Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel by Dawood, Ban B., Lowe, Gillian C., Lordkipanidzé, Marie, Bem, Danai, Daly, Martina E., Makris, Mike, Mumford, Andrew, Wilde, Jonathan T., Watson, Steve P.

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Prescribing patterns of oral antiplatelets in Wales: evolving trends from 2005 to 2016 by Protty, Majd B, Wilkins, Simon J, Hoskins, Hannah C, Dawood, Ban B, Hayes, Jamie

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A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis by Mumford, Andrew D., Dawood, Ban B., Daly, Martina E., Murden, Sherina L., Williams, Michael D., Protty, Majd B., Spalton, Jennifer C., Wheatley, Mark, Mundell, Stuart J., Watson, Steve P.

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Identification and characterization of a novel P2Y12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study by Daly, Martina E., Dawood, Ban B., Lester, William A., Peake, Ian R., Rodeghiero, Francesco, Goodeve, Anne C., Makris, Michael, Wilde, Jonathan T., Mumford, Andrew D., Watson, Stephen P., Mundell, Stuart J.

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Reference curves for aggregation and ATP secretion to aid diagnose of platelet-based bleeding disorders: effect of inhibition of ADP and thromboxane A(2) pathways by Dawood, Ban B, Wilde, Jonathan, Watson, Steve P

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Reference curves for aggregation and ATP secretion to aid diagnose of platelet-based bleeding disorders: Effect of inhibition of ADP and thromboxane A2 pathways by Dawood, Ban B., Wilde, Jonathan, Watson, Steve P.

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Reference curves for aggregation and ATP secretion to aid diagnose of platelet-based bleeding disorders: Effect of inhibition of ADP and thromboxane A 2 pathways by Dawood, Ban B., Wilde, Jonathan, Watson, Steve P.

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Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study by Daly, Martina E, Dawood, Ban B, Lester, William A, Peake, Ian R, Rodeghiero, Francesco, Goodeve, Anne C, Makris, Michael, Wilde, Jonathan T, Mumford, Andrew D, Watson, Stephen P, Mundell, Stuart J

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Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects by Johnson, Ben, Lowe, Gillian C, Futterer, Jane, Lordkipanidzé, Marie, MacDonald, David, Simpson, Michael A, Sanchez-Guiú, Isabel, Drake, Sian, Bem, Danai, Leo, Vincenzo, Fletcher, Sarah J, Dawood, Ban, Rivera, José, Allsup, David, Biss, Tina, Bolton-Maggs, Paula Hb, Collins, Peter, Curry, Nicola, Grimley, Charlotte, James, Beki, Makris, Mike, Motwani, Jayashree, Pavord, Sue, Talks, Katherine, Thachil, Jecko, Wilde, Jonathan, Williams, Mike, Harrison, Paul, Gissen, Paul, Mundell, Stuart, Mumford, Andrew, Daly, Martina E, Watson, Steve P, Morgan, Neil V

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Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders by Dovlatova, N., Lordkipanidzé, M., Lowe, G. C., Dawood, B., May, J., Heptinstall, S., Watson, S. P., Fox, S. C.

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A Germline Mutation in BLOC1S3/ Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8) by Morgan, Neil V., Pasha, Shanaz, Johnson, Colin A., Ainsworth, John R., Eady, Robin A.J., Dawood, Ban, McKeown, Carole, Trembath, Richard C., Wilde, Jonathan, Watson, Steve P., Maher, Eamonn R.

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