ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease

PD James, NT Connell, B Ameer, J Di Paola… - Blood …, 2021 - ashpublications.org
Background: von Willebrand disease (VWD) is the most common inherited bleeding disorder
known in humans. Accurate and timely diagnosis presents numerous challenges. Objective …

[HTML][HTML] The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British …

MA Laffan, W Lester, JS O'Donnell, A Will… - British journal of …, 2014 - ncbi.nlm.nih.gov
Von Willebrand factor (VWF) is a large and complex plasma glycoprotein that is essential for
normal haemostasis. It is well recognized that deficiency of VWF results in a bleeding …

Management of severe perioperative bleeding: guidelines from the European Society of Anaesthesiology: first update 2016

SA Kozek-Langenecker, AB Ahmed… - European Journal of …, 2017 - journals.lww.com
The management of perioperative bleeding involves multiple assessments and strategies to
ensure appropriate patient care. Initially, it is important to identify those patients with an …

Management of severe perioperative bleeding: guidelines from the European Society of Anaesthesiology

SA Kozek-Langenecker, A Afshari… - European Journal of …, 2013 - journals.lww.com
The aims of severe perioperative bleeding management are three-fold. First, preoperative
identification by anamesis and laboratory testing of those patients for whom the …

Guidelines for the laboratory investigation of heritable disorders of platelet function

P Harrison, I Mackie, A Mumford… - British journal of …, 2011 - Wiley Online Library
The guideline writing group was selected to be representative of UK‐based medical experts.
MEDLINE was systematically searched for publications in English up to the Summer of 2010 …

[HTML][HTML] Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH

P Gresele, P Harrison, C Gachet, C Hayward… - Journal of Thrombosis …, 2015 - Elsevier
Although rare, the prevalence of inherited platelet function disorders (IPFD) is probably
underestimated due to under‐diagnosis 1. IPFD are heterogeneous in severity, mechanisms …

[HTML][HTML] Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey

P Gresele, P Harrison, L Bury, E Falcinelli… - Journal of Thrombosis …, 2014 - Elsevier
Background Diagnosis of inherited platelet function disorders (IPFDs) is important for
appropriate management and to improve epidemiologic and clinical knowledge. However …

Inherited platelet disorders: toward DNA-based diagnosis

C Lentaigne, K Freson, MA Laffan… - Blood, The Journal …, 2016 - ashpublications.org
Variations in platelet number, volume, and function are largely genetically controlled, and
many loci associated with platelet traits have been identified by genome-wide association …

[HTML][HTML] Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: a communication from the Platelet Physiology SSC

P Gresele, S Orsini, P Noris, E Falcinelli… - Journal of Thrombosis …, 2020 - Elsevier
Background Careful assessment of bleeding history is the first step in the evaluation of
patients with mild/moderate bleeding disorders, and the use of a bleeding assessment tool …

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

SK Westbury, E Turro, D Greene, C Lentaigne… - Genome medicine, 2015 - Springer
Background Heritable bleeding and platelet disorders (BPD) are heterogeneous and
frequently have an unknown genetic basis. The BRIDGE-BPD study aims to discover new …