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New mutation found to cause hereditary thrombotic thrombocytopenic purpura in a patient presenting with seizures in adulthood

Platelets (Edinburgh), 2020-11, Vol.31 (8), p.1-1096

2020

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Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?

Platelets (Edinburgh), 2018-02, Vol.29 (2), p.148-155

2018

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Incidence of thrombotic microangiopathies in Quebec: insight from a laboratory centralizing ADAMTS-13 testing

Orphanet journal of rare diseases, 2022-08, Vol.17 (1), p.1-11, Article 308

2022

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Clinical Use of Complement, Inflammation, and Fibrosis Biomarkers in Autoimmune Glomerulonephritis

Kidney international reports, 2020-10, Vol.5 (10), p.1690-1699

2020

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Requirements for membrane attack complex formation and anaphylatoxins binding to collagen-activated platelets

PloS one, 2011-04, Vol.6 (4), p.e18812-e18812

2011

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Comparing Pathways of Bradykinin Formation in Whole Blood From Healthy Volunteers and Patients With Hereditary Angioedema Due to C1 Inhibitor Deficiency

Frontiers in immunology, 2018-10, Vol.9, p.2183-2183

2018

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Thrombospondin-1-Derived Peptide RFYVVMWK Improves the Adhesive Phenotype of CD34+ Cells from Atherosclerotic Patients with Type 2 Diabetes

Cell transplantation, 2017-02, Vol.26 (2), p.327-337

2017

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Clinical Value of Complement Activation Biomarkers in Overt Diabetic Nephropathy

Kidney international reports, 2019-06, Vol.4 (6), p.797-805

2019

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Pexelizumab fails to inhibit assembly of the terminal complement complex in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention. Insight from a substudy of the Assessment of Pexelizumab in Acute Myocardial Infarction (APEX-AMI) trial

The American heart journal, 2012-07, Vol.164 (1), p.43-51

2012

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Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene Variants

Frontiers in medicine, 2020-07, Vol.7, p.358-358

2020

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Blocking the terminal complement complex: Mismatch and misconception

The American heart journal, 2012-12, Vol.164 (6), p.e21-e21

2012

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Proteolysis of Subendothelial Adhesive Glycoproteins (Fibronectin, Thrombospondin, and von Willebrand Factor) by Plasmin, Leukocyte Cathepsin G, and Elastase

Thrombosis research, 2000-05, Vol.98 (4), p.323-332

2000

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Thrombospondin-1 in von Willebrand factor function

Current drug targets, 2008-10, Vol.9 (10), p.822-832

2008

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Overexpression of the platelet P2X1 ion channel in transgenic mice generates a novel prothrombotic phenotype

Blood, 2003-05, Vol.101 (10), p.3969-3976

2003

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Involvement of the Mitogen-activated Protein Kinase c-Jun NH2-terminal Kinase 1 in Thrombus Formation

The Journal of biological chemistry, 2007-11, Vol.282 (44), p.31990-31999

2007

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Platelets, thrombospondin-1 and human dermal fibroblasts cooperate for stimulation of endothelial cell tubulogenesis through VEGF and PAI-1 regulation

Experimental cell research, 2007-02, Vol.313 (3), p.486-499

2007

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Differential Involvement of ERK2 and p38 in Platelet Adhesion to Collagen

The Journal of biological chemistry, 2005-07, Vol.280 (28), p.26002-26010

2005

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Urinary Biomarkers as a Tool for Monitoring Remissions and Predicting Relapses in Autoimmune Glomerulonephritis: PO1732

Journal of the American Society of Nephrology, 2020-10, Vol.31 (10S), p.543-543

2020

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Incidence of Thrombotic Microangiopathies in Quebec: An 8-Year Overview from a Laboratory Centralizing Adamts-13 Testing

Blood, 2021-11, Vol.138 (Supplement 1), p.4222-4222

2021

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Initial Clinical Presentation and Predictors of Thrombotic Thrombocytopenic Purpura in Quebec

Blood, 2021-11, Vol.138 (Supplement 1), p.4224-4224

2021

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Abstract 11378: Reference Intervals of Activated Clotting Time in Pediatric Patients Undergoing Cardiac Surgery

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

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A Model of Platelet Aggregation Involving Multiple Interactions of Thrombospondin-1, Fibrinogen, and GPIIbIIIa Receptor

The Journal of biological chemistry, 2001-02, Vol.276 (8), p.5605-5612

2001

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Specific inhibition of P-selectin–mediated cell adhesion by phage display–derived peptide antagonists

Blood, 2002-11, Vol.100 (10), p.3570-3577

2002

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Predictive significance of anti‐FVIII immunoglobulin patterns on bleeding phenotype and outcomes in acquired hemophilia A: Results from the Quebec Reference Center for Inhibitors

Journal of thrombosis and haemostasis, 2021-12, Vol.19 (12), p.2947-2956

2021

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Iron-Refractory Iron Deficiency Anemia May Not Lead to Neurocognitive Dysfunction: A Case Report

Pediatrics (Evanston), 2016-07, Vol.138 (1)

2016

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New mutation found to cause hereditary thrombotic thrombocytopenic purpura in a patient presenting with seizures in adulthood

Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?

Incidence of thrombotic microangiopathies in Quebec: insight from a laboratory centralizing ADAMTS-13 testing

Clinical Use of Complement, Inflammation, and Fibrosis Biomarkers in Autoimmune Glomerulonephritis

Requirements for membrane attack complex formation and anaphylatoxins binding to collagen-activated platelets

Comparing Pathways of Bradykinin Formation in Whole Blood From Healthy Volunteers and Patients With Hereditary Angioedema Due to C1 Inhibitor Deficiency

Thrombospondin-1-Derived Peptide RFYVVMWK Improves the Adhesive Phenotype of CD34+ Cells from Atherosclerotic Patients with Type 2 Diabetes

Clinical Value of Complement Activation Biomarkers in Overt Diabetic Nephropathy

Pexelizumab fails to inhibit assembly of the terminal complement complex in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention. Insight from a substudy of the Assessment of Pexelizumab in Acute Myocardial Infarction (APEX-AMI) trial

Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene Variants

Blocking the terminal complement complex: Mismatch and misconception

Proteolysis of Subendothelial Adhesive Glycoproteins (Fibronectin, Thrombospondin, and von Willebrand Factor) by Plasmin, Leukocyte Cathepsin G, and Elastase

Thrombospondin-1 in von Willebrand factor function

Overexpression of the platelet P2X1 ion channel in transgenic mice generates a novel prothrombotic phenotype

Involvement of the Mitogen-activated Protein Kinase c-Jun NH2-terminal Kinase 1 in Thrombus Formation

Platelets, thrombospondin-1 and human dermal fibroblasts cooperate for stimulation of endothelial cell tubulogenesis through VEGF and PAI-1 regulation

Differential Involvement of ERK2 and p38 in Platelet Adhesion to Collagen

Urinary Biomarkers as a Tool for Monitoring Remissions and Predicting Relapses in Autoimmune Glomerulonephritis: PO1732

Incidence of Thrombotic Microangiopathies in Quebec: An 8-Year Overview from a Laboratory Centralizing Adamts-13 Testing

Initial Clinical Presentation and Predictors of Thrombotic Thrombocytopenic Purpura in Quebec

Abstract 11378: Reference Intervals of Activated Clotting Time in Pediatric Patients Undergoing Cardiac Surgery

A Model of Platelet Aggregation Involving Multiple Interactions of Thrombospondin-1, Fibrinogen, and GPIIbIIIa Receptor

Specific inhibition of P-selectin–mediated cell adhesion by phage display–derived peptide antagonists

Predictive significance of anti‐FVIII immunoglobulin patterns on bleeding phenotype and outcomes in acquired hemophilia A: Results from the Quebec Reference Center for Inhibitors

Iron-Refractory Iron Deficiency Anemia May Not Lead to Neurocognitive Dysfunction: A Case Report

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