Einträge von Philippi, Heike 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.

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 und 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), S. 399-406. Volltext nicht vorhanden.