طبيب كيث سبسن

Towner, S., Berger, Z., Titman, P., New, H., Theodore, K., Brown, G., Sibson, K. 2017. The psychological profile of children with immune thrombocytopenia. Submitted to Br J Haematol. 

Sibson, K., Biss, T., Furness, C., Grainger, J., Hough, R., Macartney, C., Payne, J., Chalmers, E. 2017. BSH Guideline: Management of thombotic and haemostatic issues in paediatric malignancy. Br J Haematol [in print].  

Alwan, F., Vendramin, C., Vanhoorelbeke, K., Langley, K., McDonald, V., Austin, S., Clark, A., Lester, W., Gooding, R., Biss, T., Dutt, T., Cooper, N., Chapman, O., Cranfield, T., Douglas, K., Watson, H., van Veen, J., Sibson, K., Thomas, W., Manson, L., Hill, Q., Benjamin, S., Ellis, D., Westwood, J., Thomas, M., Scully, M. 2017. Presenting ADAMTS13 antibody and antigen levels predict prognosis in immune-mediated thrombotic thrombocytopenic purpura. Blood  

Thachil, J., Bagot, C., Bradbury, C., Cooper, N., Lester, W., Grainger, J., Lowe, G., Evans, G., Talks, K., Sibson, K., Garg, M., Murphy, M., Watson, H., Bolton-Maggs, P., Watson, S., Scully, M., Provan, D., Newland, A., Hill, Q. 2017. A United Kingdom Immune Thrombocytopenia Forum review of practice: thrombopoietin receptor agonists. Br J Haematol [Epub ahead of print]. 

Fosbury, E., Szychot, E., Slater, O., Mathias, M., Sibson, K. 2017. An 11-year experience of acquired von Willebrand syndrome in children diagnosed with Wilms tumour in a tertiary referral centre. Pediatr Blood Cancer [Epub ahead of print].  

Biss, T., Payne, J., Hough, R., Grainger, J., Macartney, C., Sibson, K., Chalmers, E. 2016. Strategies to prevent and manage thrombotic complications of acute lymphoblastic leukaemia in children and young people vary between centres in the United Kingdom. J Pediatr Hematol Oncol. 

Fosbury, E., Blumberg, R., Liesner, R., Sibson, K. 2016. Lessons from a neonate with unusual bleeding. J Haem Pract. 

Smith, F., Brawand, D., Steedman, L., Oakley, M., Wall, C., Rushton, P., Allchurch, M., Sibson, K., Hemmaway, C., Thein, S., Rees, D., Clark, B. 2015. A comprehensive next generation sequencing gene panel focused on unexplained anaemia. ASH abstract 946.  

Shahni, R., Wedatilake, Y., Cleary, M., Lindley, K., Sibson, K., Rahman, S. 2013. A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anaemia (MLASA) phenotype associates with YARS2 mutations. American Journal of Medical Genetics.  

O’Connor, D., Sibson, K., Caswell, M., Connor, P., Cummins, M,. Mitchell, C., Motwani, J., Taj, M., Vora, A., Wynn, R., Kearns, P. 2011. Early UK experience in the use of clofarabine in the treatment of relapsed and refractory paediatric acute lymphoblastic leukaemia. British Journal of Haematology.