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Blood|October 1, 1994
Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counselingP V Jenkins, P W Collins, E Goldman, et al.
Diabete & Metabolisme|July 1, 1989
Serum fructosamine in diabetic pregnancyK J Pasi, M J Toop, B L Cockrill, et al.
Vox Sanguinis|January 1, 1990
Transmission of human parvovirus B19 by coagulation factor concentratesM D Williams, B J Cohen, A C Beddall, et al.
British Journal of Haematology|December 1, 1995
Induction of tissue factor expression in human monocyte/endothelium coculturesP W Collins, K E Noble, J R Reittie, et al.
Gene Therapy|December 1, 1995
Expression of factor VII by muscle cells in vitro and in vivo following direct gene transfer: modelling gene therapy for haemophiliaG Miller, R A Steinbrecher, P J Murdock, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 18, 2016
The use of enhanced half-life coagulation factor concentrates in routine clinical practice: guidance from UKHCDOP Collins, E Chalmers, P Chowdary, et al.
Thrombosis and Haemostasis|January 12, 2001
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modellingI C Nitu-Whalley, A Riddell, C A Lee, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 17, 2004
The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' OrganizationM Laffan, S A Brown, P W Collins, et al.
British Journal of Haematology|November 25, 2010
Non-malignant haematology research in the UK: looking forward to new opportunitiesP W Collins, T P Baglin, R Dang, et al.
Blood|July 27, 2001
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand diseaseM S Enayat, A M Guilliatt, G K Surdhar, et al.
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