C. Hayward

发表

Diagnostic evaluation of platelet function disorders.

C. Hayward, 2011, Blood reviews.

Thrombocytopenic platelet disorders.

C. Hayward, N. Bunimov, 2011, Seminars in thrombosis and hemostasis.

Serum-induced platelet procoagulant activity: an assay for the characterization of prothrombotic disorders.

J. Kelton, M. Warner, T. Warkentin, 1999, The Journal of laboratory and clinical medicine.

Screening and diagnosis of inherited platelet disorders

S. Tasneem, C. Hayward, Alex Bourguignon, 2022, Critical reviews in clinical laboratory sciences.

Sera from patients with heparin-induced thrombocytopenia generate platelet-derived microparticles with procoagulant activity: an explanation for the thrombotic complications of heparin-induced thrombocytopenia.

J. Kelton, T. Warkentin, Aurelio V. Santos, 1994, Blood.

Heparin‐induced thrombocytopenia and thrombosis: clinical and laboratory studies

J. Kelton, M. Andrew, T. Warkentin, 1993, British journal of haematology.

Investigation of the mechanisms of monoclonal antibody-induced platelet activation

J. Kelton, P. Horsewood, T. Warkentin, 1991 .

Investigation of the mechanisms of monoclonal antibody-induced platelet activation.

J. Kelton, P. Horsewood, T. Warkentin, 1991, Blood.

Platelet adhesion to multimerin 1 in vitro: influences of platelet membrane receptors, von Willebrand factor and shear

J. Miller, F. Adam, S. Tasneem, 2009, Journal of thrombosis and haemostasis : JTH.

Platelet Aggregation

C. Hayward, K. Moffat, 2019, Platelets.

Platelet function analyzer (PFA)‐100® closure time in the evaluation of platelet disorders and platelet function

T. Ortel, M. Cattaneo, P. Harrison, 2006, Journal of thrombosis and haemostasis : JTH.

An acquired factor V inhibitor associated with defective factor V function, storage and binding to multimerin 1

E. Krakow, S. Tasneem, C. Hayward, 2008, Journal of thrombosis and haemostasis : JTH.

A diagnostic test for heparin‐induced thrombocytopenia: detection of platelet microparticles using flow cytometry

J. Kelton, G. Denomme, T. Warkentin, 1996, British journal of haematology.

Global haemostasis and point of care testing

C. Négrier, M. Shima, A. Srivastava, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Thrombin generation abnormalities in commonly encountered platelet function disorders

Stephanie A. Smith, S. Tasneem, J. Morrissey, 2021, International journal of laboratory hematology.

Report on the International Society for Laboratory Hematology Survey on guidelines to support clinical hematology laboratory practice

T. George, C. Hayward, K. Moffat, 2016, International journal of laboratory hematology.

Critical values in the coagulation laboratory: results of a survey of the North American Specialized Coagulation Laboratory Association.

M. Pai, C. Hayward, K. Moffat, 2009, American journal of clinical pathology.

Endocytosis and storage of plasma factor V by human megakaryocytes

Y. Motomura, C. Hayward, E. Cramer, 2005, Thrombosis and Haemostasis.

Electron microscopy examination of platelet whole mount preparations to quantitate platelet dense granule numbers: Implications for diagnosing suspected platelet function disorders due to dense granule deficiency

J. Iyer, C. Hayward, K. Moffat, 2018, International journal of laboratory hematology.

Variability in platelet dense granule adenosine triphosphate release findings amongst patients tested multiple times as part of an assessment for a bleeding disorder

J. Iyer, C. Hayward, K. Moffat, 2016, International journal of laboratory hematology.

Platelet Aggregation

C. Hayward, K. Moffat, 2019, Platelets.

Recommendations for the standardization of light transmission aggregometry: a consensus of the working party from the platelet physiology subcommittee of SSC/ISTH

A. Schmaier, P. Nurden, C. Cerletti, 2013, Journal of thrombosis and haemostasis : JTH.

Simultaneous measurement of adenosine triphosphate release and aggregation potentiates human platelet aggregation responses for some subjects, including persons with Quebec platelet disorder

Jean-François Castilloux, G. Rivard, S. Tasneem, 2012, Thrombosis and Haemostasis.

Determinants of donor platelet variability when testing for heparin-induced thrombocytopenia.

J. Kelton, T. Warkentin, C. Hayward, 1992, The Journal of laboratory and clinical medicine.

The epitope specificity of heparin‐induced thrombocytopenia

J. Kelton, P. Horsewood, T. Warkentin, 1996, British journal of haematology.

Immunoglobulin G from patients with heparin-induced thrombocytopenia binds to a complex of heparin and platelet factor 4.

J. Kelton, James W. Smith, P. Horsewood, 1994, Blood.

Further complexities in diagnosing acquired thrombocytopenia: unexpected parallels between antibody-mediated delayed thrombocytopenia with abciximab and heparin induced thrombocytopenia.

C. Hayward, 2004, Thrombosis and haemostasis.

The cDNA Sequence of Human Endothelial Cell Multimerin

J. Kelton, J. Hassell, G. Denomme, 1995, The Journal of Biological Chemistry.

Laboratory Investigations for Bleeding Disorders

C. Hayward, K. Moffat, Yang Liu, 2012, Seminars in Thrombosis & Hemostasis.

Diagnostic approach to platelet function disorders.

C. Hayward, 2008, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Human platelets contain forms of factor V in disulfide-linkage with multimerin

F. Adam, M. Quinn-Allen, W. Kane, 2004, Thrombosis and Haemostasis.

An evaluation of methods for determining reference intervals for light transmission platelet aggregation tests on samples with normal or reduced platelet counts

N. Heddle, R. Cook, K. Webert, 2008, Thrombosis and Haemostasis.

Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator.

T. Podor, G. Rivard, M. Pai, 2001, Blood.

Calpain activity in patients with thrombotic thrombocytopenic purpura is associated with platelet microparticles.

J. Kelton, T. Warkentin, W. Murphy, 1992, Blood.

An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect.

J. Kelton, G. Rivard, J. Drouin, 1996, Blood.

Factor V Is Complexed with Multimerin in Resting Platelet Lysates and Colocalizes with Multimerin in Platelet α-Granules (*)

J. Kelton, D. Bainton, M. Nesheim, 1995, The Journal of Biological Chemistry.

Diagnostic utility of light transmission platelet aggregometry: results from a prospective study of individuals referred for bleeding disorder assessments

N. Heddle, R. Cook, R. Cook, 2009, Journal of thrombosis and haemostasis : JTH.

Analyses of cellular multimerin 1 receptors: in vitro evidence of binding mediated by αΙΙbβ3 and αvβ3

F. Adam, J. Kelton, Aurelio V. Santos, 2005, Thrombosis and Haemostasis.

Development of North American consensus guidelines for medical laboratories that perform and interpret platelet function testing using light transmission aggregometry.

J. Zehnder, S. Israels, C. Hayward, 2010, American journal of clinical pathology.

Diagnostic Assessment of Platelet Disorders: What Are the Challenges to Standardization?

M. Pai, C. Hayward, Menaka Pai1, 2009, Seminars in thrombosis and hemostasis.

Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey

C. Gachet, D. Kenny, A. Mumford, 2014, Journal of thrombosis and haemostasis : JTH.

Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment

M. Cattaneo, C. Hayward, A. Rao, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Inherited disorders of platelet alpha-granules.

C. Hayward, 1997, Platelets.

Diagnosis and management of mild bleeding disorders.

C. Hayward, 2005, Hematology. American Society of Hematology. Education Program.

Laboratory testing for heparin-induced thrombocytopenia is inconsistent in North America: A survey of North American specialized coagulation laboratories

J. Zehnder, T. Warkentin, C. Hayward, 2007, Thrombosis and Haemostasis.

Intracellular activation of the fibrinolytic cascade in the Quebec Platelet Disorder

G. Rivard, W. Kahr, P. Sheth, 2003, Thrombosis and Haemostasis.

Advances in Understanding “High on-Treatment Platelet Reactivity”

C. Hayward, 2009, Thrombosis and Haemostasis.

Variability in clinical laboratory practice in testing for disorders of platelet function

W. Nichols, C. Hayward, M. Ledford-Kraemer, 2005, Thrombosis and Haemostasis.

A prospective cohort study of light transmission platelet aggregometry for bleeding disorders: Is testing native platelet-rich plasma non-inferior to testing platelet count adjusted samples?

Jean-François Castilloux, M. Pai, C. Hayward, 2011, Thrombosis and Haemostasis.

Failure of pulse high‐dose dexamethasone in chronic idiopathic immune thrombocytopenia

J. Kelton, M. Warner, P. Wasi, 1997, American journal of hematology.

Expert Approaches to Common Bleeding and Thrombotic Problems, Part II

K. Webert, C. Hayward, 2012, Seminars in Thrombosis & Hemostasis.

Multimerin: a series of large disulfide-linked multimeric proteins within platelets.

J. Kelton, P. Horsewood, T. Warkentin, 1991, Blood.

External Quality Assessment of Platelet Disorder Investigations: Results of International Surveys on Diagnostic Tests for Dense Granule Deficiency and Platelet Aggregometry Interpretation

P. Meijer, E. V. Van Cott, C. Hayward, 2012, Seminars in Thrombosis & Hemostasis.

p-155, a multimeric platelet protein that is expressed on activated platelets.

J. Kelton, P. Horsewood, J. Smith, 1991, The Journal of biological chemistry.

Are laboratories following published recommendations for lupus anticoagulant testing?

P. Meijer, W. Nichols, C. Hayward, 2008, Thrombosis and Haemostasis.

Studies of multimerin in human endothelial cells.

R. Stead, T. Podor, C. Hayward, 1998, Blood.

Multimerin: A Multimeric Protein Stored in Platelet Alpha-granules.

J. Kelton, C. Hayward, 1995, Platelets.

Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders.

J. Kelton, T. Warkentin, C. Hayward, 2001, Blood.

Prospective screening of 205 patients with ITP, including diagnosis, serological markers, and the relationship between platelet counts, endogenous thrombopoietin, and circulating antithrombopoietin antibodies

J. Bussel, L. Aledort, C. Hayward, 2004, American journal of hematology.

Bacterial infection‐associated improvement of platelet counts in two patients with chronic and unresponsive idiopathic thrombocytopenic purpura with normal platelet survival studies

J. Kelton, James W. Smith, P. Wasi, 1995, British journal of haematology.

Isolation and characterization of cysteine proteinase in thrombotic thrombocytopenic purpura

J. Kelton, T. Warkentin, C. Hayward, 1996, British journal of haematology.

Results of a worldwide survey on the assessment of platelet function by light transmission aggregometry: a report from the platelet physiology subcommittee of the SSC of the ISTH

A. Michelson, M. Cattaneo, C. Hayward, 2009, Journal of thrombosis and haemostasis : JTH.

An Assessment of the State of Current Practice in Coagulation Laboratories.

E. V. Van Cott, C. Hayward, K. Smock, 2016, American journal of clinical pathology.

Multimerin 1 supports platelet function in vivo and binds to specific GPAGPOGPX motifs in fibrillar collagens that enhance platelet adhesion

B. Doble, H. Ni, D. Lillicrap, 2020, Journal of thrombosis and haemostasis : JTH.

Illustrated State‐of‐the‐Art Capsules of the ISTH 2022 Congress

A. Balduini, R. Ahrends, N. Mackman, 2022, Research and practice in thrombosis and haemostasis.

Platelet factor V New York: A defect in factor V distinct from that in factor V Quebec resulting in impaired prothrombinase generation

H. Weiss, B. Lages, C. Hayward, 2001, American journal of hematology.

Improved platelet counts during prolonged tranexamic therapy for Quebec platelet disorder implicate the underlying fibrinolytic defect as the cause of lower platelet counts

G. Rivard, S. Tasneem, C. Hayward, 2020, International journal of laboratory hematology.

Mice with deleted multimerin 1 and alpha-synuclein genes have impaired platelet adhesion and impaired thrombus formation that is corrected by multimerin 1.

H. Ni, S. Tasneem, C. Hayward, 2010, Thrombosis research.

The storage defects in grey platelet syndrome and αδ‐storage pool deficiency affect α‐granule factor V and multimerin storage without altering their proteolytic processing

Paul J. Harrison, H. Weiss, B. Lages, 2001 .

The storage defects in grey platelet syndrome and alphadelta-storage pool deficiency affect alpha-granule factor V and multimerin storage without altering their proteolytic processing.

B. Lages, P. Harrison, C. Hayward, 2001, British journal of haematology.

Factor XIII Assays and Associated Problems for Laboratory Diagnosis of Factor XIII Deficiency: An Analysis of International Proficiency Testing Results

P. Meijer, Xinmin Zhang, E. V. Van Cott, 2014, Seminars in Thrombosis & Hemostasis.

Laboratory testing for bleeding disorders: strategic uses of high and low‐yield tests

C. Hayward, K. Moffat, 2013, International journal of laboratory hematology.

Dissociation between the level of von Willebrand factor‐cleaving protease activity and disease in a patient with congenital thrombotic thrombocytopenic purpura

J. Kelton, T. Warkentin, C. Hayward, 2004, American journal of hematology.

Update on platelet procoagulant mechanisms in health and in bleeding disorders

S. Tasneem, C. Hayward, Alex Bourguignon, 2022, International journal of laboratory hematology.

Thrombin generation abnormalities in Quebec platelet disorder

Michael D. Wilson, G. Rivard, Minggao Liang, 2020, International journal of laboratory hematology.

PROTEOLYTIC DEGRADATION OF HIGH MOLECULAR WEIGHT KININOGEN IN ACUTE THROMBOTIC THROMBOCYTOPENIC PURPURA

J. Kelton, M. Warner, T. Warkentin, 1997, British journal of haematology.

Improving blood disorder diagnosis: reflections on the challenges

C. Hayward, 2013, International journal of laboratory hematology.

Multimerin processing by cells with and without pathways for regulated protein secretion.

M. Pai, C. Hayward, E. Cramer, 1999, Blood.

Studies of multimerin in patients with von Willebrand disease and platelet von Willebrand factor deficiency

Pille Harrison, P. Mannucci, A. Federici, 1998, British journal of haematology.

Studies of a second family with the Quebec platelet disorder: evidence that the degradation of the alpha-granule membrane and its soluble contents are not secondary to a defect in targeting proteins to alpha-granules.

G. Rivard, C. Hayward, E. Cramer, 1997, Blood.

Multimerin is found in the alpha-granules of resting platelets and is synthesized by a megakaryocytic cell line.

R. Stead, J. Kelton, T. Podor, 1993, The Journal of clinical investigation.

Multimerin

J. Kelton, C. Hayward, 1995, Current opinion in hematology.

Inherited platelet disorders

C. Hayward, 2003, Current opinion in hematology.

Evaluation of an automated method for measuring von Willebrand factor activity in clinical samples without ristocetin

A. Chan, A. Giulivi, C. Hayward, 2014, International journal of laboratory hematology.

Bleeding risks associated with inheritance of the Quebec platelet disorder.

F. Adam, S. Whittaker, N. Heddle, 2004, Blood.

Quebec platelet disorder: features, pathogenesis and treatment

M. Diamandis, E. Maurer-Spurej, G. Rivard, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

New developments in laboratory diagnosis and monitoring

C. Négrier, S. Kitchen, Y. Dargaud, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Genomic approaches to bleeding disorders

F. Peyvandi, C. Hayward, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Laboratory issues in bleeding disorders

F. Rodeghiero, A. Ruiz-Sáez, C. Hayward, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Prevalence and diagnosis of haemorrhagic disorders and evaluation of effectiveness of WFH laboratory training workshops in Latin America

F. Rodeghiero, A. Ruiz-Sáez, C. Hayward, 2008 .

Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation

A. Paterson, G. Paré, J. Iyer, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Analytical Performance of COVID-19 Detection Methods (RT-PCR): Scientific and Societal Concerns

M. Bizzarri, A. Fuso, A. Angeloni, 2021, Life.

Results of an external proficiency testing exercise on platelet dense-granule deficiency testing by whole mount electron microscopy.

S. Israels, C. Hayward, K. Moffat, 2009, American journal of clinical pathology.

The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes

Michael D. Wilson, A. Paterson, G. Rivard, 2017, PloS one.

Diagnostic usefulness of a lumi-aggregometer adenosine triphosphate release assay for the assessment of platelet function disorders.

N. Heddle, K. Webert, M. Pai, 2011, American journal of clinical pathology.

Morphological analysis of microparticle generation in heparin-induced thrombocytopenia.

K. Chorneyko, J. Kelton, P. Horsewood, 2000, Blood.

Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes.

A. Paterson, J. Rommens, D. Bulman, 2009, Blood.

Insights into abnormal hemostasis in the Quebec platelet disorder from analyses of clot lysis

K. Chorneyko, F. Adam, A. Arsenault, 2006, Journal of thrombosis and haemostasis : JTH.

Update on diagnostic testing for platelet function disorders: What is practical and useful?

J. Zehnder, P. Meijer, C. Hayward, 2019, International journal of laboratory hematology.

Genetic Loci Associated with Platelet Traits and Platelet Disorders

C. Hayward, N. Bunimov, N. Fuller, 2013, Seminars in Thrombosis & Hemostasis.

Chapter 28 – Platelet Aggregation

C. Hayward, K. Moffat, 2013 .

Approaches to investigating common bleeding disorders: An evaluation of North American coagulation laboratory practices

C. Hayward, ElizabethM Van Cott, K. Moffat, 2012, American journal of hematology.

Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene.

A. Paterson, J. Rommens, I. Wong, 2010, Blood.

Enhancer-gene rewiring in the pathogenesis of Quebec Platelet Disorder.

Michael D. Wilson, Jennifer A. Mitchell, A. Paterson, 2020, Blood.

Thrombocytopenia caused by passive transfusion of anti-glycoprotein Ia/IIa alloantibody (anti-HPA-5b).

J. Kelton, James W. Smith, J. Smith, 1992, Blood.

Treatment outcomes in patients with adult thrombotic thrombocytopenic purpura-hemolytic uremic syndrome.

E. D. Campbell, W. H. Carter, M. A. Baker, 1994, Archives of internal medicine.

Laboratory testing for fibrinogen abnormalities

M. Verhovsek, C. Hayward, K. Moffat, 2008, American journal of hematology.

Thrombocytopenia caused by passive transfusion of anti-glycoprotein

J. Kelton, James W. Smith, T. Warkentin, 2011 .

Maternal immunization to Gov system alloantigens on human platelets

J. Kelton, James W. Smith, M. Warner, 1997, Transfusion.

ABH antigens on human platelets: expression on the glycosyl phosphatidylinositol-anchored protein CD109.

J. Kelton, R. Finberg, James W. Smith, 1998, The Journal of laboratory and clinical medicine.

The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysis

J. Kelton, James W. Smith, P. Horsewood, 1995, British journal of haematology.

Characterization and localization of the Gova/b alloantigens to the glycosylphosphatidylinositol-anchored protein CDw109 on human platelets.

J. Kelton, P. Horsewood, G. Denomme, 1995, Blood.

Investigation of human platelet alloantigens and glycoproteins using non-radioactive immunoprecipitation.

J. Kelton, P. Horsewood, J. Smith, 1993, Journal of immunological methods.

Gova/b alloantigen system on human platelets.

J. Kelton, P. Horsewood, J. Smith, 1990, Blood.

Clinician investigator training in Canada: a review.

D. Danoff, C. Hayward, Stacey Brzezina, 2011, Clinical and investigative medicine. Medecine clinique et experimentale.

Urokinase-Type Plasminogen Activator Production by Cultured Megakaryocytes and Blood Outgrowth Endothelial Cells in the Quebec Platelet Disorder.

Ping Wang, M. Diamandis, G. Rivard, 2006 .

The Pathogenesis of Venous Limb Gangrene Associated with Heparin-Induced Thrombocytopenia

J. Kelton, M. Johnston, C. Hayward, 1997, Annals of Internal Medicine.

platelet disorder is linked to megakaryocyte differentiation Increased expression of urokinase plasminogen activator in Quebec

M. Diamandis, G. Rivard, C. Hayward, 2013 .

Increased expression of urokinase plasminogen activator in Quebec platelet disorder is linked to megakaryocyte differentiation.

M. Diamandis, G. Rivard, C. Hayward, 2009, Blood.

Technological advances in diagnostic testing for von Willebrand disease: new approaches and challenges

C. Hayward, K. Moffat, L. Graf, 2014, International journal of laboratory hematology.

Fibrinogen degradation products in patients with the Quebec platelet disorder

G. Rivard, C. Hayward, S. Zheng, 1997, British journal of haematology.

Multimerin 1 binds factor V and activated factor V with high affinity and inhibits thrombin generation

G. Nicolaes, K. Segers, R. Camire, 2008, Thrombosis and Haemostasis.

Multimerin 1

S. Tasneem, C. Hayward, E. Cramer, 2008, Platelets.

Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for ultra-rare inherited bleeding disorders

M. Recht, K. Baumann, C. Bedrosian, 2023, Expert review of hematology.

How I investigate for bleeding disorders

C. Hayward, C. Hayward, 2018, International journal of laboratory hematology.

Platelet Function Testing: Quality Assurance

J. Eikelboom, C. Hayward, Catherine Hayward1 , 2, 2007, Seminars in thrombosis and hemostasis.

Unraveling von Willebrand factor deficiency.

C. Hayward, 2021, Blood.

Platelet Multimerin and Its Proteolytic Processing

C. Hayward, 1999, Thrombosis and Haemostasis.

Platelet function analyzer (PFA)‐100®closure time in the evaluation of platelet disorders and platelet function: reply to a rebuttal

Paul J. Harrison, T. Ortel, M. Cattaneo, 2006 .

Platelet function analyzer (PFA)‐100® closure time in the evaluation of platelet disorders and platelet function: reply to a rebuttal

Paul J. Harrison, T. Ortel, M. Cattaneo, 2006 .

Sensitivity of rabbit platelet and aortic cyclooxygenase to inhibition by aspirin.

C. Hayward, J. McDonald, M. Ali, 1983, Prostaglandins, leukotrienes, and medicine.

Quebec platelet disorder: update on pathogenesis, diagnosis, and treatment.

G. Rivard, C. Hayward, N. Bunimov, 2011, Seminars in thrombosis and hemostasis.

Location of the multimerin 1 binding site in coagulation factor V: an update.

W. Kane, C. Hayward, S. Jeimy, 2008, Thrombosis research.

Analyses of cellular multimerin 1 receptors: in vitro evidence of binding mediated by alphaIIbbeta3 and alphavbeta3.

F. Adam, J. Kelton, Aurelio V. Santos, 2005, Thrombosis and haemostasis.

Bleeding risks for uncharacterized platelet function disorders

A. Paterson, G. Paré, J. Iyer, 2020, Research and practice in thrombosis and haemostasis.

Thrombopoietin levels in Quebec platelet disorder—Implications for the mechanism of thrombocytopenia

G. Rivard, S. Tasneem, C. Hayward, 2018, International journal of laboratory hematology.

Evaluation of urokinase plasminogen activator in urine from individuals with Quebec platelet disorder.

M. Diamandis, G. Rivard, C. Hayward, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Quebec platelet disorder

G. Rivard, C. Hayward, 2011, Expert review of hematology.

Rare inherited coagulation and fibrinolytic defects that challenge diagnostic laboratories

S. Tasneem, C. Hayward, Natalie Mathews, 2023, International journal of laboratory hematology.

Management of a left atrial appendage thrombus due to atrial fibrillation complicating Quebec platelet disorder.

R. Whitlock, G. Rivard, N. Chan, 2022, The Canadian journal of cardiology.

The Functions of the A1A2A3 Domains in Von Willebrand Factor Include Multimerin 1 Binding

P. D. de Groot, D. Bihan, R. Farndale, 2016, Thrombosis and Haemostasis.

The functions of the A 1 A 2 A 3 domains in von Willebrand factor include multimerin 1 binding SHORTENED TITLE ( 50 Characters ) : VWF A 1 A 2 A 3 domains support MMRN 1 binding

Dominique, R. Farndale, J. Sadler, 2016 .

Severe thrombophilia in a factor V‐deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)

P. Morange, K. Wichapong, M. Poggi, 2021, Journal of thrombosis and haemostasis : JTH.

Measurement of endogenous and exogenous alpha‐granular platelet proteins in patients with immune and nonimmune thrombocytopenia

J. Kelton, P. Horsewood, T. Warkentin, 1999, British journal of haematology.

Platelet activation in the pathogenesis of obesity and vascular disease

C. Hayward, 2011, Thrombosis and Haemostasis.

Multimerin: a bench-to-bedside chronology of a unique platelet and endothelial cell protein--from discovery to function to abnormalities in disease.

C. Hayward, 1997, Clinical and investigative medicine. Medecine clinique et experimentale.

Extending knowledge on inherited platelet disorders associated with thrombocytopenia

C. Hayward, 2003, Thrombosis and Haemostasis.

Platelet factor V New York: A defect in factor V distinct from that in factor V Quebec resulting in impaired prothrombinase generation

H. Weiss, B. Lages, C. Hayward, 2001, American journal of hematology.

Assembly and evaluation of an inventory of guidelines that are available to support clinical hematology laboratory practice

C. Hayward, K. Moffat, M. Proytcheva, 2015, International journal of laboratory hematology.

Illustrated State‐of‐the‐Art Capsules of the ISTH 2022 Congress

A. Balduini, C. Denis, R. Ahrends, 2022, Research and Practice in Thrombosis and Haemostasis.

Location of the multimerin 1 binding site in coagulation factor V: an update.

M. Quinn-Allen, W. Kane, C. Hayward, 2008, Thrombosis research.

Identification of the MMRN1 Binding Region within the C2 Domain of Human Factor V*

B. Dahlbäck, G. Nicolaes, M. Quinn-Allen, 2004, Journal of Biological Chemistry.

J. Bussel, L. Aledort, C. Hayward, 2004, American journal of hematology.

Diagnostic usefulness of a lumi-aggregometer adenosine triphosphate release assay for the assessment of platelet function disorders.

N. Heddle, K. Webert, M. Pai, 2011, American journal of clinical pathology.

Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey

C. Gachet, D. Kenny, A. Mumford, 2014, Journal of thrombosis and haemostasis : JTH.

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

G. Paré, G. Rivard, C. Hayward, 2016 .