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Platelets Volume 27, 2016 - Issue 8
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Meeting Report

ISTH Advanced Training Course on platelet bleeding disorders: How should they be investigated?

St. Anne’s College, Oxford, 6–9th September 2016

Steve P. WatsonInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UKCorrespondence[email protected]
,
Martina E. DalyDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK
,
Paul HarrisonInstitute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK
,
Gillian C. LoweInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK;Haemophilia Comprehensive Care Centre, University Hospital Birmingham, Edgbaston, Birmingham, UK
,
Andrew PatersonProgram in Genetics & Genomic Biology, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada
,
Jose RiveraServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Arrixaca, CIBERER, Murcia30003, Spain
,
Tim D. WarnerThe William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK
&
Neil V. MorganInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK
 show all
Pages 719-721 | Published online: 14 Nov 2016

References

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  • Watson SP, Lowe GC, Lordkipanidze M, Morgan NV. Genotyping and phenotyping of platelet function disorders. J Thromb Haemost 2013;11:351–363.
  • Fletcher SJ, Johnson B, Lowe GC, Bem D, Drake S, Lordkipanidzé M, Sánchez Guiú I, Dawood B, Rivera J, Simpson MA, et al. SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. J Clin Invest 2015;125:3600–3605.
  • Stockley J, Morgan NV, Bem D, Lowe GC, Lordkipanidze M, Dawood B, Simpson MA, Macfarlane K, Horner K, Leo VC, et al. Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects. Blood 2013;122:4090–4093.
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  • Stevenson WS, Rabbolini DJ, Beutler L, Chen Q, Gabrielli S, Mackay JP, Brighton TA, Ward CM, Morel-Kopp MC. Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1. Blood 2015;126:2027–2030.
  • Daly ME, Dawood BB, Lester WA, Peake IR, Rodeghiero F, Goodeve AC, Makris M, Wilde JT, Mumford AD, Watson SP, et al. 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. Blood 2009;113:4110–4113.

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