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Journal Articles

Thrombin Generation Impairments in Platelet Function Disorders

Justin Brunet, BSc, Subia Tasneem, PhD, Georges E. Rivard, MD FRCPC, Catherine P.M. Hayward, MD

Blood (2018) 132 (Supplement 1): 1150.

https://doi.org/10.1182/blood-2018-99-110247

Published: 2018

Journal Articles

Immune Tolerance Induction in Hemophilia A Patients Using Wilate® —a Canadian 10 Year Study (PREVAIL)

Paul Moorehead, MD, Mark J. Belletrutti, MD MSc, David Lillicrap, MD FRCPC, Robert J Klaassen, MD FRCPC, Manuel Carcao, MDMSc, Georges E. Rivard, MD FRCPC

Blood (2017) 130 (Supplement 1): 3679.

https://doi.org/10.1182/blood.V130.Suppl_1.3679.3679

Published: 2017

Journal Articles

Transcriptional Landscape of APL Identifies Aberrant Podoplanin Expression As a Defining Feature and Missing Link for the Bleeding Disorder of This Disease

Vincent-Philippe Lavallée, MD, Miriam Marquis, PhD, Marie-Ève Bordeleau, PhD, Jalila Chagraoui, PhD, Tara MacRae, M.Sc., Isabel Boivin, M.Sc, Geneviève Boucher, M.Sc, Patrick Gendron, M.Sc, Sébastien Lemieux, PhD, Arnaud Bonnefoy, PhD, Georges E. Rivard, MD, Josée Hébert, MD, Guy Sauvageau, MD, PhD

Blood (2016) 128 (22): 1075.

https://doi.org/10.1182/blood.V128.22.1075.1075

Published: 2016

Journal Articles

Bleeding Risks Associated with Confirmed Platelet Dense Granule Deficiency and/or Impaired Aggregation Responses

Janaki Iyer, PhD, Matthew Badin, Lucas Graf, Georges E. Rivard, MD, A. D. Paterson, Guillaume Pare, Catherine P.M. Hayward, MD PhD

Blood (2016) 128 (22): 3728.

https://doi.org/10.1182/blood.V128.22.3728.3728

Published: 2016

Journal Articles

An Unusual Case of Acquired Hemophilia a and Factor XIII Consumption

Brett L. Houston, MD, Christine M. Cserti-Gazdewich, MD, Richard Ward, MBBS, Jean St. Louis, MD, Georges E. Rivard, MD, Jerome M. Teitel, MD, Michelle Sholzberg, MD

Blood (2015) 126 (23): 4701.

https://doi.org/10.1182/blood.V126.23.4701.4701

Published: 2015

Journal Articles

Quebec Platelet Disorder Is Associated With Greater Than Expected Increases In Urokinase Plasminogen Activator In Granulocytes and Monocytes

Jessica Blavignac, PhD(c), H.BSc., Subia Tasneem, PhD, Andrew D Paterson, MD, John S Waye, Ph.D, Bhupinder Bharaj, PhD, Georges E Rivard, MD, Catherine P. M. Hayward, MD, PhD

Blood (2013) 122 (21): 3573.

https://doi.org/10.1182/blood.V122.21.3573.3573

Published: 2013

Journal Articles

Dysregulation of C10orf55 Expression in Megakaryocytic Cell Lineage From Quebec Platelet Disorder Individuals

Natalia Bunimov, PhD, Jessica Blavignac, BSc, Subia Tasneem, PhD, John S Waye, PhD, Andrew D Paterson, MD, Georges E Rivard, MD, Catherine PM Hayward, MD, PhD

Blood (2011) 118 (21): 2274.

https://doi.org/10.1182/blood.V118.21.2274.2274

Published: 2011

Journal Articles

Quantitation of Non-Inhibitory Anti-Factor VIII Antibodies in human Plasma

Jolanta Krudysz-Amblo, Behnaz Parhami-Seren, Ph.D., Saulius Butenas, Ph.D., Kathleen E. Brummel-Ziedins, PhD, Edward D. Gomperts, MBBCH, MD, Georges E. Rivard, MD, Kenneth G. Mann, PhD

Blood (2008) 112 (11): 1025.

https://doi.org/10.1182/blood.V112.11.1025.1025

Published: 2008

Journal Articles

Quebec Platelet Disorder Is Caused by a Cis-Acting Mutation near the Plasminogen Activator Gene (PLAU) That Increases PLAU Transcription by Megakaryocytes.

Maria Diamandis, Andrew D Paterson, PhD, Johanna M Rommens, PhD, D. Kika Veljkovic, MD, Jessica Blavignac, John S Waye, PhD, Francine Derome, Georges E. Rivard, MD, Catherine PM Hayward, MD, PhD

Blood (2008) 112 (11): 3394.

https://doi.org/10.1182/blood.V112.11.3394.3394

Published: 2008

Journal Articles

Use of Factor VIII/Von Willebrand Factor Complex for Inducing Immune Tolerance in Hemophilia a Patients Who Have Failed with Recombinant Fviii: Recent Canadian Experience

Anne-Marie Vincent, M.D., FRCPC, Anthony Chan, MBBS, Sara J. Israels, MD, Man-Chiu Poon, MD, John K. Wu, MBBS, FRCPC, Georges E. Rivard, MD

Blood (2008) 112 (11): 4520.

https://doi.org/10.1182/blood.V112.11.4520.4520

Published: 2008

Journal Articles

Proteomics in the Study of Qualitative Platelet Defects: Validation of the Approach in the Gray Platelet Syndrome and Quebec Platelet Disorder.

Raj S. Kasthuri, MBBS, Lorraine B. Anderson, PhD, LeeAnn Higgins, PhD, Jorge Di Paola, MD, Georges E. Rivard, MD, FRCP(C), Catherine P.M. Hayward, MD, PhD, FRCP(C), Nigel S. Key, MB, FRCP

Blood (2007) 110 (11): 3900.

https://doi.org/10.1182/blood.V110.11.3900.3900

Published: 2007

Journal Articles

Insights into Disturbed Hemostasis in the Quebec Platelet Disorder Using Thromboelastography, Blood Clots Formed at Low Shear, and Perfusion Studies of Fibrinolysis.

Maria Diamandis, Hon., BSc, Frederic Adam, PhD, Georges E. Rivard, MD, Walter H.A. Kahr, MD, PhD, Catherine P.M. Hayward, MD, PhD

Blood (2005) 106 (11): 2135.

https://doi.org/10.1182/blood.V106.11.2135.2135

Published: 2005

Journal Articles

Efficacy of Alphanate ® (Human Factor VIII/Von Willebrand Factor Concentrate) in Preventing Excessive Bleeding during Surgery or Invasive Procedures in Patients with Congenital Von Willebrand Disease. A Multicenter Retrospective Study.

M. Elaine Eyster, MD, Charles L. Sexauer, MD, Simon Brown, MD, Richard A. Lipton, MD, Craig M. Kessler, MD, Louis M. Aledort, MD, Georges E. Rivard, MD

Blood (2005) 106 (11): 3951.

https://doi.org/10.1182/blood.V106.11.3951.3951

Published: 2005

Journal Articles

Ten-Year Follow-Up of Inhibitor Induction in Previously Untreated Patients (PUPs) on Recombinate.

Louis M. Aledort, MD, Gilbert C. White, II, MD, Georges E. Rivard, MD

Blood (2004) 104 (11): 4004.

https://doi.org/10.1182/blood.V104.11.4004.4004

Published: 2004

Journal Articles

Evaluation of the Profile of Thrombin Generation during the Process of Whole Blood Clotting as Assessed by Thromboelastography.

Georges E. Rivard, MD, Brummel Kathleen, PhD, Fan Li, PhD, Hofer Angelique, RT, Cohen Eli, PhD, Mann G. Kenneth, PhD

Blood (2004) 104 (11): 2981.

https://doi.org/10.1182/blood.V104.11.2981.2981

Published: 2004

NARROW

Thrombin Generation Impairments in Platelet Function Disorders

Immune Tolerance Induction in Hemophilia A Patients Using Wilate® —a Canadian 10 Year Study (PREVAIL)

Transcriptional Landscape of APL Identifies Aberrant Podoplanin Expression As a Defining Feature and Missing Link for the Bleeding Disorder of This Disease

Bleeding Risks Associated with Confirmed Platelet Dense Granule Deficiency and/or Impaired Aggregation Responses

An Unusual Case of Acquired Hemophilia a and Factor XIII Consumption

Quebec Platelet Disorder Is Associated With Greater Than Expected Increases In Urokinase Plasminogen Activator In Granulocytes and Monocytes

Dysregulation of C10orf55 Expression in Megakaryocytic Cell Lineage From Quebec Platelet Disorder Individuals

Quantitation of Non-Inhibitory Anti-Factor VIII Antibodies in human Plasma

Quebec Platelet Disorder Is Caused by a Cis-Acting Mutation near the Plasminogen Activator Gene (PLAU) That Increases PLAU Transcription by Megakaryocytes.

Use of Factor VIII/Von Willebrand Factor Complex for Inducing Immune Tolerance in Hemophilia a Patients Who Have Failed with Recombinant Fviii: Recent Canadian Experience

Proteomics in the Study of Qualitative Platelet Defects: Validation of the Approach in the Gray Platelet Syndrome and Quebec Platelet Disorder.

Insights into Disturbed Hemostasis in the Quebec Platelet Disorder Using Thromboelastography, Blood Clots Formed at Low Shear, and Perfusion Studies of Fibrinolysis.

Efficacy of Alphanate ® (Human Factor VIII/Von Willebrand Factor Concentrate) in Preventing Excessive Bleeding during Surgery or Invasive Procedures in Patients with Congenital Von Willebrand Disease. A Multicenter Retrospective Study.

Ten-Year Follow-Up of Inhibitor Induction in Previously Untreated Patients (PUPs) on Recombinate.

Evaluation of the Profile of Thrombin Generation during the Process of Whole Blood Clotting as Assessed by Thromboelastography.

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American Society of Hematology

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American Society of Hematology

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