Performance and safety of an integrated bihormonal artificial pancreas for fully automated glucose control at home von Blauw, H., van Bon, A. C., Koops, R., DeVries, J. H.

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An exercise programme for patients with diabetic complications: a study on feasibility and preliminary effectiveness von Otterman, N. M., van Schie, C. H. M., van der Schaaf, M., van Bon, A. C., Busch-Westbroek, T. E., Nollet, F.

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Evaluation of Endocrine Tests. D: the prolonged fasting test for insulinoma von VAN BON, A. C, BENHADI, N, ENDERT, E, FLIERS, E, WIERSINGA, W. M

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Bihormonal fully closed-loop system for the treatment of type 1 diabetes: a real-world multicentre, prospective, single-arm trial in the Netherlands von van Bon, A C, Blauw, H, Jansen, T J P, Laverman, G D, Urgert, T, Geessink-Mennink, J, Mulder, A H, Out, M, Groote Veldman, R, Onvlee, A J, Schouwenberg, B J J W, Vermeulen, M A R, Diekman, M J M, Gerding, M N, van Wijk, J P H, Klaassen, M, Witkop, M, DeVries, J H

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Goserelin-induced transient thyrotoxicosis in a hypothyroid woman on L-thyroxine replacement von VAN BON, A. C, WIERSINGA, W. M

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A woman with haemolytic anaemia von VAN BON, A. C, GOEY, S. H, STUYT, P. M. J

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Clindamycin-resistant Staphylococcus aureus in foot ulcers of patients with diabetes von Regeer, M.V, van Bon, A.C, Spanjaard, L, Busch-Westbroek, T.E, van Schie, C.H.M, Geerlings, S.E, DeVries, J.H

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The changing treatment paradigm in prolactinoma - a prospective series of 100 consecutive neurosurgical cases von van Trigt, Victoria R, Bakker, Leontine E H, Pelsma, Iris C M, Zandbergen, Ingrid M, Jentus, Maaia M, Kruit, Mark C, Dekkers, Olaf M, van Furth, Wouter R, Verstegen, Marco J T, Biermasz, Nienke R

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Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy von McMichael, G, Bainbridge, M N, Haan, E, Corbett, M, Gardner, A, Thompson, S, van Bon, B W M, van Eyk, C L, Broadbent, J, Reynolds, C, O'Callaghan, M E, Nguyen, L S, Adelson, D L, Russo, R, Jhangiani, S, Doddapaneni, H, Muzny, D M, Gibbs, R A, Gecz, J, MacLennan, A H

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Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID von van Bon, B W M, Coe, B P, Bernier, R, Green, C, Gerdts, J, Witherspoon, K, Kleefstra, T, Willemsen, M H, Kumar, R, Bosco, P, Fichera, M, Li, D, Amaral, D, Cristofoli, F, Peeters, H, Haan, E, Romano, C, Mefford, H C, Scheffer, I, Gecz, J, de Vries, B B A, Eichler, E E

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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations von Ockeloen, Charlotte W, Willemsen, Marjolein H, de Munnik, Sonja, van Bon, Bregje W M, de Leeuw, Nicole, Verrips, Aad, Kant, Sarina G, Jones, Elizabeth A, Brunner, Han G, van Loon, Rosa L E, Smeets, Eric E J, van Haelst, Mieke M, van Haaften, Gijs, Nordgren, Ann, Malmgren, Helena, Grigelioniene, Giedre, Vermeer, Sascha, Louro, Pedro, Ramos, Lina, Maal, Thomas J J, van Heumen, Celeste C, Yntema, Helger G, Carels, Carine E L, Kleefstra, Tjitske

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Electrophysiologic Remodeling of the Left Ventricle in Pressure Overload-Induced Right Ventricular Failure von Hardziyenka, Maxim, MD, PhD, Campian, Maria E., MD, Verkerk, Arie O., PhD, Surie, Sulaiman, MD, van Ginneken, Antoni C.G., PhD, Hakim, Sara, BSc, Linnenbank, André C., PhD, de Bruin-Bon, H.A.C.M. Rianne, BSc, Beekman, Leander, BSc, van der Plas, Mart N., MSc, Remme, Carol A., MD, PhD, van Veen, Toon A.B., PhD, Bresser, Paul, MD, PhD, de Bakker, Jacques M.T., PhD, Tan, Hanno L., MD, PhD

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Refining analyses of copy number variation identifies specific genes associated with developmental delay von Coe, Bradley P, Witherspoon, Kali, Rosenfeld, Jill A, van Bon, Bregje W M, Vulto-van Silfhout, Anneke T, Bosco, Paolo, Friend, Kathryn L, Baker, Carl, Buono, Serafino, Vissers, Lisenka E L M, Schuurs-Hoeijmakers, Janneke H, Hoischen, Alex, Pfundt, Rolph, Krumm, Nik, Carvill, Gemma L, Li, Deana, Amaral, David, Brown, Natasha, Lockhart, Paul J, Scheffer, Ingrid E, Alberti, Antonino, Shaw, Marie, Pettinato, Rosa, Tervo, Raymond, de Leeuw, Nicole, Reijnders, Margot R F, Torchia, Beth S, Peeters, Hilde, Thompson, Elizabeth, O'Roak, Brian J, Fichera, Marco, Hehir-Kwa, Jayne Y, Shendure, Jay, Mefford, Heather C, Haan, Eric, Gécz, Jozef, de Vries, Bert B A, Romano, Corrado, Eichler, Evan E

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Impact of bosentan on exercise capacity in adults after the Fontan procedure: a randomized controlled trial von Schuuring, Mark J., Vis, Jeroen C., van Dijk, Arie P.J., van Melle, Joost P., Vliegen, Hubert W., Pieper, Petronella G., Sieswerda, Gertjan T., de Bruin-Bon, Rianne H.A.C.M., Mulder, Barbara J.M., Bouma, Berto J.

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Cantú Syndrome Is Caused by Mutations in ABCC9 von van Bon, Bregje W.M., Gilissen, Christian, Grange, Dorothy K., Hennekam, Raoul C.M., Kayserili, Hülya, Engels, Hartmut, Reutter, Heiko, Ostergaard, John R., Morava, Eva, Tsiakas, Konstantinos, Isidor, Bertrand, Le Merrer, Martine, Eser, Metin, Wieskamp, Nienke, de Vries, Petra, Steehouwer, Marloes, Veltman, Joris A., Robertson, Stephen P., Brunner, Han G., de Vries, Bert B.A., Hoischen, Alexander

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Concept mapping as a promising method to bring practice into science von van Bon-Martens, M.J.H, van de Goor, L.A.M, Holsappel, J.C, Kuunders, T.J.M, Jacobs-van der Bruggen, M.A.M, te Brake, J.H.M, van Oers, J.A.M

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Induced Hypertension for Delayed Cerebral Ischemia After Aneurysmal Subarachnoid Hemorrhage: A Randomized Clinical Trial von Gathier, Celine S, van den Bergh, Walter M, van der Jagt, Mathieu, Verweij, Bon H, Dankbaar, Jan Willem, Müller, Marcella C, Oldenbeuving, Annemarie W, Rinkel, Gabriel J.E, Slooter, Arjen J.C

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ER stress causes rapid loss of intestinal epithelial stemness through activation of the unfolded protein response von Heijmans, Jarom, van Lidth de Jeude, Jooske F, Koo, Bon-Kyoung, Rosekrans, Sanne L, Wielenga, Mattheus C B, van de Wetering, Marc, Ferrante, Marc, Lee, Amy S, Onderwater, Jos J M, Paton, James C, Paton, Adrienne W, Mommaas, A Mieke, Kodach, Liudmila L, Hardwick, James C, Hommes, Daniël W, Clevers, Hans, Muncan, Vanesa, van den Brink, Gijs R

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Differentiated Troy+ Chief Cells Act as Reserve Stem Cells to Generate All Lineages of the Stomach Epithelium von Stange, Daniel E., Koo, Bon-Kyoung, Huch, Meritxell, Sibbel, Greg, Basak, Onur, Lyubimova, Anna, Kujala, Pekka, Bartfeld, Sina, Koster, Jan, Geahlen, Jessica H., Peters, Peter J., van Es, Johan H., van de Wetering, Marc, Mills, Jason C., Clevers, Hans

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The interferon type I signature is present in systemic sclerosis before overt fibrosis and might contribute to its pathogenesis through high BAFF gene expression and high collagen... von Brkic, Zana, van Bon, Lenny, Cossu, Marta, van Helden-Meeuwsen, Cornelia G, Vonk, Madelon C, Knaapen, Hanneke, van den Berg, Wim, Dalm, Virgil A, Van Daele, Paul L, Severino, Adriana, Maria, Naomi I, Guillen, Samara, Dik, Willem A, Beretta, Lorenzo, Versnel, Marjan A, Radstake, Timothy

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