Related references
Note: Only part of the references are listed.Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care
Julie Kanter et al.
JAMA NETWORK OPEN (2020)
A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department
Elizabeth A. Linton et al.
ANNALS OF EMERGENCY MEDICINE (2020)
Clinical outcomes and healthcare utilization in patients with sickle cell disease: a nationwide cohort study of Medicaid beneficiaries
Rishi J. Desai et al.
ANNALS OF HEMATOLOGY (2020)
Intentional and unintentional nonadherence to hydroxyurea among people with sickle cell disease: a qualitative study
Jason R. Hodges et al.
BLOOD ADVANCES (2020)
Discordant Beliefs, Perceptions, and Experiences between Patients with Sickle Cell Disease and Their Care Teams: Insights from a Pilot Program to Support Shared Decision-Making
Kim Smith-Whitley et al.
BLOOD (2020)
The REDCap consortium: Building an international community of software platform partners
Paul A. Harris et al.
JOURNAL OF BIOMEDICAL INFORMATICS (2019)
Barriers and facilitators to care for individuals with sickle cell disease in central North Carolina: The emergency department providers' perspective
Rita Vanessa Masese et al.
PLOS ONE (2019)
Reducing Health Care Disparities in Sickle Cell Disease: A Review
LaTasha Lee et al.
PUBLIC HEALTH REPORTS (2019)
Stigma of Sickle Cell Disease: A Systematic Review
Dominique Bulgin et al.
ISSUES IN MENTAL HEALTH NURSING (2018)
The sickle cell disease implementation consortium: Translating evidence-based guidelines into practice for sickle cell disease
Lisa D. DiMartino et al.
AMERICAN JOURNAL OF HEMATOLOGY (2018)
Barriers to Care for Persons With Sickle Cell Disease: The Case Manager's Opportunity to Improve Patient Outcomes
Jill Brennan-Cook et al.
PROFESSIONAL CASE MANAGEMENT (2018)
The Effects of Race and Racial Concordance on Patient-Physician Communication: A Systematic Review of the Literature
Megan Johnson Shen et al.
JOURNAL OF RACIAL AND ETHNIC HEALTH DISPARITIES (2018)
Barriers to Care and Health Care Utilization Among the Publicly Insured
Elizabeth M. Allen et al.
MEDICAL CARE (2017)
Barriers to care and quality of primary care services in children with sickle cell disease
Eufemia Jacob et al.
JOURNAL OF ADVANCED NURSING (2016)
Perceptions of young adults with sickle cell disease concerning their disease experience
Nadine Matthie et al.
JOURNAL OF ADVANCED NURSING (2016)
Community Health Workers as Support for Sickle Cell Care
Lewis L. Hsu et al.
AMERICAN JOURNAL OF PREVENTIVE MEDICINE (2016)
Mounting Evidence of the Effectiveness and Versatility of Community Health Workers
Stewart Landers et al.
AMERICAN JOURNAL OF PUBLIC HEALTH (2016)
Using an Intersectional Approach to Study the Impact of Social Determinants of Health for African American Mothers Living With HIV
Courtney Caiola et al.
ADVANCES IN NURSING SCIENCE (2014)
An unequal burden: Poor patient-provider communication and sickle cell disease
Carlton Haywood et al.
PATIENT EDUCATION AND COUNSELING (2014)
Among emergency physicians, use of the term Sickler is associated with negative attitudes toward people with sickle cell disease
Jeffrey Glassberg et al.
AMERICAN JOURNAL OF HEMATOLOGY (2013)
Shared Decision Making to Improve Care and Reduce Costs
Emily Oshima Lee et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Age-related treatment patterns in sickle cell disease patients and the associated sickle cell complications and healthcare costs
Morey A. Blinder et al.
PEDIATRIC BLOOD & CANCER (2013)
Women's health, men's health, and gender and health: Implications of intersectionality
Olena Hankivsky
SOCIAL SCIENCE & MEDICINE (2012)
Integrating Interactive Web-Based Technology to Assess Adherence and Clinical Outcomes in Pediatric Sickle Cell Disease
Lori E. Crosby et al.
ANEMIA (2012)
When children with sickle-cell disease become adults: lack of outpatient care leads to increased use of the emergency department
Bradd G. Hemker et al.
AMERICAN JOURNAL OF HEMATOLOGY (2011)
Population Estimates of Sickle Cell Disease in the US
Kathryn L. Hassell
AMERICAN JOURNAL OF PREVENTIVE MEDICINE (2010)
Acute Care Utilization and Rehospitalizations for Sickle Cell Disease
David C. Brousseau et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)
Changes in Ambulatory Health Care Use During the Transition to Young Adulthood
S. Todd Callahan et al.
JOURNAL OF ADOLESCENT HEALTH (2010)
Research electronic data capture (REDCap)-A metadata-driven methodology and workflow process for providing translational research informatics support
Paul A. Harris et al.
JOURNAL OF BIOMEDICAL INFORMATICS (2009)
Perceived Barriers to Clinic Appointments for Adolescents With Sickle Cell Disease
Lori E. Crosby et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2009)
A primary care provider's guide to preventive and acute care management of adults and children with sickle cell disease
Ardie Pack-Mabien et al.
JOURNAL OF THE AMERICAN ACADEMY OF NURSE PRACTITIONERS (2009)
Share Paper
