To Disclose or Not to Disclose: A Multi-stakeholder Focus Group Study on Mental Health Issues in the Work Environment von Brouwers, E. P. M., Joosen, M. C. W., van Zelst, C., Van Weeghel, J.

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Histoplasma capsulatum reactivation with haemophagocytic syndrome in a patient with chronic lymphocytic leukaemia von van Koeveringe, M P, Brouwer, R E

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Investigating spatial concentration of sustainable restaurants: It is all about good food von Enthoven, Margo P. M., Brouwer, Aleid E.

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Decomposition in situ of the sublittoral Antarctic macroalga Desmarestia anceps Montagne von BROUWER, P. E. M

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Vertical heterogeneity in physiological characteristics of Ulva spp. mats von MALTA, E, RIJSTENBIL, J. W, BROUWER, P. E. M, KROMKAMP, J. C

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Return-to-Work Self-Efficacy and Actual Return to Work Among Long-Term Sick-Listed Employees von Volker, D., Zijlstra-Vlasveld, M. C., Brouwers, E. P. M., van Lomwel, A. G. C., van der Feltz-Cornelis, C. M.

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Long-term cardiac follow-up in survivors of a malignant bone tumour von Brouwer, CAJ, Gietema, JA, van den Berg, MP, Bink-Boelkens, MTE, Elzenga, NJ, Haaksma, J, Kamps, WA, Vonk, JM, de Vries, EGE, Postma, A

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Recovery Is Up to You, a peer-run course von van Gestel-Timmermans, J. A. W. M, Brouwers, E. P. M, van Nieuwenhuizen, Ch

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Associations between maternal long-chain polyunsaturated fatty acid concentrations and child cognition at 7 years of age: The MEFAB birth cohort von Brouwer-Brolsma, E.M., van de Rest, O., Godschalk, R., Zeegers, M.P.A., Gielen, M., de Groot, R.H.M.

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Description of the SMR cycle, which combines fluid elements of steam and organic Rankine cycles von Verschoor, M.J.E., Brouwer, E.P.

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Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability von Kleefstra, Tjitske, Kramer, Jamie M., Neveling, Kornelia, Willemsen, Marjolein H., Koemans, Tom S., Vissers, Lisenka E.L.M., Wissink-Lindhout, Willemijn, Fenckova, Michaela, van den Akker, Willem M.R., Kasri, Nael Nadif, Nillesen, Willy M., Prescott, Trine, Clark, Robin D., Devriendt, Koenraad, van Reeuwijk, Jeroen, de Brouwer, Arjan P.M., Gilissen, Christian, Zhou, Huiqing, Brunner, Han G., Veltman, Joris A., Schenck, Annette, van Bokhoven, Hans

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Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome von Koolen, David A, Kramer, Jamie M, Neveling, Kornelia, Nillesen, Willy M, Moore-Barton, Heather L, Elmslie, Frances V, Toutain, Annick, Amiel, Jeanne, Malan, Valérie, Tsai, Anne Chun-Hui, Cheung, Sau Wai, Gilissen, Christian, Verwiel, Eugene T P, Martens, Sarah, Feuth, Ton, Bongers, Ernie M H F, de Vries, Petra, Scheffer, Hans, Vissers, Lisenka E L M, de Brouwer, Arjan P M, Brunner, Han G, Veltman, Joris A, Schenck, Annette, Yntema, Helger G, de Vries, Bert B A

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Recurrent De Novo Mutations in PACS1 Cause Defective Cranial-Neural-Crest Migration and Define a Recognizable Intellectual-Disability Syndrome von Schuurs-Hoeijmakers, Janneke H.M., Oh, Edwin C., Vissers, Lisenka E.L.M., Swinkels, Mariëlle E.M., Gilissen, Christian, Willemsen, Michèl A., Holvoet, Maureen, Steehouwer, Marloes, Veltman, Joris A., de Vries, Bert B.A., van Bokhoven, Hans, de Brouwer, Arjan P.M., Katsanis, Nicholas, Devriendt, Koenraad, Brunner, Han G.

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Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness von Wortmann, Saskia B, Vaz, Frédéric M, Gardeitchik, Thatjana, Vissers, Lisenka E L M, Renkema, G Herma, Schuurs-Hoeijmakers, Janneke H M, Kulik, Wim, Lammens, Martin, Christin, Christin, Kluijtmans, Leo A J, Rodenburg, Richard J, Nijtmans, Leo G J, Grünewald, Anne, Klein, Christine, Gerhold, Joachim M, Kozicz, Tamas, van Hasselt, Peter M, Harakalova, Magdalena, Kloosterman, Wigard, Barić, Ivo, Pronicka, Ewa, Ucar, Sema Kalkan, Naess, Karin, Singhal, Kapil K, Krumina, Zita, Gilissen, Christian, van Bokhoven, Hans, Veltman, Joris A, Smeitink, Jan A M, Lefeber, Dirk J, Spelbrink, Johannes N, Wevers, Ron A, Morava, Eva, de Brouwer, Arjan P M

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Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly von Giannandrea, Maila, Bianchi, Veronica, Mignogna, Maria Lidia, Sirri, Alessandra, Carrabino, Salvatore, D'Elia, Errico, Vecellio, Matteo, Russo, Silvia, Cogliati, Francesca, Larizza, Lidia, Ropers, Hans-Hilger, Tzschach, Andreas, Kalscheuer, Vera, Oehl-Jaschkowitz, Barbara, Skinner, Cindy, Schwartz, Charles E., Gecz, Jozef, Van Esch, Hilde, Raynaud, Martine, Chelly, Jamel, de Brouwer, Arjan P.M., Toniolo, Daniela, D'Adamo, Patrizia

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OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin von Coene, Karlien L.M., Roepman, Ronald, Doherty, Dan, Afroze, Bushra, Kroes, Hester Y., Letteboer, Stef J.F., Ngu, Lock H., Budny, Bartlomiej, van Wijk, Erwin, Gorden, Nicholas T., Azhimi, Malika, Thauvin-Robinet, Christel, Veltman, Joris A., Boink, Mireille, Kleefstra, Tjitske, Cremers, Frans P.M., van Bokhoven, Hans, de Brouwer, Arjan P.M.

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PRPS1 Mutations: Four Distinct Syndromes and Potential Treatment von de Brouwer, Arjan P.M., van Bokhoven, Hans, Nabuurs, Sander B., Arts, Willem Frans, Christodoulou, John, Duley, John

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The Applicability of the International Classification of Functioning, Disability, and Health to Study Lifestyle and Quality of Life of Colorectal Cancer Survivors von VAN ROEKEL, Eline H, BOURS, Martijn J. L, DE BROUWER, Carin P. M, NAPEL, Huib Ten, SANDULEANU, Silvia, BEETS, Geerard L, KANT, Ijmert, WEIJENBERG, Matty P

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Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency von Banka, Siddharth, Blom, Henk J., Walter, John, Aziz, Majid, Urquhart, Jill, Clouthier, Christopher M., Rice, Gillian I., de Brouwer, Arjan P.M., Hilton, Emma, Vassallo, Grace, Will, Andrew, Smith, Desirée E.C., Smulders, Yvo M., Wevers, Ron A., Steinfeld, Robert, Heales, Simon, Crow, Yanick J., Pelletier, Joelle N., Jones, Simon, Newman, William G.

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Profiles of individually defined recovery of people with major psychiatric problems von van Gestel-Timmermans, J. A. W. M., Brouwers, E. P. M., Bongers, I. L., van Assen, M. A. L. M., van Nieuwenhuizen, Ch

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