The definition, diagnosis and management of mild hemophilia A: communication from the SSC of the ISTH von Makris, M., Oldenburg, J., Mauser‐Bunschoten, E. P., Peerlinck, K., Castaman, G., Fijnvandraat, K.

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Guidelines for the management of hemophilia von Srivastava, A., Brewer, A. K., Mauser-Bunschoten, E. P., Key, N. S., Kitchen, S., Llinas, A., Ludlam, C. A., Mahlangu, J. N., Mulder, K., Poon, M. C., Street, A.

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Clinically relevant differences between assays for von Willebrand factor activity von Boender, J., Eikenboom, J., Bom, J. G., Meijer, K., Meris, J., Fijnvandraat, K., Cnossen, M. H., Laros‐van Gorkom, B. A. P., Heerde, W. L., Mauser‐Bunschoten, E. P., Maat, M. P. M., Leebeek, F. W. G.

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Reduced prevalence of arterial thrombosis in von Willebrand disease von Sanders, Y. V., Eikenboom, J., Wee, E. M., Bom, J. G., Cnossen, M. H., Degenaar‐Dujardin, M. E. L., Fijnvandraat, K., Kamphuisen, P. W., Laros‐van Gorkom, B. A. P., Meijer, K., Mauser‐Bunschoten, E. P., Leebeek, F. W. G.

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Clinical severity of haemophilia A: does the classification of the 1950s still stand? von Den UIJL, I. E. M., MAUSER BUNSCHOTEN, E. P., ROOSENDAAL, G., SCHUTGENS, R. E. G., BIESMA, D. H., GROBBEE, D. E., FISCHER, K.

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von Willebrand disease and aging: an evolving phenotype von Sanders, Y. V., Giezenaar, M. A., Laros‐van Gorkom, B. A. P., Meijer, K., Bom, J. G., Cnossen, M. H., Nijziel, M. R., Ypma, P. F., Fijnvandraat, K., Eikenboom, J., Mauser‐Bunschoten, E. P., Leebeek, F. W. G.

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Cardiovascular disease in patients with hemophilia von TUINENBURG, A., MAUSER‐BUNSCHOTEN, E. P., VERHAAR, M. C., BIESMA, D. H., SCHUTGENS, R. E. G.

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Continuous infusion of extended half‐life factor VIII (efmoroctocog alpha) for surgery in severe haemophilia A von Kremer Hovinga, I. C. L., Schutgens, R. E. G., Valk, P. R., Vulpen, L. F. D., Mauser‐Bunschoten, E. P., Fischer, K.

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CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease von Sanders, Y. V., Bom, J. G., Isaacs, A., Cnossen, M. H., Maat, M. P. M., Laros‐van Gorkom, B. A. P., Fijnvandraat, K., Meijer, K., Duijn, C. M., Mauser‐Bunschoten, E. P., Eikenboom, J., Leebeek, F. W. G., Coppens, M., Kors, A., Meris, J., Nijziel, M. R., Tamminga, R. Y. J., Ypma, P. F., Smiers, F. J. W., Granzen, B., Hamulyák, K., Brons, P.

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Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study von van Galen, K. P. M., Sanders, Y. V., Vojinovic, U., Eikenboom, J., Cnossen, M. H., Schutgens, R. E. G., van der Bom, J. G., Fijnvandraat, K., Laros-Van Gorkom, B. A. P., Meijer, K., Leebeek, F. W. G., Mauser-Bunschoten, E. P.

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Health‐related quality of life among adult patients with moderate and severe von Willebrand disease von DE WEE, E. M., MAUSER‐BUNSCHOTEN, E. P., VAN DER BOM, J. G., DEGENAAR‐DUJARDIN, M. E. L., EIKENBOOM, H. C. J., FIJNVANDRAAT, K., DE GOEDE‐BOLDER, A., LAROS‐VAN GORKOM, B. A. P., MEIJER, K., RAAT, H., LEEBEEK, F. W. G

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The association of haemophilic arthropathy with Health-Related Quality of Life: a post hoc analysis von Fischer, K., de Kleijn, P., Negrier, C., Mauser-Bunschoten, E. P., van der Valk, P. R., van Galen, K. P. M., Willemze, A., Schutgens, R.

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Mortality and causes of death in patients with hemophilia, 1992-2001: a prospective cohort study von Plug, I, Van Der Bom, J G, Peters, M, Mauser-Bunschoten, E P, De Goede-Bolder, A, Heijnen, L, Smit, C, Willemse, J, Rosendaal, F R

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Long-term effects of joint bleeding before starting prophylaxis in severe haemophilia von Nijdam, A., Foppen, W., van der Schouw, Y. T., Mauser-Bunschoten, E. P., Schutgens, R. E. G., Fischer, K.

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Cardiovascular disease in haemophilia patients: a contemporary issue von MANNUCCI, P. M., MAUSER-BUNSCHOTEN, E. P.

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Co-morbidity in the ageing haemophilia patient: the down side of increased life expectancy von MAUSER-BUNSCHOTEN, E. P., FRANSEN VAN DE PUTTE, D. E., SCHUTGENS, R. E. G.

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Evidence for and cost-effectiveness of physiotherapy in haemophilia: a Dutch perspective von de Kleijn, P., Mauser-Bunschoten, E. P., Fischer, K., Smit, C., Holtslag, H., Veenhof, C.

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Hemophilic arthropathy in patients with von Willebrand disease von van Galen, K.P.M, Mauser-Bunschoten, E.P, Leebeek, F.W.G

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Treatment of ischaemic heart disease in haemophilia patients: an institutional guideline von SCHUTGENS, R. E. G., TUINENBURG, A., ROOSENDAAL, G., GUYOMI, S. Hoseyni, MAUSER-BUNSCHOTEN, E. P.

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Risk of inhibitor development in mild haemophilia A increases with age von MAUSER-BUNSCHOTEN, E. P., DEN UIJL, I. E. M, SCHUTGENS, R. E. G, ROOSENDAAL, G., FISCHER, K.

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