Mutations of DEPDC5 cause autosomal dominant focal epilepsies von Ishida, Saeko, Picard, Fabienne, Rudolf, Gabrielle, Noé, Eric, Achaz, Guillaume, Thomas, Pierre, Genton, Pierre, Mundwiller, Emeline, Wolff, Markus, Marescaux, Christian, Miles, Richard, Baulac, Michel, Hirsch, Edouard, Leguern, Eric, Baulac, Stéphanie

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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy von Syrbe, Steffen, Hedrich, Ulrike B S, Riesch, Erik, Djémié, Tania, Müller, Stephan, Møller, Rikke S, Maher, Bridget, Hernandez-Hernandez, Laura, Synofzik, Matthis, Caglayan, Hande S, Arslan, Mutluay, Serratosa, José M, Nothnagel, Michael, May, Patrick, Krause, Roland, Löffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Krämer, Günter, Schöls, Ludger, Mullis, Primus E, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C, Hoffman-Zacharska, Dorota, Korff, Christian M, Weber, Yvonne G, Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K, Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M, Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R

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Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies von Masnada, Silvia, Hedrich, Ulrike B S, Gardella, Elena, Schubert, Julian, Kaiwar, Charu, Klee, Eric W, Lanpher, Brendan C, Gavrilova, Ralitza H, Synofzik, Matthis, Bast, Thomas, Gorman, Kathleen, King, Mary D, Allen, Nicholas M, Conroy, Judith, Ben Zeev, Bruria, Tzadok, Michal, Korff, Christian, Dubois, Fanny, Ramsey, Keri, Narayanan, Vinodh, Serratosa, Jose M, Giraldez, Beatriz G, Helbig, Ingo, Marsh, Eric, O'Brien, Margaret, Bergqvist, Christina A, Binelli, Adrian, Porter, Brenda, Zaeyen, Eduardo, Horovitz, Dafne D, Wolff, Markus, Marjanovic, Dragan, Caglayan, Hande S, Arslan, Mutluay, Pena, Sergio D J, Sisodiya, Sanjay M, Balestrini, Simona, Syrbe, Steffen, Veggiotti, Pierangelo, Lemke, Johannes R, Møller, Rikke S, Lerche, Holger, Rubboli, Guido

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Severe Myoclonic Epilepsy of Infants (Dravet Syndrome): Natural History and Neuropsychological Findings von Wolff, Markus, Cassé‐Perrot, Catherine, Dravet, Charlotte

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Optimized Inferencing and Integration with AI on IBM zSystems: Introduction, Methodology, and Use Cases von Makenzie Manna, Erhan Mengusoglu, Artem Minin, Krishna Teja Rekapalli, Thomas Rüter, Pia Velazco, Markus Wolff

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Targeted next generation sequencing as a diagnostic tool in epileptic disorders von Lemke, Johannes R., Riesch, Erik, Scheurenbrand, Tim, Schubach, Max, Wilhelm, Christian, Steiner, Isabelle, Hansen, Jörg, Courage, Carolina, Gallati, Sabina, Bürki, Sarah, Strozzi, Susi, Simonetti, Barbara Goeggel, Grunt, Sebastian, Steinlin, Maja, Alber, Michael, Wolff, Markus, Klopstock, Thomas, Prott, Eva C., Lorenz, Rüdiger, Spaich, Christiane, Rona, Sabine, Lakshminarasimhan, Maya, Kröll, Judith, Dorn, Thomas, Krämer, Günter, Synofzik, Matthis, Becker, Felicitas, Weber, Yvonne G., Lerche, Holger, Böhm, Detlef, Biskup, Saskia

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A De Lellis–Müller type estimate on the Minkowski lightcone von Wolff, Markus

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Ricci flow on surfaces along the standard lightcone in the 3+1-Minkowski spacetime von Wolff, Markus

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A multicenter, matched case‐control analysis comparing burden‐of‐illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany von Strzelczyk, Adam, Schubert‐Bast, Susanne, Bast, Thomas, Bettendorf, Ulrich, Fiedler, Barbara, Hamer, Hajo M., Herting, Arne, Kalski, Malin, Kay, Lara, Kieslich, Matthias, Klein, Karl Martin, Kluger, Gerhard, Kurlemann, Gerhard, Mayer, Thomas, Neubauer, Bernd A., Polster, Tilman, von Spiczak, Sarah, Stephani, Ulrich, Trollmann, Regina, Wiemer‐Kruel, Adelheid, Wolff, Markus, Irwin, John, Carroll, Joe, Pritchard, Clive, Rosenow, Felix

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On effects of the null energy condition on totally umbilic hypersurfaces in a class of static spacetimes von Wolff, Markus

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Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany von Maltseva, Margarita, Schubert-Bast, Susanne, Zöllner, Johann Philipp, Bast, Thomas, Mayer, Thomas, von Spiczak, Sarah, Ruf, Susanne, Trollmann, Regina, Wolff, Markus, Hornemann, Frauke, Klotz, Kerstin A, Jacobs, Julia, Kurlemann, Gerhard, Neubauer, Bernd A, Polster, Tilman, Syrbe, Steffen, Bertsche, Astrid, Bettendorf, Ulrich, Kluger, Gerhard, Flege, Silke, Rosenow, Felix, Kay, Lara, Strzelczyk, Adam

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Benign Partial Epilepsy in Childhood: Selective Cognitive Deficits Are Related to the Location of Focal Spikes Determined by Combined EEG/MEG von Wolff, Markus, Weiskopf, Nikolaus, Serra, Emilio, Preissl, Hubert, Birbaumer, Niels, Kraegeloh‐Mann, Ingeborg

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Network for Therapy in Rare Epilepsies (NETRE): Lessons From the Past 15 Years von von Stülpnagel, Celina, van Baalen, Andreas, Borggraefe, Ingo, Eschermann, Kirsten, Hartlieb, Till, Kiwull, Lorenz, Pringsheim, Milka, Wolff, Markus, Kudernatsch, Manfred, Wiegand, Gert, Striano, Pasquale, Kluger, Gerhard

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Some new perspectives on the Kruskal–Szekeres extension with applications to photon surfaces von Cederbaum, Carla, Wolff, Markus

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Auditory stimulation during sleep suppresses spike activity in benign epilepsy with centrotemporal spikes von Klinzing, Jens G., Tashiro, Lilian, Ruf, Susanne, Wolff, Markus, Born, Jan, Ngo, Hong-Viet V.

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KCNC1‐related disorders: new de novo variants expand the phenotypic spectrum von Park, Joohyun, Koko, Mahmoud, Hedrich, Ulrike B. S., Hermann, Andreas, Cremer, Kirsten, Haberlandt, Edda, Grimmel, Mona, Alhaddad, Bader, Beck‐Woedl, Stefanie, Harrer, Merle, Karall, Daniela, Kingelhoefer, Lisa, Tzschach, Andreas, Matthies, Lars C., Strom, Tim M., Ringelstein, Erich Bernd, Sturm, Marc, Engels, Hartmut, Wolff, Markus, Lerche, Holger, Haack, Tobias B.

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Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome von Strzelczyk, Adam, Kurlemann, Gerhard, Bast, Thomas, Bettendorf, Ulrich, Kluger, Gerhard, Mayer, Thomas, Neubauer, Bernd A, Polster, Tilman, von Spiczak, Sarah, Trollmann, Regina, Wolff, Markus, Toward, Toby, Gruenert, Jens, Gibson, Eddie, Pritchard, Clive, Carroll, Joe, Rosenow, Felix, Schubert-Bast, Susanne

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Functional correlates of clinical phenotype and severity in recurrent SCN2A variants von Berecki, Géza, Howell, Katherine B., Heighway, Jacqueline, Olivier, Nelson, Rodda, Jill, Overmars, Isabella, Vlaskamp, Danique R. M., Ware, Tyson L., Ardern-Holmes, Simone, Lesca, Gaetan, Alber, Michael, Veggiotti, Pierangelo, Scheffer, Ingrid E., Berkovic, Samuel F., Wolff, Markus, Petrou, Steven

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The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood von Döring, Jan Henje, Saffari, Afshin, Bast, Thomas, Brockmann, Knut, Ehrhardt, Laura, Fazeli, Walid, Janzarik, Wibke G., Kluger, Gerhard, Muhle, Hiltrud, Møller, Rikke S., Platzer, Konrad, Santos, Joana Larupa, Bache, Iben, Bertsche, Astrid, Bonfert, Michaela, Borggräfe, Ingo, Broser, Philip J., Datta, Alexandre N., Hammer, Trine Bjørg, Hartmann, Hans, Hasse-Wittmer, Anette, Henneke, Marco, Kühne, Hermann, Lemke, Johannes R., Maier, Oliver, Matzker, Eva, Merkenschlager, Andreas, Opp, Joachim, Patzer, Steffi, Rostasy, Kevin, Stark, Birgit, Strzelczyk, Adam, von Stülpnagel, Celina, Weber, Yvonne, Wolff, Markus, Zirn, Birgit, Hoffmann, Georg Friedrich, Kölker, Stefan, Syrbe, Steffen

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Phenotypic spectrum and genetics of SCN2A‐related disorders, treatment options, and outcomes in epilepsy and beyond von Wolff, Markus, Brunklaus, Andreas, Zuberi, Sameer M.

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