Pregnancy outcomes in women with mechanical prosthetic heart valves: a prospective descriptive population based study using the United Kingdom Obstetric Surveillance System (UKOSS)... von Vause, S, Clarke, B, Tower, CL, Hay, CRM, Knight, M

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Thrombosis and recombinant factor VIIa von Hay, C.R.M.

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The impact of sport on health status, psychological well-being and physical performance of adults with haemophilia von von Mackensen, S., Harrington, C., Tuddenham, E., Littley, A., Will, A., Fareh, M., Hay, C. R. M., Khair, K.

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Evaluation of the use of global haemostasis assays to monitor treatment in factor XI deficiency von Pike, G. N., Cumming, A. M., Thachil, J., Hay, C. R. M., Burthem, J., Bolton‐Maggs, P. H. B.

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Central venous access device (CVAD) complications in Haemophilia with inhibitors undergoing immune tolerance induction: Lessons from the international immune tolerance study von Rodriguez, V., Mancuso, M. E., Warad, D., Hay, C. R. M., DiMichele, D. M., Valentino, L., Kenet, G., Kulkarni, R.

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The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977–99 von Darby, S. C., Keeling, D. M., Spooner, R. J. D., Wan Kan, S., Giangrande, P. L. F., Collins, P. W., Hill, F. G. H., Hay, C. R. M.

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Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization von Pasi, K. J., Collins, P. W., Keeling, D. M., Brown, S. A., Cumming, A. M., Dolan, G. C., Hay, C. R. M., Hill, F. G. H., Laffan, M., Peake, I. R.

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Clinical evaluation of an advanced category antihaemophilic factor prepared using a plasma/albumin-free method: pharmacokinetics, efficacy, and safety in previously treated patient... von Tarantino, M. D., Collins, P. W., Hay, C. R. M., Shapiro, A.D., Gruppo, R. A., Berntorp, E., Bray, G. L., Tonetta, S. A., Schroth, P. C., Retzios, A. D., Rogy, S. S., Sensel, M. G., Ewenstein, B. M.

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The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the North West of England von SUTHERLAND, M. S., KEENEY, S., BOLTON-MAGGS, P. H. B., HAY, C. R. M., WILL, A., CUMMING, A. M.

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The diagnosis and management of factor VIII and IX inhibitors : A guideline from the UK Haemophilia Centre Doctors' Organization (UKHCDO) von HAY, C. R. M, BAGLIN, T. P, COLLINS, P. W, HILL, F. G. H, KEELING, D. M

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Acquired Glanzmann's thrombasthenia without thrombocytopenia: a severe acquired autoimmune bleeding disorder von Tholouli, Eleni, Hay, Charles R. M., O'Gorman, Peter, Makris, Michael

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The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population von CUMMING, A. M., KEENEY, S., SALDEN, A., BHAVNANI, M., SHWE, K. H., HAY, C. R. M.

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Factor VIII inhibitors in mild and moderate-severity haemophilia A von Lee, C. A., Kessler, C. M., Varon, D., Martinowitz, U., Heim, M., HAY, C. R. M.

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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 Incre... von SMITH, Mark P, LUDLAM, Christopher A, COLLINS, Peter W, HAY, Charles R. M, WILDE, Jonathan T, GRIGERI, Alessandro, MELSEN, Tina, SAVIDGE, Geoffrey F

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Insights into the mechanism of haemorrhage caused by snake venom metalloproteinases von Kamiguti, Aura S., Hay, Charles R.M., Theakston, R.David G., Zuzel, Mirko

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Aplasia cutis congenita and low molecular weight heparin von Sharif, Saba, Hay, Charles R.M., Clayton‐Smith, Jill

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Von Willebrand factor, thrombomodulin, thromboxane, beta-thromboglobulin and markers of fibrinolysis in primary Raynaud's phenomenon and systemic sclerosis von Herrick, A L, Illingworth, K, Blann, A, Hay, C R, Hollis, S, Jayson, M I

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Porcine factor VIII: current status and future developments von Hay, C.R.M.

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Hormone implants and tachyphylaxis von Yoong, Ann, Rugman, F. P., Hay, C. R. M.

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The Treatment of Bleeding in Hemophilic Patients with Inhibitors with Recombinant Factor VIIa von Negrier, Claude, Hay, Charles R.

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