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Anzahl der Publikationen: 59

Zeitschriftenartikel

Schader, Carla ORCID logoORCID: https://orcid.org/0000-0002-8675-8191; Schmidlechner, Tristan ORCID logoORCID: https://orcid.org/0009-0006-0915-5983; Cornell, Sonia; Gerstl, Lucia ORCID logoORCID: https://orcid.org/0000-0003-4490-5357; Trollmann, Regina ORCID logoORCID: https://orcid.org/0000-0001-6031-8537 und Borggraefe, Ingo ORCID logoORCID: https://orcid.org/0000-0002-8484-5945 (2024): Risk of behavioral disturbances in pediatric patients with epilepsy and mild to moderate cognitive impairment: A cross‐sectional study. In: Epileptic Disorders, Bd. 26, Nr. 5: S. 676-684 [PDF, 418kB]

Schmidlechner, Tristan; Zaddach, Malin ORCID logoORCID: https://orcid.org/0000-0001-7584-0811; Heinen, Florian ORCID logoORCID: https://orcid.org/0000-0002-3872-6136; Cornell, Sonia; Ramantani, Georgia ORCID logoORCID: https://orcid.org/0000-0002-7931-2327; Rémi, Jan ORCID logoORCID: https://orcid.org/0000-0003-1527-9350; Vollmar, Christian ORCID logoORCID: https://orcid.org/0000-0002-4630-7484; Kunz, Mathias ORCID logoORCID: https://orcid.org/0000-0003-1641-450X und Borggraefe, Ingo ORCID logoORCID: https://orcid.org/0000-0002-8484-5945 (2024): IQ changes after pediatric epilepsy surgery: a systematic review and meta-analysis. In: Journal of Neurology, Bd. 271, Nr. 1: S. 177-187 [PDF, 2MB]

Borggraefe, Ingo ORCID logoORCID: https://orcid.org/0000-0002-8484-5945; Tacke, Moritz; Kunz, Mathias ORCID logoORCID: https://orcid.org/0000-0003-1641-450X; Vollmar, Christian ORCID logoORCID: https://orcid.org/0000-0002-4630-7484 und Rémi, Jan ORCID logoORCID: https://orcid.org/0000-0003-1527-9350 (2023): Epilepsy surgery in pediatric refractory status epilepticus. In: Clinical Epileptology, Bd. 36, Nr. 4: S. 304-309 [PDF, 1MB]

Tacke, Moritz; Janson, Katharina; Vill, Katharina; Heinen, Florian; Gerstl, Lucia; Reiter, Karl und Borggraefe, Ingo (17. März 2022): Effects of a reduction of the number of electrodes in the EEG montage on the number of identified seizure patterns. In: Scientific Reports, Bd. 12 [PDF, 1MB]

Johannesen, Katrine M.; Liu, Yuanyuan; Koko, Mahmoud; Gjerulfsen, Cathrine E.; Sonnenberg, Lukas; Schubert, Julian; Fenger, Christina D.; Eltokhi, Ahmed; Rannap, Maert; Koch, Nils A.; Lauxmann, Stephan; Krüger, Johanna; Kegele, Josua; Canafoglia, Laura; Franceschetti, Silvana; Mayer, Thomas; Rebstock, Johannes; Zacher, Pia; Ruf, Susanne; Alber, Michael; Sterbova, Katalin; Lassuthova, Petra; Vlckova, Marketa; Lemke, Johannes R.; Platzer, Konrad; Krey, Ilona; Heine, Constanze; Wieczorek, Dagmar; Kroell-Seger, Judith; Lund, Caroline; Klein, Karl Martin; Au, P. Y. Billie; Rho, Jong M.; Ho, Alice W.; Masnada, Silvia; Veggiotti, Pierangelo; Giordano, Lucio; Accorsi, Patrizia; Hoei-Hansen, Christina E.; Striano, Pasquale; Zara, Federico; Verhelst, Helene; Verhoeven, Judith S.; Braakman, Hilde M. H.; Zwaag, Bert van der; Harder, Aster V. E.; Brilstra, Eva; Pendziwiat, Manuela; Lebon, Sebastian; Vaccarezza, Maria; Ngoc, Minh Le; Christensen, Jakob; Gronborg, Sabine; Scherer, Stephen W.; Howe, Jennifer; Fazeli, Walid; Howell, Katherine B.; Leventer, Richard; Stutterd, Chloe; Walsh, Sonja; Gerard, Marion; Gerard, Benedicte; Matricardi, Sara; Bonardi, Claudia M.; Sartori, Stefano; Berger, Andrea; Hoffman-Zacharska, Dorota; Mastrangelo, Massimo; Darra, Francesca; Vollo, Arve; Motazacker, M. Mahdi; Lakeman, Phillis; Nizon, Mathilde; Betzler, Cornelia; Altuzarra, Cecilia; Caume, Roseline; Roubertie, Agathe; Gelisse, Philippe; Marini, Carla; Guerrini, Renzo; Bilan, Frederic; Tibussek, Daniel; Koch-Hogrebe, Margarete; Perry, M. Scott; Ichikawa, Shoji; Dadali, Elena; Sharkov, Artem; Mishina, Irina; Abramov, Mikhail; Kanivets, Ilya; Korostelev, Sergey; Kutsev, Sergey; Wain, Karen E.; Eisenhauer, Nancy; Wagner, Monisa; Savatt, Juliann M.; Müller-Schlüter, Karen; Bassan, Haim; Borovikov, Artem; Nassogne, Marie-Cecile; Destree, Anne; Schoonjans, An-Sofie; Meuwissen, Marije; Buzatu, Marga; Jansen, Anna; Scalais, Emmanuel; Srivastava, Siddharth; Tan, Wen-Hann; Olson, Heather E.; Loddenkemper, Tobias; Poduri, Annapurna; Helbig, Katherine L.; Helbig, Ingo; Fitzgerald, Mark P.; Goldberg, Ethan M.; Roser, Timo; Borggraefe, Ingo; Brunger, Tobias; May, Patrick; Lal, Dennis; Lederer, Damien; Rubboli, Guido; Heyne, Henrike O.; Lesca, Gaetan; Hedrich, Ulrike B. S.; Benda, Jan; Gardella, Elena; Lerche, Holger und Moller, Rikke S. (2022): Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications. In: Brain, Bd. 145, Nr. 9: S. 2991-3009

Moorhouse, Frederik Jan; Cornell, Sonia; Gerstl, Lucia; Wagner, Johanna; Tacke, Moritz; Roser, Timo; Heinen, Florian; Stuelpnagel, Celina von; Vollmar, Christian; Kunz, Mathias; Ramantani, Georgia und Borggraefe, Ingo (2022): Cognitive profiles in pediatric unilobar vs. multilobar epilepsy. In: European Journal of Paediatric Neurology, Bd. 41: S. 48-54

Gerstl, Lucia; Borggraefe, Ingo; Heinen, Florian und Olivieri, Martin (2022): Arteriell ischämischer Schlaganfall im Kindes- und Jugendalter. Zeitkritischer Notfall in der Pädiatrie. In: Nervenarzt, Bd. 93, Nr. 12: S. 1258-1270

Bonfert, Michaela V.; Wagner, Johanna; Goettler, Catherina; Bidlingmaier, Christoph; Borggraefe, Ingo; Landgraf, Mirjam N.; Hoffmann, Florian; Gersing, Alexandra; Koerte, Inga K.; Terpolilli, Nicole; Holler, Anne-Sophie; Froeba-Pohl, Alexandra; Muensterer, Oliver und Heinen, Florian (2022): Leichtes Schädel-Hirn-Trauma im Kindes- und Jugendalter – Update Gehirnerschütterung. In: Monatsschrift Kinderheilkunde, Bd. 170, Nr. 8: S. 746-757

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]

Borggraefe, Ingo und Remi, Jan (2021): Normvarianten im kindlichen EEG: Pitfalls in der Praxis. In: Klinische Neurophysiologie, Bd. 52, Nr. 3: S. 150-160

Olivieri, Martin; Sorg, Anna-Lisa; Weinberger, Raphael; Kurnik, Karin; Bidlingmaier, Christoph; Juranek, Sabrina; Hoffmann, Florian; Reiter, Karl; Bonfert, Michaela; Tacke, Moritz; Borggraefe, Ingo; Heinen, Florian und Gerstl, Lucia (2021): Recanalization strategies in childhood stroke in Germany. In: Scientific reports, Bd. 11, Nr. 1, 13314 [PDF, 937kB]

Mirza-Schreiber, Nazanin ORCID logoORCID: https://orcid.org/0000-0003-0836-8267; Zech, Michael; Wilson, Rory; Brunet, Theresa; Wagner, Matias ORCID logoORCID: https://orcid.org/0000-0002-4454-8823; Jech, Robert; Boesch, Sylvia; Škorvánek, Matej; Necpál, Ján; Weise, David; Weber, Sandrina; Mollenhauer, Brit; Trenkwalder, Claudia; Maier, Esther M; Borggraefe, Ingo; Vill, Katharina; Hackenberg, Annette; Pilshofer, Veronika; Kotzaeridou, Urania; Schwaibold, Eva Maria Christina; Hoefele, Julia; Waldenberger, Melanie; Gieger, Christian; Peters, Annette ORCID logoORCID: https://orcid.org/0000-0001-6645-0985; Meitinger, Thomas; Schormair, Barbara; Winkelmann, Juliane und Oexle, Konrad ORCID logoORCID: https://orcid.org/0000-0001-7447-2252 (2021): Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset. In: Brain, Bd. 145, Nr. 2: S. 644-654 [PDF, 1MB]

Balestrini, Simona; Chiarello, Daniela; Gogou, Maria; Silvennoinen, Katri; Puvirajasinghe, Clinda; Jones, Wendy D.; Reif, Philipp; Klein, Karl Martin; Rosenow, Felix; Weber, Yvonne G.; Lerche, Holger; Schubert-Bast, Susanne; Borggraefe, Ingo; Coppola, Antonietta; Troisi, Serena; Moller, Rikke S.; Riva, Antonella; Striano, Pasquale; Zara, Federico; Hemingway, Cheryl; Marini, Carla; Rosati, Anna; Mei, Davide; Montomoli, Martino; Guerrini, Renzo; Cross, J. Helen und Sisodiya, Sanjay M. (2021): Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies. In: Journal of Neurology Neurosurgery and Psychiatry, Bd. 92, Nr. 10: S. 1044-1052

Brunet, Theresa; Jech, Robert; Brugger, Melanie; Kovacs, Reka; Alhaddad, Bader; Leszinski, Gloria; Riedhammer, Korbinian M.; Westphal, Dominik S.; Mahle, Isabella; Mayerhanser, Katharina; Skorvanek, Matej; Weber, Sandrina; Graf, Elisabeth; Berutti, Riccardo; Necpal, Jan; Havrankova, Petra; Pavelekova, Petra; Hempel, Maja; Kotzaeridou, Urania; Hoffmann, Georg F.; Leiz, Steffen; Makowski, Christine; Roser, Timo; Schroeder, Sebastian A.; Steinfeld, Robert; Strobl-Wildemann, Gertrud; Hoefele, Julia; Borggraefe, Ingo; Distelmaier, Felix; Strom, Tim M.; Winkelmann, Juliane; Meitinger, Thomas; Zech, Michael und Wagner, Matias (2021): De novo variants in neurodevelopmental disorders-experiences from a tertiary care center. In: Clinical Genetics, Bd. 100, Nr. 1: S. 14-28 [PDF, 2MB]

Mirza-Schreiber, Nazanin; Zech, Michael; Wilson, Rory; Brunet, Theresa; Wagner, Matias; Jech, Robert; Boesch, Sylvia; Skorvanek, Matej; Necpal, Jan; Weise, David; Weber, Sandrina; Mollenhauer, Brit; Trenkwalder, Claudia; Maier, Esther M.; Borggraefe, Ingo; Vill, Katharina; Hackenberg, Annette; Pilshofer, Veronika; Kotzaeridou, Urania; Schwaibold, Eva Maria Christina; Hoefele, Julia; Waldenberger, Melanie; Gieger, Christian; Peters, Annette; Meitinger, Thomas; Schormair, Barbara; Winkelmann, Juliane und Oexle, Konrad (2021): Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset. In: Brain, Bd. 145, Nr. 2: S. 644-654 [PDF, 1MB]

Olivieri, Martin; Sorg, Anna-Lisa; Weinberger, Raphael; Kurnik, Karin; Bidlingmaier, Christoph; Juranek, Sabrina; Hoffmann, Florian; Reiter, Karl; Bonfert, Michaela; Tacke, Moritz; Borggraefe, Ingo; Heinen, Florian und Gerstl, Lucia (2021): Recanalization strategies in childhood stroke in Germany. In: Scientific Reports, Bd. 11, Nr. 1, 13314

Tacke, Moritz; Janson, Katharina; Vill, Katharina; Heinen, Florian; Gerstl, Lucia; Reiter, Karl; Remi, Jan und Borggraefe, Ingo (2021): The influence of information about the circumstances of EEG recordings on the ability to identify seizure patterns. In: Seizure-European Journal of Epilepsy, Bd. 88: S. 125-129

Zech, Michael; Jech, Robert; Boesch, Sylvia; Skorvanek, Matej; Weber, Sandrina; Wagner, Matias; Zhao, Chen; Jochim, Angela; Necpal, Jan; Dincer, Yasemin; Vill, Katharina; Disteimaier, Felix; Stoklosa, Malgorzata; Krenn, Martin; Grunwald, Stephan; Bock-Bierbaum, Tobias; Fecikova, Anna; Havrankova, Petra; Roth, Jan; Prihodova, Iva; Adamovicova, Miriam; Ulmanova, Olga; Bechyne, Karel; Danhofer, Pavlina; Vesely, Branislav; Han, Vladimir; Pavelekova, Petra; Gdovinova, Zuzana; Mantel, Tobias; Meindl, Tobias; Sitzberger, Alexandra; Schröder, Sebastian; Blaschek, Astrid; Roser, Timo; Bonfert, Michaela V.; Haberlandt, Edda; Plecko, Barbara; Leineweber, Birgit; Berweck, Steffen; Herberhold, Thomas; Langguth, Berthold; Svantnerova, Jana; Minar, Michal; Ramos-Rivera, Gonzalo Alonso; Wojcik, Monica H.; Pajusalu, Sander; Ounap, Katrin; Schatz, Ulrich A.; Pölsler, Laura; Milenkovic, Ivan; Laccone, Franco; Pilhofer, Veronika; Colombo, Roberto; Patzer, Steffi; Iuso, Arcangela; Vera, Julia; Troncoso, Monica; Fang, Fang; Prokisch, Holger; Wilbert, Friederike; Eckenweiler, Matthias; Graf, Elisabeth; Westphal, Dominik S.; Riedhammer, Korbinian M.; Brunet, Theresa; Alhaddad, Bader; Berutti, Riccardo; Strom, Tim M.; Hecht, Martin; Baumann, Matthias; Wolf, Marc; Telegrafi, Aida; Person, Richard E.; Zamora, Francisca Milian; Henderson, Lindsay B.; Weise, David; Musacchio, Thomas; Volkmann, Jens; Szuto, Anna; Becker, Jessica; Cremer, Kirsten; Sycha, Thomas; Zimprich, Fritz; Kraus, Verena; Makowski, Christine; Gonzalez-Alegre, Pedro; Bardakjian, Tanya M.; Ozelius, Laurie J.; Vetro, Annafisa; Guerrini, Renzo; Maier, Esther; Borggraefe, Ingo; Kuster, Alice; Wortmann, Saskia B.; Hackenberg, Annette; Steinfeld, Robert; Assmann, Birgit; Staufner, Christian; Opladen, Thomas; Ruzicka, Evzen; Cohn, Ronald D.; Dyment, David; Chung, Wendy K.; Engels, Hartmut; Ceballos-Baumann, Andres; Ploski, Rafai; Daumke, Ofiver; Haslinger, Bernhard; Mall, Volker; Oexle, Konrad und Winkehnann, Juliane (2020): Monogenic variants in dystonia: an exome-wide sequencing study. In: Lancet Neurology, Bd. 19, Nr. 11: S. 908-918

Zech, Michael; Jech, Robert; Boesch, Sylvia; Skorvanek, Matej; Weber, Sandrina; Wagner, Matias; Zhao, Chen; Jochim, Angela; Necpal, Jan; Dincer, Yasemin; Vill, Katharina; Distelmaier, Felix; Stoklosa, Malgorzata; Krenn, Martin; Grunwald, Stephan; Bock-Bierbaum, Tobias; Fecikova, Anna; Havrankova, Petra; Roth, Jan; Prihodova, Iva; Adamovicova, Miriam; Ulmanova, Olga; Bechyne, Karel; Danhofer, Pavlina; Vesely, Branislav; Han, Vladimir; Pavelekova, Petra; Gdovinova, Zuzana; Mantel, Tobias; Meindl, Tobias; Sitzberger, Alexandra; Schroeder, Sebastian; Blaschek, Astrid; Roser, Timo; Bonfert, Michaefa; Haberlandt, Edda; Plecko, Barbara; Leineweber, Birgit; Berweck, Steffen; Herberhold, Thomas; Langguth, Berthold; Svantnerova, Jana; Minar, Michal; Ramos-Rivera, Gonzalo Alonso; Wojcik, Monica H.; Pajusalu, Sander; Ounap, Katrin; Schatz, Ulrich A.; Poelsler, Laura; Milenkovic, Ivan; Laccone, Franco; Pilhofer, Veronika; Colombo, Roberto; Patzer, Steffi; Iuso, Arcangela; Vera, Julia; Troncoso, Monica; Fang, Fang; Prokisch, Holger; Wilbert, Friederike; Eckenweiler, Matthias; Graf, Elisabeth; Westphal, Dominik S.; Riedhammer, Korbinian M.; Brunet, Theresa; Alhaddad, Bader; Berutti, Riccardo; Strom, Tim M.; Hecht, Martin; Baumann, Matthias; Wolf, Marc; Telegrafi, Aida; Person, Richard E.; Zamora, Francisca Milian; Henderson, Lindsay B.; Weise, David; Musacchio, Thomas; Volkmann, Jens; Szuto, Anna; Becker, Jessica; Cremer, Kirsten; Sycha, Thomas; Zimprich, Fritz; Kraus, Verena; Makowski, Christine; Gonzalez-Alegre, Pedro; Bardakjian, Tanya M.; Ozelius, Laurie J.; Vetro, Annafisa; Guerrini, Renzo; Maier, Esther; Borggraefe, Ingo; Kuster, Alice; Wortmann, Saskia B.; Hackenberg, Annette; Steinfeld, Robert; Assmann, Birgit; Staufner, Christian; Opladen, Thomas; Ruzicka, Evzen; Cohn, Ronald D.; Dyment, David; Chung, Wendy K.; Engels, Hartmut; Ceballos-Baumann, Andres; Ploski, Rafai; Daumke, Ofiver; Haslinger, Bernhard; Mall, Volker; Oexle, Konrad und Winkehnann, Juliane (2020): Monogenic variants in dystonia: an exome-wide sequencing study. In: Lancet Neurology, Bd. 19, Nr. 11: S. 908-918 [PDF, 1MB]

Gerstl, Lucia; Bonfert, Michaela V.; Heinen, Florian; Olivieri, Martin; Schroeder, Andreas Sebastian; Tacke, Moritz; Kurnik, Karin; Bidlingmaier, Christoph; Reiter, Karl und Borggraefe, Ingo (2020): Childhood Arterial Ischaemic Stroke: Clinical Presentation, Risk Factors and Management. In: Hamostaseologie, Bd. 40, Nr. 2: S. 165-173

Doering, Jan Henje; Saffari, Afshin; Bast, Thomas; Brockmann, Knut; Ehrhardt, Laura; Fazeli, Walid; Janzarik, Wibke G.; Kluger, Gerhard; Muhle, Hiltrud; Moller, Rikke S.; Platzer, Konrad; Santos, Joana Larupa; Bache, Iben; Bertsche, Astrid; Bonfert, Michaela; Borggraefe, Ingo; Broser, Philip J.; Datta, Alexandre N.; Hammer, Trine Bjorg; Hartmann, Hans; Hasse-Wittmer, Anette; Henneke, Marco; Kuehne, Hermann; Lemke, Johannes R.; Maier, Oliver; Matzker, Eva; Merkenschlager, Andreas; Opp, Joachim; Patzer, Steffi; Rostasy, Kevin; Stark, Birgit; Strzelczyk, Adam; Stülpnagel, Celina von; Weber, Yvonne; Wolff, Markus; Zirn, Birgit; Hoffmann, Georg Friedrich; Koelker, Stefan und Syrbe, Steffen (2020): The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood. In: Biomedicines, Bd. 8, Nr. 11, 456

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; Wandinger, Klaus-Peter; Leypoldt, Frank und Bien, Christian G. (2020): CASPR2 autoimmunity in children expanding to mild encephalopathy with hypertension. In: Neurology, Bd. 94, Nr. 22, E2290-E2301

Remi, Jan; Shen, Sophie; Tacke, Moritz; Probst, Philipp; Gerstl, Lucia; Peraud, Aurelia; Kunz, Mathias; Vollmar, Christian; Noachtar, Soheyl und Borggraefe, Ingo (2020): Congruence and Discrepancy of Interictal and Ictal EEG With MRI Lesions in Pediatric Epilepsies. In: Clinical Eeg and Neuroscience, Bd. 51, Nr. 6: S. 412-419 [PDF, 563kB]

Lorenz, Robin; Ahting, Uwe; Betzler, Cornelia; Heimering, Sigrid; Borggraefe, Ingo und Lange-Sperandio, Baerbel (2020): Homoplasmy of the Mitochondrial DNA Mutation m.616T>C Leads to Mitochondrial Tubulointerstitial Kidney Disease and Encephalopathia. In: Nephron, Bd. 144, Nr. 3: S. 156-160

Willimsky, Eva-Katharina; Munzig, Anna; Mayer, Karin; Biskup, Saskia; Abicht, Angela; Hoertnagel, Konstanze; Voss, Hubertus von; Klein, Hanns-Georg; Rost, Imma; Larsen, Line H. G.; Dahl, Hanns Atli; Hoelz, Hannes; Stülpnagel, Celina von und Borggraefe, Ingo (2020): Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters. In: Neuropediatrics, Bd. 52, Nr. 02: S. 92-97

Moorhouse, Frederik Jan; Cornell, Sonia; Gerstl, Lucia; Tacke, Moritz; Roser, Timo; Heinen, Florian; Bonfert, Michaela; Stülpnagel, Celina von; Wagner, Matias und Borggraefe, Ingo (2020): Cognitive performance and behavior across idiopathic/genetic epilepsies in children and adolescents. In: Scientific Reports, Bd. 10, Nr. 1, 21543 [PDF, 1MB]

Klotz, Kerstin Alexandra; Schoenberger, Jan; Nakamura, Lea; San Antonio-Arce, Victoria; Bast, Thomas; Wiemer-Kruel, Adelheid; Schubert-Bast, Susanne; Borggraefe, Ingo; Syrbe, Steffen und Jacobs, Julia (2020): Expectations and knowledge of cannabidiol therapy for childhood epilepsy - A German caregiver survey. In: Epilepsy & Behavior, Bd. 111, 107268

Gasser, Marius; Boonsimma, Ponghatai; Netbaramee, Wiracha; Wechapinan, Thanin; Srichomthomg, Chalurmpon; Ittiwut, Chupong; Krenn, Martin; Zimprich, Fritz; Milenkovic, Ivan; Abicht, Angela; Biskup, Saskia; Roser, Timo; Shotelersuk, Vorasuk; Tacke, Moritz; Kuersten, Marianne; Wagner, Matias; Borggraefe, Ingo; Suphapeetiporn, Kanya und Stulpnagel, Celina von (2020): ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response. In: Journal of Clinical Neuroscience, Bd. 72: S. 31-38

Boonsimma, Ponghatai; Gasser, Marius Michael; Netbaramee, Wiracha; Wechapinan, Thanin; Srichomthong, Chalurmpon; Ittiwut, Chupong; Wagner, Matias; Krenn, Martin; Zimprich, Fritz; Abicht, Angela; Biskup, Saskia; Roser, Timo; Borggraefe, Ingo; Suphapeetiporn, Kanya und Shotelersuk, Vorasuk (2020): Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases. In: Gene, Bd. 749, 144709

Brugger, Melanie; Becker-Dettling, Fiona; Brunet, Theresa; Strom, Tim; Meitinger, Thomas; Lurz, Eberhard; Borggraefe, Ingo und Wagner, Matias (2020): A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy. In: Annals of Clinical and Translational Neurology, Bd. 8, Nr. 1: S. 278-283

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

Borggraefe, Ingo; Tacke, Moritz; Gerstl, Lucia; Leiz, Steffen; Coras, Roland; Blumcke, Ingmar; Giese, Armin; Ertl-Wagner, Birgit; Thiel, Christian T.; Noachtar, Soheyl und Peraud, Aurelia (2019): Epilepsy surgery in the first months of life: a large type IIb focal cortical dysplasia causing neonatal drug-resistant epilepsy. In: Epileptic Disorders, Bd. 21, Nr. 1: S. 122-127

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

Hölz, Hannes; Herdl, Christian; Gerstl, Lucia; Tacke, Moritz; Vill, Katharina; Stuelpnagel, Celina von; Rost, Imma; Hoertnagel, Konstanze; Abicht, Angela; Hollizeck, Sebastian; Larsen, Line H. G. und Borggraefe, Ingo (2019): Impact on Clinical Decision Making of Next-Generation Sequencing in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center. In: Clinical Eeg and Neuroscience, Bd. 51, Nr. 1: S. 61-69

Gerstl, Lucia; Weinberger, Raphael; Heinen, Florian; Bonfert, Michaela V.; Borggraefe, Ingo; Schröder, A. Sebastian; Tacke, Moritz; Landgraf, Mirjam N.; Vill, Katharina; Kurnik, Karin; Sorg, Anna-Lisa und Olivieri, Martin (2019): Arterial ischemic stroke in infants, children, and adolescents: results of a Germany-wide surveillance study 2015-2017. In: Journal of Neurology, Bd. 266, Nr. 12: S. 2929-2941

Tacke, Moritz; Borggraefe, Ingo; Gerstl, Lucia; Heinen, Florian; Vill, Katharina; Bonfert, Michaela; Bast, Thomas; Neubauer, Bernd Axel; Baumeister, Friedrich; Baethmann, Martina; Bentele, Karl; Blank, Christian; Blank, Harald M.; Bode, Harald; Bosch, Friedrich; Brandl, Ulrich; Brockmann, Knut; Dahlem, Peter; Ernst, Jan-Peter; Feldmann, Evemarie; Fiedler, Andreas; Gerigk, Michael; Hess, Sören; Hikel, Christiane; Hoffmann, Hans -Georg; Kieslich, Matthias; Klepper, Jörg; Kluger, Gerhard; Koch, Hartmut; Koch, Walter; Korinthenberg, Rudolf; Krois, Ilona; Kuehne, Hermann; Kurlemann, Gerhard; Mandl, Michaela; Mause, Ulrike; Navratil, Peter; Opp, Joachim; Penzien, Johann; Prietsch, Viola; Quattlaender, Axel; Rating, Dietz; Schara, Ulrike; Shamdeen, Mohammed G.; Sprinz, Andreas; Wendker-Magrabi, Hildegard; Stephani, Ulrich; Muhle, Hiltrud; Strassburg, Hans-Michael; Toepke, Baerbel; Trollmann, Regina; Tuschen-Hofstaetter, Elisabeth; Waltz, Stephan; Weber, Gabriele; Wien, Frank U.; Wolff', Markus; Polster, Tilman; Freitag, Hedwig; Soenmez, Otzcam; Reinhardt, Klaus; Traus, Marion und Hoovey, Zeecam (2018): Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial. In: Seizure-European Journal of Epilepsy, Bd. 56: S. 115-120

Kotlarz, Daniel; Marquardt, Benjamin; Baroy, Tuva; Lee, Way S.; Konnikova, Liza; Hollizeck, Sebastian; Magg, Thomas; Lehle, Anna S.; Walz, Christoph; Borggraefe, Ingo; Hauck, Fabian; Bufler, Philip; Conca, Raffaele; Wall, Sarah M.; Schumacher, Eva M.; Misceo, Doriana; Frengen, Eirik; Bentsen, Beint S.; Uhlig, Holm H.; Hopfner, Karl-Peter; Muise, Aleixo M.; Snapper, Scott B.; Stromme, Petter und Klein, Christoph (2018): Human TGF-beta 1 deficiency causes severe inflammatory bowel disease and encephalopathy. In: Nature Genetics, Bd. 50, Nr. 3: S. 344-348

Tacke, Moritz; Rupp, Nina; Gerstl, Lucia; Heinen, Florian; Vill, Katharina; Bonfert, Michaela; Neubauer, Bernd Axel; Bast, Thomas und Borggraefe, Ingo (2018): Benign epilepsy with centrotemporal spikes: Correlating spike frequency and neuropsychology. In: Acta Neurologica Scandinavica, Bd. 138, Nr. 6: S. 475-481

Borggraefe, Ingo; Müller-Felber, Wolfgang; Schmid, Irene und Huetker, Sebastian (2018): Unilateral Tongue Fasciculation Associated with Genetic Paraganglioma Syndrome. In: Neuropediatrics, Bd. 49, Nr. 1: S. 78-79

Gerstl, Lucia; Weinberger, Raphael; Kries, Rüdiger von; Heinen, Florian; Schröder, A. Sebastian; Bonfert, Michaela V.; Borggraefe, Ingo; Tacke, Moritz; Vill, Katharina; Landgraf, Mirjam N.; Kurnik, Karin und Olivieri, Martin (2018): Risk factors in childhood arterial ischaemic stroke: Findings from a population-based study in Germany. In: European Journal of Paediatric Neurology, Bd. 22, Nr. 3: S. 380-386

Gerstl, Lucia; Weinberger, Raphael; Kries, Rüdiger von; Heinen, Florian; Schröder, Andreas Sebastian; Bonfert, Michaela Veronika; Borggraefe, Ingo; Tacke, Moritz; Vill, Katharina; Landgraf, Mirjam N.; Kurnik, Karin und Olivieri, Martin (2018): Symptom patterns in childhood arterial ischemic stroke: Analysis of a population-based study in Germany. In: Klinische Pädiatrie, Bd. 230, Nr. 6: S. 319-325

Hölz, Hannes; Coppenrath, Eva; Hoertnagel, Konstanze; Roser, Timo; Tacke, Moritz; Gerstl, Lucia und Borggraefe, Ingo (2018): Childhood-Onset Epileptic Encephalopathy Associated With Isolated Focal Cortical Dysplasia and a Novel TSC1 Germline Mutation. In: Clinical Eeg and Neuroscience, Bd. 49, Nr. 3: S. 187-191 [PDF, 388kB]

Bonfert, Michaela V.; Badura, Katharina; Gerstl, Julia; Borggraefe, Ingo; Heinen, Florian; Schröder, Sebastian; Olivieri, Martin; Weinberger, Raphael; Landgraf, Mirjam N.; Vill, Katharina; Tacke, Moritz; Berweck, Steffen; Reiter, Karl; Hoffmann, Florian; Nicolai, Thomas und Gerstl, Lucia (2018): Childhood Stroke: Awareness, Interest, and Knowledge Among the Pediatric Community. In: Frontiers in Pediatrics, Bd. 6, 182 [PDF, 842kB]

Baker, Kate; Gordon, Sarah L.; Melland, Holly; Bumbak, Fabian; Scott, Daniel J.; Jiang, Tess J.; Owen, David; Turner, Bradley J.; Boyd, Stewart G.; Rossi, Mari; Al-Raqad, Mohammed; Elpeleg, Orly; Peck, Dawn; Mancini, Grazia M. S.; Wilke, Martina; Zollino, Marcella; Marangi, Giuseppe; Weigand, Heike; Borggraefe, Ingo; Haack, Tobias; Stark, Zornitza; Sadedin, Simon; Tan, Tiong Yang; Jiang, Yunyun; Gibbs, Richard A.; Ellingwood, Sara; Amaral, Michelle; Kelley, Whitley; Kurian, Manju A.; Cousin, Michael A. und Raymond, F. Lucy (2018): SYT1-associated neurodevelopmental disorder: a case series. In: Brain, Bd. 141: S. 2576-2591

Surges, Rainer; Alber, Michael; Bast, Thomas; Baier, Hartmut; Bien, Christian G.; Borggraefe, Ingo; Boesebeck, Frank; Brandl, Ulrich; Hamer, Hajo M.; Hethey, Sven; Holtkamp, Martin; Jacobs, Julia; Kellinghaus, Christoph; Kerling, Frank; Knake, Susanne; Kunze, Albrecht; Kurlemann, Gerhard; Laufs, Helmut; Lerche, Holger; Mayer, Thomas; Moeddel, Gabriel; Neubauer, Bernd. A.; Noachtar, Soheyl; Panzer, Axel; Podewils, Felix von; Polster, Tilman; Rona, Sabine; Rosenow, Felix; Schmitz, Bettina; Schulze-Bonhage, Andreas; Spiczak, Sarah von; Staudt, Martin; Steinhoff, Bernhard J.; Stephani, Ulrich; Stodieck, Stefan R. G.; Straub, Hans-Beatus; Strzelczyk, Adam; Wellmer, Jörg und Elger, Christian E. (2018): Aufgaben und Struktur moderner Epilepsiezentren in Deutschland. In: Aktuelle Neurologie, Bd. 45, Nr. 7: S. 513-533

Schiergens, Katharina A.; Staudigl, Michael; Borggraefe, Ingo und Maier, Esther M. (2018): Neurological Sequelae due to Inborn Metabolic Diseases in Pediatric Refugees: Challenges in Treating the Untreated. In: Neuropediatrics, Bd. 49, Nr. 6: S. 363-368

Møller, Rikke S.; Wuttke, Thomas V.; Helbig, Ingo; Marini, Carla; Johannesen, Katrine M.; Brilstra, Eva H.; Vaher, Ulvi; Borggraefe, Ingo; Talvik, Inga; Talvik, Tiina; Kluger, Gerhard; Francois, Laurence L.; Lesca, Gaetan; Bellescize, Julitta de; Blichfeldt, Susanne; Chatron, Nicolas; Holert, Nils; Jacobs, Julia; Swinkels, Marielle; Betzler, Cornelia; Syrbe, Steffen; Nikanorova, Marina; Myers, Candace T.; Larsen, Line H. G.; Vejzovic, Sabina; Pendziwiat, Manuela; Spiczak, Sarah von; Hopkins, Sarah; Dubbs, Holly; Mang, Yuan; Mukhin, Konstantin; Holthausen, Hans; Gassen, Koen L. van; Dahl, Hans A.; Tommerup, Niels; Mefford, Heather C.; Rubboli, Guido; Guerrini, Renzo; Lemke, Johannes R.; Lerche, Holger; Muhle, Hiltrud und Maljevic, Snezana (2017): Mutations in GABRB3. From febrile seizures to epileptic encephalopathies. In: Neurology, Bd. 88, Nr. 5: S. 483-492 [PDF, 805kB]

Kovel, Carolien G. F. de; Syrbe, Steffen; Brilstra, Eva H.; Verbeek, Nienke; Kerr, Bronwyn; Dubbs, Holly; Bayat, Allan; Desai, Sonal; Naidu, Sakkubai; Srivastava, Siddharth; Cagaylan, Hande; Yis, Uluc; Saunders, Carol; Rook, Martin; Plugge, Susanna; Muhle, Hiltrud; Afawi, Zaid; Klein, Karl-Martin; Jayaraman, Vijayakumar; Rajagopalan, Ramakrishnan; Goldberg, Ethan; Marsh, Eric; Kessler, Sudha; Bergqvist, Christina; Conlin, Laura K.; Krok, Bryan L.; Thiffault, Isabelle; Pendziwiat, Manuela; Helbig, Ingo; Polster, Tilman; Borggraefe, Ingo; Lemke, Johannes R.; Boogaardt, Marie-Jose van den; Moller, Rikke S. und Koeleman, Bobby P. C. (2017): Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes. In: Jama Neurology, Bd. 74, Nr. 10: S. 1228-1236

Gerstl, Lucia; Heinen, Florian; Schroeder, A. Sebastian; Tacke, Moritz; Olivieri, Martin; Dorn, Franziska; Voll, Christian und Borggraefe, Ingo (2016): The "seagull cry": An initial sign in a child with intracranial carotid stenosis. In: Neurology, Bd. 87, Nr. 8: S. 850-851

Zech, Michael; Boesch, Sylvia; Maier, Esther M.; Borggraefe, Ingo; Vill, Katharina; Laccone, Franco; Pilshofer, Veronika; Ceballos-Baumann, Andres; Alhaddad, Bader; Berutti, Riccardo; Poewe, Werner; Haack, Tobias B.; Haslinger, Bernhard; Strom, Tim M. und Winkelmann, Juliane (2016): Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia. In: American Journal of Human Genetics, Bd. 99, Nr. 6: S. 1377-1387

Borggraefe, Ingo; Catarino, Claudia B.; Rémi, Jan; Vollmar, Christian; Peraud, Aurelia; Winkler, Peter A. und Noachtar, Soheyl (2016): Lateralization of cortical negative motor areas. In: Clinical Neurophysiology, Bd. 127, Nr. 10: S. 3314-3321

Gerstl, Lucia; Olivieri, Martin; Heinen, Florian; Borggraefe, Ingo; Schroeder, Andreas Sebastian; Tacke, Moritz; Vill, Katharina; Dalla-Pozza, Robert; Reiter, Karl; Lutz, Juergen; Brueckmann, Hartmut und Janssen, Hendrik (2016): Successful mechanical thrombectomy in a three-year-old boy with cardioembolic occlusion of both the basilar artery and the left middle cerebral artery. In: European Journal of Paediatric Neurology, Bd. 20, Nr. 6: S. 962-965

Tacke, Moritz; Gerstl, Lucia; Heinen, Florian; Heukaeufer, Isabel; Bonfert, Michaela; Bast, Thomas; Cornell, Sonia; Neubauer, Bernd Axel und Borggraefe, Ingo (2016): Effect of anticonvulsive treatment on neuropsychological performance in children with BECTS. In: European Journal of Paediatric Neurology, Bd. 20, Nr. 6: S. 874-879

Herbst, Saskia M.; Proepper, Christiane R.; Geis, Tobias; Borggraefe, Ingo; Hahn, Andreas; Debus, Otfried; Haeussler, Martin; Gersdorff, Gero von; 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. In: Brain & Development, Bd. 38, Nr. 4: S. 399-406

Johannesen, Katrine; Marini, Carla; Pfeffer, Siona; Møller, Rikke S.; Dorn, Thomas; Niturad, Christina; Gardella, Elena; Weber, Yvonne; Søndergård, Marianne; Hjalgrim, Helle; Nikanorova, Mariana; Becker, Felicitas; Larsen, Line H. G.; Dahl, Hans A.; Maier, Oliver; Mei, Davide; Biskup, Saskia; Klein, Karl M.; Reif, Philipp S.; Rosenow, Felix; Elias, Abdallah F.; Hudson, Cindy; Helbig, Katherine L.; Schubert-Bast, Susanne; Scordo, Maria R.; Craiu, Dana; Djémié, Tania; Hoffman-Zacharska, Dorota; Caglayan, Hande; Helbig, Ingo; Serratosa, Jose; Striano, Pasquale; Jonghe, Peter de; Weckhuysen, Sarah; Suls, Arvid; Muru, Kai; Talvik, Inga; Talvik, Tiina; Muhle, Hiltrud; Borggraefe, Ingo; Rost, Imma; Guerrini, Renzo; Lerche, Holger; Lemke, Johannes R.; Rubboli, Guido und Maljevic, Snezana (2016): Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. In: Neurology, Bd. 87, Nr. 11: S. 1140-1151

Langhagen, Thyra; Lehrer, Nicole; Borggraefe, Ingo; Heinen, Florian und Jahn, Klaus (2015): Vestibular migraine in children and adolescents: clinical findings and laboratory tests. In: Frontiers in Neurology, Bd. 5, UNSP 292 [PDF, 439kB]

Koerte, Inga; Pelavin, Paula; Kirmess, Berit; Fuchs, Teresa; Berweck, Steffen; Laubender, Rüdiger P.; Borggraefe, Ingo; Schroeder, Sebastian; Danek, Adrian; Rummeny, Claudia; Reiser, Maximilian; Kubicki, Marek; Shenton, Martha E.; Ertl-Wagner, Birgit und Heinen, Florian (2011): Anisotropy of transcallosal motor fibres indicates functional impairment in children with periventricular leukomalacia. In: Developmental medicine and child neurology, Bd. 53, Nr. 2: S. 179-186

Mehrkens, Jan Hinnerk; Borggraefe, Ingo; Feddersen, Berend; Heinen, Florian und Bötzel, Kai (2010): Early Globus Pallidus Internus Stimulation in Pediatric Patients With Generalized Primary Dystonia: Long-Term Efficacy and Safety. In: Journal of Child Neurology, Bd. 25, Nr. 11: S. 1355-1361 [PDF, 313kB]

Meyer-Heim, A.; Ammann-Reiffer, C.; Schmartz, A.; Schäfer, Jan; Sennhauser, F. H.; Heinen, Florian; Knecht, B.; Dabrowski, E. und Borggraefe, Ingo (2009): Improvement of walking abilities after robotic-assisted locomotion training in children with cerebral palsy. In: Archives of Disease in Childhood, Bd. 94: S. 615-620 [PDF, 248kB]

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