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William Lester

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Martina E Daly; Ban B Dawood; William A Lester; Ian R Peake; Francesco Rodeghiero; Anne C Goodeve; Michael Makris; Jonathan T Wilde; Andrew D Mumford; Stephen P Watson; Stuart J Mundell
Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study.
William A Lester; Andrea M Guilliatt; Pamela Grundy; Said M Enayat; Carolyn Millar; Frank Hill; Tony Cumming; Peter Collins
Is VWF R924Q a benign polymorphism, a marker of a null allele or a factor VIII-binding defect? The debate continues with results from the UKHCDO VWD study.
William A Lester; Andrea M Guilliatt; MOHAMMAD ENAYAT; Peter Rose; Frank G H Hill
The R2464C missense mutation in the von Willebrand factor gene causes a novel abnormality of multimer electrophoretic mobility and falls into the subgroup of type 2 von Willebrand disease 'unclassified'.

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All Publications

2009: Martina E Daly; Ban B Dawood; William A Lester; Ian R Peake; Francesco Rodeghiero; Anne C Goodeve; Michael Makris; Jonathan T Wilde; Andrew D Mumford; Stephen P Watson; Stuart J Mundell
Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study.
Blood 2009;113(17):4110-3.
2008: William A Lester; Andrea M Guilliatt; Pamela Grundy; Said M Enayat; Carolyn Millar; Frank Hill; Tony Cumming; Peter Collins
Is VWF R924Q a benign polymorphism, a marker of a null allele or a factor VIII-binding defect? The debate continues with results from the UKHCDO VWD study.
Thrombosis and haemostasis 2008;100(4):716-8.
2007: William A Lester; Andrea M Guilliatt; MOHAMMAD ENAYAT; Peter Rose; Frank G H Hill
The R2464C missense mutation in the von Willebrand factor gene causes a novel abnormality of multimer electrophoretic mobility and falls into the subgroup of type 2 von Willebrand disease 'unclassified'.
Thrombosis and haemostasis 2007;97(1):159-60.
2007: Anne C Goodeve; J C J Eikenboom; Giancarlo Castaman; Francesco Rodeghiero; Augusto B Federici; Javier Batlle; Dominique Meyer; Claudine Mazurier; Jenny Goudemand; Reinhard Schneppenheim; Ulrich Budde; Jørgen Ingerslev; David Habart; Zdena Vorlova; Lars Holmberg; Stefan Lethagen; John Pasi; Frank Hill; Mohammad Hashemi Soteh; Luciano Baronciani; Christer Hallden; Andrea M Guilliatt; William A Lester; Ian R Peake
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).
Blood 2007;109(1):112-21.
2006: Anthony M Cumming; Pamela Grundy; Steven Keeney; William A Lester; Said M Enayat; Andrea M Guilliatt; Derrick Bowen; John Pasi; David Keeling; Frank Hill; Paula H B Bolton-Maggs; Charles R M Hay; Peter Collins
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease.
Thrombosis and haemostasis 2006;96(5):630-41.
2006: William A Lester; Andrea M Guilliatt; Gurcharan K Surdhar; Said M Enayat; Jonathan T Wilde; Sara Willoughby; Pamela Grundy; Anthony M Cumming; Peter W Collins; Frank G H Hill
Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation: diagnostic pitfalls and new insights.
British journal of haematology 2006;135(1):91-6.
2006: MOHAMMAD ENAYAT; Andrea M Guilliatt; William A Lester; Jonathan T Wilde; Michael D Williams; Frank G H Hill
Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance.
British journal of haematology 2006;133(6):664-6.
2005: Derrick J Bowen; Peter W Collins; William A Lester; Anthony M Cumming; Steven Keeney; Pamela Grundy; Said M Enayat; Paula H B Bolton-Maggs; David Keeling; Kate Khair; R Campbell Tait; Jonathan T Wilde; K John Pasi; Frank G H Hill
The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotype.
British journal of haematology 2005;128(6):830-6.
2002: William A Lester; Michael D Williams; Sarah L Allford; MOHAMMAD ENAYAT; Samuel J Machin
Successful treatment of congenital thrombotic thrombocytopenic purpura using the intermediate purity factor VIII concentrate BPL 8Y.
British journal of haematology 2002;119(1):176-9.