Molecular diagnosis of von Willebrand disease-Reference-Cited by-同舟云学术

Molecular diagnosis of von Willebrand disease

Published:2017-02-20 Issue:2 Volume:23 Page:188-197
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Baronciani L.¹,Goodeve A.²,Peyvandi F.¹³^ORCID

Affiliation:

1. Angelo Bianchi Bonomi Hemophilia and Thrombosis Center; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico and Luigi Villa Foundation; Milan Italy

2. Department of Infection, Immunity and Cardiovascular Disease; University of Sheffield Medical School; Sheffield UK

3. Department of Pathophysiology and Transplantation; Università degli Studi di Milano; Milan Italy

Funder

Alexion Pharmaceuticals

Biotest

Kedrion Biopharma

Novo Nordisk

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13175/fullpdf

Reference40 articles.

1. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA);Nichols;Haemophilia,2008

2. Gene deletions correlate with the development of alloantibodies in von Willebrand disease;Shelton-Inloes;J Clin Invest,1987

3. Antibodies to von Willebrand factor in von Willebrand disease

4. Genetic testing for von Willebrand disease: the case against;Favaloro;J Thromb Haemost,2010

5. Genetic testing for von Willebrand disease: the case for;Peake;J Thromb Haemost,2010

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