Tom Williams/Br J Haematol

Transfusion management of severe anaemia in African children: a consensus algorithm.Maitland K, Kiguli S, Olupot-Olupot P, Opoka RO, Chimalizeni Y, Alaroker F, Uyoga S, Kyeyune-Byabazaire D, M'Baya B, Bates I, Williams TN, Munube D, Mbanya D, Molyneux EM, South A, Walker AS, Gibb DM, George EC, 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 OA, Opiyo M, Orori EN, Williams TN, 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 AN, Ajala-Agbo T, Newton CR, Marsh K, Williams TN
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 FJ, Komba A, Ajala-Agbo T, Otieno G, Fegan G, Williams TN, Marsh K, Newton CR
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 TN
Br J Haematol, (2006). 133:206-9

The membrane characteristics of Plasmodium falciparum-infected and -uninfected heterozygous alpha(0)thalassaemic erythrocytes.Williams TN, Weatherall DJ, Newbold CI
Br J Haematol, (2002). 118:663-70