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Research Christine Briscoe 12/6/25 Research Christine Briscoe 12/6/25

Motivators and barriers affecting decisions to participate in sickle cell disease clinical trials in the global Learning and Insights into Sickle Cell Trial Experiences Survey

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Research Christine Briscoe 12/6/25 Research Christine Briscoe 12/6/25

Increasing ketamine administration in children's hospitals for youth with sickle cell disease

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Research Christine Briscoe 12/1/25 Research Christine Briscoe 12/1/25

Adherence, treatment utilization, clinical and economic outcomes of patients with sickle cell disease with recurrent vaso-occlusive crises treated with recently approved chronic therapies in the US

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Research Christine Briscoe 12/1/25 Research Christine Briscoe 12/1/25

Community Health Worker and Mobile Health Interventions for Quality of Life Among Young Adults With Sickle Cell DiseaseA Randomized Clinical Trial

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Research Christine Briscoe 11/26/25 Research Christine Briscoe 11/26/25

International Variations in Body Mass Index within the CASiRe Global Cohort ofSickle Cell Disease Patients

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Research Christine Briscoe 11/17/25 Research Christine Briscoe 11/17/25

National Alliance of Sickle Cell Centers Consensus Recommendations on Sickle Cell Disease Health Maintenance: A Consensus Statement

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Research Christine Briscoe 9/14/25 Research Christine Briscoe 9/14/25

Patient Perspectives on Enhancing Clinician Communication About Pain in Sickle Cell Disease

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Research Christine Briscoe 6/11/25 Research Christine Briscoe 6/11/25

Etavopivat Reduces Incidence of Vaso-occlusive Crises inPatients With Sickle Cell Disease: Hibiscus Trial Phase 2 Results through 52 Weeks

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Research Christine Briscoe 5/15/25 Research Christine Briscoe 5/15/25

Initial evaluation of an intervention to address provider implicit bias in pediatric sickle cell disease pain care: A mixed methods pilot study

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Research Christine Briscoe 5/15/25 Research Christine Briscoe 5/15/25

Is the early use of ketamine effective as an opioid sparing adjunct for treating pain in sickle cell disease patients?

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Research Christine Briscoe 5/1/25 Research Christine Briscoe 5/1/25

An Ethical Allocation Scheme for Scarce Gene Therapies in Sickle Cell Disease andTransfusion-Dependent β-Thalassemia

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Research Christine Briscoe 4/23/25 Research Christine Briscoe 4/23/25

Screen of the ReFRAME Compound Library for Therapeutic Agents to Prevent Red Blood Cell Sickling Using an Improved High Throughput Sickling Assay

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Research Christine Briscoe 4/23/25 Research Christine Briscoe 4/23/25

Clinical and Economic Burden of Managing Patientswith Sickle Cell Disease Receiving Frequent Red BloodCell Transfusions in the United States

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Research Christine Briscoe 4/9/25 Research Christine Briscoe 4/9/25

Understanding and treating menstruation associated sickle cell pain

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Research Christine Briscoe 3/31/25 Research Christine Briscoe 3/31/25

Retinal Imaging Biomarkers and Correlation to Systemic Disease Activity in Pediatric Sickle Cell Disease

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Research Christine Briscoe 3/27/25 Research Christine Briscoe 3/27/25

Sickle Cell Trait Does Not Cause “Sickle Cell Crisis” Leading to Exertion-RelatedDeath: A Systematic Review

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Research Christine Briscoe 3/27/25 Research Christine Briscoe 3/27/25

Hematology training in Africa: from brain drain to brain gain

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Research Christine Briscoe 3/27/25 Research Christine Briscoe 3/27/25

IMPACT OF INDIVIDUALIZED VERSUS WEIGHT-BASED PAIN PROTOCOLS ON PATIENT SATISFACTION FOR PATIENTS WITH SICKLE CELL DISEASE EXPERIENCING A VASO-OCCLUSIVE EPISODE

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Research Christine Briscoe 11/17/24 Research Christine Briscoe 11/17/24

Trends in Sickle Cell Disease Mortality: 1979–2020

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Research Christine Briscoe 10/29/24 Research Christine Briscoe 10/29/24

Hematopoietic Cell Transplant compared with Standard Care in Adolescents and Young Adults with Sickle Cell Disease

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