Browsing Universitätsbibliographie by Author "Becker, Felicitas"

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Browsing Universitätsbibliographie by Author "Becker, Felicitas"

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  • Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
    Gardella, Elena; Becker, Felicitas; Moller, Rikke S.; Schubert, Julian; Lemke, Johannes R.; Larsen, Line H. G.; Eiberg, Hans; Nothnagel, Michael; Thiele, Holger; Altmueller, Janine; Syrbe, Steffen; Merkenschlager, Andreas; Bast, Thomas; Steinhoff, Bernhard; Nuernberg, Peter; Mang, Yuan; Moller, Louise Bakke; Gellert, Pia; Heron, Sarah E.; Dibbens, Leanne M.; Weckhuysen, Sarah; Dahl, Hans Atli; Biskup, Saskia; Tommerup, Niels; Hjalgrim, Helle; Lerche, Holger; Beniczky, Sandor; Weber, Yvonne G. (2016)
  • Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis
    Androsova, Ganna; Krause, Roland; Borghei, Mojgansadat; Wassenaar, Merel; Auce, Pauls; Avbersek, Andreja; Becker, Felicitas; Berghuis, Bianca; Campbell, Ellen; Coppola, Antonietta; Francis, Ben; Wolking, Stefan; Cavalleri, Gianpiero L.; Craig, John; Delanty, Norman; Koeleman, Bobby P. C.; Kunz, Wolfram S.; Lerche, Holger; Marson, Anthony G.; Sander, Josemir W.; Sills, Graeme J.; Striano, Pasquale; Zara, Federico; Sisodiya, Sanjay M.; Depondt, Chantal (2017)
  • DEPDC5 Mutations in Genetic Focal Epilepsies of Childhood
    Lal, Dennis; Reinthaler, Eva M.; Schubert, Julian; Muhle, Hiltrud; Riesch, Erik; Kluger, Gerhard; Jabbari, Kamel; Kawalia, Amit; Baeumel, Christine; Holthausen, Hans; Hahn, Andreas; Feucht, Martha; Neophytou, Birgit; Haberlandt, Edda; Becker, Felicitas; Altmueller, Janine; Thiele, Holger; Lemke, Johannes R.; Lerche, Holger; Nuernberg, Peter; Sander, Thomas; Weber, Yvonne; Zimprich, Fritz; Neubauer, Bernd A. (2014)
  • Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
    Becker, Felicitas; Schubert, Julian; Weckhuysen, Sarah; Suls, Arvid; Grueninger, Steffen; Korn-Merker, Elisabeth; Hofmann-Peters, Anne; Sperner, Juergen; Cross, Helen; Hallmann, Kerstin; Elger, Christian E.; Kunz, Wolfram S.; Madeleyen, Rene; Lerche, Holger; Weber, Yvonne G. (2015)
  • Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
    Kasperaviciute, Dalia; Catarino, Claudia B.; Matarin, Mar; Leu, Costin; Novy, Jan; Tostevin, Anna; Leal, Barbara; Hessel, Ellen V. S.; Hallmann, Kerstin; Hildebrand, Michael S.; Dahl, Hans-Henrik M.; Ryten, Mina; Trabzuni, Daniah; Ramasamy, Adaikalavan; Alhusaini, Saud; Doherty, Colin P.; Dorn, Thomas; Hansen, Joerg; Kraemer, Guenter; Steinhoff, Bernhard J.; Zumsteg, Dominik; Duncan, Susan; Kaelviaeinen, Reetta K.; Eriksson, Kai J.; Kantanen, Anne-Mari; Pandolfo, Massimo; Gruber-Sedlmayr, Ursula; Schlachter, Kurt; Reinthaler, Eva M.; Stogmann, Elisabeth; Zimprich, Fritz; Theatre, Emilie; Smith, Colin; O'Brien, Terence J.; Tan, K. Meng; Petrovski, Slave; Robbiano, Angela; Paravidino, Roberta; Zara, Federico; Striano, Pasquale; Sperling, Michael R.; Buono, Russell J.; Hakonarson, Hakon; Chaves, Joao; Costa, Paulo P.; Silva, Berta M.; da Silva, Antonio M.; de Graan, Pierre N. E.; Koeleman, Bobby P. C.; Becker, Albert; Schoch, Susanne; von Lehe, Marec; Reif, Philipp S.; Rosenow, Felix; Becker, Felicitas; Weber, Yvonne; Lerche, Holger; Roessler, Karl; Buchfelder, Michael; Hamer, Hajo M.; Kobow, Katja; Coras, Roland; Blumcke, Ingmar; Scheffer, Ingrid E.; Berkovic, Samuel F.; Weale, Michael E.; Delanty, Norman; Depondt, Chantal; Cavalleri, Gianpiero L.; Kunz, Wolfram S.; Sisodiya, Sanjay M. (2013)
  • Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy
    Lal, Dennis; Pernhorst, Katharina; Klein, Karl Martin; Reif, Philipp; Tozzi, Rossana; Toliat, Mohammad R.; Winterer, Georg; Neubauer, Bernd; Nuernberg, Peter; Rosenow, Felix; Becker, Felicitas; Lerche, Holger; Kunz, Wolfram S.; Kurki, Mitja I.; Hoffmann, Per; Becker, Albert J.; Perucca, Emilio; Zara, Federico; Sander, Thomas; Weber, Yvonne G. (2015)
  • Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature
    Wolking, Stefan; Becker, Felicitas; Bast, Thomas; Wiemer-Kruel, Adelheid; Mayer, Thomas; Lerche, Holger; Weber, Yvonne G. (2014)
  • Galanin pathogenic mutations in temporal lobe epilepsy
    Guipponi, Michel; Chentouf, Amina; Webling, Kristin E. B.; Freimann, Krista; Crespel, Arielle; Nobile, Carlo; Lemke, Johannes R.; Hansen, Jorg; Dorn, Thomas; Lesca, Gaetan; Ryvlin, Philippe; Hirsch, Edouard; Rudolf, Gabrielle; Rosenberg, Dominique Sarah; Weber, Yvonne; Becker, Felicitas; Helbig, Ingo; Muhle, Hiltrud; Salzmann, Annick; Chaouch, Malika; Oubaiche, Mohand Laid; Ziglio, Serena; Gehrig, Corinne; Santoni, Federico; Pizzato, Massimo; Langel, Ulo; Antonarakis, Stylianos E. (2015)
  • Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
    Steffens, Michael; Leu, Costin; Ruppert, Ann-Kathrin; Zara, Federico; Striano, Pasquale; Robbiano, Angela; Capovilla, Giuseppe; Tinuper, Paolo; Gambardella, Antonio; Bianchi, Amedeo; La Neve, Angela; Crichiutti, Giovanni; de Kovel, Carolien G. F.; Trenite, Dorothee Kasteleijn-Nolst; de Haan, Gerrit-Jan; Lindhout, Dick; Gaus, Verena; Schmitz, Bettina; Janz, Dieter; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Steinhoff, Bernhard J.; Kleefuss-Lie, Ailing A.; Kunz, Wolfram S.; Surges, Rainer; Elger, Christian E.; Muhle, Hiltrud; von Spiczak, Sarah; Ostertag, Philipp; Helbig, Ingo; Stephani, Ulrich; Moller, Rikke S.; Hjalgrim, Helle; Dibbens, Leanne M.; Bellows, Susannah; Oliver, Karen; Mullen, Saul; Scheffer, Ingrid E.; Berkovic, Samuel F.; Everett, Kate V.; Gardiner, Mark R.; Marini, Carla; Guerrini, Renzo; Lehesjoki, Anna-Elina; Siren, Auli; Guipponi, Michel; Malafosse, Alain; Thomas, Pierre; Nabbout, Rima; Baulac, Stephanie; Leguern, Eric; Guerrero, Rosa; Serratosa, Jose M.; Reif, Philipp S.; Rosenow, Felix; Moerzinger, Martina; Feucht, Martha; Zimprich, Fritz; Kapser, Claudia; Schankin, Christoph J.; Suls, Arvid; Smets, Katrin; De Jonghe, Peter; Jordanova, Albena; Caglayan, Hande; Yapici, Zuhal; Yalcin, Destina A.; Baykan, Betul; Bebek, Nerses; Ozbek, Ugur; Gieger, Christian; Wichmann, Heinz-Erich; Balschun, Tobias; Ellinghaus, David; Franke, Andre; Meesters, Christian; Becker, Tim; Wienker, Thomas F.; Hempelmann, Anne; Schulz, Herbert; Rueschendorf, Franz; Leber, Markus; Pauck, Steffen M.; Trucks, Holger; Toliat, Mohammad R.; Nuernberg, Peter; Avanzini, Giuliano; Koeleman, Bobby P. C.; Sander, Thomas (2012)
  • Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
    Leu, Costin; de Kovel, Carolien G. F.; Zara, Federico; Striano, Pasquale; Pezzella, Marianna; Robbiano, Angela; Bianchi, Amedeo; Bisulli, Francesca; Coppola, Antonietta; Giallonardo, Anna Teresa; Beccaria, Francesca; Trenite, Dorothee Kasteleijn-Nolst; Lindhout, Dick; Gaus, Verena; Schmitz, Bettina; Janz, Dieter; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Kleefuss-Lie, Ailing A.; Hallman, Kerstin; Kunz, Wolfram S.; Elger, Christian E.; Muhle, Hiltrud; Stephani, Ulrich; Moller, Rikke S.; Hjalgrim, Helle; Mullen, Saul; Scheffer, Ingrid E.; Berkovic, Samuel F.; Everett, Kate V.; Gardiner, Mark R.; Marini, Carla; Guerrini, Renzo; Lehesjoki, Anna-Elina; Siren, Auli; Nabbout, Rima; Baulac, Stephanie; Leguern, Eric; Serratosa, Jose M.; Rosenow, Felix; Feucht, Martha; Unterberger, Iris; Covanis, Athanasios; Suls, Arvid; Weckhuysen, Sarah; Kaneva, Radka; Caglayan, Hande; Turkdogan, Dilsad; Baykan, Betul; Bebek, Nerses; Ozbek, Ugur; Hempelmann, Anne; Schulz, Herbert; Rueschendorf, Franz; Trucks, Holger; Nuernberg, Peter; Avanzini, Giuliano; Koeleman, Bobby P. C.; Sander, Thomas (2012)
  • Investigation of GRIN2A in common epilepsy phenotypes
    Lal, Dennis; Steinbruecker, Sandra; Schubert, Julian; Sander, Thomas; Becker, Felicitas; Weber, Yvonne; Lerche, Holger; Thiele, Holger; Krause, Roland; Lehesjoki, Anna-Elina; Nuernberg, Peter; Palotie, Aarno; Neubauer, Bernd A.; Muhle, Hiltrud; Stephani, Ulrich; Helbig, Ingo; Becker, Albert J.; Schoch, Susanne; Hansen, Joerg; Dorn, Thomas; Hohl, Christin; Luescher, Nicole; von Spiczak, Sarah; Lemke, Johannes R. (2015)
  • Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsy
    Zsurka, Gabor; Becker, Felicitas; Heinen, Markus; Gdynia, Hans-Juergen; Lerche, Holger; Kunz, Wolfram S.; Weber, Yvonne G. (2013)
  • Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
    Lemke, Johannes R.; Lal, Dennis; Reinthaler, Eva M.; Steiner, Isabelle; Nothnagel, Michael; Alber, Michael; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Finsterwalder, Katrin; Franke, Andre; Schilhabel, Markus; Jaehn, Johanna A.; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; Larsen, Jan; Moller, Rikke S.; Hjalgrim, Helle; Addis, Laura; Tang, Shan; Hughes, Elaine; Pal, Deb K.; Veri, Kadi; Vaher, Ulvi; Talvik, Tiina; Dimova, Petia; Lopez, Rosa Guerrero; Serratosa, Jose M.; Linnankivi, Tarja; Lehesjoki, Anna-Elina; Ruf, Susanne; Wolff, Markus; Buerki, Sarah; Wohlrab, Gabriele; Kroell, Judith; Datta, Alexandre N.; Fiedler, Barbara; Kurlemann, Gerhard; Kluger, Gerhard; Hahn, Andreas; Haberlandt, D. Edda; Kutzer, Christina; Sperner, Juergen; Becker, Felicitas; Weber, Yvonne G.; Feucht, Martha; Steinboeck, Hannelore; Neophythou, Birgit; Ronen, Gabriel M.; Gruber-Sedlmayr, Ursula; Geldner, Julia; Harvey, Robert J.; Hoffmann, Per; Herms, Stefan; Altmueller, Janine; Toliat, Mohammad R.; Thiele, Holger; Nuernberg, Peter; Wilhelm, Christian; Stephani, Ulrich; Helbig, Ingo; Lerche, Holger; Zimprich, Fritz; Neubauer, Bernd A.; Biskup, Saskia; von Spiczak, Sarah (2013)
  • Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
    Schubert, Julian; Siekierska, Aleksandra; Langlois, Melanie; May, Patrick; Huneau, Clement; Becker, Felicitas; Muhle, Hiltrud; Suls, Arvid; Lemke, Johannes R.; de Kovel, Carolien G. F.; Thiele, Holger; Konrad, Kathryn; Kawalia, Amit; Toliat, Mohammad R.; Sander, Thomas; Rueschendorf, Franz; Caliebe, Almuth; Nagel, Inga; Kohl, Bernard; Kecskes, Angela; Jacmin, Maxime; Hardies, Katia; Weckhuysen, Sarah; Riesch, Erik; Dorn, Thomas; Brilstra, Eva H.; Baulac, Stephanie; Moller, Rikke S.; Hjalgrim, Helle; Koeleman, Bobby P. C.; Jurkat-Rott, Karin; Lehman-Horn, Frank; Roach, Jared C.; Glusman, Gustavo; Hood, Leroy; Galas, David J.; Martin, Benoit; de Witte, Peter A. M.; Biskup, Saskia; De Jonghe, Peter; Helbig, Ingo; Balling, Rudi; Nuernberg, Peter; Crawford, Alexander D.; Esguerra, Camila V.; Weber, Yvonne G.; Lerche, Holger (2014)
  • Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
    Liu, Yuanyuan; Schubert, Julian; Sonnenberg, Lukas; Helbig, Katherine L.; Hoei-Hansen, Christina E.; Koko, Mahmoud; Rannap, Maert; Lauxmann, Stephan; Huq, Mahbubul; Schneider, Michael C.; Johannesen, Katrine M.; Kurlemann, Gerhard; Gardella, Elena; Becker, Felicitas; Weber, Yvonne G.; Benda, Jan; Moller, Rikke S.; Lerche, Holger (2019)
  • No evidence for a BRD2 promoter hypermethylation inblood leukocytes of Europeans with juvenile myoclonic epilepsy
    Schulz, Herbert; Ruppert, Ann-Kathrin; Zara, Federico; Madia, Francesca; Iacomino, Michele; Vari, Maria S.; Balagura, Ganna; Minetti, Carlo; Striano, Pasquale; Marini, Carla; Guerrini, Renzo; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Kapser, Claudia; Schankin, Christoph J.; Kunz, Wolfram S.; Moller, Rikke S.; Oliver, Karen L.; Bellows, Susannah T.; Mullen, Saul A.; Berkovic, Samuel F.; Scheffer, Ingrid E.; Caglayan, Hande; Ozbek, Ugur; Hoffmann, Per; Schramm, Sara; Tsortouktzidis, Despina; Becker, Albert J.; Sander, Thomas; Bianchi, Amedeo (2019)
  • Phenotypic spectrum of GABRA1: from generalized epilepsies to severe epileptic encephalopathies
    Johannesen, Katrine; Marini, Carla; Pfeffer, Siona; Moller, Rikke S.; Dorn, Thomas; Niturad, Christina; Gardella, Elena; Weber, Yvonne; Sondergard, 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; Djemie, Tania; Hoffman-Zacharska, Dorota; Caglayan, Hande; Helbig, Ingo; Serratosa, Jose; Striano, Pasquale; De Jonghe, Peter; 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; Maljevic, Snezana (2016)
  • PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures
    Schubert, Julian; Paravidino, Roberta; Becker, Felicitas; Berger, Andrea; Bebek, Nerses; Bianchi, Amedeo; Brockmann, Knut; Capovilla, Giuseppe; Bernardina, Bernardo Dalla; Fukuyama, Yukio; Hoffmann, Georg F.; Jurkat-Rott, Karin; Anttonen, Anna-Kaisa; Kurlemann, Gerhard; Lehesjoki, Anna-Elina; Lehmann-Horn, Frank; Mastrangelo, Massimo; Mause, Ulrike; Mueller, Stephan; Neubauer, Bernd; Puest, Burkhard; Rating, Dietz; Robbiano, Angela; Ruf, Susanne; Schroeder, Christopher; Seidel, Andreas; Specchio, Nicola; Stephani, Ulrich; Striano, Pasquale; Teichler, Jens; Turkdogan, Dilsad; Vigevano, Federico; Viri, Maurizio; Bauer, Peter; Zara, Federico; Lerche, Holger; Weber, Yvonne G. (2012)
  • PRRT2-related disorders: further PKD and ICCA cases and review of the literature
    Becker, Felicitas; Schubert, Julian; Striano, Pasquale; Anttonen, Anna-Kaisa; Liukkonen, Elina; Gaily, Eija; Gerloff, Christian; Mueller, Stephan; Heussinger, Nicole; Kellinghaus, Christoph; Robbiano, Angela; Polvi, Anne; Zittel, Simone; von Oertzen, Tim J.; Rostasy, Kevin; Schoels, Ludger; Warner, Tom; Muenchau, Alexander; Lehesjoki, Anna-Elina; Zara, Federico; Lerche, Holger; Weber, Yvonne G. (2013)
  • Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies : an exome-based case-control study
    May, Patrick; Girard, Simon; Harrer, Merle; Bobbili, Dheeraj R.; Schubert, Julian; Wolking, Stefan; Becker, Felicitas; Lachance-Touchette, Pamela; Meloche, Caroline; Gravel, Micheline; Niturad, Cristina E.; Knaus, Julia; De Kovel, Carolien; Toliat, Mohamad; Polvi, Anne; Iacomino, Michele; Guerrero-Lopez, Rosa; Baulac, Stephanie; Marini, Carla; Thiele, Holger; Altmueller, Janine; Jabbari, Kamel; Ruppert, Ann-Kathrin; Jurkowski, Wiktor; Lal, Dennis; Rusconi, Raffaella; Cestele, Sandrine; Terragni, Benedetta; Coombs, Ian D.; Reid, Christopher A.; Striano, Pasquale; Caglayan, Hande; Siren, Auli; Everett, Kate; Moller, Rikke S.; Hjalgrim, Helle; Muhle, Hiltrud; Helbig, Ingo; Kunz, Wolfram S.; Weber, Yvonne G.; Weckhuysen, Sarah; De Jonghe, Peter; Sisodiya, Sanjay M.; Nabbout, Rima; Franceschetti, Silvana; Coppola, Antonietta; Vari, Maria S.; Trenite, Dorothee Kasteleijn-Nolst; Baykan, Betul; Ozbek, Ugur; Bebek, Nerses; Klein, Karl M.; Rosenow, Felix; Nguyen, Dang K.; Dubeau, Francois; Carmant, Lionel; Lortie, Anne; Desbiens, Richard; Clement, Jean-Francois; Cieuta-Walti, Cecile; Sills, Graeme J.; Auce, Pauls; Francis, Ben; Johnson, Michael R.; Marson, Anthony G.; Berghuis, Bianca; Sander, Josemir W.; Avbersek, Andreja; McCormack, Mark; Cavalleri, Gianpiero L.; Delanty, Norman; Depondt, Chantal; Krenn, Martin; Zimprich, Fritz; Peter, Sarah; Nikanorova, Marina; Kraaij, Robert; van Rooij, Jeroen; Balling, Rudi; Ikram, M. Arfan; Uitterlinden, Andre G.; Avanzini, Giuliano; Schorge, Stephanie; Petrou, Steven; Mantegazza, Massimo; Sander, Thomas; LeGuern, Eric; Serratosa, Jose M.; Koeleman, Bobby P. C.; Palotie, Aarno; Lehesjoki, Anna-Elina; Nothnagel, Michael; Nuernberg, Peter; Maljevic, Snezana; Zara, Federico; Cossette, Patrick; Krause, Roland; Lerche, Holger (2018)