Entries of von Gersdorff, Gero on the publication server

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 and 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, p. 206.

Herbst, Saskia M., Proepper, Christiane R., Geis, Tobias, Borggraefe, Ingo, Hahn, Andreas, Debus, Otfried, Haeussler, Martin, von Gersdorff, Gero, Kurlemann, Gerhard, Ensslen, Matthias, Beaud, Nathalie, Budde, Joerg, Gilbert, Michael, Heiming, Ralf, Morgner, Rita, Philippi, Heike, Ross, Sophia, Strobl-Wildemann, Gertrud, Muelleder, Kerstin, Vosschulte, Paul, Morris-Rosendahl, Deborah J. , Schuierer, Gerhard and Hehr, Ute (2016) LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs. Brain and Development 38 (4), pp. 399-406. Fulltext not available.