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Journal Articles

Congenital Aspirin-like Defect As a Result of Autosomal Recessive Variants in PTGS1

Suthesh Sivapalaratnam, MD PhD, Hayman Melissa, PhD, Claire Lentaigne, BSc, MB, MRCP, Melissa Chan, PhD, Marilena Crescente, PhD, Harriet Allan, Katherine Wedderburn, Moghees Hanif, Ernest Turro, PhD, Dan P Hart, PhD MBBChir, FRCPath, FRCP, Kathleen Freson, PhD, Kate Downes, PhD, NIHR Bioresource, Willem Ouwehand, MDPhD, Michael Laffan, DM, FRCP, FRCPath, Tim Warner, PhD

Blood (2018) 132 (Supplement 1): 1156.

https://doi.org/10.1182/blood-2018-99-118958

Published: 2018

Journal Articles

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

Suthesh Sivapalaratnam, MD PhD, Willem Ouwehand, MD PhD, Bridge Consortium, ThromboGenomics Consortium

Blood (2016) 128 (22): 1359.

https://doi.org/10.1182/blood.V128.22.1359.1359

Published: 2016

Journal Articles

A Dominant Gain-of-Function Mutation in Universal Tyrosine Kinase SRC Causes Enhanced Podosome Formation in a Syndrome with Thrombocytopenia, Myelofibrosis, Bleeding and Bone Pathologies

Kathleen Freson, Ernest Turro, Willem Ouwehand, MD, PhD

Blood (2015) 126 (23): LBA-7.

https://doi.org/10.1182/blood.V126.23.LBA-7.LBA-7

Published: 2015

Journal Articles

A Novel β3 Intracytoplasmic Domain Mutation Associated with Macrothrombocytopenia: Structural Analysis in Comparison with Previously Reported Cases

Paquita Nurden, MD PhD, Ernest Turro, PhD, Xavier Pillois, PhD, Daniel Greene, PhD, Willem Ouwehand, MD PhD, Alan Nurden, PhD

Blood (2014) 124 (21): 1454.

https://doi.org/10.1182/blood.V124.21.1454.1454

Published: 2014

Journal Articles

Functional Genomics in Zebrafish Permits Rapid Characterization of Novel Platelet Membrane Proteins

Isabelle I Salles, Marie N O’Connor, Nicholas A. Watkins, Adam Walker, Stephen F Garner, Chris I Jones, Iain Macauley, Michael Steward, Jaap Jan Zwaginga, Sarah L Bray, Ana Cvejic, Frank Dudbridge, Bernard de Bono, Hans Deckmyn, Derek L. Stemple, Willem Ouwehand, MD, PhD

Blood (2008) 112 (11): 2860.

https://doi.org/10.1182/blood.V112.11.2860.2860

Published: 2008

Journal Articles

Functional Genomics of the Platelet ADP and Collagen Signalling Pathways.

Stephen F Garner, Chris I Jones, Jonathan Stephens, Sarah L Bray, Will Angenent, Philippa Burns, Richard W Farndale, Catherine Rice, Frank Dudbridge, Nick Watkins, Bernard de Bono, Panos Deloukas, Alison H Goodall, Willem Ouwehand

Blood (2008) 112 (11): 1844.

https://doi.org/10.1182/blood.V112.11.1844.1844

Published: 2008

Journal Articles

Effect of Treatment with Rituximab in Patients with Refractory Autoimmune Cytopenias.

Moez Dungarwalla, Judith Marsh, Jenny Tooze, Geoff Lucas, Willem Ouwehand, Ruth Pettengell, Clare E. Dearden, Edward C. Gordon-Smith, Modupe O. Elebute

Blood (2005) 106 (11): 2405.

https://doi.org/10.1182/blood.V106.11.2405.2405

Published: 2005

NARROW

Congenital Aspirin-like Defect As a Result of Autosomal Recessive Variants in PTGS1

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

A Dominant Gain-of-Function Mutation in Universal Tyrosine Kinase SRC Causes Enhanced Podosome Formation in a Syndrome with Thrombocytopenia, Myelofibrosis, Bleeding and Bone Pathologies

A Novel β3 Intracytoplasmic Domain Mutation Associated with Macrothrombocytopenia: Structural Analysis in Comparison with Previously Reported Cases

Functional Genomics in Zebrafish Permits Rapid Characterization of Novel Platelet Membrane Proteins

Functional Genomics of the Platelet ADP and Collagen Signalling Pathways.

Effect of Treatment with Rituximab in Patients with Refractory Autoimmune Cytopenias.

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ASH Publications

American Society of Hematology

Congenital Aspirin-like Defect As a Result of Autosomal Recessive Variants in PTGS1

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

A Dominant Gain-of-Function Mutation in Universal Tyrosine Kinase SRC Causes Enhanced Podosome Formation in a Syndrome with Thrombocytopenia, Myelofibrosis, Bleeding and Bone Pathologies

A Novel β3 Intracytoplasmic Domain Mutation Associated with Macrothrombocytopenia: Structural Analysis in Comparison with Previously Reported Cases

Functional Genomics in Zebrafish Permits Rapid Characterization of Novel Platelet Membrane Proteins

Functional Genomics of the Platelet ADP and Collagen Signalling Pathways.

Effect of Treatment with Rituximab in Patients with Refractory Autoimmune Cytopenias.

Email alerts

ASH Publications

American Society of Hematology

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