Do We Contribute to Women's Empowerment? Insights From a Nutrition-Sensitive Agriculture Project Implemented in Nong, Laos von Gerber, Manon, Bon, Daniëlle M., Bouahom, Bounthanom, Broerse, Jacqueline E.W., Essink, Dirk

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Understanding Discrepancies in Nutritional Outcomes Among Under-Fives in Laos: A Mixed-Methods Study Using the Positive Deviance Approach von Boulom, Sayvisene, Bon, Daniëlle M., Essink, Dirk, Kounnavong, Sengchanh, Broerse, Jacqueline E. W.

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Myeloid lncRNA LOUP mediates opposing regulatory effects of RUNX1 and RUNX1-ETO in t(8;21) AML von Trinh, Bon Q., Ummarino, Simone, Zhang, Yanzhou, Ebralidze, Alexander K., Bassal, Mahmoud A., Nguyen, Tuan M., Heller, Gerwin, Coffey, Rory, Tenen, Danielle E., van der Kouwe, Emiel, Fabiani, Emiliano, Gurnari, Carmelo, Wu, Chan-Shuo, Angarica, Vladimir Espinosa, Yang, Henry, Chen, Sisi, Zhang, Hong, Thurm, Abby R., Marchi, Francisco, Levantini, Elena, Staber, Philipp B., Zhang, Pu, Voso, Maria Teresa, Pandolfi, Pier Paolo, Kobayashi, Susumu S., Chai, Li, Di Ruscio, Annalisa, Tenen, Daniel G.

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A Multicenter Randomized Controlled Trial of Zephyr Endobronchial Valve Treatment in Heterogeneous Emphysema (LIBERATE) von Criner, Gerard J, Sue, Richard, Wright, Shawn, Dransfield, Mark, Rivas-Perez, Hiram, Wiese, Tanya, Sciurba, Frank C, Shah, Pallav L, Wahidi, Momen M, de Oliveira, Hugo Goulart, Morrissey, Brian, Cardoso, Paulo F G, Hays, Steven, Majid, Adnan, Pastis, Jr, Nicholas, Kopas, Lisa, Vollenweider, Mark, McFadden, P Michael, Machuzak, Michael, Hsia, David W, Sung, Arthur, Jarad, Nabil, Kornaszewska, Malgorzata, Hazelrigg, Stephen, Krishna, Ganesh, Armstrong, Brian, Shargill, Narinder S, Slebos, Dirk-Jan

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A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency von Jansen, Sandra, Hoischen, Alexander, Coe, Bradley P, Carvill, Gemma L, Van Esch, Hilde, Bosch, Daniëlle G M, Andersen, Ulla A, Baker, Carl, Bauters, Marijke, Bernier, Raphael A, van Bon, Bregje W, Claahsen-van der Grinten, Hedi L, Gecz, Jozef, Gilissen, Christian, Grillo, Lucia, Hackett, Anna, Kleefstra, Tjitske, Koolen, David, Kvarnung, Malin, Larsen, Martin J, Marcelis, Carlo, McKenzie, Fiona, Monin, Marie-Lorraine, Nava, Caroline, Schuurs-Hoeijmakers, Janneke H, Pfundt, Rolph, Steehouwer, Marloes, Stevens, Servi J C, Stumpel, Connie T, Vansenne, Fleur, Vinci, Mirella, van de Vorst, Maartje, Vries, Petra de, Witherspoon, Kali, Veltman, Joris A, Brunner, Han G, Mefford, Heather C, Romano, Corrado, Vissers, Lisenka E L M, Eichler, Evan E, de Vries, Bert B A

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De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila von Lugtenberg, Dorien, Reijnders, Margot R F, Fenckova, Michaela, Bijlsma, Emilia K, Bernier, Raphael, van Bon, Bregje W M, Smeets, Eric, Vulto-van Silfhout, Anneke T, Bosch, Danielle, Eichler, Evan E, Mefford, Heather C, Carvill, Gemma L, Bongers, Ernie M H F, Schuurs-Hoeijmakers, Janneke Hm, Ruivenkamp, Claudia A, Santen, Gijs W E, van den Maagdenberg, Arn M J M, Peeters-Scholte, Cacha M P C D, Kuenen, Sabine, Verstreken, Patrik, Pfundt, Rolph, Yntema, Helger G, de Vries, Petra F, Veltman, Joris A, Hoischen, Alexander, Gilissen, Christian, de Vries, Bert B A, Schenck, Annette, Kleefstra, Tjitske, Vissers, Lisenka E L M

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Effect of Zephyr Endobronchial Valves on Dyspnea, Activity Levels, and Quality of Life at One Year. Results from a Randomized Clinical Trial von Dransfield, Mark T., Garner, Justin L., Bhatt, Surya P., Slebos, Dirk-Jan, Klooster, Karin, Sciurba, Frank C., Shah, Pallav L., Marchetti, Nathaniel T., Sue, Richard D., Wright, Shawn, Rivas-Perez, Hiram, Wiese, Tanya A., Wahidi, Momen M., Goulart de Oliveira, Hugo, Armstrong, Brian, Radhakrishnan, Sri, Shargill, Narinder S., Criner, Gerard J., Katz, Lewis, Criner, Gerard J., Cordova, Francis, Desai, Parag, Marchetti, Nathaniel, Kim, Victor, Shenoy, Kartik, Travaline, John, Thomas, Jiji, Criner, Lii-Yoong H., Sue, Richard, Wright, Shawn, Thornburg, Aaron, Thomas, Terry, Dransfield, Mark, Bhatt, Surya, Wells, James Michael, Seabron-Harris, Necole, Rivas-Perez, Hiram, Gauhar, Umair, Wiese, Tanya A., Despirito, Crissie, Sciurba, Frank, Bon Field, Jessica, Chandra, Divay, Leader, Joseph, Semaan, Roy, Ledezma, Christina, Shah, Pallav, Kemp, Samuel, Garner, Justin, Aboelhassan, Arafa, Srikanthan, Karthi, Tenda, Eric, Abraham, Anita, Sim, Cai, Wahidi, Momen, Mahmood, Kamran, Shofer, Scott, Coles, Kathleen, de Oliveira, Hugo Goulart, Oliveira, Guilherme Augusto, Machado, Betina, Benedetto, Igor, Svartman, Fabio, de Macedo Neto, Amarilio, Schreiner, Leonardo, Vieira, Taiane, Morrissey, Brian, Yoneda, Ken, Tham, Tina, Tompkins, Daniel, Guerreiro Cardoso, Paulo F., Athanazio, Rodrigo, Nominando, Felipe, Rached, Samia, Cassimiro, Luciana, Hays, Steven, Seeley, Eric, Shrestha, Pavan, Dincheva, Gabriela R., Majid, Adnan, Alape-Moya, Daniel, Parikh, Mihir, Paton, Alichia, Agnew, Alexis, Pastis, Nicholas, Strange, Charlie, Beiko, Tatsiana, Woodford, Danielle, Blanton, Mary, Kopas, Lisa, Connolly, Timothy, Santacruz, Jose Fernando, Shah, Bhavin, Vollenweider, Mark, Herrera, Luis, Khan, Rumi, Sernulka, Kristine, McFadden, P. Michael, Barbers, Richard, Hernandez, Michelle

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The phenotype of recurrent 10q22q23 deletions and duplications von van Bon, Bregje W M, Balciuniene, Jorune, Fruhman, Gary, Nagamani, Sandesh Chakravarthy Sreenath, Broome, Diane L, Cameron, Elizabeth, Martinet, Danielle, Roulet, Eliane, Jacquemont, Sebastien, Beckmann, Jacques S, Irons, Mira, Potocki, Lorraine, Lee, Brendan, Cheung, Sau Wai, Patel, Ankita, Bellini, Melissa, Selicorni, Angelo, Ciccone, Roberto, Silengo, Margherita, Vetro, Annalisa, Knoers, Nine V, de Leeuw, Nicole, Pfundt, Rolph, Wolf, Barry, Jira, Petr, Aradhya, Swaroop, Stankiewicz, Pawel, Brunner, Han G, Zuffardi, Orsetta, Selleck, Scott B, Lupski, James R, de Vries, Bert B A

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Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection von Chenuet, Sebastien, Martinet, Danielle, Besuchet-Schmutz, Nathalie, Wicht, Marianne, Jaccard, Nicolas, Bon, Anne-Charlotte, Derouazi, Madiha, Hacker, David L, Beckmann, Jacques S, Wurm, Florian M

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Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic... von Donger, Claire, Krejci, Eric, Pou Serradell, Adolf, Eymard, Bruno, Bon, Suzanne, Nicole, Sophie, Chateau, Danielle, Gary, Françoise, Fardeau, Michel, Massoulié, Jean, Guicheney, Pascale

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Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy von Mercuri, Eugenio, Darras, Basil T, Chiriboga, Claudia A, Day, John W, Campbell, Craig, Connolly, Anne M, Iannaccone, Susan T, Kirschner, Janbernd, Kuntz, Nancy L, Saito, Kayoko, Shieh, Perry B, Tulinius, Már, Mazzone, Elena S, Montes, Jacqueline, Bishop, Kathie M, Yang, Qingqing, Foster, Richard, Gheuens, Sarah, Bennett, C. Frank, Farwell, Wildon, Schneider, Eugene, De Vivo, Darryl C, Finkel, Richard S

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Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome: Emerging Microdeletion and Microduplication Syndromes von VAN DER AA, Nathalie, ROOMS, Liesbeth, DESTREE, Anne, MAYSTADT, Isabelle, MÄNNIK, Katrin, KURG, Ants, REIMAND, Tiia, MCMULLAN, Dom, OLEY, Christine, BRUETON, Louise, BONGERS, Ernie M. H. F, VAN BON, Bregje W. M, VANDEWEYER, Geert, PFUND, Rolph, JACQUEMONT, Sebastien, FERRARINI, Alessandra, MARTINET, Danielle, SCHRANDER-STUMPEL, Connie, STEGMANN, Alexander P. A, FRINTS, Suzanna G. M, DE VRIES, Bert B. A, CEULEMANS, Berten, KOOY, R. Frank, VAN DEN ENDE, Jenneke, REYNIERS, Edwin, FICHERA, Marco, ROMANO, Corrado, DELLE CHIAIE, Barbara, MORTIER, Geert, MENTEN, Björn

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Human metabotropic glutamate receptor 1:mRNA distribution, chromosome localization and functional expression of two splice variants von STEPHAN, D, BON, C, HOLZWARTH, J. A, GALVAN, M, PRUSS, R. M

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Les lettres de mon moulin

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Medieval Disability Sourcebook: Western Europe

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La Conquête du ciel : 5ème épisode

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Time to love

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Le Journal : 2ème épisode

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L'Affaire Lambert

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La folle de Maigret

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