A comparison of grain boundary evolution during grain growth in fcc metals von Brons, J.G., Thompson, G.B.

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Cryogenic indentation-induced grain growth in nanotwinned copper von Brons, J.G., Padilla, H.A., Thompson, G.B., Boyce, B.L.

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Abnormalities associated with grain growth in solid solution Cu(Ni) thin films von Brons, J.G., Thompson, G.B.

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The role of copper twin boundaries in cryogenic indentation-induced grain growth von Brons, J.G., Hardwick, J.A., Padilla, H.A., Hattar, K., Thompson, G.B., Boyce, B.L.

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Comparison of atom probe compositional fidelity across thin film interfaces von Brons, J.G., Herzing, A.A., Henry, K.T., Anderson, I.M., Thompson, G.B.

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Thin film underlayer effects on mass resolving power in laser-assisted atom probe tomography von Tippey, K., Brons, J.G., Kapoor, M., Fu, B., Thompson, G.B.

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Grain Boundary Evolution of Face-Centered Cubic Metals during in-situ TEM Annealing von Brons, J.G., Thompson, G.B.

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Evidence of Cryogenic Indentation-Induced Grain Growth in Highly Twinned Nanocrystalline Copper von Brons, J.G., Padilla, H.A., Thompson, G.B., Boyce, B.L.

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Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations von Loomans, J. I., Velzen, A. S., Eckhardt, C. L., Peters, M., Mäkipernaa, A., Holmstrom, M., Brons, P. P., Dors, N., Haya, S., Voorberg, J., Bom, J. G., Fijnvandraat, 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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Inhibitor development and mortality in non‐severe hemophilia A von Eckhardt, C. L., Loomans, J. I., Velzen, A. S., Peters, M., Mauser‐Bunschoten, E. P., Schwaab, R., Mazzucconi, M. G., Tagliaferri, A., Siegmund, B., Reitter‐Pfoertner, S. E., Bom, J. G., Fijnvandraat, K., Fijnvandraat, K., Peters, M., Kamphuisen, P. W., Kamphuisen, P. W., Bom, J. G., Peerlinck, K., Oldenburg, J., Santagostino, E., Astermark, J., Eckhardt, C.L, Velzen, A.S, Streefkerk, N., Loomans, J. L., Eijkelenburg, A., Jansen, A. J., Kruijt, C. C., Tienoven, B., Baar, A. C. G., Corten, I. W., Meijer, K., Nijziel, M. R., Dors, N., Hamulyak, K., Beckers, E., Brons, P. P., Laros‐van Gorkom, B. A. P., Heerde, W. L., Leebeek, F., Kruip, M., Cnossen, M. H., Mauser‐Bunschoten, E., Fischer, K., Smiers, F. J., Hermans, C., Schwaab, R., Siegmund, B., Klamroth, R., Escuriola‐Ettingshausen, C., Königs, C., Petrini, P., Holmström, M., Mäkipernaa, A., Male, C., Pabinger, I., Reitter‐Pfoertner, S. E., Keenan, R. D., Liesner, R., Khair, K., Yee, T. T., Hart, D. P., Rangarajan, S., Mitchell, M., Thompson, G., Haya, S., Moret, A., Cid, A. R., Jimenez‐Yuste, V., Mancuso, M. E., Mazzuconni, M. G., Santoro, C., Morfini, M., Castaman, G., Schinco, P., Tagliaferri, A., Rivolta, G. F., Platokouki, H., McRae, S.

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Impact of von Willebrand disease on health‐related quality of life in a pediatric population von DE WEE, E. M., FIJNVANDRAAT, K., DE GOEDE‐BOLDER, A., MAUSER‐BUNSCHOTEN, E. P., EIKENBOOM, J. C. J., BRONS, P. P., SMIERS, F. J., TAMMINGA, R., OOSTENBRINK, R., RAAT, H., VAN DER BOM, J. G., LEEBEEK, F. W. G.

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Back to base pairs: What is the genetic risk for red bloodcell alloimmunization? von Gerritsma, J.J., Oomen, I., Meinderts, S., van der Schoot, C.E., Biemond, B.J., van der Bom, J.G., Fijnvandraat, K., van Beers, E.J., Biemond, B.J., Beijlevelt, M., Brons, P.P.T., Cnossen, M.H., Dovern, L., Fijnvandraat, K., Heijboer, H., Hofstede, F., Kerkhoffs, J.L.H., Nur, E., Ootjers, C., de Pagter, P.J., Rijneveld, A.W., Schols, S.E.M., Smiers, F.J., Suiker, M.H., Teuben, S.A.M.C., van Tuijn, C.F.J., van Vliet, I., Zwagemaker, E.

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Genetic variants, thrombocytopenia, and clinical phenotype of type 2B von Willebrand disease: a median 16-year follow-up study von van Kwawegen, Calvin B., Atiq, Ferdows, Endenburg, Dara, Fijnvandraat, Karin, van Galen, Karin P.M., Cnossen, Marjon H., Schols, Saskia E.M., Kruip, Marieke J.H.A., van Heerde, Waander L., de Meris, Joke, van der Bom, Johanna G., Eikenboom, Jeroen, Meijer, Karina, Leebeek, Frank W.G., Fijnvandraat, K., Coppens, M., Kors, A., Zweegman, S., de Meris, J., Goverde, G.J., Jonkers, M.H., Dors, N., Nijziel, M.R., Nieuwenhuizen, L., Meijer, K., Tamminga, R.Y.J., van der Linden, P.W., Ypma, P.F., Eikenboom, H.C.J., van der Bom, J.G., Smiers, F.J.W., Granzen, B., Hamulyák, K., Brons, P., Laros-van Gorkom, B.A.P., Schols, S.E.M., Leebeek, F.W.G., Cnossen, M.H., Boender, J., Atiq, F., van Kwawegen, C.B., Mauser-Bunschoten, E.P., van Galen, K.P.M.

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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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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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Cyclosporin A: an immunosuppressive agent preferentially active against proliferating T cells von White, D J, Plumb, A M, Pawelec, G, Brons, G

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