Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel
Dawood, Ban B., Lowe, Gillian C., Lordkipanidzé, Marie, Bem, Danai, Daly, Martina E., Makris, Mike, Mumford, Andrew, Wilde, Jonathan T., Watson, Steve P.
Published in Blood (13.12.2012)
Published in Blood (13.12.2012)
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A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction
Nisar, Shaista P, Lordkipanidzé, Marie, Jones, Matthew L, Dawood, Ban, Murden, Sherina, Cunningham, Margaret R, Mumford, Andrew D, Wilde, Jonathan T, Watson, Steve P, Mundell, Stuart J, Lowe, Gillian C
Published in Thrombosis and haemostasis (2014)
Published in Thrombosis and haemostasis (2014)
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Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy)
Hartley, Jane Louise, Zachos, Nicholas C, Dawood, Ban, Donowitz, Mark, Forman, Julia, Pollitt, Rodney J, Morgan, Neil V, Tee, Louise, Gissen, Paul, Kahr, Walter H A, Knisely, Alex S, Watson, Steve, Chitayat, David, Booth, Ian W, Protheroe, Sue, Murphy, Stephen, de Vries, Esther, Kelly, Deirdre A, Maher, Eamonn R
Published in Gastroenterology (New York, N.Y. 1943) (01.06.2010)
Published in Gastroenterology (New York, N.Y. 1943) (01.06.2010)
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A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis
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.
Published in Blood (14.01.2010)
Published in Blood (14.01.2010)
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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
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.
Published in Blood (23.04.2009)
Published in Blood (23.04.2009)
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Prescribing patterns of oral antiplatelets in Wales: evolving trends from 2005 to 2016
Protty, Majd B, Wilkins, Simon J, Hoskins, Hannah C, Dawood, Ban B, Hayes, Jamie
Published in Future cardiology (01.07.2018)
Published in Future cardiology (01.07.2018)
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A Germline Mutation in BLOC1S3/ Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8)
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.
Published in American journal of human genetics (01.01.2006)
Published in American journal of human genetics (01.01.2006)
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Journal Article
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects
Fletcher, Sarah J, Johnson, Ben, Lowe, Gillian C, Bem, Danai, Drake, Sian, Lordkipanidzé, Marie, Guiú, Isabel Sánchez, Dawood, Ban, Rivera, José, Simpson, Michael A, Daly, Martina E, Motwani, Jayashree, Collins, Peter W, Watson, Steve P, Morgan, Neil V
Published in The Journal of clinical investigation (01.09.2015)
Published in The Journal of clinical investigation (01.09.2015)
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Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects
Stockley, Jacqueline, Morgan, Neil V., Bem, Danai, Lowe, Gillian C., Lordkipanidzé, Marie, Dawood, Ban, Simpson, Michael A., Macfarlane, Kirsty, Horner, Kevin, Leo, Vincenzo C., Talks, Katherine, Motwani, Jayashree, Wilde, Jonathan T., Collins, Peter W., Makris, Michael, Watson, Steve P., Daly, Martina E.
Published in Blood (12.12.2013)
Published in Blood (12.12.2013)
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Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects
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
Published in Haematologica (Roma) (01.10.2016)
Published in Haematologica (Roma) (01.10.2016)
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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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