Хайлтын үр дүнгүүд - Gillian Lowe

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  1. 1
    Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders

    Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders -н Gillian Lowe, Marie Lordkipanidzé, Steve P. Watson

    Хэвлэсэн 2013
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    Artigo
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  2. 2
    Genotyping and phenotyping of platelet function disorders

    Genotyping and phenotyping of platelet function disorders -н Steve P. Watson, Gillian Lowe, Marie Lordkipanidzé, Neil V. Morgan

    Хэвлэсэн 2013
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    Revisão
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  3. 3
    Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders

    Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders -н Natalia Dovlatova, Marie Lordkipanidzé, Gillian Lowe, Ban B. Dawood, Jane May, Stan Heptinstall, Steve P. Watson, Susan C. Fox

    Хэвлэсэн 2014
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    Artigo
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  4. 4
    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 -н Ban B. Dawood, Gillian Lowe, Marie Lordkipanidzé, Danai Bem, Martina E. Daly, Michael Makris, Andrew Mumford, Jonathan T. Wilde, Steve P. Watson

    Хэвлэсэн 2012
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    Artigo
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  5. 5
    Rituximab prophylaxis to prevent thrombotic thrombocytopenic purpura relapse: outcome and evaluation of dosing regimens

    Rituximab prophylaxis to prevent thrombotic thrombocytopenic purpura relapse: outcome and evaluation of dosing regimens -н John‐Paul Westwood, Mari Thomas, Ferras Alwan, Vickie McDonald, Sylvia Benjamin, Will Lester, Gillian Lowe, Tina Dutt, Quentin A. Hill, Marie Scully

    Хэвлэсэн 2017
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    Artigo
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  6. 6
    Mutation in GNE is associated with severe congenital thrombocytopenia

    Mutation in GNE is associated with severe congenital thrombocytopenia -н Jane Wong Fütterer, Amanda Dalby, Gillian Lowe, Ben Johnson, Michael A. Simpson, Jayashree Motwani, Mike Williams, Steve P. Watson, Neil V. Morgan

    Хэвлэсэн 2018
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    Carta
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  7. 7
    Disparities in menstrual bleeding management during acute venous thromboembolism treatment: A review of UK practice and a call for clinical studies

    Disparities in menstrual bleeding management during acute venous thromboembolism treatment: A review of UK practice and a call for clinical studies -н Eman Hassan, David Sutton, Richard J. Buka, Gillian Lowe, Taran K Nandra, Nkemdirim Jacob, Lucy Rose, Yasir Alhamdi, Phillip L. R. Nicolson

    Хэвлэсэн 2025
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    Revisão
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  8. 8
    Adenovirus‐associated antibodies in UK cohort of hemophilia patients: A seroprevalence study of the presence of adenovirus‐associated virus vector–serotypes AAV5 and AAV8 neutralizing activity and antibodies in patients with hemophilia A

    Adenovirus‐associated antibodies in UK cohort of hemophilia patients: A seroprevalence study of the presence of adenovirus‐associated virus vector–serotypes AAV5 and AAV8 neutraliz... -н Sophia Stanford, Ruth Pink, Desmond Creagh, Amanda Clark, Gillian Lowe, Nicola Curry, John Pasi, David J. Perry, Sylvia Fong, Gregory M. Hayes, Kandiah Chandrakumaran, Savita Rangarajan

    Хэвлэсэн 2019
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    Artigo
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  9. 9
    Practical guidance for the management of adults with immune thrombocytopenia during the COVID‐19 pandemic

    Practical guidance for the management of adults with immune thrombocytopenia during the COVID‐19 pandemic -н Sue Pavord, Thachil Jecko, Beverley J. Hunt, Michael Murphy, Gillian Lowe, Michael Laffan, Michaël Makris, Adrian C. Newland, Drew Provan, John D. Grainger, Quentin A. Hill

    Хэвлэсэн 2020
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    Revisão
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  10. 10
    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 -н 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

    Хэвлэсэн 2014
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    Artigo
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  11. 11
    Plain language summary of the GENEr8-1 clinical trial of valoctocogene roxaparvovec gene therapy for hemophilia A

    Plain language summary of the GENEr8-1 clinical trial of valoctocogene roxaparvovec gene therapy for hemophilia A -н Gillian Lowe, Simon Fletcher, Patrick James Lynch, Johnny Mahlangu, Margareth C. Ozelo, Luke Pembroke, Steven W. Pipe, Gabriela G Yamaguti-Hayakawa, Deon York, Tara M. Robinson, Hua Yu, Leonard A. Valentino

    Хэвлэсэн 2023
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    Artigo
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  12. 12
    SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects

    SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects -н Sarah J. Fletcher, Ben Johnson, Gillian Lowe, Danai Bem, Sian Drake, Marie Lordkipanidzé, Isabel Sánchez Guiú, Ban B. Dawood, José Rivera, Michael A. Simpson, Martina E. Daly, Jayashree Motwani, Peter W. Collins, Steve P. Watson, Neil V. Morgan

    Хэвлэсэн 2015
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    Artigo
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  13. 13
    Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay

    Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay -н Marie Lordkipanidzé, Gillian Lowe, Nicholas S. Kirkby, Melissa V. Chan, Martina H. Lundberg, Neil V. Morgan, Danai Bem, Shaista P. Nisar, Vincenzo Leo, Matthew L. Jones, Stuart J. Mundell, Martina E. Daly, Andrew Mumford, Timothy D. Warner, Steve P. Watson

    Хэвлэсэн 2014
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    Artigo
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  14. 14
    Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

    Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects -н Jacqueline Stockley, Neil V. Morgan, Danai Bem, Gillian Lowe, Marie Lordkipanidzé, Ban B. Dawood, Michael A. Simpson, Kirsty Macfarlane, Kevin Horner, Vincenzo Leo, Katherine Talks, Jayashree Motwani, Jonathan T. Wilde, Peter W. Collins, Michael Makris, Steve P. Watson, Martina E. Daly

    Хэвлэсэн 2013
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    Artigo
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  15. 15
    Real-World Rates of Bleeding, Factor VIII Use, and Quality of Life in Individuals with Severe Haemophilia A Receiving Prophylaxis in a Prospective, Noninterventional Study

    Real-World Rates of Bleeding, Factor VIII Use, and Quality of Life in Individuals with Severe Haemophilia A Receiving Prophylaxis in a Prospective, Noninterventional Study -н Gili Kenet, Yeu‐Chin Chen, Gillian Lowe, Charles Percy, Huyen Tran, Annette von Drygalski, Marc Trossaërt, Mark T. Reding, Johannes Oldenburg, María Eva Mingot‐Castellano, Young Shil Park, Flora Peyvandi, Margareth C. Ozelo, Johnny Mahlangu, Jennifer Quinn, Mei Huang, Divya B. Reddy, Benjamin Kim

    Хэвлэсэн 2021
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    Artigo
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  16. 16
    Real‐world use of thrombopoietin receptor agonists for the management of immune thrombocytopenia in adult patients in the United Kingdom: Results from the <scp>TRAIT</scp> study

    Real‐world use of thrombopoietin receptor agonists for the management of immune thrombocytopenia in adult patients in the United Kingdom: Results from the <scp>TRAIT</scp> study -н Nichola Cooper, Marie Scully, Charles Percy, Phillip L. R. Nicolson, Gillian Lowe, Catherine Bagot, Jecko Thachil, H. Grech, Tim Nokes, Quentin A. Hill, Charlotte Bradbury, Kate Talks, Tina Dutt, Gillian Evans, Sue Pavord, Sarah Wexler, Asad Charania, Sarah J. Collington, Andrew Ervin, Nicholas Ramscar, Drew Provan

    Хэвлэсэн 2024
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    Artigo
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  17. 17
    Efficacy, safety, and quality of life 4 years after valoctocogene roxaparvovec gene transfer for severe hemophilia A in the phase 3 GENEr8-1 trial

    Efficacy, safety, and quality of life 4 years after valoctocogene roxaparvovec gene transfer for severe hemophilia A in the phase 3 GENEr8-1 trial -н Andrew D. Leavitt, Johnny Mahlangu, Priyanka Raheja, Emily Symington, Doris Quon, Adam Giermasz, María Fernanda López Fernández, Gili Kenet, Gillian Lowe, Nigel S. Key, Carolyn M. Millar, Steven W. Pipe, Bella Madan, Sheng‐Chieh Chou, Robert Klamroth, Jane Mason, Hérvè Chambost, Flora Peyvandi, Elaine M. Majerus, Dominic Pepperell, Christine Rivat, Hua Yu, Tara M. Robinson, Margareth C. Ozelo

    Хэвлэсэн 2024
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    Artigo
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  18. 18
    Three-year outcomes of valoctocogene roxaparvovec gene therapy for hemophilia A

    Three-year outcomes of valoctocogene roxaparvovec gene therapy for hemophilia A -н Bella Madan, Margareth C Ozelo, Priyanka Raheja, Emily Symington, Doris Quon, Andrew D. Leavitt, Steven W. Pipe, Gillian Lowe, Gili Kenet, Mark T. Reding, Jane Mason, Michael Wang, Annette von Drygalski, Robert Klamroth, Susan Shapiro, Hérvè Chambost, Amy L. Dunn, Johannes Oldenburg, Sheng‐Chieh Chou, Flora Peyvandi, Carolyn M Millar, Dane Osmond, Hua Yu, Ebony Dashiell-Aje, Tara M. Robinson, Johnny Mahlangu

    Хэвлэсэн 2024
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    Artigo
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  19. 19
    Real-world experience with caplacizumab in the management of acute TTP

    Real-world experience with caplacizumab in the management of acute TTP -н Tina Dutt, Rebecca Shaw, Matthew Stubbs, Jun Yong, Benjamin Bailiff, Tanya Cranfield, Maeve P. Crowley, Michael Desborough, Toby A. Eyre, Richard Gooding, John D. Grainger, John Hanley, Joanna Haughton, Joannes Hermans, Quentin A. Hill, L. Humphrey, Gillian Lowe, Hamish Lyall, Muhammad Mohsin, Phillip L. R. Nicolson, Nicole Priddee, Alexandros Rampotas, Rachel Rayment, Susan Rhodes, A. E. Taylor, William Thomas, Oliver Tomkins, Joost J. van Veen, Steven Lane, Cheng‐Hock Toh, Marie Scully

    Хэвлэсэн 2020
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    Artigo
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  20. 20
    Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

    Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects -н Benjamin C. Johnson, Gillian Lowe, Jane Wong Fütterer, Marie Lordkipanidzé, Deborah J. MacDonald, Michael A. Simpson, Isabel Sánchez‐Guiu, Sian Drake, Danai Bem, Vincenzo Leo, Sarah J. Fletcher, Ban B. Dawood, José Rivera, David Allsup, Tina Biss, P Bolton-Maggs, Peter Collins, Nicola Curry, Charlotte Grimley, Beki James, Michael Makris, Jayashree Motwani, Sue Pavord, Katherine Talks, Jecko Thachil, J Wilde, M. Williams, Paul Harrison, Paul Gissen, Stuart J. Mundell, Andrew Mumford, Mary E. Daly, Steve P. Watson, Neil V. Morgan

    Хэвлэсэн 2016
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    Artigo
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