Biree Andemariam
Biographic Data
| ID | 92767 |
|---|---|
| NAME | Biree Andemariam |
| GIVEN NAMES | Biree |
| FAMILY NAME | Andemariam |
| SIGNATURE | ANDEMARIAM B |
| AFFILIATIONS | UConn Health |
| ORCID | 0000-0002-2540-6037 |
| VERIFIED | Yes |
| TOTAL WORKS | 4 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 4 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2016 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Motivators and Barriers Affecting Decisions to Participate in Clinical Trials for Sickle Cell Disease: United States Findings from the Quantitative Listen Survey
Sickle cell disease (SCD) is an inherited blood disorder that results in abnormal hemoglobin and crescent-shaped red blood cells. While SCD was discovered over a century ago, it has historically had fewer new drugs in development compared with other conditions, negatively impacting patients’ therapeutic options. Recently, there has been a substantial increase in the development of novel therapies for SCD, but the perception that people with SCD (…
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research
Exploring Transition to Self-Management Within the Culture of Sickle Cell Disease
Purpose: The aim of this study was to explore the meaning of transition to self-management in sickle cell disease. Design/Method: Twelve audio-recorded semistructured interviews were conducted with a sample of 21- to 25-year-olds recruited from a comprehensive sickle cell center in the northeast region of the United States. Data were analyzed using an existential framework according to van Manen’s phenomenological method. Findings: The meaning of…
Development of a New Adult Sickle Cell Disease Center Within an Academic Cancer Center: Impact on Hospital Utilization Patterns and Care Quality
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Development of a New Adult Sickle Cell Disease Center Within an Academic Cancer Center: Impact on Hospital Utilization Patterns and Care Quality
Exploring Transition to Self-Management Within the Culture of Sickle Cell Disease
Purpose: The aim of this study was to explore the meaning of transition to self-management in sickle cell disease. Design/Method: Twelve audio-recorded semistructured interviews were conducted with a sample of 21- to 25-year-olds recruited from a comprehensive sickle cell center in the northeast region of the United States. Data were analyzed using an existential framework according to van Manen’s phenomenological method. Findings: The meaning of…
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research
Motivators and Barriers Affecting Decisions to Participate in Clinical Trials for Sickle Cell Disease: United States Findings from the Quantitative Listen Survey
Sickle cell disease (SCD) is an inherited blood disorder that results in abnormal hemoglobin and crescent-shaped red blood cells. While SCD was discovered over a century ago, it has historically had fewer new drugs in development compared with other conditions, negatively impacting patients’ therapeutic options. Recently, there has been a substantial increase in the development of novel therapies for SCD, but the perception that people with SCD (…
Disease (4 works) · Hemoglobinopathies and Related Disorders (4 works) · Medicine (3 works) · Pathology (3 works) · Public health (3 works) · Epidemiology (2 works) · Health care (2 works) · Internal Medicine (2 works) · Iron Metabolism and Disorders (2 works) · Alternative medicine (1 works)