Unfavourable cardiovascular disease risk profiles in a cohort of Dutch and British haemophilia patientsFRANSEN VAN DE PUTTE, Dietje E; FISCHER, Kathelijn; MAKRIS, Michael et al.Thrombosis and haemostasis. 2013, Vol 109, Num 1, pp 16-23, issn 0340-6245, 8 p.Article

Advances in the understanding of acquired haemophilia A: implications for clinical practiceCOLLINS, Peter W; PERCY, Charles L.British journal of haematology. 2010, Vol 148, Num 2, pp 183-194, issn 0007-1048, 12 p.Article

Increased prevalence of hypertension in haemophilia patientsFRANSEN VAN DE PUTTE, Dietje E; FISCHER, Kathelijn; MAKRIS, Michael et al.Thrombosis and haemostasis. 2012, Vol 108, Num 4, pp 750-755, issn 0340-6245, 6 p.Article

Absence of platelet-dependent fibrin formation in a patient with Scott syndromeWIELDERS, Simone J. H; BROERS, Jos; TEN CATE, Hugo et al.Thrombosis and haemostasis. 2009, Vol 102, Num 1, pp 76-82, issn 0340-6245, 7 p.Article

A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDOBOLTON-MAGGS, Paula H. B; CHALMERS, Elizabeth A; WATSON, Steve P et al.British journal of haematology. 2006, Vol 135, Num 5, pp 603-633, issn 0007-1048, 31 p.Article

Diagnosis and management of acquired coagulation inhibitors: a guideline from UKHCDOCOLLINS, Peter W; CHALMERS, Elizabeth; HART, Daniel et al.British journal of haematology. 2013, Vol 162, Num 6, pp 758-773, issn 0007-1048, 16 p.Article

Laboratory monitoring of Scott SyndromePERCY, Charles L; RAYMENT, Rachel; MACARTNEY, Nicola et al.British journal of haematology. 2010, Vol 149, Num 6, issn 0007-1048, p. 803Article

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 phenotypeBOWEN, Derrick J; COLLINS, Peter W; TAIT, R. Campbell et al.British journal of haematology. 2005, Vol 128, Num 6, pp 830-836, issn 0007-1048, 7 p.Article

Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation : diagnostic pitfalls and new insightsLESTER, William A; GUILLIATT, Andrea M; SURDHAR, Gurcharan K et al.British journal of haematology. 2006, Vol 135, Num 1, pp 91-96, issn 0007-1048, 6 p.Article

Heterogeneous detection of A-antigen on von willebrand factor derived from platelets, endothelial cells and plasmaBROWN, Simon A; COLLINS, Peter W; BOWEN, Derrick J et al.Thrombosis and haemostasis. 2002, Vol 87, Num 6, pp 990-996, issn 0340-6245Article

A new polymorphism in the human factor VIII gene : implications for linkage analysis in haemophilia A and for the evolution of int22h sequencesBOWEN, Derrick J; DE BRASI, Carlos D; LARRIPA, Irene B et al.British journal of haematology. 2000, Vol 111, Num 2, pp 544-548, issn 0007-1048Article

Population pharmacokinetics of recombinant factor VIII: the relationships of pharmacokinetics to age and body weightBJÖRKMAN, Sven; OH, Myungshin; SPOTTS, Gerald et al.Blood. 2012, Vol 119, Num 2, pp 612-618, issn 0006-4971, 7 p.Article

Incidence of factor VIII inhibitors throughout life in severe hemophilia A in the United KingdomHAY, Charles R. M; PALMER, Ben; CHALMERS, Elizabeth et al.Blood. 2011, Vol 117, Num 23, pp 6367-6370, issn 0006-4971, 4 p.Article

Acquired hemophilia A in the United Kingdom : A 2-year national surveillance study by the United Kingdom haemophilia centre Doctors' organisation. CommentaryKYRIAKIDES, Themis R; COLLINS, Peter W; HAY, Charles R. M et al.Blood. 2007, Vol 109, Num 5, issn 0006-4971, 1793, 1870-1877 [9 p.]Article

Store-mediated calcium entry in the regulation of phosphatidylserine exposure in blood cells from Scott patientsMUNNIX, Imke C. A; HARMSMA, Marjan; GIDDINGS, John C et al.Thrombosis and haemostasis. 2003, Vol 89, Num 4, pp 687-695, issn 0340-6245, 9 p.Article

Factor viia induced release of von Willebrand factor from human umbilical vein endothelial cells by a tyrosine kinase dependent pathwayBROWN, Simon A; BOWEN, Derrick J; HALLETT, Maurice B et al.Thrombosis and haemostasis. 2002, Vol 87, Num 6, pp 1057-1061, issn 0340-6245Article

Diagnosis and treatment of factor VIII and IX inhibitors in congenital haemophilia: (4th edition)COLLINS, Peter W; CHALMERS, Elizabeth; HART, Daniel P et al.British journal of haematology. 2013, Vol 160, Num 2, pp 153-170, issn 0007-1048, 18 p.Article

A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3SUTHERLAND, Megan S; CUMMING, Anthony M; BOWMAN, Mackenzie et al.Blood. 2009, Vol 114, Num 5, pp 1091-1098, issn 0006-4971, 8 p.Article

Global tests of haemostasis in critically ill patients with severe sepsis syndrome compared to controlsCOLLINS, Peter W; MACCHIAVELLO, Luis I; LEWIS, Sarah J et al.British journal of haematology. 2006, Vol 135, Num 2, pp 220-227, issn 0007-1048, 8 p.Article

Efficacy of standard dose and 30 ml/kg fresh frozen plasma in correcting laboratory parameters of haemostasis in critically ill patientsCHOWDHURY, Pratima; SAAYMAN, Anton G; PAULUS, Ulrike et al.British journal of haematology. 2004, Vol 125, Num 1, pp 69-73, issn 0007-1048, 5 p.Article

High concentrations of coagulation factor VIII and thrombosis : is the factor VIII-binding domain of von Willebrand factor implicated?BOWEN, Derrick J; MACLEAN, Rhona M; PELLARD, Sarah et al.British journal of haematology. 2001, Vol 113, Num 3, pp 655-657, issn 0007-1048Article

Elective surgery on factor VIII inhibitor patients using continuous infusion of recombinant activated factor VII: Plasma factor VII activity of 10 IU/ml is associated with an increased incidence of bleedingSMITH, Mark P; LUDLAM, Christopher A; COLLINS, Peter W et al.Thrombosis and haemostasis. 2001, Vol 86, Num 4, pp 949-953, issn 0340-6245Article