Browse by People

Up a level
Export as [feed] Atom [feed] RSS [feed] RSSPD
Group by: Item Type | No Grouping
Number of items: 6.

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

Nash, M.J., Camilleri, Raymond, Liesner, R., Mackie, I.J., Machin, S.J. and Cohen, Hannah (2003) Paradoxical association between the 316 Trp to Ser beta 2-glycoprotein I (Beta2GPI) polymorphism and anti-Beta2GPI antibodies. British Journal of Haematology, 120 (3). pp. 529-531. ISSN 0007-1048

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..

Camilleri, Raymond, Nash, M.J., Liesner, R., Mackie, I.J., Machin, S.J. and Cohen, Hannah (2002) Ser316Ser ?2-glycoprotein I variant with reduced binding to phospholipid associated with anti-?2-glycoprotein I antibodies in a patient with pregnancy complications. In: 10th International congress on antiphospholipid antibodies, Taormina, Sicily, Italy. (Submitted)

This list was generated on Thu Dec 8 23:45:51 2016 GMT.