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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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An unequal burden: Poor patient–provider communication and sickle cell disease

Patient education and counseling, 2014-08, Vol.96 (2), p.159-164

2014

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Improving Emergency Providers’ Attitudes Toward Sickle Cell Patients in Pain

Journal of pain and symptom management, 2016-03, Vol.51 (3), p.628-632.e3

2016

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Racial differences in acute kidney injury of hospitalized adults with diabetes

Journal of diabetes and its complications, 2016-08, Vol.30 (6), p.1129-1136

2016

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Prediction of onset and course of high hospital utilization in sickle cell disease

Journal of hospital medicine, 2011-05, Vol.6 (5), p.248-255

2011

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Acute Pain and Depressive Symptoms: Independent Predictors of Insomnia Symptoms among Adults with Sickle Cell Disease

Pain management nursing, 2016-02, Vol.17 (1), p.38-46

2016

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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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Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers

Advanced emergency nursing journal, 2014-10, Vol.36 (4), p.335-347

2014

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The impact of depressive symptoms on patient-provider communication in HIV care

AIDS care, 2013-09, Vol.25 (9), p.1185-1192

2013

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What does shared decision making look like in natural settings? A mixed methods study of patient–provider conversations

Communication & medicine, 2017, Vol.14 (3), p.217-228

2017

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Mortality Rates and Age at Death from Sickle Cell Disease: U.S., 1979—2005

Public health reports (1974), 2013-03, Vol.128 (2), p.110-116

2013

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Patient reactions to personalized medicine vignettes: An experimental design

Genetics in medicine, 2011-05, Vol.13 (5), p.421-428

2011

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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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Sickle cell trait diagnosis: clinical and social implications

Hematology, 2015-12, Vol.2015 (1), p.160-167

2015

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Examining the effectiveness of hydroxyurea in people with sickle cell disease

Journal of health care for the poor and underserved, 2010-02, Vol.21 (1), p.277-286

2010

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Venous Thromboembolism in Adults with Sickle Cell Disease: A Serious and Under-recognized Complication

The American journal of medicine, 2013-05, Vol.126 (5), p.443-449

2013

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The burden of emergency department use for sickle‐cell disease: An analysis of the national emergency department sample database

American journal of hematology, 2010-10, Vol.85 (10), p.797-799

2010

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Social and Behavioral Implications of National Collegiate Athletic Association Sickle Cell Trait Screening: The Athletes’ Perspective

Journal of the Georgia Public Health Association, 2015-10, Vol.5 (2)

2015

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Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review

Annals of internal medicine, 2018-11, Vol.169 (9), p.619

2018

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The five key things you need to know to manage adult patients with sickle cell disease

Hematology, 2015-12, Vol.2015 (1), p.420-425

2015

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An evaluation of central sensitization in patients with sickle cell disease

The journal of pain, 2016-05, Vol.17 (5), p.617-627

2016

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Chronic Opioid Therapy and Central Sensitization in Sickle Cell Disease

American journal of preventive medicine, 2016-07, Vol.51 (1), p.S69-S77

2016

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Mortality and Access to Kidney Transplantation in Patients with Sickle Cell Disease-Associated Kidney Failure

Clinical journal of the American Society of Nephrology, 2021-03, Vol.16 (3), p.407-414

2021

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Perceived Discrimination in Health Care Is Associated With a Greater Burden of Pain in Sickle Cell Disease

Journal of pain and symptom management, 2014-11, Vol.48 (5), p.934-943

2014

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

An unequal burden: Poor patient–provider communication and sickle cell disease

Improving Emergency Providers’ Attitudes Toward Sickle Cell Patients in Pain

Racial differences in acute kidney injury of hospitalized adults with diabetes

Prediction of onset and course of high hospital utilization in sickle cell disease

Acute Pain and Depressive Symptoms: Independent Predictors of Insomnia Symptoms among Adults with Sickle Cell Disease

Problematic hospital experiences among adult patients with sickle cell disease

Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers

The impact of depressive symptoms on patient-provider communication in HIV care

What does shared decision making look like in natural settings? A mixed methods study of patient–provider conversations

Mortality Rates and Age at Death from Sickle Cell Disease: U.S., 1979—2005

Patient reactions to personalized medicine vignettes: An experimental design

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

Sickle cell trait diagnosis: clinical and social implications

Examining the effectiveness of hydroxyurea in people with sickle cell disease

Venous Thromboembolism in Adults with Sickle Cell Disease: A Serious and Under-recognized Complication

The burden of emergency department use for sickle‐cell disease: An analysis of the national emergency department sample database

Social and Behavioral Implications of National Collegiate Athletic Association Sickle Cell Trait Screening: The Athletes’ Perspective

Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review

The five key things you need to know to manage adult patients with sickle cell disease

An evaluation of central sensitization in patients with sickle cell disease

Chronic Opioid Therapy and Central Sensitization in Sickle Cell Disease

Mortality and Access to Kidney Transplantation in Patients with Sickle Cell Disease-Associated Kidney Failure

Perceived Discrimination in Health Care Is Associated With a Greater Burden of Pain in Sickle Cell Disease

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

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