Area of research
Genetics · Hematology
Research interest
Research interests include Medicine, Disease, Emergency department, Sickle cell anemia, Acute chest syndrome, and Health care.
Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registry
The clinical spectrum of <scp>HbSC</scp> sickle cell disease‐not a benign condition
DISPLACE study shows poor quality of transcranial doppler ultrasound for stroke risk screening in sickle cell anemia
Hereditary Spherocytosis with Mitochondrial Retention, Increased Oxidative Stress, and Alterations to Bioactive Membrane Lipids
Intranasal fentanyl and discharge from the emergency department among children with sickle cell disease and vaso‐occlusive pain: A multicenter pediatric emergency medicine perspective
A multilevel mHealth intervention boosts adherence to hydroxyurea in individuals with sickle cell disease
“The project did not come to us with a solution”: Perspectives of research teams on implementing a study about electronic health record-embedded individualized pain plans for emergency department treatment of vaso-occlusive episodes in adults with sickle cell disease
Perspectives of individuals with sickle cell disease on barriers to care
COVID-19 and Sickle Cell Disease–Related Deaths Reported in the United States
Consensus definition of essential, optimal, and suggested components of a pediatric sickle cell disease center
Motivators and Barriers to Physical Activity among Youth with Sickle Cell Disease: Brief Review
Adherence to <scp>NHLBI</scp> guidelines for the emergent management of <scp>vaso‐occlusive</scp> episodes in children with sickle cell disease: A multicenter perspective
Implementation of Complex Interventions
Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease
Patient‐reported neurocognitive symptoms influence instrumental activities of daily living in sickle cell disease
Safety of maximal cardiopulmonary exercise testing in individuals with sickle cell disease: a systematic review
A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department
Paediatric to adult transition care for patients with sickle cell disease: a global perspective
Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment
Normal saline bolus use in pediatric emergency departments is associated with poorer pain control in children with sickle cell anemia and vaso‐occlusive pain
Design of the patient navigator to Reduce Readmissions (PArTNER) study: A pragmatic clinical effectiveness trial
“Maximum tolerated dose” vs “fixed low‐dose” hydroxyurea for treatment of adults with sickle cell anemia
A Phase 3 Trial of <scp>l</scp> -Glutamine in Sickle Cell Disease
The sickle cell disease implementation consortium: Translating evidence‐based guidelines into practice for sickle cell disease
White Paper: Pathways to Progress in Newborn Screening for Sickle Cell Disease in Sub-Saharan Africa
Red blood cell alloimmunization in sickle cell disease: assessment of transfusion protocols during two time periods
A dose‐ranging study of ticagrelor in children aged 3‐17 years with sickle cell disease: A 2‐part phase 2 study
Health-Related Quality of Life and Personal Life Goals of Adults With Sickle Cell Disease After Hematopoietic Stem Cell Transplantation
Fixed low‐dose hydroxyurea for the treatment of adults with sickle cell anemia in<scp>N</scp>igeria
Oral tetrahydrouridine and decitabine for non-cytotoxic epigenetic gene regulation in sickle cell disease: A randomized phase 1 study