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Journal Articles

Homozygous Mutation of the ETS DNA-Binding Domain of FLI1 Causes a Bleeding Disorder with Giant Alpha Granules Similar to Paris-Trousseau Thrombocytopenia

William S Stevenson, MBBS, PhD FRACP, FRCPA, David John Rabbolini, BSc,MBBChir, Timothy Brighton, Joel Mackay, Christopher M Ward, MBChB, PhD FRACP, FRCPA, Marie-Christine Morel-Kopp, PhD

Blood (2015) 126 (23): 78.

https://doi.org/10.1182/blood.V126.23.78.78

Published: 2015

Journal Articles

Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1

William S. Stevenson, David J. Rabbolini, Lucinda Beutler, Qiang Chen, Sara Gabrielli, Joel P. Mackay, Timothy A. Brighton, Christopher M. Ward, Marie-Christine Morel-Kopp

Blood (2015) 126 (17): 2027–2030.

https://doi.org/10.1182/blood-2015-06-650887

Published: 2015

Includes: Supplemental data

Journal Articles

GFI1B Mutation Causes a Platelet Function Defect With Reduced Alpha-Granule Content and Abnormal Aggregation Response

Christopher M Ward, MB, CHB, PhD, Marie-Christine Morel-Kopp, PhD, Qiang Chen, BMed MSc, Hai Po Liang, PhD, Ashley P. Ng, MBBS, BMedSc, PhD, FRACP, FRCPA, Andrew W. Roberts, MBBS, PhD, Melanie Bahlo, PhD, William s Stevenson, MBBS, PhD

Blood (2013) 122 (21): 566.

https://doi.org/10.1182/blood.V122.21.566.566

Published: 2013

Journal Articles

The Overall Haemostatic Potential (OHP) Assay Detects Abnormalities in Fibrinolytic Factors

Jennifer L Curnow, MBBS, Marie-Christine Morel-Kopp, PhD, Christopher Ward, MB CHB, PhD

Blood (2008) 112 (11): 4093.

https://doi.org/10.1182/blood.V112.11.4093.4093

Published: 2008

Journal Articles

Patients with the Antiphospholipid Syndrome (APLS) Show Hypercoagulability Due to Hypofibrinolysis and Increased Fibrin Generation, but Thrombin Generation Is Variable

Jennifer L Curnow, MD, Marie-Christine Morel-Kopp, PhD, Ninfa Rojas, MD, Margaret Aboud, MSci, Christopher Ward, MB CHB, PhD

Blood (2008) 112 (11): 3833.

https://doi.org/10.1182/blood.V112.11.3833.3833

Published: 2008

Journal Articles

Identifying Hypercoagulable States with the Overall Haemostatic Potential (OHP), a Simple Global Haemostasis Assay.

Jennifer L. Curnow, MBBS, Marie-Christine Morel-Kopp, PhD, Margaret Aboud, FAIMS, Christopher Ward, PhD, MBBS, BMSc

Blood (2004) 104 (11): 3505.

https://doi.org/10.1182/blood.V104.11.3505.3505

Published: 2004

Journal Articles

A Three Amino Acid Deletion in Glycoprotein IIIa Is Responsible for Type I Glanzmann's Thrombasthenia: Importance of Residues Ile 325 Pro 326 Gly 327 for β3 Integrin Subunit Association

Marie-Christine Morel-Kopp, Cécile Kaplan, Valérie Proulle, Vincent Jallu, Chantal Melchior, Olivier Peyruchaud, Marie-Hélène Aurousseau, Nelly Kieffer

Blood (1997) 90 (2): 669–677.

https://doi.org/10.1182/blood.V90.2.669

Published: 1997

NARROW

Homozygous Mutation of the ETS DNA-Binding Domain of FLI1 Causes a Bleeding Disorder with Giant Alpha Granules Similar to Paris-Trousseau Thrombocytopenia

Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1

GFI1B Mutation Causes a Platelet Function Defect With Reduced Alpha-Granule Content and Abnormal Aggregation Response

The Overall Haemostatic Potential (OHP) Assay Detects Abnormalities in Fibrinolytic Factors

Patients with the Antiphospholipid Syndrome (APLS) Show Hypercoagulability Due to Hypofibrinolysis and Increased Fibrin Generation, but Thrombin Generation Is Variable

Identifying Hypercoagulable States with the Overall Haemostatic Potential (OHP), a Simple Global Haemostasis Assay.

A Three Amino Acid Deletion in Glycoprotein IIIa Is Responsible for Type I Glanzmann's Thrombasthenia: Importance of Residues Ile 325 Pro 326 Gly 327 for β3 Integrin Subunit Association

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ASH Publications

American Society of Hematology

Homozygous Mutation of the ETS DNA-Binding Domain of FLI1 Causes a Bleeding Disorder with Giant Alpha Granules Similar to Paris-Trousseau Thrombocytopenia

Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1

GFI1B Mutation Causes a Platelet Function Defect With Reduced Alpha-Granule Content and Abnormal Aggregation Response

The Overall Haemostatic Potential (OHP) Assay Detects Abnormalities in Fibrinolytic Factors

Patients with the Antiphospholipid Syndrome (APLS) Show Hypercoagulability Due to Hypofibrinolysis and Increased Fibrin Generation, but Thrombin Generation Is Variable

Identifying Hypercoagulable States with the Overall Haemostatic Potential (OHP), a Simple Global Haemostasis Assay.

A Three Amino Acid Deletion in Glycoprotein IIIa Is Responsible for Type I Glanzmann's Thrombasthenia: Importance of Residues Ile 325 Pro 326 Gly 327 for β3 Integrin Subunit Association

Email alerts

ASH Publications

American Society of Hematology

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