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Anzahl der Publikationen: 5
Zeitschriftenartikel
Stuelpnagel, Celina von; Baalen, Andreas van; Borggraefe, Ingo; Eschermann, Kirsten; Hartlieb, Till; Kiwull, Lorenz; Pringsheim, Milka; Wolff, Markus; Kudernatsch, Manfred; Wiegand, Gert; Striano, Pasquale und Kluger, Gerhard
(14. Januar 2021):
Network for Therapy in Rare Epilepsies (NETRE): Lessons From the Past 15 Years.
In: Frontiers in Neurology, Bd. 11, 622510
[PDF, 563kB]
Tiefes, Anna M.; Hartlieb, Till; Tacke, Moritz; Stuelpnagel-Steinbeis, Celina von; Larsen, Line H. G.; Hao, Quin; Dahl, Hans Atli; Neubauer, Bernd A.; Gerstl, Lucia; Kudernatsch, Manfred; Kluger, Gerhard J. und Borggraefe, Ingo
(2019):
Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies.
In: Clinical Eeg and Neuroscience, Bd. 50, Nr. 4: S. 267-272
Kluger, Gerhard; Stuelpnagel-Steinbeis, Celina von; Arnold, Stephan; Eschermann, Kirsten und Hartlieb, Till
(2019):
Positive Short-Term Effect of Low-Dose Rosuvastatin in a Patient with SYNGAP1 -Associated Epilepsy.
In: Neuropediatrics, Bd. 50, Nr. 4: S. 266-267
Stuelpnagel, Celina von; Hartlieb, Till; Borggraefe, Ingo; Coppola, Antonietta; Gennaro, Elena; Eschermann, Kirsten; Kiwull, Lorenz; Kluger, Felicitas; Krois, Ilona; Moller, Rikke S.; Rossler, Franziska; Santulli, Lia; Schwermer, Constanze; Wallacher-Scholz, Barbara; Zara, Federico; Wolf, Peter und Kluger, Gerhard
(2019):
Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.
In: Seizure-European Journal of Epilepsy, Bd. 65: S. 131-137
Zagaglia, Sara; Selch, Christina; Nisevic, Jelena Radic; Mei, Davide; Michalak, Zuzanna; Hernandez-Hernandez, Laura; Krithika, S.; Vezyroglou, Katharina; Varadkar, Sophia M.; Pepler, Alexander; Biskup, Saskia; Leao, Miguel; Gärtner, Jutta; Merkenschlager, Andreas; Jaksch, Michaela; Moller, Rikke S.; Gardella, Elena; Schlott Kristiansen, Britta; Kjaersgaard Hansen, Lars; Vari, Maria Stella; Helbig, Katherine L.; Desai, Sonal; Smith-Hicks, Constance L.; Hino-Fukuyo, Naomi; Talvik, Tiina; Laugesaar, Rael; Ilves, Pilvi; Ounap, Katrin; Körber, Ingrid; Hartlieb, Till; Kudernatsch, Manfred; Winkler, Peter; Schimmel, Mareike; Hasse, Anette; Knuf, Markus; Heinemeyer, Jan; Makowski, Christine; Ghedia, Sondhya; Subramanian, Gopinath M.; Striano, Pasquale; Thomas, Rhys H.; Micallef, Caroline; Thom, Maria; Werring, David J.; Kluger, Gerhard Josef; Cross, J. Helen; Guerrini, Renzo; Balestrini, Simona und Sisodiya, Sanjay M.
(2018):
Neurologic phenotypes associated with COL4A1/2 mutations Expanding the spectrum of disease.
In: Neurology, Bd. 91, Nr. 22, E2078-E2088
[PDF, 1MB]