Publications
Journals
Telfer P, Anie KA, Kotsiopoulou S, et al., 2024, The acute pain crisis in sickle cell disease: What can be done to improve outcomes?, Blood Rev, Vol:65
Munung NS, Kamga KK, Treadwell MJ, et al., 2024, Perceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania., Eur J Hum Genet
Munung NS, Treadwell M, Kamga KK, et al., 2024, Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries., Qual Life Res, Vol:33, Pages:423-432
Paintsil V, Ally M, Isa H, et al., 2023, Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica, Frontiers in Genetics, Vol:13
Munung NS, Nembaware V, Osei-Tutu L, et al., 2022, Assent, parental consent and reconsent for health research in Africa: thematic analysis of national guidelines and lessons from the SickleInAfrica registry., Bmc Med Ethics, Vol:23