia: Results from a mixed-methods study of caregivers.
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Variability in sickle cell knowledge by sickle cell status.
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Health Literacy, Perceived Stigma, Self-Efficacy, and HRQOL in Sickle Cell Disease.
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A Health Literate Approach to Address Health Disparities: a Virtual Program for Parents of Children with Sickle Cell Trait.
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Chronic pediatric diseases and risk for reading difficulties: a narrative review with recommendations.
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The CDC Clear Communication Index is a new evidence-based tool to prepare and review health information.
Health Promot Pract. 2014 Sep;15(5):629-37. doi: 10.1177/1524839914538969. Epub 2014 Jun 20.
4
A qualitative study of staff perspectives of patient non-attendance in a regional primary healthcare setting.
Australas Med J. 2014 May 31;7(5):218-26. doi: 10.4066/AMJ.2014.2056. eCollection 2014.
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Six components necessary for effective public health program implementation.
Am J Public Health. 2014 Jan;104(1):17-22. doi: 10.2105/AJPH.2013.301608. Epub 2013 Nov 14.
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Low health literacy and health outcomes: an updated systematic review.
Ann Intern Med. 2011 Jul 19;155(2):97-107. doi: 10.7326/0003-4819-155-2-201107190-00005.
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Improving Americans' health literacy.
N Engl J Med. 2010 Dec 9;363(24):2283-5. doi: 10.1056/NEJMp1008755.
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Population estimates of sickle cell disease in the U.S.
Am J Prev Med. 2010 Apr;38(4 Suppl):S512-21. doi: 10.1016/j.amepre.2009.12.022.
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JAMA patient page. Sickle cell vasculopathy.
JAMA. 2008 Dec 10;300(22):2690. doi: 10.1001/jama.300.22.2690.

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