1. Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. Issue 3 (13th February 2016) Authors: Gardella, Elena; Becker, Felicitas; Møller, Rikke S.; Schubert, Julian; Lemke, Johannes R.; Larsen, Line H. G.; Eiberg, Hans; Nothnagel, Michael; Thiele, Holger; Altmüller, Janine; Syrbe, Steffen; Merkenschlager, Andreas; Bast, Thomas; Steinhoff, Bernhard; Nürnberg, Peter; Mang, Yuan; Bakke Mølle... Journal: Annals of neurology Issue: Volume 79:Issue 3(2016:Mar.) Page Start: 428 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CASPR2 autoimmunity in children expanding to mild encephalopathy with hypertension. (2nd June 2020) Authors: Syrbe, Steffen; Stettner, Georg M.; Bally, Julien; Borggraefe, Ingo; Bien, Corinna I.; Ferfoglia, Ruxandra Iancu; Huppke, Peter; Kern, Jan; Polster, Tilman; Probst-Müller, Elisabeth; Schmid, Silvia; Steinfeld, Robert; Strozzi, Susi; Weichselbaum, Annette; Weitz, Marcus; Ziegler, Andreas; Wandinge... Journal: Neurology Issue: Volume 94:Number 22(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseases. (December 2016) Authors: Baumann, Matthias; Hennes, Eva-Maria; Schanda, Kathrin; Karenfort, Michael; Kornek, Barbara; Seidl, Rainer; Diepold, Katharina; Lauffer, Heinz; Marquardt, Iris; Strautmanis, Jurgis; Syrbe, Steffen; Vieker, Silvia; Höftberger, Romana; Reindl, Markus; Rostásy, Kevin Journal: Multiple sclerosis Issue: Volume 22:Number 14(2016) Page Start: 1821 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical spectrum and treatment outcome of 95 children with continuous spikes and waves during sleep (CSWS). (January 2021) Authors: Sonnek, Benedikt; Döring, Jan Henje; Mütze, Ulrike; Schubert-Bast, Susanne; Bast, Thomas; Balke, Doreen; Reuner, Gitta; Schuler, Elisabeth; Klabunde-Cherwon, Annick; Hoffmann, Georg F.; Kölker, Stefan; Syrbe, Steffen Journal: European journal of paediatric neurology Issue: Volume 30(2021) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. (7th June 2016) Authors: Lemke, Johannes R.; Geider, Kirsten; Helbig, Katherine L.; Heyne, Henrike O.; Schütz, Hannah; Hentschel, Julia; Courage, Carolina; Depienne, Christel; Nava, Caroline; Heron, Delphine; Møller, Rikke S.; Hjalgrim, Helle; Lal, Dennis; Neubauer, Bernd A.; Nürnberg, Peter; Thiele, Holger; Kurlemann, G... Journal: Neurology Issue: Volume 86:Number 23(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Efficacy, Tolerability, and Retention of Antiseizure Medications in PRRT2-Associated Infantile Epilepsy. (28th October 2022) Authors: Döring, Jan H.; Saffari, Afshin; Bast, Thomas; Brockmann, Knut; Ehrhardt, Laura; Fazeli, Walid; Janzarik, Wibke G.; Klabunde-Cherwon, Annick; Kluger, Gerhard; Muhle, Hiltrud; Pendziwiat, Manuela; Møller, Rikke S.; Platzer, Konrad; Santos, Joana Larupa; Schröter, Julian; Hoffmann, Georg F.; Kölker... Journal: Neurology Issue: Volume 8:Number 5(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Epilepsy surgery: Late seizure recurrence after initial complete seizure freedom. (29th March 2021) Authors: Petrik, Stephan; San Antonio‐Arce, Victoria; Steinhoff, Bernhard J.; Syrbe, Steffen; Bast, Thomas; Scheiwe, Christian; Brandt, Armin; Beck, Juergen; Schulze‐Bonhage, Andreas Journal: Epilepsia Issue: Volume 62:issue 5(2021) Page Start: 1092 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder. Issue 9 (5th July 2021) Authors: Semino, Francesca; Schröter, Julian; Willemsen, Marjolein H.; Bast, Thomas; Biskup, Saskia; Beck‐Woedl, Stefanie; Brennenstuhl, Heiko; Schaaf, Christian P.; Kölker, Stefan; Hoffmann, Georg F.; Haack, Tobias B.; Syrbe, Steffen Journal: Human mutation Issue: Volume 42:Issue 9(2021) Page Start: 1094 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic testing before epilepsy surgery – An exploratory survey and case collection from German epilepsy centers. (February 2022) Authors: Boßelmann, Christian Malte; San Antonio-Arce, Victoria; Schulze-Bonhage, Andreas; Fauser, Susanne; Zacher, Pia; Mayer, Thomas; Aparicio, Javier; Albers, Kristina; Cloppenborg, Thomas; Kunz, Wolfram; Surges, Rainer; Syrbe, Steffen; Weber, Yvonne; Wolking, Stefan Journal: Seizure Issue: Volume 95(2022) Page Start: 4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genotype-phenotype correlation on 45 individuals with West syndrome. (March 2020) Authors: Krey, Ilona; Krois-Neudenberger, Janna; Hentschel, Julia; Syrbe, Steffen; Polster, Tilman; Hanker, Britta; Fiedler, Barbara; Kurlemann, Gerhardt; Lemke, Johannes R. Journal: European journal of paediatric neurology Issue: Volume 25(2020) Page Start: 134 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗