The ADAMTS13 missense mutant R1060W, found in six patients with adult onset TTP, exhibits a secretion defect in vitroĬamilleri, R., Mackie, I.J., Scully, M., Starke, R.D., Crawley, J.T.B., Lane, D.A., Machin, S.J. XXIst Congress of the International Society on Thrombosis and Haemostasis. Six adult onset TTP patients with several ADAMTS13 polymorphisms and a missense mutation (R1060W) that exhibits defective secretion in vitro. Six adult onset TTP patients with several ADAMTS13 polymorphisms and a missense mutation (R1060W) that exhibits defective secretion in vitroĬamilleri, R., Cohen, H., Mackie, I.J., Scully, M., Starke, R.D., Crawley, J.T.B., Lane, D.A. British Society for Haemostasis & Thrombosis Annual Meeting. Three interesting cases demonstrating the continued heterogeneity of ADAMTS13 abnormalities. Three interesting cases demonstrating the continued heterogeneity of ADAMTS13 abnormalitiesĬamilleri, R., Mackie, I.J., Liesner, R., Chen, W., Manns, K., Hunt, B.J., Machin, S.J. Late onset adult thrombotic thrombocytopenic purpura. Prevalence of the ADAMTS-13 missense mutation R1060W in Late onset adult thrombotic thrombocytopenic purpuraĬamilleri, R., Cohen, H., Mackie, I.J., Skully, M., Starke, R.D., Crawley, J.T.B., Lane, D.A. PP-TH-088-XXIInd Congress of the International Society on Thrombosis and Haemostasis (ISTH). Eight novel ADAMTS13 missense mutations in childhood and adult onset congenital TTP. Newcastle Įight novel ADAMTS13 missense mutations in childhood and adult onset congenital TTPĬamilleri, R., Mackie, I.J., Liesner, R., Chen, W., Manns, K., Machin, S.J. British Society for Haemostasis and Thrombosis, Scientific Meeting. Phenotype-genotype correlation in congenital TTP. Phenotype-genotype correlation in congenital TTPĬamilleri, R., Mackie, I.J., Liesner, R., Chen, W., Manns, K., Machin, S.J. XXIIIrd Congress of the International Society on Thrombosis and Haemostasis (ISTH). Thrombotic Thrombocytopenic Purpura (TTP) and pregnancy in the UK: indentification of subtype, manangement and outcome of subsequent pregnancies. Thomas, M., Camilleri, R., Machin, S.J., Clark, A., Creagh, D., Evans, G. Thrombotic Thrombocytopenic Purpura (TTP) and pregnancy in the UK: indentification of subtype, manangement and outcome of subsequent pregnancies British society for haemostasis and thrombosis (BSHT) scientific meeting. Thrombotic thrombocytopenic purpura (TTP) and pregnancy in the UK: identification of subtype, management and outcome of subsequent pregnancies. Thrombotic thrombocytopenic purpura (TTP) and pregnancy in the UK: identification of subtype, management and outcome of subsequent pregnancies ADAMTS-13 deficiency: can it cause chronic renal failure? Nephrology, Dialysis, Transplantation. ĪDAMTS-13 deficiency: can it cause chronic renal failure?īramham, K., Hilton, R., Horsfield, C., McDonald, V., Camilleri, R. A phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom. Ī phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United KingdomĬamilleri, R., Scully, M., Thomas, M., Mackie, I.J., Liesner, R., Chen, W., Manns, K. Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes. and O Brien P collaborators of the UK TTP Registry 2014. Scully, M., Thomas, M., Underwood, M., Watson, H., Langley, K., Camilleri, R., Clark, A., Creagh, D., Rayment, R., McDonald, V., Roy, A., Evans, G., McGuckin, S., Ni Ainle, F., Maclean, R., Lester, W., Nash, M., Scott, R. Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes
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