Biotherapies: are they just like any other drugs? von Paintaud, Gilles, Tonelli, Dominique, Postaire, Eric

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Biotherapies: Are they Just Like any Other Drugs? von Paintaud, Gilles, Tonelli, Dominique, Postaire, Eric, Amalric, François, Bassompierre, François, Becquemont, Laurent, Cartron, Guillaume, Cellier, Dominic, Dagher, Georges, Demerens, Thierry, Dessein, Alain, Girault, Danièle, Grognet, Jean-Marc, Le Gros, Vincent, Lemoine, François, Moachon, Laurence, Pallardy, Marc, Pathak, Atul, Peschanski, Marc, Ségard, Lionel, Squiban, Patrick, Vasmant, Daniel, Vermeesch, Luc, HervéWatier, Zorzi, Pierrette

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Biothérapies : des médicaments comme les autres ? von Paintaud, Gilles, Tonelli, Dominique, Postaire, Eric, Amalric, François, Bassompierre, François, Becquemont, Laurent, Cartron, Guillaume, Cellier, Dominic, Dagher, Georges, Demerens, Thierry, Dessein, Alain, Girault, Danièle, Grognet, Jean-Marc, Le Gros, Vincent, Lemoine, François, Moachon, Laurence, Pallardy, Marc, Pathak, Atul, Peschanski, Marc, Ségard, Lionel, Squiban, Patrick, Vasmant, Daniel, Vermeesch, Luc, HervéWatier, Zorzi, Pierrette

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Non-invasive detection of genomic imbalances in Hodgkin/Reed-Sternberg cells in early and advanced stage Hodgkin's lymphoma by sequencing of circulating cell-free DNA: a technical... von Vandenberghe, Peter, Prof, Wlodarska, Iwona, Prof, Tousseyn, Thomas, Prof, Dehaspe, Luc, PhD, Dierickx, Daan, Prof, Verheecke, Magali, MD, Uyttebroeck, Anne, Prof, Bechter, Oliver, Prof, Delforge, Michel, Prof, Vandecaveye, Vincent, Prof, Brison, Nathalie, PhD, Verhoef, Gregor EG, Prof, Legius, Eric, Prof, Amant, Frederic, Prof, Vermeesch, Joris R, Prof

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Rare Autosomal Trisomies and Adverse Perinatal Outcomes von Lannoo, Lore, Van Den Bogaert, Kris, Brison, Nathalie, Dehaspe, Luc, Dimitriadou, Eftychia, Fieuws, Steffen, Melotte, Cindy, Duquenne, Armelle, Parijs, Ilse, Sznajer, Yves, Vancoillie, Leen, Vandecruys, Hilde, Vermeesch, Joris R., Devriendt, Koen, Van Calsteren, Kristel

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Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients von Thienpont, Bernard, Mertens, Luc, de Ravel, Thomy, Eyskens, Benedicte, Boshoff, Derize, Maas, Nicole, Fryns, Jean-Pierre, Gewillig, Marc, Vermeesch, Joris R., Devriendt, Koen

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Preimplantation genetic screening for aneuploidy of embryos after in vitro fertilization in women aged at least 35 years: a prospective randomized trial von Debrock, Sophie, Ph.D, Melotte, Cindy, M.Sc, Spiessens, Carl, Ph.D, Peeraer, Karen, M.D, Vanneste, Evelyne, M.Sc, Meeuwis, Luc, M.D, Meuleman, Christel, M.D, Frijns, Jean-Pierre, M.D., Ph.D, Vermeesch, Joris R., Ph.D, D'Hooghe, Thomas M., M.D., Ph.D

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Response to a comment on “Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing” von Brison, Nathalie, Dehaspe, Luc, Vermeesch, Joris R.

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Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management von Bayindir, Baran, Dehaspe, Luc, Brison, Nathalie, Brady, Paul, Ardui, Simon, Kammoun, Molka, Van der Veken, Lars, Lichtenbelt, Klaske, Van den Bogaert, Kris, Van Houdt, Jeroen, Peeters, Hilde, Van Esch, Hilde, de Ravel, Thomy, Legius, Eric, Devriendt, Koen, Vermeesch, Joris R

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Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia von Brady, P.D, Moerman, Philippe, De Catte, Luc, Deprest, J, Devriendt, K, Vermeesch, J.R

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Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing von Brison, Nathalie, Neofytou, Maria, Dehaspe, Luc, Bayindir, Baran, Van Den Bogaert, Kris, Dardour, Leila, Peeters, Hilde, Van Esch, Hilde, Van Buggenhout, Griet, Vogels, Annick, Ravel, Thomy, Legius, Eric, Devriendt, Koen, Vermeesch, Joris R.

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Maternal liver transplant: Another cause of discordant fetal sex determination using cell‐free DNA von Neofytou, Maria, Brison, Nathalie, Van den Bogaert, Kris, Dehaspe, Luc, Devriendt, Koen, Geerts, Anja, Vermeesch, Joris R.

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Response to a comment on "Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing" von Brison, Nathalie, Dehaspe, Luc, Vermeesch, Joris R

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Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies von Brison, Nathalie, Van Den Bogaert, Kris, Dehaspe, Luc, van den Oever, Jessica M.E., Janssens, Katrien, Blaumeiser, Bettina, Peeters, Hilde, Van Esch, Hilde, Van Buggenhout, Griet, Vogels, Annick, de Ravel, Thomy, Legius, Eric, Devriendt, Koen, Vermeesch, Joris R.

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Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge von Lannoo, Lore, van Straaten, Khaila, Breckpot, Jeroen, Brison, Nathalie, De Catte, Luc, Dimitriadou, Eftychia, Legius, Eric, Peeters, Hilde, Parijs, Ilse, Tsuiko, Olga, Vancoillie, Leen, Vermeesch, Joris Robert, Van Buggenhout, Griet, Van Den Bogaert, Kris, Van Calsteren, Kristel, Devriendt, Koenraad

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Accuracy and Clinical Value of Maternal Incidental Findings During Noninvasive Prenatal Testing for Fetal Aneuploidies von Brison, Nathalie, van den Bogaert, Kris, Dehaspe, Luc, van den Oever, Jessica M E, Janssens, Katrien, Blaumeiser, Bettina, Peeters, Hilde, van Esch, Hilde, van Buggenhout, Griet, Vogels, Annick, de Ravel, Thomy, Legius, Eric, Devriendt, Koen, Vermeesch, Joris R

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Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening von Brison, Nathalie, Storms, Jazz, Villela, Darine, Claeys, Kristl G., Dehaspe, Luc, de Ravel, Thomy, De Waele, Liesbeth, Goemans, Nathalie, Legius, Eric, Peeters, Hilde, Van Esch, Hilde, Race, Valerie, Robert Vermeesch, Joris, Devriendt, Koenraad, Van Den Bogaert, Kris

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Rare Autosomal Trisomies and Adverse Perinatal Outcomes von Lannoo, Lore, van den Bogaert, Kris, Brison, Nathalie, Dehaspe, Luc, Dimitriadou, Eftychia, Fieuws, Steffen, Melotte, Cindy, Duquenne, Armelle, Parijs, Ilse, Sznajer, Yves, Vancoillie, Leen, Vandecruys, Hilde, Vermeesch, Joris R, Devriendt, Koen, Van Calsteren, Kristel

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The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects von Jia, Yaojuan, Louw, Jacoba J., Breckpot, Jeroen, Callewaert, Bert, Barrea, Catherine, Sznajer, Yves, Gewillig, Marc, Souche, Erika, Dehaspe, Luc, Vermeesch, Joris Robert, Lambrechts, Diether, Devriendt, Koenraad, Corveleyn, Anniek

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Breast Cancer Detection and Treatment Monitoring Using a Noninvasive Prenatal Testing Platform: Utility in Pregnant and Nonpregnant Populations von Lenaerts, Liesbeth, Che, Huiwen, Brison, Nathalie, Neofytou, Maria, Jatsenko, Tatjana, Lefrere, Hanne, Maggen, Charlotte, Villela, Darine, Verheecke, Magali, Dehaspe, Luc, Croitor, Anca, Hatse, Sigrid, Wildiers, Hans, Neven, Patrick, Vandecaveye, Vincent, Floris, Giuseppe, Vermeesch, Joris Robert, Amant, Frederic

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