Assisted reproductive techniques and the risk of anorectal malformations: a German case-control study

por Zwink, Nadine, Jenetzky, Ekkehart, Schmiedeke, Eberhard, Schmidt, Dominik, Märzheuser, Stefanie, Grasshoff-Derr, Sabine, Holland-Cunz, Stefan, Weih, Sandra, Hosie, Stuart, Reifferscheid, Peter, Ameis, Helen, Kujath, Christina, Rißmann, Anke, Obermayr, Florian, Schwarzer, Nicole, Bartels, Enrika, Reutter, Heiko, Brenner, Hermann
Publicado 2012

Inter- and Intraobserver Variation in the Assessment of Preoperative Colostograms in Male Anorectal Malformations: An ARM-Net Consortium Survey

por Midrio, Paola, van Rooij, Iris A. L. M., Brisighelli, Giulia, Garcia, Aracelli, Fanjul, Maria, Broens, Paul, Iacobelli, Barbara D., Giné, Carlos, Lisi, Gabriele, Sloots, Cornelius E. J., Fascetti Leon, Francesco, Morandi, Anna, van der Steeg, Herjan, Giuliani, Stefan, Grasshoff-Derr, Sabine, Lacher, Martin, de Blaauw, Ivo, Jenetzky, Ekkehart
Publicado 2020

European consensus meeting of ARM-Net members concerning diagnosis and early management of newborns with anorectal malformations

por van der Steeg, H. J. J., Schmiedeke, E., Bagolan, P., Broens, P., Demirogullari, B., Garcia–Vazquez, A., Grasshoff-Derr, S., Lacher, M., Leva, E., Makedonsky, I., Sloots, C. E. J., Schwarzer, N., Aminoff, D., Schipper, M., Jenetzky, E., van Rooij, I. A. L. M., Giuliani, S., Crétolle, C., Holland Cunz, S., Midrio, P., de Blaauw, I.
Publicado 2015

Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across...

por Wijers, Charlotte H. W., de Blaauw, Ivo, Marcelis, Carlo L. M., Wijnen, Rene M. H., Brunner, Han, Midrio, Paola, Gamba, Piergiorgio, Clementi, Maurizio, Jenetzky, Ekkehart, Zwink, Nadine, Reutter, Heiko, Bartels, Enrika, Grasshoff-Derr, Sabine, Holland-Cunz, Stefan, Hosie, Stuart, Märzheuser, Stefanie, Schmiedeke, Eberhard, Crétolle, Célia, Sarnacki, Sabine, Levitt, Marc A., Knoers, Nine V. A. M., Roeleveld, Nel, van Rooij, Iris A. L. M.
Publicado 2010

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

por Nuzhat, Nafisa, Van Schil, Kristof, Liakopoulos, Sandra, Bauwens, Miriam, Rey, Alfredo Dueñas, Käseberg, Stephan, Jäger, Melanie, Willer, Jason R., Winter, Jennifer, Truong, Hanh M., Gruartmoner, Nuria, Van Heetvelde, Mattias, Wolf, Joachim, Merget, Robert, Grasshoff-Derr, Sabine, Van Dorpe, Jo, Hoorens, Anne, Stöhr, Heidi, Mansard, Luke, Roux, Anne-Françoise, Langmann, Thomas, Dannhausen, Katharina, Rosenkranz, David, Wissing, Karl M., Van Lint, Michel, Rossmann, Heidi, Häuser, Friederike, Nürnberg, Peter, Thiele, Holger, Zechner, Ulrich, Pearring, Jillian N., De Baere, Elfride, Bolz, Hanno J.
Publicado 2023

Whole exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

por Saisawat, Pawaree, Kohl, Stefan, Hilger, Alina C., Hwang, Daw-Yang, Gee, Heon Yung, Dworschak, Gabriel C., Tasic, Velibor, Pennimpede, Tracie, Natarajan, Sivakumar, Sperry, Ethan, Matassa, Danilo S., Stajić, Nataša, Bogdanovic, Radovan, de Blaauw, Ivo, Marcelis, Carlo L.M., Wijers, Charlotte H.W., Bartels, Enrika, Schmiedeke, Eberhard, Schmidt, Dominik, Mäzheuser, Stefanie, Grasshoff-Derr, Sabine, Holland-Cunz, Stefan, Ludwig, Michael, Nöhen, Markus M., Draaken, Markus, Brosens, Erwin, Heij, Hugo, Tibboel, Dick, Herrmann, Bernhard G., Solomon, Benjamin D., de Klein, Annelies, van Rooij, Iris A.L.M., Esposito, Franca, Reutter, Heiko M., Hildebrandt, Friedhelm
Publicado 2013