Shawn Bediako
Affiliations: | Psychology | University of Maryland, Baltimore County, Baltimore, MD, United States |
Area:
Developmental Psychology, Physiological Psychology, Social PsychologyGoogle:
"Shawn Bediako"Mean distance: 106866
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Publications
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Wilson JD, Lanzkron S, Pecker LH, et al. (2020) Psychosocial and Clinical Risk Factors Associated with Substance Use in Observational Cohort of Patients with Sickle Cell Disease. Substance Use & Misuse. 1-8 |
Robbins MA, McGill LS, Holloway BM, et al. (2019) Sickle Cell Disease, More Than Just Pain: The Mediating Role of Psychological Symptoms. Southern Medical Journal. 112: 253-258 |
Bediako SM. (2018) Interpersonal Contexts of Communication Between Sickle Cell Disease Patients and Providers. Southern Medical Journal. 109: 573-5 |
Bediako SM, Harris C. (2017) Communalism Moderates the Association Between Racial Centrality and Emergency Department Use for Sickle Cell Disease Pain. The Journal of Black Psychology. 43: 659-668 |
Holloway BM, McGill LS, Bediako SM. (2017) Depressive symptoms and sickle cell pain: The moderating role of internalized stigma. Stigma and Health. 2: 271-280 |
Mathur VA, Kiley KB, Haywood C, et al. (2016) Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell Disease. The Clinical Journal of Pain |
Haywood C, Lanzkron S, Bediako S, et al. (2014) Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease. Journal of General Internal Medicine. 29: 1657-62 |
Bediako SM, Lanzkron S, Diener-West M, et al. (2014) The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study. Journal of Health Psychology |
Haywood C, Bediako S, Lanzkron S, et al. (2014) An unequal burden: poor patient-provider communication and sickle cell disease. Patient Education and Counseling. 96: 159-64 |
Haywood C, Diener-West M, Strouse J, et al. (2014) Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease. Journal of Pain and Symptom Management. 48: 934-43 |