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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 7, 2020
Confounding effect of therapeutic protamine and heparin levels on routine and special coagulation testingAditi Khandelwal, Chai W Phua, Hina R Chaudhry, et al.
Blood|July 30, 2005
Aminoglycoside suppression of nonsense mutations in severe hemophiliaPaula D James, Sanj Raut, Georges E Rivard, et al.
International Journal of Laboratory Hematology|August 8, 2020
Thrombin generation abnormalities in Quebec platelet disorderJustin G Brunet, Tanmya Sharma, Subia Tasneem, et al.
Thrombosis and Haemostasis|July 31, 2003
Intracellular activation of the fibrinolytic cascade in the Quebec Platelet DisorderPrameet M Sheth, Walter H A Kahr, M Anwar Haq, et al.
Pediatric Blood & Cancer|February 5, 2011
Platelet disorders in children: A diagnostic approachSara J Israels, Walter H A Kahr, Victor S Blanchette, et al.
Blood|January 16, 2009
Quantitation of anti-factor VIII antibodies in human plasmaJolanta Krudysz-Amblo, Behnaz Parhami-Seren, Saulius Butenas, et al.
Plos One|March 17, 2017
The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytesCatherine P M Hayward, Minggao Liang, Subia Tasneem, et al.
Blood|March 18, 2004
Bleeding risks associated with inheritance of the Quebec platelet disorderHeather McKay, Francine Derome, M Anwar Haq, et al.
Research and Practice in Thrombosis and Haemostasis|July 21, 2020
Bleeding risks for uncharacterized platelet function disordersJustin Brunet, Matthew Badin, Michael Chong, et al.
Blood|December 17, 2009
Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator geneAndrew D Paterson, Johanna M Rommens, Bhupinder Bharaj, et al.
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