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Illness Intrusiveness in Adults with Sickle Cell Disease: The Role of Fatigue

Journal of clinical psychology in medical settings, 2023-12, Vol.30 (4), p.866-875

2023

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Marijuana use and health behaviors in a US clinic sample of patients with sickle cell disease

PloS one, 2020-07, Vol.15 (7), p.e0235192-e0235192

2020

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Herman G. Canady: A reintroduction

History of psychology, 2024-09

Bediako, Shawn M

2024

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Daily Loneliness Affects Quality of Life in Sickle Cell Disease

International journal of behavioral medicine, 2024-06, Vol.31 (3), p.393-398

2024

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In memoriam: Dr. Carlton Haywood, Jr. (1976–2021)

American journal of hematology, 2022-12, Vol.97 (12), p.1671-1672

2022

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Interpersonal Contexts of Communication Between Sickle Cell Disease Patients and Providers

Southern medical journal (Birmingham, Ala.), 2016-09, Vol.109 (9), p.573-575

Bediako, Shawn M.

2016

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The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study

Journal of health psychology, 2016-05, Vol.21 (5), p.808-820

2016

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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, 2016-12, Vol.32 (12), p.1076-1085

2016

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Communalism Moderates the Association Between Racial Centrality and Emergency Department Use for Sickle Cell Disease Pain

Journal of black psychology, 2017-10, Vol.43 (7), p.659-668

2017

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Psychosocial and Clinical Risk Factors Associated with Substance Use in Observational Cohort of Patients with Sickle Cell Disease

Substance use & misuse, 2020-01, Vol.55 (13), p.2205-2212

2020

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Sickle Cell Disease, More Than Just Pain: The Mediating Role of Psychological Symptoms

Southern medical journal (Birmingham, Ala.), 2019-05, Vol.112 (5), p.253-258

2019

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The Association of Provider Communication with Trust among Adults with Sickle Cell Disease

Journal of general internal medicine : JGIM, 2010-06, Vol.25 (6), p.543-548

2010

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Metabolic syndrome among adults living with sickle cell disease

Blood cells, molecules, & diseases, 2019-02, Vol.74, p.25-29

2019

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Race and social attitudes about sickle cell disease

Ethnicity & health, 2011-08, Vol.16 (4-5), p.423-429

2011

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Sickle Cell Disease in a "Postracial" America

Journal of the National Medical Association, 2009-10, Vol.101 (10), p.1065-1066

2009

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Predictors of employment status among African Americans with sickle cell disease

Journal of health care for the poor and underserved, 2010-11, Vol.21 (4), p.1124-1137

Bediako, Shawn M

2010

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Public Support for Sickle-Cell Disease Funding: Does Race Matter?

Race and social problems, 2016-06, Vol.8 (2), p.186-195

2016

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Assessing Psychosocial Risk and Resilience to Support Readiness for Gene Therapy in Sickle Cell Disease: A Consensus Statement

JAMA network open, 2024-08, Vol.7 (8), p.e2429443

2024

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Daily Mood and Stress Predict Pain, Health Care Use, and Work Activity in African American Adults With Sickle-Cell Disease

Health psychology, 2004-05, Vol.23 (3), p.267-274

2004

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Problematic hospital experiences among adult patients with sickle cell disease

Journal of health care for the poor and underserved, 2010-11, Vol.21 (4), p.1114-1123

2010

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Health care provider attitudes toward patients with acute vaso-occlusive crisis due to sickle cell disease: Development of a scale

Patient education and counseling, 2009-08, Vol.76 (2), p.272-278

2009

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Religious coping and hospital admissions among adults with sickle cell disease

Journal of behavioral medicine, 2011-04, Vol.34 (2), p.120-127

2011

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Depressive Symptoms and Sickle Cell Pain: The Moderating Role of Internalized Stigma

Stigma and health (Washington, D.C.), 2017-11, Vol.2 (4), p.271-280

2017

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Hospital self-discharge among adults with sickle-cell disease (SCD): Associations with trust and interpersonal experiences with care

Journal of hospital medicine, 2010-05, Vol.5 (5), p.289-294

2010

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Optimism and Perceived Stress in Sickle-Cell Disease: The Role of an Afrocultural Social Ethos

Journal of black psychology, 2011-05, Vol.37 (2), p.234-253

2011

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Illness Intrusiveness in Adults with Sickle Cell Disease: The Role of Fatigue

Marijuana use and health behaviors in a US clinic sample of patients with sickle cell disease

Herman G. Canady: A reintroduction

Daily Loneliness Affects Quality of Life in Sickle Cell Disease

In memoriam: Dr. Carlton Haywood, Jr. (1976–2021)

Interpersonal Contexts of Communication Between Sickle Cell Disease Patients and Providers

The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study

Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell Disease

Communalism Moderates the Association Between Racial Centrality and Emergency Department Use for Sickle Cell Disease Pain

Psychosocial and Clinical Risk Factors Associated with Substance Use in Observational Cohort of Patients with Sickle Cell Disease

Sickle Cell Disease, More Than Just Pain: The Mediating Role of Psychological Symptoms

The Association of Provider Communication with Trust among Adults with Sickle Cell Disease

Metabolic syndrome among adults living with sickle cell disease

Race and social attitudes about sickle cell disease

Sickle Cell Disease in a "Postracial" America

Predictors of employment status among African Americans with sickle cell disease

Public Support for Sickle-Cell Disease Funding: Does Race Matter?

Assessing Psychosocial Risk and Resilience to Support Readiness for Gene Therapy in Sickle Cell Disease: A Consensus Statement

Daily Mood and Stress Predict Pain, Health Care Use, and Work Activity in African American Adults With Sickle-Cell Disease

Problematic hospital experiences among adult patients with sickle cell disease

Health care provider attitudes toward patients with acute vaso-occlusive crisis due to sickle cell disease: Development of a scale

Religious coping and hospital admissions among adults with sickle cell disease

Depressive Symptoms and Sickle Cell Pain: The Moderating Role of Internalized Stigma

Hospital self-discharge among adults with sickle-cell disease (SCD): Associations with trust and interpersonal experiences with care

Optimism and Perceived Stress in Sickle-Cell Disease: The Role of an Afrocultural Social Ethos

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