Einträge von Diepold, Katharina auf dem Publikationsserver

Proepper, Christiane R. , Schwarz, Lisa-Maria, Schuetz, Sofia M., von Au, Katja, Bast, Thomas, Beaud, Nathalie, Borggraefe, Ingo, Bosch, Friedrich, Busse, Melanie, Chung, Jena, Debus, Otfried, Diepold, Katharina, Fries, Thomas, von Gersdorff, Gero, Haeussler, Martin, Hahn, Andreas, Hartlieb, Till, Heiming, Ralf, Herkenrath, Peter, Kluger, Gerhard, Kreth, Jonas H., Kurlemann, Gerhard, Moeller, Peter, Morris-Rosendahl, Deborah J. , Panzer, Axel, Philippi, Heike, Ruegner, Sophia, Toepfer, Carolina, Vieker, Silvia, Wiemer-Kruel, Adelheid, Winter, Anika, Schuierer, Gerhard, Hehr, Ute und Geis, Tobias (2026) Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly. Orphanet Journal of Rare Diseases 21, S. 206.

Lange, Max, Kasper, Burkhard, Bohring, Axel, Rutsch, Frank, Kluger, Gerhard, Hoffjan, Sabine, Spranger, Stephanie, Behnecke, Anne, Ferbert, Andreas, Hahn, Andreas, Oehl-Jaschkowitz, Barbara, Graul-Neumann, Luitgard, Diepold, Katharina, Schreyer, Isolde, Bernhard, Matthias K., Mueller, Franziska, Siebers-Renelt, Ulrike, Beleza-Meireles, Ana, Uyanik, Goekhan, Janssens, Sandra, Boltshauser, Eugen, Winkler, Juergen, Schuierer, Gerhard und Hehr, Ute (2015) 47 patients with FLNA associated periventricular nodular heterotopia. Orphanet Journal of Rare Diseases 10 (1). Volltext nicht vorhanden.