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Procoagulant Phosphatidylserine-Exposing Platelets in vitro and in vivo

Frontiers in cardiovascular medicine, 2020-03, Vol.7, p.15-15

2020

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Professor Victor S. Blanchette, MA, MB, BChir (Cantab), FRCP(C), FRCP (1945-2024)

Journal of thrombosis and haemostasis, 2024-09

2024

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Dr. Victor Stanley Blanchette (1945-2024): a titan at Toronto's SickKids

Pediatric research, 2024-10

2024

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IVIg treatment increases thrombin activation of platelets and thrombin generation in paediatric patients with immune thrombocytopenia

British journal of haematology, 2023-06, Vol.201 (6), p.1209-1219

2023

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Plasma fibronectin supports hemostasis and regulates thrombosis

The Journal of clinical investigation, 2014-10, Vol.124 (10), p.4281-4293

2014

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Omi/HtrA2 and XIAP are components of platelet apoptosis signalling

Thrombosis and haemostasis, 2013-03, Vol.109 (3), p.532-539

2013

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Comparative pharmacokinetics of two extended half‐life FVIII concentrates (Eloctate and Adynovate) in adolescents with hemophilia A: Is there a difference?

Journal of thrombosis and haemostasis, 2019-07, Vol.17 (7), p.1085-1096

2019

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Apolipoprotein A-IV polymorphisms Q360H and T347S attenuate its endogenous inhibition of thrombosis

Biochemical and biophysical research communications, 2024-06, Vol.712-713, p.149946, Article 149946

2024

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Professor Marian A. Packham, CM, PhD, DSc, FRSC (1927–2020)

Journal of thrombosis and haemostasis, 2021-01, Vol.19 (1), p.311-312

2021

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Bleeding Severity and Phenotype in 22q11.2 Deletion Syndrome—A Cross-Sectional Investigation

The Journal of pediatrics, 2021-08, Vol.235, p.220-225

2021

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A Practical, One-Clinic Visit Protocol for Pharmacokinetic Profile Generation with the ADVATE myPKFiT Dosing Tool in Severe Hemophilia A Subjects

Thrombosis and haemostasis, 2021-10, Vol.121 (10), p.1326-1336

2021

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Moderate-intensity aerobic exercise vs desmopressin in adolescent males with mild hemophilia A: a randomized trial

Blood, 2022-09, Vol.140 (10), p.1156-1166

2022

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Increased levels of IL-10 and IL-1Ra counterbalance the proinflammatory cytokine pattern in acute pediatric immune thrombocytopenia

Cytokine (Philadelphia, Pa.), 2020-06, Vol.130, p.155078-155078, Article 155078

2020

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Decreased numbers of dense granules in fetal and neonatal platelets

Haematologica (Roma), 2017-02, Vol.102 (2), p.e36-e38

2017

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Laboratory diagnosis of inherited platelet function disorders

Transfusion and apheresis science, 2018-08, Vol.57 (4), p.485-493

2018

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Altered coagulation profile in peripheral artery disease patients

Vascular, 2020-08, Vol.28 (4), p.368-377

2020

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Constitutive hypercoagulability in pediatric sickle cell disease patients with hemoglobin SS genotype

Research and practice in thrombosis and haemostasis, 2024-03, Vol.8 (3), p.102374-102374, Article 102374

2024

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Glanzmann thrombasthenia platelets compete with transfused platelets, reducing the haemostatic impact of platelet transfusions

British journal of haematology, 2018-05, Vol.181 (3), p.410-413

2018

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EspP, an Extracellular Serine Protease from Enterohemorrhagic E. coli, Reduces Coagulation Factor Activities, Reduces Clot Strength, and Promotes Clot Lysis

PloS one, 2016-03, Vol.11 (3), p.e0149830-e0149830

2016

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Idiopathic pulmonary arterial hypertension – a unrecognized cause of high‐shear high‐flow haemostatic defects (otherwise referred to as acquired von Willebrand syndrome) in children

British journal of haematology, 2018-10, Vol.183 (2), p.267-275

2018

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Generation and optimization of the self‐administered pediatric bleeding questionnaire and its validation as a screening tool for von Willebrand disease

Pediatric blood & cancer, 2017-10, Vol.64 (10), p.n/a

2017

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Impact of aerobic exercise on haemostatic indices in paediatric patients with haemophilia: Results from a prospective cohort study

Thrombosis and haemostasis, 2016-06, Vol.115 (6), p.1120-1128

2016

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Low-dose aspirin and rivaroxaban combination therapy to overcome aspirin non-sensitivity in patients with vascular disease

Frontiers in cardiovascular medicine, 2022-08, Vol.9, p.912114-912114

2022

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Procoagulant Phosphatidylserine-Exposing Platelets in vitro and in vivo

Professor Victor S. Blanchette, MA, MB, BChir (Cantab), FRCP(C), FRCP (1945-2024)

Dr. Victor Stanley Blanchette (1945-2024): a titan at Toronto's SickKids

IVIg treatment increases thrombin activation of platelets and thrombin generation in paediatric patients with immune thrombocytopenia

Plasma fibronectin supports hemostasis and regulates thrombosis

Omi/HtrA2 and XIAP are components of platelet apoptosis signalling

Comparative pharmacokinetics of two extended half‐life FVIII concentrates (Eloctate and Adynovate) in adolescents with hemophilia A: Is there a difference?

Apolipoprotein A-IV polymorphisms Q360H and T347S attenuate its endogenous inhibition of thrombosis

Professor Marian A. Packham, CM, PhD, DSc, FRSC (1927–2020)

Bleeding Severity and Phenotype in 22q11.2 Deletion Syndrome—A Cross-Sectional Investigation

A Practical, One-Clinic Visit Protocol for Pharmacokinetic Profile Generation with the ADVATE myPKFiT Dosing Tool in Severe Hemophilia A Subjects

Moderate-intensity aerobic exercise vs desmopressin in adolescent males with mild hemophilia A: a randomized trial

Increased levels of IL-10 and IL-1Ra counterbalance the proinflammatory cytokine pattern in acute pediatric immune thrombocytopenia

Decreased numbers of dense granules in fetal and neonatal platelets

Laboratory diagnosis of inherited platelet function disorders

Altered coagulation profile in peripheral artery disease patients

Expanding the Mutation Spectrum Affecting alpha IIb beta 3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort

Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort

Constitutive hypercoagulability in pediatric sickle cell disease patients with hemoglobin SS genotype

Glanzmann thrombasthenia platelets compete with transfused platelets, reducing the haemostatic impact of platelet transfusions

EspP, an Extracellular Serine Protease from Enterohemorrhagic E. coli, Reduces Coagulation Factor Activities, Reduces Clot Strength, and Promotes Clot Lysis

Idiopathic pulmonary arterial hypertension – a unrecognized cause of high‐shear high‐flow haemostatic defects (otherwise referred to as acquired von Willebrand syndrome) in children

Generation and optimization of the self‐administered pediatric bleeding questionnaire and its validation as a screening tool for von Willebrand disease

Impact of aerobic exercise on haemostatic indices in paediatric patients with haemophilia: Results from a prospective cohort study

Low-dose aspirin and rivaroxaban combination therapy to overcome aspirin non-sensitivity in patients with vascular disease

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