Reactive surfactants in heterophase polymerization for high performance polymers von Schipper, E. T. W. M., Sindt, O., Hamaide, T., Lacroix-Desmazes, P., Müller, B., Guyot, A., van den Enden, M. J. W. A., Vidal, F., van Es, J. J. G. S., German, A. L., Montaya Goñi, A., Sherrington, D. C., Schoonbrood, H. A. S., Asua, J. M., Sjöberg, M.

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Seeded emulsion polymerization of butylacrylate: "Zero-one or pseudo-bulk?" von Zirkzee, H. F., Van den Enden, M. J. W. A., Van Kilsdonk, W. T., Van Herk, A. M., German, A. L.

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Reactive surfactants in heterophase polymerization for high performance polymers. Part 1. Synthesis of functionalized poly(ethylene oxide)-b-poly(butylene oxide) copolymers as surf... von SCHIPPER, E. T. W. M, SINDT, O, MONTAYA GONI, A, SHERRINGTON, D. C, SCHOONBROOD, H. A. S, ASUA, J. M, SJÖBERG, M, HAMAIDE, T, LACROIX DESMAZES, P, MÜLLER, B, GUYOT, A, VAN DEN ENDEN, M. J. W. A, VIDAL, F, VAN ES, J. J. G. S, GERMAN, A. L

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Reactive surfactants in heterophase polymerization for high performance polymers: Part 1.Synthesis of functionalized poly(ethylene oxide)- b-poly(butylene oxide) copolymers as surf... von Schipper, E T W M, Sindt, O, Hamaide, T, Lacroix-desmazes, P, Müller, B, Guyot, A, van den Enden, M J W A, Vidal, F, van Es, J J G S, German, A L, Montaya Goñi, A, Sherrington, D C, Schoonbrood, H A S, Asua, J M, Sjöberg, M

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A mutation update for the FLNC gene in myopathies and cardiomyopathies von Verdonschot, Job A. J., Vanhoutte, Els K., Claes, Godelieve R. F., Helderman‐van den Enden, Apollonia T. J. M., Hoeijmakers, Janneke G. J., Hellebrekers, Debby M. E. I., Haan, Amber, Christiaans, Imke, Lekanne Deprez, Ronald H., Boen, Hanne M., Craenenbroeck, Emeline M., Loeys, Bart L., Hoedemaekers, Yvonne M., Marcelis, Carlo, Kempers, Marlies, Brusse, Esther, Waning, Jaap I., Baas, Annette F., Dooijes, Dennis, Asselbergs, Folkert W., Barge‐Schaapveld, Daniela Q. C. M., Koopman, Pieter, Wijngaard, Arthur, Heymans, Stephane R. B., Krapels, Ingrid P. C., Brunner, Han G.

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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study von Dierick, Ines, Baets, Jonathan, Irobi, Joy, Jacobs, An, De Vriendt, Els, Deconinck, Tine, Merlini, Luciano, Van den Bergh, Peter, Rasic, Vedrana Milic, Robberecht, Wim, Fischer, Dirk, Morales, Raul Juntas, Mitrovic, Zoran, Seeman, Pavel, Mazanec, Radim, Kochanski, Andrzej, Jordanova, Albena, Auer-Grumbach, Michaela, Helderman-van den Enden, A. T. J. M., Wokke, John H. J., Nelis, Eva, De Jonghe, Peter, Timmerman, Vincent

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Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: deter... von Christiaans, Imke, Birnie, Erwin, Bonsel, Gouke J, Mannens, Marcel M A M, Michels, Michelle, Majoor-Krakauer, Daniëlle, Dooijes, Dennis, van Tintelen, J Peter, van den Berg, Maarten P, Volders, Paul G A, Arens, Yvonne H, van den Wijngaard, Arthur, Atsma, Douwe E, Helderman-van den Enden, Apollonia T J M, Houweling, Arjan C, de Boer, Karin, van der Smagt, Jasper J, Hauer, Richard N W, Marcelis, Carlo L M, Timmermans, Janneke, van Langen, Irene M, Wilde, Arthur A M

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Perioperative outcome, long-term mortality and time trends in elderly patients undergoing low-, intermediate- or major non-cardiac surgery von Tjeertes, E. K. M., Simoncelli, T. F. W., van den Enden, A. J. M., Mattace-Raso, F. U. S., Stolker, R. J., Hoeks, S. E.

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Update on Kleefstra Syndrome von Willemsen, M.H., Vulto-van Silfhout, A.T., Nillesen, W.M., Wissink-Lindhout, W.M., van Bokhoven, H., Philip, N., Berry-Kravis, E.M., Kini, U., van Ravenswaaij-Arts, C.M.A., Delle Chiaie, B., Innes, A.M.M., Houge, G., Kosonen, T., Cremer, K., Fannemel, M., Stray-Pedersen, A., Reardon, W., Ignatius, J., Lachlan, K., Mircher, C., Helderman van den Enden, P.T.J.M., Mastebroek, M., Cohn-Hokke, P.E., Yntema, H.G., Drunat, S., Kleefstra, T.

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Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy von Verhagen, Judith M A, Veldman, Job H, van der Zwaag, Paul A, von der Thüsen, Jan H, Brosens, Erwin, Christiaans, Imke, Dooijes, Dennis, Helderman-van den Enden, Apollonia T J M, Lekanne Deprez, Ronald H, Michels, Michelle, van Mil, Anneke M, Oldenburg, Rogier A, van der Smagt, Jasper J, van den Wijngaard, Arthur, Wessels, Marja W, Hofstra, Robert M W, van Slegtenhorst, Marjon A, Jongbloed, Jan D H, van de Laar, Ingrid M B H

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Acute Muscular Sarcocystosis: An International Investigation Among Ill Travelers Returning From Tioman Island, Malaysia, 2011-2012 von Esposito, Douglas H., Stich, August, Epelboin, Loïc, Malvy, Denis, Han, Pauline V., Bottieau, Emmanuel, da Silva, Alexandre, Zanger, Philipp, Slesak, Günther, van Genderen, Perry J. J., Rosenthal, Benjamin M., Cramer, Jakob P., Visser, Leo G., Muñoz, José, Drew, Clifton P., Goldsmith, Cynthia S., Steiner, Florian, Wagner, Noémie, Grobusch, Martin P., Plier, D. Adam, Tappe, Dennis, Sotir, Mark J., Brown, Clive, Brunette, Gary W., Fayer, Ronald, von Sonnenburg, Frank, Neumayr, Andreas, Kozarsky, Phyllis E.

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Mortality Risk Associated With Truncating Founder Mutations in Titin von Jansen, Mark, Baas, Annette F, van Spaendonck-Zwarts, Karin Y, Ummels, Amber S, van den Wijngaard, Arthur, Jongbloed, Jan D H, van Slegtenhorst, Marjon A, Lekanne Deprez, Ronald H, Wessels, Marja W, Michels, Michelle, Houweling, Arjan C, Hoorntje, Edgar T, Helderman-van den Enden, Paula J T M, Barge-Schaapveld, Daniela Q C M, Peter van Tintelen, J, van den Berg, Maarten P, Wilde, Arthur A M, Ploos van Amstel, Hans K, Hennekam, Eric A M, Asselbergs, Folkert W, Sijbrands, Eric J G, Dooijes, Dennis

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Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7 von van Engelen, K., Postma, A. V., van de Meerakker, J. B. A., Roos-Hesselink, J. W., Helderman-van den Enden, A. T. J. M., Vliegen, H. W., Rahman, T., Baars, M. J. H., Sels, J-W, Bauer, U., Pickardt, T., Sperling, S. R., Moorman, A. F. M., Keavney, B., Goodship, J., Klaassen, S., Mulder, B. J. M.

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A mutation update for the FLNC gene in myopathies and cardiomyopathies von Verdonschot, Job A J, Vanhoutte, Els K, Claes, Godelieve R F, Helderman-van den Enden, Apollonia T J M, Hoeijmakers, Janneke G J, Hellebrekers, Debby M E I, de Haan, Amber, Christiaans, Imke, Lekanne Deprez, Ronald H, Boen, Hanne M, van Craenenbroeck, Emeline M, Loeys, Bart L, Hoedemaekers, Yvonne M, Marcelis, Carlo, Kempers, Marlies, Brusse, Esther, van Waning, Jaap I, Baas, Annette F, Dooijes, Dennis, Asselbergs, Folkert W, Barge-Schaapveld, Daniela Q C M, Koopman, Pieter, van den Wijngaard, Arthur, Heymans, Stephane R B, Krapels, Ingrid P C, Brunner, Han G

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Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients von Demirdas, Serwet, van den Bersselaar, Lisa M, Lechner, Rosan, Bos, Jessica, Alsters, Suzanne I M, Baars, Marieke J H, Baas, Annette F, Baysal, Özlem, van der Crabben, Saskia N, Dulfer, Eelco, Giesbertz, Noor A A, Helderman-van den Enden, Apollonia T J M, Hilhorst-Hofstee, Yvonne, Kempers, Marlies J E, Komdeur, Fenne L, Loeys, Bart, Majoor-Krakauer, Daniëlle, Ockeloen, Charlotte W, Overwater, Eline, van Tintelen, Peter J, Voorendt, Marsha, de Waard, Vivian, Maugeri, Alessandra, Brüggenwirth, Hennie T, van de Laar, Ingrid M B H, Houweling, Arjan C

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Improving recognition and referral of patients with an increased familial risk of colorectal cancer: results from a randomized controlled trial von Dekker, N., Hermens, R. P., de Wilt, J. H., van Zelst-Stams, W. A., Hoogerbrugge, N.

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Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition von Mikropoulos, C, Selkirk, CGH, Bancroft, E, Vertosick, E, Dadaev, T, Brendler, C, Page, E, Dias, A, Evans, DG, Rothwell, J, Maehle, L, Axcrona, K, Richardson, K, Eccles, D, Jensen, T, Osther, PJ, Van Asperen, CJ, Vasen, H, Kiemeney, LA, Ringelberg, J, Cybulski, C, Wokolorczyk, D, Hart, R, Glover, W, Lam, J, Taylor, L, Salinas, M, Feliubadalo, L, Oldenburg, R, Cremers, R, Verhaegh, G, Van Zelst-Stams, WA, Oosterwijk, JC, Cook, J, Rosario, DJ, Buys, SS, Conner, T, Powers, J, Ausems, MGEM, Teixeira, MR, Maia, S, Rhiem, K, Foulkes, WD, Boshari, T, Davidson, R, Ruijs, M, Helderman-van den Enden, ATJM, Walker, L, Snape, K, Jobson, I, Liljegren, A, Harris, M, Adank, MA, Kirk, J, Taylor, A, Susman, R, Pachter, N, Spigelman, A, Zgajnar, J, Mora, J, Brewer, C, Gallagher, D, Van Os, T, Donaldson, A, Stefansdottir, V, James, PA, Murphy, D, Friedman, E, Greenhalgh, L, Obeid, E, Murthy, V, Copakova, L, McGrath, J, Teo, S-H, Strom, S, Kast, K, Pope, J, Ardern-Jones, A, Bangma, C, Castro, E, Dearnaley, D, Eyfjord, J, Falconer, A, Gronberg, H, Hamdy, FC, Johannsson, O, Khoo, V, Lubinski, J, Grindedal, EM, McKinley, J, Shackleton, K, Moynihan, C, Rennert, G, Suri, M, Tricker, K, Moss, S, Kote-Jarai, Z, Vickers, A, Helfand, BT, Eeles, RA

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Animal model of human disease: multiple myeloma von RADL, J, CROESE, J. W, ZURCHER, C, VAN DEN ENDEN-VIEVEEN, M. H. M, DE LEEUW, A. M

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A near false-negative finding of mosaic trisomy 21-a cautionary tale von Beverstock, G. C., Hansson, Kerstin, Helderman-Van Den Enden, Apollonia T. J. M., Bröcker-Vriends, Annette, Klumper, F., Bartelings, Margot, Dobbe-Van Meerendonk, Willemijn, Roosmalen, J. V., Kolkman, P. H., Kanhai, H. H. H.

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The 5T mouse multiple myeloma model: absence of c-myc oncogene rearrangement in early transplant generations von Radl, J, Punt, YA, van den Enden-Vieveen, MH, Bentvelzen, PA, Bakkus, MH, van den Akker, TW, Benner, R

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