Bone scintigraphy in children with persistent pain in an extremity, suggesting algoneurodystrophy von OUD, C. F, LEGEIN, J, EVERAERT, H, DE BOECK, H, PINTELON, H, PIEPSZ, A

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Bone scintigraphy in children with persistent pain in an extremity, suggesting algoneurodystrophy von OUD, C. F, LEGEIN, J, EVERAERT, H, DE BOECK, H, PINTELON, H, PIEPSZ, A

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Variant PNLDC1, Defective piRNA Processing, and Azoospermia von Nagirnaja, Liina, Mørup, Nina, Nielsen, John E, Stakaitis, Rytis, Golubickaite, Ieva, Oud, Manon S, Winge, Sofia B, Carvalho, Filipa, Aston, Kenneth I, Khani, Francesca, van der Heijden, Godfried W, Marques, C. Joana, Skakkebaek, Niels E, Rajpert–De Meyts, Ewa, Schlegel, Peter N, Jørgensen, Niels, Veltman, Joris A, Lopes, Alexandra M, Conrad, Donald F, Almstrup, Kristian

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C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome von Arts, Heleen H, Bongers, Ernie M H F, Mans, Dorus A, van Beersum, Sylvia E C, Oud, Machteld M, Bolat, Emine, Spruijt, Liesbeth, Cornelissen, Elisabeth A M, Schuurs-Hoeijmakers, Janneke H M, de Leeuw, Nicole, Cormier-Daire, Valérie, Brunner, Han G, Knoers, Nine V A M, Roepman, Ronald

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Lack of evidence for a role of PIWIL1 variants in human male infertility von Oud, M.S., Volozonoka, L., Friedrich, C., Kliesch, S., Nagirnaja, L., Gilissen, C., O’Bryan, M.K., McLachlan, R.I., Aston, K.I., Tüttelmann, F., Conrad, D.F., Veltman, J.A.

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Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling von Chaki, Moumita, Airik, Rannar, Ghosh, Amiya K., Giles, Rachel H., Chen, Rui, Slaats, Gisela G., Wang, Hui, Hurd, Toby W., Zhou, Weibin, Cluckey, Andrew, Gee, Heon Yung, Ramaswami, Gokul, Hong, Chen-Jei, Hamilton, Bruce A., Červenka, Igor, Ganji, Ranjani Sri, Bryja, Vitezslav, Arts, Heleen H., van Reeuwijk, Jeroen, Oud, Machteld M., Letteboer, Stef J.F., Roepman, Ronald, Husson, Hervé, Ibraghimov-Beskrovnaya, Oxana, Yasunaga, Takayuki, Walz, Gerd, Eley, Lorraine, Sayer, John A., Schermer, Bernhard, Liebau, Max C., Benzing, Thomas, Le Corre, Stephanie, Drummond, Iain, Janssen, Sabine, Allen, Susan J., Natarajan, Sivakumar, O’Toole, John F., Attanasio, Massimo, Saunier, Sophie, Antignac, Corinne, Koenekoop, Robert K., Ren, Huanan, Lopez, Irma, Nayir, Ahmet, Stoetzel, Corinne, Dollfus, Helene, Massoudi, Rustin, Gleeson, Joseph G., Andreoli, Sharon P., Doherty, Dan G., Lindstrad, Anna, Golzio, Christelle, Katsanis, Nicholas, Pape, Lars, Abboud, Emad B., Al-Rajhi, Ali A., Lewis, Richard A., Omran, Heymut, Lee, Eva Y.-H.P., Wang, Shaohui, Sekiguchi, JoAnn M., Saunders, Rudel, Johnson, Colin A., Garner, Elizabeth, Vanselow, Katja, Andersen, Jens S., Shlomai, Joseph, Nurnberg, Gudrun, Nurnberg, Peter, Levy, Shawn, Smogorzewska, Agata, Otto, Edgar A., Hildebrandt, Friedhelm

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Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19 von Bredrup, Cecilie, Saunier, Sophie, Oud, Machteld M., Fiskerstrand, Torunn, Hoischen, Alexander, Brackman, Damien, Leh, Sabine M., Midtbø, Marit, Filhol, Emilie, Bole-Feysot, Christine, Nitschké, Patrick, Gilissen, Christian, Haugen, Olav H., Sanders, Jan-Stephan F., Stolte-Dijkstra, Irene, Mans, Dorus A., Steenbergen, Eric J., Hamel, Ben C.J., Matignon, Marie, Pfundt, Rolph, Jeanpierre, Cécile, Boman, Helge, Rødahl, Eyvind, Veltman, Joris A., Knappskog, Per M., Knoers, Nine V.A.M., Roepman, Ronald, Arts, Heleen H.

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Awareness in children: a secondary analysis of five cohort studies von Davidson, A. J., Smith, K. R., Blussé van Oud‐Alblas, H. J., Lopez, U., Malviya, S., Bannister, C. F., Galinkin, J. L., Habre, W., Ironfield, C., Voepel‐Lewis, T., Weber, F.

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Risk of Four Geriatric Syndromes: A Comparison of Mental Health Care and General Hospital Inpatients von Douairi, J, Bos, E G T, van Munster, B C, Boudestein, K, Benraad, C, Disselhorst, L, Oude Voshaar, R C, Oud, F M M, Kok, R M

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Recognition of cognitive impairment and depressive symptoms in older patients with heart failure von Oud, F. M. M., Spies, P. E., Braam, R. L., van Munster, B. C.

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Real-World Effectiveness of Reslizumab in Patients With Severe Eosinophilic Asthma – First Initiators and Switchers von Hashimoto, Simone, Kroes, Johannes A., Eger, Katrien A., Mau Asam, Pearl F., Hofstee, Hendrik B., Bendien, Sarah A., Braunstahl, Gert Jan, Broeders, Marielle E.A.C., Imming, Leonie M., Langeveld, Bas, Maitland-van der Zee, Anke H., Oud, Karen T.M., Patberg, Kornelis Wiebe, Smeenk, Frank W.J.M., Romme, Elisabeth A.P.M., van Bezouw, Maarten J., van de Ven, Marjo J., van Veen, Anneke, van Velzen, Edwin, van Veen, Ilonka H.P.A.A., Weersink, Els J.M., Ten Brinke, Anneke, Sont, Jacob K., Bel, Elisabeth H.

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Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility von Wyrwoll, Margot J., Temel, Şehime G., Nagirnaja, Liina, Oud, Manon S., Lopes, Alexandra M., van der Heijden, Godfried W., Heald, James S., Rotte, Nadja, Wistuba, Joachim, Wöste, Marius, Ledig, Susanne, Krenz, Henrike, Smits, Roos M., Carvalho, Filipa, Gonçalves, João, Fietz, Daniela, Türkgenç, Burcu, Ergören, Mahmut C., Çetinkaya, Murat, Başar, Murad, Kahraman, Semra, McEleny, Kevin, Xavier, Miguel J., Turner, Helen, Pilatz, Adrian, Röpke, Albrecht, Dugas, Martin, Kliesch, Sabine, Neuhaus, Nina, Aston, Kenneth I., Conrad, Donald F., Veltman, Joris A., Friedrich, Corinna, Tüttelmann, Frank

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A de novo paradigm for male infertility von Oud, M. S., Smits, R. M., Smith, H. E., Mastrorosa, F. K., Holt, G. S., Houston, B. J., de Vries, P. F., Alobaidi, B. K. S., Batty, L. E., Ismail, H., Greenwood, J., Sheth, H., Mikulasova, A., Astuti, G. D. N., Gilissen, C., McEleny, K., Turner, H., Coxhead, J., Cockell, S., Braat, D. D. M., Fleischer, K., D’Hauwers, K. W. M., Schaafsma, E., Nagirnaja, L., Conrad, D. F., Friedrich, C., Kliesch, S., Aston, K. I., Riera-Escamilla, A., Krausz, C., Gonzaga-Jauregui, C., Santibanez-Koref, M., Elliott, D. J., Vissers, L. E. L. M., Tüttelmann, F., O’Bryan, M. K., Ramos, L., Xavier, M. J., van der Heijden, G. W., Veltman, J. A.

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Interaction between geriatric syndromes in predicting three months mortality risk von Oud, F. M.M., Schut, M.C., Spies, P.E., van der Zaag-Loonen, H.J., de Rooij, S.E., Abu-Hanna, A., van Munster, B.C.

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Intraoperative awareness during paediatric anaesthesia von Blussé van Oud-Alblas, H.J., van Dijk, M., Liu, C., Tibboel, D., Klein, J., Weber, F.

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Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia von Oud, Manon S., Ramos, Liliana, O'Bryan, Moira K., McLachlan, Robert I., Okutman, Özlem, Viville, Stephane, Vries, Petra F., Smeets, Dominique F.C.M., Lugtenberg, Dorien, Hehir‐Kwa, Jayne Y., Gilissen, Christian, de Vorst, Maartje, Vissers, Lisenka E.L.M., Hoischen, Alexander, Meijerink, Aukje M., Fleischer, Kathrin, Veltman, Joris A., Noordam, Michiel J.

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Does the Dutch Safety Management Program predict adverse outcomes for older patients in the emergency department? von Schuijt, H-J, Oud, F. M. M., Bruns, E. J. R., van Duijvendijk, P., Van der Zaag-Loonen, H. J., Spies, P. E., van Munster, B. C.

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Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement von Schmidts, Miriam, Arts, Heleen H, Bongers, Ernie M H F, Yap, Zhimin, Oud, Machteld M, Antony, Dinu, Duijkers, Lonneke, Emes, Richard D, Stalker, Jim, Yntema, Jan-Bart L, Plagnol, Vincent, Hoischen, Alexander, Gilissen, Christian, Forsythe, Elisabeth, Lausch, Ekkehart, Veltman, Joris A, Roeleveld, Nel, Superti-Furga, Andrea, Kutkowska-Kazmierczak, Anna, Kamsteeg, Erik-Jan, Elçioğlu, Nursel, van Maarle, Merel C, Graul-Neumann, Luitgard M, Devriendt, Koenraad, Smithson, Sarah F, Wellesley, Diana, Verbeek, Nienke E, Hennekam, Raoul C M, Kayserili, Hulya, Scambler, Peter J, Beales, Philip L, Knoers, Nine VAM, Roepman, Ronald, Mitchison, Hannah M

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De novo mutations in children born after medical assisted reproduction von Smits, R M, Xavier, M J, Oud, M S, Astuti, G D N, Meijerink, A M, de Vries, P F, Holt, G S, Alobaidi, B K S, Batty, L E, Khazeeva, G, Sablauskas, K, Vissers, L E L M, Gilissen, C, Fleischer, K, Braat, D D M, Ramos, L, Veltman, J A

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Whole exome sequencing of intracranial aneurysm von Foroud, Tatiana

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