Prevalidation of the cAMP-PTx reporter assay for quantitative assessment of pertussis toxin activity von de Brouwer, L., David, D., Espitia Ballestas, M., Sloots, A., Hoonakker, M.E.

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Measurement of immunological parameters in blood of Gottingen Minipigs super(()R) and the T cell-dependent immune response to KLH von van Mierlo, G, Schijf, M, de Zeeuw-Brouwer, ML, van Bilsen, J, Penninks, A

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Development of methods to measure immunological parameters in blood of Beagle dogs von van Mierlo, Geertje, Schijf, Marcel, de Zeeuw-Brouwer, Mary-Lène, van Och, François, Penninks, André

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Jugements derniers von de Brouwer, Jérôme, Ost, François, Rousseaux, Xavier

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Human Ontogeny of Drug Transporters: Review and Recommendations of the Pediatric Transporter Working Group von Brouwer, KLR, Aleksunes, LM, Brandys, B, Giacoia, GP, Knipp, G, Lukacova, V, Meibohm, B, Nigam, SK, Rieder, M, de Wildt, SN

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Hérésies : : une construction d'identités religieuses

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How nurses and their work environment affect patient experiences of the quality of care: a qualitative study von Kieft, Renate Amm, de Brouwer, Brigitte B J M, Francke, Anneke L, Delnoij, Diana M J

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Subcutaneous or Transvenous Defibrillator Therapy von Knops, Reinoud E, Olde Nordkamp, Louise R.A, Delnoy, Peter-Paul H.M, Boersma, Lucas V.A, Kuschyk, Jürgen, El-Chami, Mikhael F, Bonnemeier, Hendrik, Behr, Elijah R, Brouwer, Tom F, Kääb, Stefan, Mittal, Suneet, Quast, Anne-Floor B.E, Smeding, Lonneke, van der Stuijt, Willeke, de Weger, Anouk, de Wilde, Koen C, Bijsterveld, Nick R, Richter, Sergio, Brouwer, Marc A, de Groot, Joris R, Kooiman, Kirsten M, Lambiase, Pier D, Neuzil, Petr, Vernooy, Kevin, Alings, Marco, Betts, Tim R, Bracke, Frank A.L.E, Burke, Martin C, de Jong, Jonas S.S.G, Wright, David J, Tijssen, Jan G.P, Wilde, Arthur A.M

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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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Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability von Riazuddin, S, Hussain, M, Razzaq, A, Iqbal, Z, Shahzad, M, Polla, D L, Song, Y, van Beusekom, E, Khan, A A, Tomas-Roca, L, Rashid, M, Zahoor, M Y, Wissink-Lindhout, W M, Basra, M A R, Ansar, M, Agha, Z, van Heeswijk, K, Rasheed, F, Van de Vorst, M, Veltman, J A, Gilissen, C, Akram, J, Kleefstra, T, Assir, M Z, Grozeva, D, Carss, K, Raymond, F L, O'Connor, T D, Riazuddin, S A, Khan, S N, Ahmed, Z M, de Brouwer, A P M, van Bokhoven, H, Riazuddin, S

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Lifetime medical costs of obesity: prevention no cure for increasing health expenditure von van Baal, Pieter H M, Polder, Johan J, de Wit, G Ardine, Hoogenveen, Rudolf T, Feenstra, Talitha L, Boshuizen, Hendriek C, Engelfriet, Peter M, Brouwer, Werner B F

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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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Low vitamin D status is associated with reduced muscle mass and impaired physical performance in frail elderly people von Tieland, M, Brouwer-Brolsma, E M, Nienaber-Rousseau, C, van Loon, L J C, De Groot, L C P G M

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Human fetal microglia acquire homeostatic immune-sensing properties early in development von Kracht, L., Borggrewe, M., Eskandar, S., Brouwer, N., Chuva de Sousa Lopes, S. M., Laman, J. D., Scherjon, S. A., Prins, J. R., Kooistra, S. M., Eggen, B. J. L.

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Mutations in MED12 Cause X-Linked Ohdo Syndrome von Vulto-van Silfhout, Anneke T., de Vries, Bert B.A., van Bon, Bregje W.M., Hoischen, Alexander, Ruiterkamp-Versteeg, Martina, Gilissen, Christian, Gao, Fangjian, van Zwam, Marloes, Harteveld, Cornelis L., van Essen, Anthonie J., Hamel, Ben C.J., Kleefstra, Tjitske, Willemsen, Michèl A.A.P., Yntema, Helger G., van Bokhoven, Hans, Brunner, Han G., Boyer, Thomas G., de Brouwer, Arjan P.M.

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Streptococcus suis Meningitis: A Systematic Review and Meta-analysis von van Samkar, Anusha, Brouwer, Matthijs C, Schultsz, Constance, van der Ende, Arie, van de Beek, Diederik

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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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Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction between CYP2C19 and CYP2D6 and SSRIs von Brouwer, Jurriaan M J L, Nijenhuis, Marga, Soree, Bianca, Guchelaar, Henk-Jan, Swen, Jesse J, van Schaik, Ron H N, Weide, Jan van der, Rongen, Gerard A P J M, Buunk, Anne-Marie, de Boer-Veger, Nienke J, Houwink, Elisa J F, van Westrhenen, Roos, Wilffert, Bob, Deneer, Vera H M, Mulder, Hans

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Disease‐Associated Changes in Drug Transporters May Impact the Pharmacokinetics and/or Toxicity of Drugs: A White Paper From the International Transporter Consortium von Evers, Raymond, Piquette‐Miller, Micheline, Polli, Joseph W., Russel, Frans G.M., Sprowl, Jason A., Tohyama, Kimio, Ware, Joseph A., Wildt, Saskia N., Xie, Wen, Brouwer, Kim L.R.

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Distinct amyloid-β and tau-associated microglia profiles in Alzheimer’s disease von Gerrits, Emma, Brouwer, Nieske, Kooistra, Susanne M., Woodbury, Maya E., Vermeiren, Yannick, Lambourne, Mirjam, Mulder, Jan, Kummer, Markus, Möller, Thomas, Biber, Knut, Dunnen, Wilfred F. A. den, De Deyn, Peter P., Eggen, Bart J. L., Boddeke, Erik W. G. M.

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