Результаты поиска - Andrew Mumford

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  1. 1
    Guidelines for the laboratory investigation of heritable disorders of platelet function

    Guidelines for the laboratory investigation of heritable disorders of platelet function по Paul Harrison, Ian Mackie, Andrew Mumford, Carol Briggs, Ri Liesner, Mark Winter, Sam Machin

    Опубликовано 2011
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    Artigo
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  2. 2
    Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia

    Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia по Susan Shapiro, Emma Phillips, Richard A. Manning, Colin Morse, Sherina L. Murden, Michael Laffan, Andrew Mumford

    Опубликовано 2012
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    Artigo
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  3. 3
    Pharmacodynamic resistance to warfarin associated with a Val66Met substitution in vitamin K epoxide reductase complex subunit 1

    Pharmacodynamic resistance to warfarin associated with a Val66Met substitution in vitamin K epoxide reductase complex subunit 1 по Dominic J. Harrington, Sarah Underwood, C. MORSE, Martin J. Shearer, Edward G. D. Tuddenham, Andrew Mumford

    Опубликовано 2004
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    Artigo
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  4. 4
    Bleeding symptoms and coagulation abnormalities in 337 patients with AL‐amyloidosis

    Bleeding symptoms and coagulation abnormalities in 337 patients with AL‐amyloidosis по Andrew Mumford, James S. O’Donnell, Julian D. Gillmore, Richard A. Manning, Philip N. Hawkins, Michael Laffan

    Опубликовано 2000
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    Artigo
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  5. 5
    Inverse agonism at the P2Y12 receptor and ENT1 transporter blockade contribute to platelet inhibition by ticagrelor

    Inverse agonism at the P2Y12 receptor and ENT1 transporter blockade contribute to platelet inhibition by ticagrelor по Riyaad Aungraheeta, Alexandra E. Conibear, Mark Butler, Eamonn Kelly, Sven Nylander, Andrew Mumford, Stuart J. Mundell

    Опубликовано 2016
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    Artigo
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  6. 6
    Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders

    Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders по Daniel Greene, Chantal Thys, Ian Berry, Joanna Jarvis, Els Ortibus, Andrew Mumford, Kathleen Freson, Ernest Turro

    Опубликовано 2024
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    Artigo
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  7. 7
    Pharmacodynamic resistance to warfarin is associated with nucleotide substitutions inVKORC1

    Pharmacodynamic resistance to warfarin is associated with nucleotide substitutions inVKORC1 по D.J. HARRINGTON, Renata Górska, Ruth B. Wheeler, Simon Davidson, Sherina L. Murden, C. MORSE, M. J. Shearer, Andrew Mumford

    Опубликовано 2008
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    Artigo
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  8. 8
    Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

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

    Опубликовано 2012
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    Artigo
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  9. 9
    Guidelines for the use of platelet transfusions

    Guidelines for the use of platelet transfusions по Lise J Estcourt, Janet Birchall, Shubha Allard, Stephen J. Bassey, Peter Hersey, Jonathan P. Kerr, Andrew Mumford, Simon Stanworth, Hazel Tinegate

    Опубликовано 2016
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    Artigo
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  10. 10
    Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH

    Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH по Paolo Gresele, Paul Harrison, Christian Gachet, Catherine P.M. Hayward, Dermot Kenny, Diego Mezzano, Andrew Mumford, Diane J. Nugent, Alan T. Nurden, Marco Cattaneo

    Опубликовано 2014
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    Revisão
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  11. 11
    The rare coagulation disorders – review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation

    The rare coagulation disorders – review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation по Paula Bolton‐Maggs, David J. Perry, Elizabeth Chalmers, L. A. Parapia, J Wilde, Michael D. Williams, Peter W. Collins, Steve Kitchen, Gerard Dolan, Andrew Mumford

    Опубликовано 2004
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    Revisão
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  12. 12
    Identification and characterization of a novel P2Y12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

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

    Опубликовано 2009
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    Artigo
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  13. 13
    Investigation of human haemotropic Mycoplasma infections using a novel generic haemoplasma qPCR assay on blood samples and blood smears

    Investigation of human haemotropic Mycoplasma infections using a novel generic haemoplasma qPCR assay on blood samples and blood smears по Séverine Tasker, Iain R. Peters, Andrew Mumford, Michael Day, Timothy J. Gruffydd-Jones, Sarinder Day, Anne-Marié Pretorius, Richard J. Birtles, Chris R. Helps, Harold Neimark

    Опубликовано 2010
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    Artigo
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  14. 14
    A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis

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

    Опубликовано 2009
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    Artigo
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  15. 15
    A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome

    A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome по Christiane Albrecht, John H. McVey, James I. Elliott, Alessandro Sardini, Ildikó Kasza, Andrew Mumford, R.P. Naoumova, Edward G. D. Tuddenham, Katalin Szabó, Christopher F. Higgins

    Опубликовано 2005
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    Artigo
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  16. 16
    Coronary Artery-Bypass-Graft Surgery Increases the Plasma Concentration of Exosomes Carrying a Cargo of Cardiac MicroRNAs: An Example of Exosome Trafficking Out of the Human Heart with Potential for Cardiac Biomarker Discovery

    Coronary Artery-Bypass-Graft Surgery Increases the Plasma Concentration of Exosomes Carrying a Cargo of Cardiac MicroRNAs: An Example of Exosome Trafficking Out of the Human Heart... по Costanza Emanueli, Andrew I.U. Shearn, Abas H. Laftah, Francesca Fiorentino, Barnaby C Reeves, Cristina Beltrami, Andrew Mumford, Aled Clayton, Mark Gurney, Saran Shantikumar, Gianni D. Angelini

    Опубликовано 2016
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    Artigo
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  17. 17
    Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH

    Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH по Adrian Minford, Leonardo R. Brandão, Maha Othman, Christoph Male, Rezan A. Kadir, Paul Monagle, Andrew Mumford, Dorothy M. Adcock, Björn Dahlbäck, Predrag Miljić, Maria T. DeSancho, Jun Teruya

    Опубликовано 2022
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    Artigo
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  18. 18
    A multicentre randomised controlled trial of Transfusion Indication Threshold Reduction on transfusion rates, morbidity and health-care resource use following cardiac surgery (TITRe2)

    A multicentre randomised controlled trial of Transfusion Indication Threshold Reduction on transfusion rates, morbidity and health-care resource use following cardiac surgery (TITR... по Barnaby C Reeves, Katie Pike, Chris Rogers, Rachel Brierley, Elizabeth A Stokes, Sarah Wordsworth, Rachel Nash, Alice Miles, Andrew Mumford, Alan Cohen, Gianni D. Angelini, Gavin J. Murphy

    Опубликовано 2016
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    Artigo
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  19. 19
    Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey

    Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey по Paolo Gresele, Paul Harrison, Loredana Bury, Emanuela Falcinelli, Christian Gachet, Catherine P.M. Hayward, Dermot Kenny, Diego Mezzano, Andrew Mumford, Diane J. Nugent, Alan T. Nurden, Sara Orsini, Marco Cattaneo

    Опубликовано 2014
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    Artigo
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  20. 20
    Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

    Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders по Vincenzo Leo, Neil V. Morgan, Danai Bem, Matthew L. Jones, Gillian Lowe, Marie Lordkipanidzé, Sian Drake, Michael A. Simpson, Paul Gissen, Andrew Mumford, Steve P. Watson, Mary E. Daly

    Опубликовано 2014
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    Artigo
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