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British Journal of Haematology|June 26, 2024
Seeing haemoglobin SC: Challenging the misperceptionsCatherine Segbefia, Lori Luchtman-Jones
Pharmacogenomics and Personalized Medicine|March 18, 2022
Association Between Selected Single Nucleotide Polymorphisms in Globin and Related Genes and Response to Hydroxyurea Therapy in Ghanaian Children with Sickle Cell DiseaseGloria Pokuaa Manu, Catherine Segbefia, Benoit Banga N'guessan, et al.
Journal of Pediatric Hematology/Oncology|November 20, 2015
Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-ThalassemiaMarianne E M Yee, Maa-Ohui Quarmyne, Catherine Segbefia, et al.
Journal of Sickle Cell Disease|March 30, 2026
Prevalence of ocular complications of sickle cell disease in children seen at a tertiary health facility in Southern GhanaImoro Zeba Braimah, Vera M Beyuo, Catherine Segbefia, et al.
Advances in Hematology|June 25, 2026
Incidence of Induction Toxicities in Childhood Acute Lymphoblastic Leukaemia in GhanaLily Gloria Tagoe, Emmanuella Amoako, Ernestina Schandorf, et al.
Journal of Pain Research|May 18, 2026
A Multidimensional Digital Approach to Pain Assessment in Sickle Cell Disease: A Feasibility Study in GhanaModesty E Obasohan, Eugenia Vicky Asare, Charles Jonassaint, et al.
Journal of Racial and Ethnic Health Disparities|May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical ResearchAndrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
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