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