Inhibitory influence of Enterococcus faecium on the propagation of swine influenza A virus in vitro von Wang, Zhenya, Chai, Weidong, Burwinkel, Michael, Twardziok, Sven, Wrede, Paul, Palissa, Christiane, Esch, Bettina, Schmidt, Michael F G

Volltext

Antiviral effects of a probiotic Enterococcus faecium strain against transmissible gastroenteritis coronavirus von Chai, Weidong, Burwinkel, Michael, Wang, Zhenya, Palissa, Christiane, Esch, Bettina, Twardziok, Sven, Rieger, Juliane, Wrede, Paul, Schmidt, Michael F. G.

Volltext

Severe Dysbiosis and Specific Haemophilus and Neisseria Signatures as Hallmarks of the Oropharyngeal Microbiome in Critically Ill Coronavirus Disease 2019 (COVID-19) Patients von de Castilhos, Juliana, Zamir, Eli, Hippchen, Theresa, Rohrbach, Roman, Schmidt, Sabine, Hengler, Silvana, Schumacher, Hanna, Neubauer, Melanie, Kunz, Sabrina, Müller-Esch, Tonia, Hiergeist, Andreas, Gessner, André, Khalid, Dina, Gaiser, Rogier, Cullin, Nyssa, Papagiannarou, Stamatia M, Beuthien-Baumann, Bettina, Krämer, Alwin, Bartenschlager, Ralf, Jäger, Dirk, Müller, Michael, Herth, Felix, Duerschmied, Daniel, Schneider, Jochen, Schmid, Roland M, Eberhardt, Johann F, Khodamoradi, Yascha, Vehreschild, Maria J G T, Teufel, Andreas, Ebert, Matthias P, Hau, Peter, Salzberger, Bernd, Schnitzler, Paul, Poeck, Hendrik, Elinav, Eran, Merle, Uta, Stein-Thoeringer, Christoph K

Volltext

Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation von Jensen, Lars Riff, Amende, Marion, Gurok, Ulf, Moser, Bettina, Gimmel, Verena, Tzschach, Andreas, Janecke, Andreas R., Tariverdian, Gholamali, Chelly, Jamel, Fryns, Jean-Pierre, Van Esch, Hilde, Kleefstra, Tjitske, Hamel, Ben, Moraine, Claude, Gécz, Jozef, Turner, Gillian, Reinhardt, Richard, Kalscheuer, Vera M., Ropers, Hans-Hilger, Lenzner, Steffen

Volltext

Amino Acid Substitutions within HLA-B27-Restricted T Cell Epitopes Prevent Recognition by Hepatitis Delta Virus-Specific CD8 + T Cells von Karimzadeh, Hadi, Kiraithe, Muthamia M, Kosinska, Anna D, Glaser, Manuel, Fiedler, Melanie, Oberhardt, Valerie, Salimi Alizei, Elahe, Hofmann, Maike, Mok, Juk Yee, Nguyen, Melanie, van Esch, Wim J E, Budeus, Bettina, Grabowski, Jan, Homs, Maria, Olivero, Antonella, Keyvani, Hossein, Rodríguez-Frías, Francisco, Tabernero, David, Buti, Maria, Heinold, Andreas, Alavian, Seyed Moayed, Bauer, Tanja, Schulze Zur Wiesch, Julian, Raziorrouh, Bijan, Hoffmann, Daniel, Smedile, Antonina, Rizzetto, Mario, Wedemeyer, Heiner, Timm, Jörg, Antes, Iris, Neumann-Haefelin, Christoph, Protzer, Ulrike, Roggendorf, Michael

Volltext

Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 ( CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation von Tao, Jiong, Van Esch, Hilde, Hagedorn-Greiwe, M., Hoffmann, Kirsten, Moser, Bettina, Raynaud, Martine, Sperner, Jürgen, Fryns, Jean-Pierre, Schwinger, Eberhard, Gécz, Jozef, Ropers, Hans-Hilger, Kalscheuer, Vera M.

Volltext

Phenotypic spectrum associated with CASK loss-of-function mutations von Moog, Ute, Kutsche, Kerstin, Kortüm, Fanny, Chilian, Bettina, Bierhals, Tatjana, Apeshiotis, Neophytos, Balg, Stefanie, Chassaing, Nicolas, Coubes, Christine, Das, Soma, Engels, Hartmut, Van Esch, Hilde, Grasshoff, Ute, Heise, Marisol, Isidor, Bertrand, Jarvis, Joanna, Koehler, Udo, Martin, Thomas, Oehl-Jaschkowitz, Barbara, Ortibus, Els, Pilz, Daniela T, Prabhakar, Prab, Rappold, Gudrun, Rau, Isabella, Rettenberger, Günther, Schlüter, Gregor, Scott, Richard H, Shoukier, Moonef, Wohlleber, Eva, Zirn, Birgit, Dobyns, William B, Uyanik, Gökhan

Volltext

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.

Volltext

Identification of phosphatases that dephosphorylate the co-chaperone BAG3 von Kokot, Thomas, Zimmermann, Johannes P, Chand, Yamini, Krier, Fabrice, Reimann, Lena, Scheinost, Laura, Höfflin, Nico, Esch, Alessandra, Höhfeld, Jörg, Warscheid, Bettina, Köhn, Maja

Volltext

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

Volltext

Correction to: Severe Dysbiosis and Specific Haemophilus and Neisseria Signatures as Hallmarks of the Oropharyngeal Microbiome in Critically Ill Coronavirus Disease 2019 (COVID-19)... von de Castilhos, Juliana, Zamir, Eli, Hippchen, Theresa, Rohrbach, Roman, Schmidt, Sabine, Hengler, Silvana, Schumacher, Hanna, Neubauer, Melanie, Kunz, Sabrina, Müller-Esch, Tonia, Hiergeist, Andreas, Gessner, André, Khalid, Dina, Gaiser, Rogier, Cullin, Nyssa, Papagiannarou, Stamatia M, Beuthien-Baumann, Bettina, Krämer, Alwin, Bartenschlager, Ralf, Jäger, Dirk, Müller, Michael, Herth, Felix, Duerschmied, Daniel, Schneider, Jochen, Schmid, Roland M, Eberhardt, Johann F, Khodamoradi, Yascha, Vehreschild, Maria J G T, Teufel, Andreas, Ebert, Matthias P, Hau, Peter, Salzberger, Bernd, Schnitzler, Paul, Poeck, Hendrik, Elinav, Eran, Merle, Uta, Stein-Thoeringer, Christoph K

Volltext

Severe dysbiosis and specific Haemophilus and Neisseria signatures as hallmarks of the oropharyngeal microbiome in critically ill COVID-19 patients von de Castilhos, Juliana, Zamir, Eli, Hippchen, Theresa, Rohrbach, Roman, Schmidt, Sabine, Hengler, Silvana, Schumacher, Hanna, Neubauer, Melanie, Kunz, Sabrina, Müller-Esch, Tonia, Hiergeist, Andreas, Gessner, André, Khalid, Dina, Gaiser, Rogier, Cullin, Nyssa, Papagiannarou, Stamatia M, Beuthien-Baumann, Bettina, Krämer, Alwin, Bartenschlager, Ralf, Jäger, Dirk, Müller, Michael, Herth, Felix, Duerschmied, Daniel, Schneider, Jochen, Schmid, Roland M, Eberhardt, Johann F, Khodamoradi, Yascha, Vehreschild, Maria J G T, Teufel, Andreas, Ebert, Matthias P, Hau, Peter, Salzberger, Bernd, Schnitzler, Paul, Poeck, Hendrik, Elinav, Eran, Merle, Uta, Stein-Thoeringer, Christoph K

Volltext

Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy von Duerinckx, Sarah, Désir, Julie, Perazzolo, Camille, Badoer, Cindy, Jacquemin, Valérie, Soblet, Julie, Maystadt, Isabelle, Tunca, Yusuf, Blaumeiser, Bettina, Ceulemans, Berten, Courtens, Winnie, Debray, François‐Guillaume, Destree, Anne, Devriendt, Koenraad, Jansen, Anna, Keymolen, Kathelijn, Lederer, Damien, Loeys, Bart, Meuwissen, Marije, Moortgat, Stéphanie, Mortier, Geert, Nassogne, Marie‐Cécile, Sekhara, Tayeb, Van Coster, Rudy, Van Den Ende, Jenny, Van der Aa, Nathalie, Van Esch, Hilde, Vanakker, Olivier, Verhelst, Helene, Vilain, Catheline, Weckhuysen, Sarah, Passemard, Sandrine, Verloes, Alain, Aeby, Alec, Deconinck, Nicolas, Van Bogaert, Patrick, Pirson, Isabelle, Abramowicz, Marc

Volltext

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 de l'Argentière, Thomy, Legius, Eric, Devriendt, Koenraad, Vermeesch, Joris

Volltext

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1 von JENSEN, Lars R, WEI CHEN, VAN ESCH, Hilde, CHELLY, Jamel, DE BROUWER, Arjan Pm, HACKETT, Anna, VAN DER HAAR, Sigrun, HENN, Wolfram, GECZ, Jozef, RIESS, Olaf, BONIN, Michael, REINHARDT, Richard, MOSER, Bettina, ROPERS, Hans-Hilger, KUSS, Andreas W, LIPKOWITZ, Bettina, SCHROEDER, Christopher, MUSANTE, Luciana, TZSCHACH, Andreas, KALSCHEUER, Vera M, MELONI, Ilaria, RAYNAUD, Martine

Volltext

Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy von Duerinckx, Sarah, Desir, Julie, Perazzolo, Camille, Badoer, Cindy, Jacquemin, Valerie, Soblet, Julie, Maystadt, Isabelle, Tunca, Yusuf, Blaumeiser, Bettina, Ceulemans, Berten, Courtens, Winnie, Debray, Francois-Guillaume, Destree, Anne, Devriendt, Koenraad, Jansen, Anna, Keymolen, Kathelijn, Lederer, Damien, Loeys, Bart, Meuwissen, Marije, Moortgat, Stephanie, Mortier, Geert, Nassogne, Marie-Cecile, Sekhara, Tayeb, Van Coster, Rudy, van den Ende, Jenny, van der Aa, Nathalie, Van Esch, Hilde, Vanakker, Olivier, Verhelst, Helene, Vilain, Catheline, Weckhuysen, Sarah, Passemard, Sandrine, Verloes, Alain, Aeby, Alec, Deconinck, Nicolas, Van Bogaert, Patrick, Pirson, Isabelle, Abramowicz, Marc

Volltext

Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy von Duerinckx, Sarah, Désir, Julie, Perazzolo, Camille, Badoer, Cindy, Jacquemin, Valérie, Soblet, Julie, Maystadt, Isabelle, Tunca, Yusuf, Blaumeiser, Bettina, Ceulemans, Berten, Courtens, Winnie, Debray, François‐Guillaume, Destree, Anne, Devriendt, Koenraad, Jansen, Anna, Keymolen, Kathelijn, Lederer, Damien, Loeys, Bart, Meuwissen, Marije, Moortgat, Stéphanie, Mortier, Geert, Nassogne, Marie‐Cécile, Sekhara, Tayeb, Van Coster, Rudy, Van Den Ende, Jenny, Van der Aa, Nathalie, Van Esch, Hilde, Vanakker, Olivier, Verhelst, Helene, Vilain, Catheline, Weckhuysen, Sarah, Passemard, Sandrine, Verloes, Alain, Aeby, Alec, Deconinck, Nicolas, Van Bogaert, Patrick, Pirson, Isabelle, Abramowicz, Marc

Volltext

Reflections by Former Editors von Herrmann, Sebastian M., Schoppmeier, Sören, Freitag, Katharina, Polkau, Marianna, Schuster, Bettina, Vogel, Christiane, Krug, Ines, Esch, Linda, Pruessing, Heather, Ravizza, Eleonora, Vatonne, Silane, Wilke, Miriam, Bast, Florian

Volltext

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1 von Jensen, Lars R, Chen, Wei, Moser, Bettina, Lipkowitz, Bettina, Schroeder, Christopher, Musante, Luciana, Tzschach, Andreas, Kalscheuer, Vera M, Meloni, Ilaria, Raynaud, Martine, Van Esch, Hilde, Chelly, Jamel, de Brouwer, Arjan P.M, Hackett, Anna, van der Haar, Sigrun, Henn, Wolfram, Gecz, Jozef, Riess, Olaf, Bonin, Michael, Reinhardt, Richard, Ropers, Hans-Hilger, Kuss, Andreas W

Volltext

Phenotypic spectrum associated with CASK loss-of-function mutations von Moog, Ute, Kutsche, Kerstin, Kortüm, Fanny, Chilian, Bettina, Bierhals, Tatjana, Apeshiotis, Neophytos, Balg, Stefanie, Chassaing, Nicolas, Coubes, Christine, Das, Soma, Engels, Hartmut, Van Esch, Hilde, Grasshoff, Ute, Heise, Marisol, Isidor, Bertrand, Jarvis, Joanna, Koehler, Udo, Martin, Thomas, Oehl-Jaschkowitz, Barbara, Ortibus, Els, Pilz, Daniela T, Prabhakar, Prab, Rappold, Gudrun, Rau, Isabella, Rettenberger, Günther, Schlüter, Gregor, Scott, Richard H, Shoukier, Moonef, Wohlleber, Eva, Zirn, Birgit, Dobyns, William B, Uyanik, Gökhan

Volltext