Correlation between Disease Biomarkers and Hemoglobin F Levels in Sickle Cell Patients
Casey Gazza(Augusta University), Abdullah Kutlar(Augusta University), Asim Ahmed(Augusta University), Elena Wernecke(Augusta University), Neha Balachandran, Siera Gollan(Augusta University), Daniel Herrera(Augusta University), Heath Aston(Augusta University), Faizan Boghani(Augusta University), Satya Jella(Augusta University), Ahmed Shetewi(Augusta University), Hongyan Xu(Augusta University), Emma Hazenberg(Augusta University), Girindra Raval(Augusta University)
Cited by 4
Related Papers
Depression, sleep and pain affect instrumental activities of daily living through cognitive functioning in adults with sickle cell disease: A report from the Sickle Cell Disease Implementation Consortium
|British Journal of Haematology|2024|5
Burden of Aging: Health Outcomes Among Adolescents and Young Adults With Sickle Cell Disease
|HemaSphere|2023|4
The role of hemoglobin F in sickle cell disease complications: a descriptive secondary analysis
|Blood Vessels Thrombosis & Hemostasis|2025|1