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Baba Inusa
Project Scientific Coordinator and PMT Member
Professor Baba P D Inusa
Graduated MBBS, ABU Zaria, Nigeria 1984
Chair, National Haemoglobinopathy Panel; www.nationalhaempanel-nhs.net
Founder, Academy for sickle cell and thalassaemia (ASCAT) https://www.ascat2022.com
Founder of the sickle cell cohort research foundation, Nigeria (SCORE): www.scorecharity.com
Co-Chair Treatment Subcommittee of Consortium on Newborn Screening Africa (CONSA) and ASH Visitors training programme supervisor. Consortium on Newborn Screening in Africa – Hematology.org
Principal Investigator, African Research and Innovative Initiative for sickle cell education: improving research for service (ARISE) EU, Africa, Lebanon and UIC at Chicago.
His research interest includes Newborn screening, stroke and renal impairment in sickle cell disease, with special interest in global haematology
He has published over 130 peer review papers and edited a book and book chapters as well as a reviewer and editorial board member of high impact journals.
He supervises Masters and PhD students at KCL.
Latest News & Events
Keep updated on all the initiatives and events of the ARISE project
Join the HELIOS Webinar Series and Advance Your Knowledge on Haemoglobinopathies
The ARISE Initiative is pleased to inform you about the webinar series on haemoglobinopathies organised by HELIOS, the European network dedicated to raising awareness on haemoglobinopathies (HBs) and improving access to expert knowledge. As part of its efforts to...
Participate in a Study on Sickle Cell Disease Management in Nigeria
ARISE is conducting a questionnaire-based study, with the aim to map and analyse the organisation of the healthcare centres managing SCD in in relation with accessibility and readiness of specific health technologies (i.e., blood transfusion service, Magnetic...
An interview with a Sickle cell disease patient living in Portugal
Living with a rare disease like sickle cell disease is not easy. We asked a Portuguese patient to tell us about his experience with this disease. Read his story.