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Items where Author is Manns, K.

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Number of items: 4.

2012

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

2009

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..

2008

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..

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