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Number of items: 4.

Article

Camilleri, Raymond, Scully, M., Thomas, M., Mackie, I.J., Liesner, R., Chen, W.J., Manns, K. and Machin, S.J. (2012) A phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom. Journal of Thrombosis and Haemostasis, 10 (9). pp. 1792-1801. ISSN 1538-7933

Conference or Workshop Item

Camilleri, R., Mackie, I.J., Liesner, R., Chen, W., Manns, K., Machin, S.J. and Scully, M. (2009) Eight novel ADAMTS13 missense mutations in childhood and adult onset congenital TTP. In: PP-TH-088-XXIInd Congress of the International Society on Thrombosis and Haemostasis (ISTH), Boston, USA..

Camilleri, Raymond, Mackie, I.J., Liesner, R., Chen, W., Manns, K., Machin, S. and Scully, M. (2009) Phenotype-genotype correlation in congenital TTP. In: British Society for Haemostasis and Thrombosis, Scientific Meeting, Newcastle.

Camilleri, R., Mackie, I.J., Liesner, R., Chen, W., Manns, K., Hunt, B.J., Machin, S.J. and Scully, M. (2008) Three interesting cases demonstrating the continued heterogeneity of ADAMTS13 abnormalities. In: British Society for Haemostasis & Thrombosis Annual Meeting, Nottingham, UK..

This list was generated on Mon Jul 25 23:27:28 2016 BST.