Transfusion management of severe anaemia in African children: a consensus algorithm.Maitland, K. Kiguli, S. Olupot-Olupot, P. Opoka, R. O. Chimalizeni, Y. Alaroker, F. Uyoga, S. Kyeyune-Byabazaire, D. M'Baya, B. Bates, I. Williams, T. N. Munube, D. Mbanya, D. Molyneux, E. M. South, A. Walker, A. S. Gibb, D. M. George, E. C. Tract Stakeholders meeting group
Br J Haematol, (2021). 193:1247-1259

Transfer of 4-hydroxynonenal from parasitized to non-parasitized erythrocytes in rosettes. Proposed role in severe malaria anemia.Uyoga, S. Skorokhod, O. A. Opiyo, M. Orori, E. N. Williams, T. N. Arese, P. Schwarzer, E.
Br J Haematol, (2012). 157:116-24

An observational study of children with sickle cell disease in Kilifi, Kenya.Sadarangani, M. Makani, J. Komba, A. N. Ajala-Agbo, T. Newton, C. R. Marsh, K. Williams, T. N.
Br J Haematol, (2009). 146:675-82

Risk factors for high cerebral blood flow velocity and death in Kenyan children with Sickle Cell Anaemia: role of haemoglobin oxygen saturation and febrile illness.Makani, J. Kirkham, F. J. Komba, A. Ajala-Agbo, T. Otieno, G. Fegan, G. Williams, T. N. Marsh, K. Newton, C. R.
Br J Haematol, (2009). 145:529-32

Co-inheritance of alpha+-thalassaemia and sickle trait results in specific effects on haematological parameters.Wambua, S. Mwacharo, J. Uyoga, S. Macharia, A. Williams, T. N.
Br J Haematol, (2006). 133:206-9

The membrane characteristics of Plasmodium falciparum-infected and -uninfected heterozygous alpha(0)thalassaemic erythrocytes.Williams, T. N. Weatherall, D. J. Newbold, C. I.
Br J Haematol, (2002). 118:663-70