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Journal Articles

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

Brief Report
Suthesh Sivapalaratnam, Sarah K. Westbury, Jonathan C. Stephens, Daniel Greene, Kate Downes, Anne M. Kelly, Claire Lentaigne, William J. Astle, Eric G. Huizinga, Paquita Nurden, Sofia Papadia, Kathelijne Peerlinck, Christopher J. Penkett, David J. Perry, Catherine Roughley, Ilenia Simeoni, Kathleen Stirrups, Daniel P. Hart, R. Campbell Tait, Andrew D. Mumford, NIHR BioResource, Michael A. Laffan, Kathleen Freson, Willem H. Ouwehand, Shinji Kunishima, Ernest Turro
Journal: Blood
Blood (2017) 129 (4): 520–524.
https://doi.org/10.1182/blood-2016-08-732248
Published: 2017
Includes: Supplemental data
Journal Articles

Renal Status and Hematuria in Older Patients with Hemophilia

Pal André Holme, PhDMD, Robert Campbell Tait, MD, Christophe Combescure, PhD, Erik Berntorp, MD PhD, Annarita Tagliaferri, Peter Staritz, MD, Roger E.G. Schutgens, MD PhD, Robert Klamroth, Natascha Marquardt, Stephan Rauchensteiner, Philippe De Moerloose, MD PhD
Journal: Blood
Blood (2015) 126 (23): 2290.
https://doi.org/10.1182/blood.V126.23.2290.2290
Published: 2015
Journal Articles

Antithrombin Alfa in Hereditary Antithrombin Deficient Patients at High Risk for Thromboembolic Complications

Robert Campbell Tait, Johan TM Frieling
Journal: Blood
Blood (2008) 112 (11): 986.
https://doi.org/10.1182/blood.V112.11.986.986
Published: 2008
Journal Articles

Identification of Ten Novel Mutations Associated with Inherited Coagulation Factor V Deficiency.

Rinku Patel, Jacky Cutler, Campbell Tait, Geoffrey Savidge
Journal: Blood
Blood (2004) 104 (11): 1030.
https://doi.org/10.1182/blood.V104.11.1030.1030
Published: 2004