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Items where Author is Manns, K.

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Number of items: 4.

Article

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

Camilleri, Raymond and Mackie, I.J. and Liesner, R. and Chen, W. and Manns, K. and Machin, S. 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 and Mackie, I.J. and Liesner, R. and Chen, W. and Manns, K. and Hunt, B. and Machin, S. 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 Wed Jul 30 08:03:35 2014 BST.