Literature DB >> 27405677

State of the art: von Willebrand disease.

A H James1,2, J Eikenboom3, A B Federici4.   

Abstract

The State of the Art in von Willebrand disease (VWD) has been impacted not only by discoveries in the field of haemostasis, but also by changes in practice in other fields. The development of bleeding assessment tools has led to the clarification of bleeding symptoms and phenotype in VWD. New discoveries in the biology and genetics of von Willebrand factor (VWF) are challenging our existing diagnostics and classification(s). An improved understanding of reproductive physiology and the pathology of VWD along with changing obstetric, gynaecologic and haemostatic therapies necessitate an evolving response to the care of women with VWD. The survival of patients with autoimmune disease, malignancies and congenital heart disease along with increasing use of circulatory support devices and extracorporeal membrane oxygenation is increasing the prevalence of acquired von Willebrand syndrome. In each of these challenges, there are opportunities to improve the care of our patients with VWD.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  acquired von Willebrand syndrome; childbirth; diagnostic assays; heavy menstrual bleeding; laboratory assessment; von Willebrand disease

Mesh:

Substances:

Year:  2016        PMID: 27405677     DOI: 10.1111/hae.12984

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  5 in total

1.  Von Willebrand factor multimers during transcatheter aortic valve replacement-an additional clue for detecting post-procedural aortic regurgitation?

Authors:  Andras Peter Durko; Arie Pieter Kappetein
Journal:  J Thorac Dis       Date:  2016-12       Impact factor: 2.895

2.  The impact of bicuspid aortic valve morphology on von Willebrand factor function in patients with severe aortic stenosis and its change after TAVI.

Authors:  Carsten Jungbauer; Kurt Debl; Nastasia Roth; Carolin Heidel; Congde Xu; Ute Hubauer; Stefan Wallner; Christine Meindl; Andreas Holzamer; Michael Hilker; Marcus Creutzenberg; Samuel Sossalla; Lars Maier
Journal:  Clin Res Cardiol       Date:  2022-07-15       Impact factor: 6.138

3.  Combination of acquired von Willebrand syndrome (AVWS) and Glanzmann thrombasthenia in monoclonal gammopathy of uncertain significance (MGUS), a case report.

Authors:  Elizabeth Sarah Mayne; Malcolm Tait; Barry Frank Jacobson; Evashin Pillay; Susan J Louw
Journal:  Thromb J       Date:  2018-11-26

4.  Crystal structure of ADAMTS13 CUB domains reveals their role in global latency.

Authors:  H J Kim; Y Xu; A Petri; K Vanhoorelbeke; J T B Crawley; J Emsley
Journal:  Sci Adv       Date:  2021-04-16       Impact factor: 14.136

5.  [Chinese guideline on the diagnosis and management of von Willebrand disease (2022)].

Authors: 
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2022-01-14
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.