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8/11/2016 11:29:00 AM | Browse: 667 | Download: 1426
Publication Name World Journal of Hematology
Manuscript ID 23508
Country/Territory Netherlands
Received
2015-11-26 16:25
Peer-Review Started
2015-11-30 10:18
To Make the First Decision
2016-01-14 17:11
Return for Revision
2016-01-15 16:54
Revised
Second Decision
2016-04-08 09:52
Accepted by Journal Editor-in-Chief
2016-04-08 10:12
Accepted by Company Editor-in-Chief
2016-04-18 13:41
Articles in Press
2016-04-18 13:41
Publication Fee Transferred
Edit the Manuscript by Language Editor
2016-04-26 04:49
Typeset the Manuscript
2016-08-04 15:33
Publish the Manuscript Online
2016-08-06 17:31
ISSN 2218-6204 (online)
Open Access This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Copyright © The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Gastroenterology & Hepatology
Manuscript Type Review
Article Title Changing insights in the diagnosis and classification of autosomal recessive and dominant von Willebrand diseases 1980-2015
Manuscript Source Invited Manuscript
All Author List Jan Jacques Michiels, Angelika Batorova, Tatiana Prigancova, Petr Smejkal, Miroslav Penka, Inge Vangenechten and Alain Gadisseur
Funding Agency and Grant Number
Corresponding Author Jan Jacques Michiels, MD, PhD, Investigator, Senior Internist, Goodheart Institute and Foundation in Nature Medicine and Health, Blood Coagulation and Vascular Medicine Research Center, Erasmus Tower, Veenmos 13, 3069 Rotterdam, The Netherlands. goodheartcenter.@upcmail.nl
Key Words Von Willebrand disease; Von Willebrand factor; ADAMTS13; DDAVP; Von Willebrand factor assays; Von Willebrand gene mutations
Core Tip The European Clinical Laboratory and Mole-cular criteria define at least 10 distinct phenotypes of von Willebrand diseases (VWD) that have significant therapeutic implications. High quality von Willebrand factor (VWF) multimeric analysis and responses to desmopressin of FVIII:C and VWF parameters are of critical diagnostic importance to document the contribution of VWF secretion, clearance, proteolysis and multimerization defects to real life phenotyping of each individual VWD patient.
Publish Date 2016-08-06 17:31
Citation Michiels JJ, Batorova A, Prigancova T, Smejkal P, Penka M, Vangenechten I, Gadisseur A. Changing insights in the diagnosis and classification of autosomal recessive and dominant von Willebrand diseases 1980-2015. World J Hematol 2016; 5(3): 61-74
URL http://www.wjgnet.com/2218-6204/full/v5/i3/61.htm
DOI http://dx.doi.org/10.5315/wjh.v5.i3.61
Full Article (PDF) WJH-5-61.pdf
Full Article (Word) WJH-5-61.doc
Manuscript File 23508-Review.docx
Answering Reviewers 23508-Answering reviewers.pdf
Audio Core Tip 23508-Audio core tip.mp3
Conflict-of-Interest Disclosure Form 23508-Conflict-of-interest statement.pdf
Copyright License Agreement 23508-Copyright assignment.pdf
Peer-review Report 23508-Peer-review(s).pdf
Journal Editor-in-Chief Review Report 23508-Journal editor-in-chief review report.pdf
Scientific Misconduct Check 23508-Scientific misconduct check.pdf
Scientific Editor Work List 23508-Scientific editor work list.pdf