PT-VWD.org
22 Aug
May 30 2008
Preleminary data from the Canadian PT-VWD project is presented in the WFH congress Istanbul 1-6 2008
22 Aug
April 16 2008
RCPA-QAP:
QMP-LS:
LEECH:
NASCOLA:
22 Aug
March 15 2008
QMP-LS (Quality Mangament Program - Labaoratory Service) distributes an announcement regarding a project to investigate the occurrence of platelet type von Willebrand Disease (PT-VWD) and differential identification from the closely similar, type 2B VWD to laboratories performing von Willebrand investigations in Ontario, Canada
22 Aug
April 15 2008
Hemophilia Today Announces Participation in the Platelet Type VWD Project and Canadian Hemophilia Society approved second year funding in its Spring 2008 Edition, Vol. 2.
Hemophilia Today is the official publicartion of the Canadian Hemophilia society.
6 Dec
June 12 2006
Dears
The overall aim of the PT-VWD database/ registry project is to determine the frequency of this rare bleeding disorder in the world and to collect data about the molecular pathology, phenotype/ genotype correlations as well as treatment. Therefore, we invite you to complete a form that includes the main information in order to allow us to learn about your experience with PT-VWD patients and if you would like to participate in the Canadian PT-VWD project.
The objectives of the PT-VWD Registry are:
Physicians worldwide are encouraged to collaborate, share observations, and evaluation data in an effort to guide and assess future diagnostic/therapeutic interventions.
Please do not hesitate to contact us by phone or by email in case any further details are required.
Yours sincerely,
Maha Othman MD MSc PhD
othman@queensu.ca
Department of Pathology and Molecular Medicine
Queen’s University
Kingston, Ontario
Canada
This project is funded by:
