A prospective clinical trial of HIFU hemiablation for clinically localized prostate cancer von van Velthoven, R, Aoun, F, Marcelis, Q, Albisinni, S, Zanaty, M, Lemort, M, Peltier, A, Limani, K

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Development and application of a novel method to assess exposure levels of sensitizing and irritating substances leaching from menstrual hygiene products von Marcelis, Q., Gatzios, A., Deconinck, E., Rogiers, V., Vanhaecke, T., Desmedt, B.

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P24-06: Applicability of the DPRA on mixture testing: Challenges and opportunities von Marcelis, Q., Rogiers, V., Deconinck, E., Desmedt, B., Vanhaecke, T.

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Minimally invasive devices for treating lower urinary tract symptoms in benign prostate hyperplasia: technology update von Aoun, Fouad, Marcelis, Quentin, Roumeguère, Thierry

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Risque d’invasion ganglionnaire après prostatectomie radicale cœlioscopique robot-assistée : validation externe du nomogramme de Briganti von Marcelis, Q., Albisinni, S., Van Velthoven, R., Peltier, A., Roumeguère, T., Quackels, T.

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Hémi-ablation focale pour cancer de prostate localisé par ultrasons focalisés de haute intensité (HIFU) : expérience monocentrique sur dix ans von Van Velthoven, R., Albisinni, S., Diamand, R., Limani, K., Marcelis, Q., Lemort, M., Peltier, A., Roumeguère, T.

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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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Lamin A/C-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation von Hoorntje, Edgar T, Bollen, Ilse A, Barge-Schaapveld, Daniela Q, van Tienen, Florence H, te Meerman, Gerard J, Jansweijer, Joeri A, van Essen, Anthonie J, Volders, Paul G, Constantinescu, Alina A, van den Akker, Peter C, van Spaendonck-Zwarts, Karin Y, Oldenburg, Rogier A, Marcelis, Carlo L, van der Smagt, Jasper J, Hennekam, Eric A, Vink, Aryan, Bootsma, Marianne, Aten, Emmelien, Wilde, Arthur A, van den Wijngaard, Arthur, Broers, Jos L, Jongbloed, Jan D, van der Velden, Jolanda, van den Berg, Maarten P, van Tintelen, J Peter

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Chronic Q fever: Review of the literature and a proposal of new diagnostic criteria von Wegdam-Blans, M.C.A, Kampschreur, L.M, Delsing, C.E, Bleeker-Rovers, C.P, Sprong, T, van Kasteren, M.E.E, Notermans, D.W, Renders, N.H.M, Bijlmer, H.A, Lestrade, P.J, Koopmans, M.P.G, Nabuurs-Franssen, M.H, Oosterheert, J.J

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Towards mismatched DNA photoprobes and photoreagents: “elbow-shaped” Ru( ii ) complexes von Deraedt, Q., Marcélis, L., Loiseau, F., Elias, B.

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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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Lamin A/C-Related Cardiac Disease von Hoorntje, Edgar T, Bollen, Ilse A, Barge-Schaapveld, Daniela Q, van Tienen Florence H, te Meerman Gerard J, Jansweijer, Joeri A, van Essen Anthonie J, Volders, Paul G, Constantinescu, Alina A, van den Akker Peter C, van Spaendonck-Zwarts Karin Y, Oldenburg, Rogier A, Marcelis, Carlo L, van der Smagt Jasper J, Hennekam, Eric A, Vink Aryan, Bootsma, Marianne, Aten Emmelien, Wilde, Arthur A, van den Wijngaard Arthur, Broers, Jos L, Jongbloed, Jan D, van der Velden Jolanda, van den Berg Maarten P, van Tintelen J Peter

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Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification von van der Meulen, Marijke H., Herkert, Johanna C., den Boer, Susanna L., du Marchie Sarvaas, Gideon J., Blom, Nico A., ten Harkel, Arend D.J., Breur, Hans M.P.J., Rammeloo, Lukas A.J., Tanke, Ronald B., Marcelis, Carlo, van de Laar, Ingrid M.B.H., Verhagen, Judith M.A., Lekanne dit Deprez, Ronald H., Barge-Schaapveld, Daniela Q.C.M., Baas, Annette F., Sammani, Arjan, Christiaans, Imke, van Tintelen, J. Peter, Dalinghaus, Michiel

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Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant von Hoorntje, Edgar T., Burns, Charlotte, Marsili, Luisa, Corden, Ben, Parikh, Victoria N., te Meerman, Gerard J., Gray, Belinda, Adiyaman, Ahmet, Bagnall, Richard D., Barge-Schaapveld, Daniela Q.C.M., van den Berg, Maarten P., Bootsma, Marianne, Bosman, Laurens P., Correnti, Gemma, Duflou, Johan, Eppinga, Ruben N., Fatkin, Diane, Fietz, Michael, Haan, Eric, Jongbloed, Jan D.H., Hauer, Arnaud D., Lam, Lien, van Lint, Freyja H.M., Lota, Amrit, Marcelis, Carlo, McCarthy, Hugh J., van Mil, Anneke M., Oldenburg, Rogier A., Pachter, Nicholas, Planken, R. Nils, Reuter, Chloe, Semsarian, Christopher, van der Smagt, Jasper J., Thompson, Tina, Vohra, Jitendra, Volders, Paul G.A., van Waning, Jaap I., Whiffin, Nicola, van den Wijngaard, Arthur, Amin, Ahmad S., Wilde, Arthur A.M., van Woerden, Gijs, Yeates, Laura, Zentner, Dominica, Ashley, Euan A., Wheeler, Matthew T., Ware, James S., van Tintelen, J. Peter, Ingles, Jodie

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Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification von van der Meulen, Marijke H, Herkert, Johanna C, den Boer, Susanna L, du Marchie Sarvaas, Gideon J, Blom, Nico, Ten Harkel, Arend D J, Breur, Hans M P J, Rammeloo, Lukas A J, Tanke, Ronald, Marcelis, Carlo, van de Laar, Ingrid M B H, Verhagen, Judith M A, Lekanne Dit Deprez, Ronald H, Barge-Schaapveld, Daniela Q C M, Baas, Annette, Sammani, Arjan, Christiaans, Imke, van Tintelen, J Peter, Dalinghaus, Michiel

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Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family von Dai, J, Kim, O-H, Cho, T-J, Schmidt-Rimpler, M, Tonoki, H, Takikawa, K, Haga, N, Miyoshi, K, Kitoh, H, Yoo, W-J, Choi, I-H, Song, H-R, Jin, D-K, Kim, H-T, Kamasaki, H, Bianchi, P, Grigelioniene, G, Nampoothiri, S, Minagawa, M, Miyagawa, S-i, Fukao, T, Marcelis, C, Jansweijer, M C E, Hennekam, R C M, Bedeschi, F, Mustonen, A, Jiang, Q, Ohashi, H, Furuichi, T, Unger, S, Zabel, B, Lausch, E, Superti-Furga, A, Nishimura, G, Ikegawa, S

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Towards mismatched DNA photoprobes and photoreagents: "elbow-shaped" Ru(ii) complexesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6qi00223d von Deraedt, Q, Marcélis, L, Loiseau, F, Elias, B

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Intelligence, educational attainment, and brain structure in those at familial high‐risk for schizophrenia or bipolar disorder von de Zwarte, SMC, Brouwer, RM, Agartz, I, Alda, M, Alonso-Lana, S, Bearden, CE, Bertolino, A, Bonvino, A, Bramon, E, Buimer, EEL, Cahn, W, Canales-Rodríguez, EJ, Cannon, DM, Cannon, TD, Caseras, X, Castro-Fornieles, J, Chen, Q, Chung, Y, De la Serna, E, Del Mar Bonnin, C, Demro, C, Di Giorgio, A, Doucet, GE, Eker, MC, Erk, S, Fatjó-Vilas, M, Fears, SC, Foley, SF, Frangou, S, Fullerton, JM, Glahn, DC, Goghari, VM, Goikolea, JM, Goldman, AL, Gonul, AS, Gruber, O, Hajek, T, Hawkins, EL, Heinz, A, Hidiroglu Ongun, C, Hillegers, MHJ, Houenou, J, Hulshoff Pol, HE, Hultman, CM, Ingvar, M, Johansson, V, Jönsson, EG, Kane, F, Kempton, MJ, Koenis, MMG, Kopecek, M, Krämer, B, Lawrie, SM, Lenroot, RK, Marcelis, M, Mattay, VS, McDonald, C, Meyer-Lindenberg, A, Michielse, S, Mitchell, PB, Moreno, D, Murray, RM, Mwangi, B, Nabulsi, L, Newport, J, Olman, CA, van Os, J, Overs, BJ, Ozerdem, A, Pergola, G, Picchioni, MM, Piguet, C, Pomarol-Clotet, E, Radua, J, Ramsay, IS, Richter, A, Roberts, G, Salvador, R, Saricicek Aydogan, A, Sarró, S, Schofield, PR, Simsek, F, Soares, JC, Sponheim, SR, Sugranyes, G, Toulopoulou, T, Tronchin, G, Vieta, E, Walter, H, Whalley, HC, Wu, M-J, Yalin, N, Andreassen, OA, Ching, CRK, Thomopoulos, SI, van Erp, TGM, Jahanshad, N, Thompson, PM, Kahn, RS, van Haren, NEM

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The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder von de Zwarte, SMC, Brouwer, RM, Agartz, I, Alda, M, Aleman, A, Alpert, KI, Bearden, CE, Bertolino, A, Bois, C, Bonvino, A, Bramon, E, Buimer, EEL, Cahn, W, Cannon, DM, Cannon, TD, Caseras, X, Castro-Fornieles, J, Chen, Q, Chung, Y, De la Serna, E, Di Giorgio, A, Doucet, GE, Eker, MC, Erk, S, Fears, SC, Foley, SF, Frangou, S, Frankland, A, Fullerton, JM, Glahn, DC, Goghari, VM, Goldman, AL, Gonul, AS, Gruber, O, de Haan, L, Hajek, T, Hawkins, EL, Heinz, A, Hillegers, MHJ, Hulshoff Pol, HE, Hultman, CM, Ingvar, M, Johansson, V, Jönsson, EG, Kane, F, Kempton, MJ, Koenis, MMG, Kopecek, M, Krabbendam, L, Krämer, B, Lawrie, SM, Lenroot, RK, Marcelis, M, Marsman, JBC, Mattay, VS, McDonald, C, Meyer-Lindenberg, A, Michielse, S, Mitchell, PB, Moreno, D, Murray, RM, Mwangi, B, Najt, P, Neilson, E, Newport, J, van Os, J, Overs, B, Ozerdem, A, Picchioni, MM, Richter, A, Roberts, G, Aydogan, AS, Schofield, PR, Simsek, F, Soares, JC, Sugranyes, G, Toulopoulou, T, Tronchin, G, Walter, H, Wang, L, Weinberger, DR, Whalley, HC, Yalin, N, Andreassen, OA, Ching, CRK, van Erp, TGM, Turner, JA, Jahanshad, N, Thompson, PM, Kahn, RS, van Haren, NEM

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The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder von de Zwarte, SMC, Brouwer, RM, Agartz, I, Alda, M, Aleman, A, Alpert, KI, Bearden, CE, Bertolino, A, Bois, C, Bonvino, A, Bramon, E, Buimer, EEL, Cahn, W, Cannon, DM, Cannon, TD, Caseras, X, Castro-Fornieles, J, Chen, Q, Chung, Y, De la Serna, E, Di Giorgio, A, Doucet, GE, Eker, MC, Erk, S, Fears, SC, Foley, SF, Frangou, S, Frankland, A, Fullerton, JM, Glahn, DC, Goghari, VM, Goldman, AL, Gonul, AS, Gruber, O, de Haan, L, Hajek, T, Hawkins, EL, Heinz, A, Hillegers, MHJ, Pol, HEH, Hultman, CM, Ingvar, M, Johansson, V, Jonsson, EG, Kane, F, Kempton, MJ, Koenis, MMG, Kopecek, M, Krabbendam, L, Kraemer, B, Lawrie, SM, Lenroot, RK, Marcelis, M, Marsman, J-BC, Mattay, VS, McDonald, C, Meyer-Lindenberg, A, Michielse, S, Mitchell, PB, Moreno, D, Murray, RM, Mwangi, B, Najt, P, Neilson, E, Newport, J, van Os, J, Overs, B, Ozerdem, A, Picchioni, MM, Richter, A, Roberts, G, Aydogan, AS, Schofield, PR, Simsek, F, Soares, JC, Sugranyes, G, Toulopoulou, T, Tronchin, G, Walter, H, Wang, L, Weinberger, DR, Whalley, HC, Yalin, N, Andreassen, OA, Ching, CRK, van Erp, TGM, Turner, JA, Jahanshad, N, Thompson, PM, Kahn, RS, van Haren, NEM

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