Publications by authors named "Anthony Cumming"

Claim this Profile
S
Sample conditions determine the ability of thrombin generation parameters to identify bleeding phenotype in FXI deficiency.
Gillian N Pike, Anthony M Cumming, Charles R M Hay, Paula H B Bolton-Maggs, John Burthem

Blood· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Diagnosis and management of von Willebrand disease in the United Kingdom.
Steve Keeney, Peter Collins, Anthony Cumming, Anne Goodeve, John Pasi

Semin Thromb Hemost· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical utility gene card for: von Willebrand disease.
Anthony M Cumming, Stephen Keeney, P Vincent Jenkins, Michael J Nash, James S O'Donnell

Eur J Hum Genet· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3.
Megan S Sutherland, Anthony M Cumming, Mackenzie Bowman, Paula H B Bolton-Maggs, Derrick J Bowen

Blood· July 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease.
Anthony Cumming, Pamela Grundy, Stephen Keeney, William Lester, Said Enayat

Thromb Haemost· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation: diagnostic pitfalls and new insights.
William A Lester, Andrea M Guilliatt, Gurcharan K Surdhar, Said M Enayat, Jonathan T Wilde, Anthony M Cumming

Br J Haematol· October 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
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.
Derrick J Bowen, Peter W Collins, Will Lester, Anthony M Cumming, Steven Keeney

Br J Haematol· March 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis