Sample conditions determine the ability of thrombin generation parameters to identify bleeding phenotype in FXI deficiency

Authors: Pike, Gillian N. ^*, Cumming, Anthony M., Hay, Charles R.M., Bolton-Maggs, Paula H.B., Burthem, John

Source: In Blood 16 July 2015 126(3):397-405

A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3

Authors: Sutherland, Megan S., Cumming, Anthony M., Bowman, Mackenzie, Bolton-Maggs, Paula H.B., Bowen, Derrick J., Collins, Peter W., Hay, Charles R.M., Will, Andrew M., Keeney, Stephen

Source: In Blood 30 July 2009 114(5):1091-1098

The Molecular Basis of Type 3 von Willebrand Disease.

Authors: Cumming, Anthony M.¹ tony.cumming@cmft.nhs.uk, Sutherland, Megan S.¹, Keeney, Stephen¹

Source: Journal of Coagulation Disorders. 2010, Vol. 2 Issue 2, p29-35. 7p. 2 Diagrams, 1 Graph.

Subject Terms: *VON Willebrand disease, *VON Willebrand factor, *NOSEBLEED, *MENORRHAGIA, *JOINT diseases, *GENETIC mutation, *EXONS (Genetics), *THROMBOSIS, *HEMOSTASIS

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Two Factor XI Concentrates Correct Impaired Thrombin Generation in Major FXI Deficiency but Are Not Equivalent in Their Effect

Authors: Pike, Gillian N ^*, Cumming, Anthony M ^*, Hay, Charles R.M ^*, Sempasa, Brenda ^*, Sutherland, Megan ^*, Thachil, Jecko ^*, Burthem, John ^*, Bolton-Maggs, Paula H. B

Source: In Blood 6 December 2014 124(21):1519-1519

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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.

Authors: Bowen, Derrick J., Collins, Peter W., Lester, Will, Cumming, Anthony M., Keeney, Steven, Grundy, Pamela, Enayat, Saad M., Bolton-Maggs, Paula H. B., Keeling, David M., Khair, Kate, Campbell Tait, R., Wilde, Jonathon T., John Pasi, K., Hill, Frank G. H.

Source: British Journal of Haematology; Mar2005, Vol. 128 Issue 6, p830-836, 7p

Subject Terms: VON Willebrand factor, BLOOD coagulation factors, PROTEOLYSIS, GENOTYPE-environment interaction, THROMBOSPONDINS, BLOOD transfusion

Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: application to family studies in von Willebrand disease

Authors: Cumming, Anthony M., Armstrong, John G., Pendry, Kate, Burn, Aileen M, Wensley, Richard T.

Source: Human Genetics; May 1992, Vol. 89 Issue: 2 p194-198, 5p

Diagnosis of APC resistance during pregnancy.

Authors: Cumming, Anthony M., Campbell Tait, R., Fildes, Sheila, Hay, Charles R. M.

Source: British Journal of Haematology; Mar1996, Vol. 92 Issue 4, p1026-1027, 2p