Literature DB >> 24762277

von Willebrand disease and platelet disorders.

E J Favaloro1, I Bodó, S J Israels, S A Brown.   

Abstract

The diagnosis and management of bleeding disorders is made difficult by the complexity and variety of disorders, clinical symptoms and bleeding type and severity. von Willebrand disease (VWD) and platelet disorders are disorders of primary haemostasis and together represent the most common inherited bleeding disorders. In this article, we describe the diagnosis of VWD and platelet disorders and the treatment options for VWD.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  desmopressin; platelet aggregation; platelet disorders; von Willebrand disease; von Willebrand factor

Mesh:

Substances:

Year:  2014        PMID: 24762277     DOI: 10.1111/hae.12414

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


  4 in total

1.  Peri-operative DDAVP Use Leading to Severe Hyponatremia after Total Shoulder Replacement in a Patient with von Willebrand's Disease.

Authors:  James S MacKenzie; Stuart C Kozinn
Journal:  HSS J       Date:  2015-07-17

Review 2.  Towards personalised therapy for von Willebrand disease: a future role for recombinant products.

Authors:  Emmanuel J Favaloro
Journal:  Blood Transfus       Date:  2016-03-22       Impact factor: 3.443

3.  Preclinical evaluation of a semi-automated and rapid commercial electrophoresis assay for von Willebrand factor multimers.

Authors:  Marika Pikta; Galina Zemtsovskaja; Hector Bautista; Georges Nouadje; Timea Szanto; Margus Viigimaa; Valdas Banys
Journal:  J Clin Lab Anal       Date:  2018-02-17       Impact factor: 2.352

Review 4.  Why Do Patients Bleed?

Authors:  Jennifer Curnow; Leonardo Pasalic; Emmanuel J Favaloro
Journal:  Surg J (N Y)       Date:  2016-02-24
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.