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Number of items: 21.

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

Camilleri, Raymond, Cohen, H., Mackie, I.J., Skully, M., Starke, R.D., Crawley, J.T., Lane, D.A. and Machin, S.J. (2008) Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura. Journal of Thrombosis and Haemostasis, 6 (2). pp. 331-338. ISSN 1538-7933

Nash, M.J., Camilleri, Raymond, Kunka, S., Mackie, I.J., Machin, S.J. and Cohen, Hannah (2004) The anticardiolipin assay is required for sensitive screening for antiphospholipid antibodies. Journal of Thrombosis and Haemostasis, 2 (7). pp. 1077-1081. ISSN 1538-7933

Camilleri, Raymond, Mackie, I.J., Humphries, Steve E., Machin, S.J. and Cohen, Hannah (2003) Lack of association of ?2-glycoprotein I polymorphisms Val247Leu and Trp316Ser with antiphospholipid antibodies in patients with thrombosis and pregnancy complications. British Journal of Haematology, 120 (6). pp. 1066-1072. ISSN 0007-1048

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

Starke, Richard, Drummond, Olive, MacGregor, Ian, Biggerstaff, John, Gale, Rosemary, Camilleri, Raymond, Mackie, I.J., Machin, S.J. and Harrison, Paul (2002) The expression of prion protein by endothelial cells: a source of the plasma form of prion protein? British Journal of Haematology, 119 (3). pp. 863-873. 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, Cohen, Hannah, Mackie, I.J., Scully, M., Starke, R.D., Crawley, J.T.B., Lane, D.A. and Machin, S.J. (2007) Six adult onset TTP patients with several ADAMTS13 polymorphisms and a missense mutation (R1060W) that exhibits defective secretion in vitro. In: XXIst Congress of the International Society on Thrombosis and Haemostasis, Geneva, Switzerland. (Submitted)

Camilleri, Raymond, Mackie, I.J., Scully, M., Starke, R.D., Crawley, J.T.B., Lane, D.A., Machin, S.J. and Cohen, Hannah (2006) The ADAMTS13 missense mutant R1060W, found in six patients with adult onset TTP, exhibits a secretion defect in vitro. In: British society for haemostasis and thrombosis (BSHT) scientific meeting, Jersey, UK. (Submitted)

Camilleri, Raymond, Mackie, I.J., Scully, M., Machin, S.J. and Cohen, Hannah (2005) ADAMTS13 gene mutations and polymorphisms in acquired thrombotic thrombocytopenic purpura (TTP) patients. In: XXth Congress of the international society on thrombosis and haemostasis, Sydney, Australia. (Submitted)

Camilleri, Raymond, Mackie, I.J., Scully, M., Machin, S.J. and Cohen, Hannah (2005) A genetic basis for adult onset TTP? In: American society of haematology 47th annual meeting, Atlanta, Georgia, USA.. (Submitted)

Camilleri, Raymond, Mackie, I.J., Scully, M., Machin, S.J. and Cohen, Hannah (2005) A novel mutation in the ADAMTS13 gene of patients with adult onset TTP. In: British society for haemostasis and thrombosis (BSHT) scientific meeting, Chester, UK. (Submitted)

Camilleri, Raymond, Mackie, I.J. and Cohen, Hannah (2004) ADAMTS13 gene mutations and polymorphisms in thrombotic thrombocytopenic purpura patients. In: British society for haemostasis and thrombosis (BSHT) scientific meeting, Edinburgh, UK. (Submitted)

Nash, M.J., Camilleri, Raymond, Kunka, S., Mackie, I.J., Machin, S.J. and Cohen, Hannah (2003) A proposed ISTH revised classification for the antiphospholipid syndrome. In: XIXth Congress of the International Society on Thrombosis and Haemostasis (ISTH), , Birmingham, UK. (Submitted)

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)

Camilleri, Raymond, Al-Mulla, N., Mackie, I.J. and Cohen, Hannah (2001) The ?2-glycoprotein I Trp316Ser polymorphism does not protect against the development of primary antiphospholipid syndrome. In: 41st Annual Scientific Meeting, British society for haematology (BSH), Harrogate, UK. (Submitted)

Camilleri, Raymond, Al-Mulla, N., Mackie, I.J. and Cohen, Hannah (2001) Clinical significance of ?2-glycoprotein I polymorphisms Trp316Ser and Val247Leu in a PAPS population. In: European forum for antiphospholipid antibodies, Utrecht, Netherlands. (Submitted)

Camilleri, Raymond, Al-Mulla, N., Mackie, I.J., Humphries, Steve E. and Cohen, Hannah (2001) Clinical significance of ?2-glycoprotein I polymorphisms Val247Leu and Trp316Ser in an antiphospholipid syndrome (APS) population. In: British society for haemostasis and thrombosis (BSHT) scientific meeting, Bath, UK. (Submitted)

Camilleri, Raymond, Al-Mulla, N., Mackie, I.J. and Cohen, Hannah (2001) Lack of a protective effect of the ?2-glycoprotein I Trp316Ser polymorphism on the development of primary antiphospholipid syndrome. In: XVIIIth Congress of the international society on thrombosis and haemostasis (ISTH), Paris, France. (Submitted)

This list was generated on Fri Jul 22 23:31:41 2016 BST.