Einträge von Wiemer-Kruel, Adelheid 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.

Disse, Sigrid , Ramantani, Georgia, Küpper, Hanna, Bock, Annette, Korenke, Georg-Christoph, Weidner, Birgit, Preisel, Martin, Trollmann, Regina, Wiemer-Kruel, Adelheid, Wellmann, Sven , Brockmann, Knut, Schroeder, Simone und Meyer, Sascha (2025) Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types. Orphanet Journal of Rare Diseases 20 (1).

Disse, Sigrid Claudia, Küpper, Hanna, Bock, Annette, Korenke, Georg-Christoph, Ramantani, Georgia, Weidner, Birgit, Preisel, Martin, Trollmann, Regina, Wiemer-Kruel, Adelheid, Brockmann, Knut, Schroeder, Simone und Meyer, Sascha (2025) The natural history of pediatric Sturge-Weber Syndrome: A multinational cross-sectional study. European Journal of Paediatric Neurology 54, S. 200-209.

Martin*, Peter, Uyanik*, G�khan, Wiemer-Kruel, Adelheid, Schneider, Silvia, Gross, Claudia, Hehr, Ute und Winkler, J�rgen (2004) Different clinical and morphological phenotypes in monozygotic twins with identical DCX mutation. Journal of Neurology 251 (1), S. 108-110. Volltext nicht vorhanden.