The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology.

نویسندگان

  • Mike A Laffan
  • Will Lester
  • James S O'Donnell
  • Andrew Will
  • Robert Campbell Tait
  • Anne Goodeve
  • Carolyn M Millar
  • David M Keeling
چکیده

Mike A. Laffan, Will Lester, James S. O’Donnell, Andrew Will, Robert Campbell Tait, Anne Goodeve, Carolyn M. Millarand David M. Keeling Centre for Haematology, Imperial College London, London, Department of Haematology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK, National Centre for Coagulation Disorders, St James’s Hospital, Dublin, Ireland, Royal Manchester Children’s Hospital, Manchester, Department of Haematology, Royal Infirmary, Glasgow, Sheffield Diagnostic Genetics Service, Sheffield Children’s NHS Foundation Trust & Department of Cardiovascular Science, University of Sheffield, Sheffield, and Oxford University Hospitals, Oxford, UK

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منابع مشابه

The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization.

von Willebrand disease (VWD) is the commonest inherited bleeding disorder. However, despite an increasing understanding of the pathophysiology of VWD, the diagnosis of VWD is frequently difficult because of uncertainty regarding the relationship between laboratory assays and function in vivo. The objective of this guideline is to provide contemporary advice on a rational approach to the diagnos...

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Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization.

von Willebrand disease (VWD) is the commonest inherited bleeding disorder. The aim of therapy for VWD is to correct the two defects of haemostasis in this disorder, impaired primary haemostasis because of defective platelet adhesion and aggregation and impaired coagulation as a result of low levels of factor VIII. The objective of this guideline is to inform individuals making choices about the...

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Characterisation of W1745C and S1783A: two novel mutations causing defective collagen binding in the A3 domain of von Willebrand Factor. Short title: Von Willebrand factor mutants W1745C and S1783A

Katharine Dormandy Haemophilia Centre and Thrombosis Unit, The Royal Free and University College Medical School, London NW3 2QG, United Kingdom. Department of Haematology, Imperial College Academic Health Sciences Centre, Hammersmith Hospital, London W12 0NN, United Kingdom Department of Haematology, Royal Children’s Hospital and Royal Brisbane and Women’s Hospital, Brisbane, Queensland, Austra...

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عنوان ژورنال:
  • British journal of haematology

دوره 167 4  شماره 

صفحات  -

تاریخ انتشار 2014