Genotyping and phenotyping of platelet function disorders
Watson, S. P., Lowe, G. C., Lordkipanidzé, M., Morgan, N. V.
Published in Journal of thrombosis and haemostasis (01.06.2013)
Published in Journal of thrombosis and haemostasis (01.06.2013)
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Journal Article
Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders
Leo, V. C., Morgan, N. V., Bem, D., Jones, M. L., Lowe, G. C., Lordkipanidzé, M., Drake, S., Simpson, M. A., Gissen, P., Mumford, A., Watson, S. P., Daly, M. E.
Published in Journal of thrombosis and haemostasis (01.04.2015)
Published in Journal of thrombosis and haemostasis (01.04.2015)
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Journal Article
Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders
Dovlatova, N., Lordkipanidzé, M., Lowe, G. C., Dawood, B., May, J., Heptinstall, S., Watson, S. P., Fox, S. C.
Published in Journal of thrombosis and haemostasis (01.05.2014)
Published in Journal of thrombosis and haemostasis (01.05.2014)
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A novel mutation in the P2Y12 receptor and a function‐reducing polymorphism in protease‐activated receptor 1 in a patient with chronic bleeding
Patel, Y. M., Lordkipanidzé, M., Lowe, G. C., Nisar, S. P., Garner, K., Stockley, J., Daly, M. E., Mitchell, M., Watson, S. P., Austin, S. K., Mundell, S. J.
Published in Journal of thrombosis and haemostasis (01.05.2014)
Published in Journal of thrombosis and haemostasis (01.05.2014)
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Journal Article