Auflistung Universitätsbibliographie nach Autor "Lerche, Holger"

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Auflistung Universitätsbibliographie nach Autor "Lerche, Holger"

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  • Genetik der idiopathischen Epilepsien
    Weber, Y. G.; Lerche, H. (2013)
  • 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)
  • Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
    Abou-Khalil, Bassel; Auce, Pauls; Avbersek, Andreja; Bahlo, Melanie; Balding, David J.; Bast, Thomas; Baum, Larry; Becker, Albert J.; Becker, Felicitas; Berghuis, Bianca; Berkovic, Samuel F.; Boysen, Katja E.; Bradfield, Jonathan P.; Brody, Lawrence C.; Buono, Russell J.; Campbell, Ellen; Cascino, Gregory D.; Catarino, Claudia B.; Cavalleri, Gianpiero L.; Cherny, Stacey S.; Chinthapalli, Krishna; Coffey, Alison J.; Compston, Alastair; Coppola, Antonietta; Cossette, Patrick; Craig, John J.; de Haan, Gerrit-Jan; De Jonghe, Peter; de Kovel, Carolien G. F.; Delanty, Norman; Depondt, Chantal; Devinsky, Orrin; Dlugos, Dennis J.; Doherty, Colin P.; Elger, Christian E.; Eriksson, Johan G.; Ferraro, Thomas N.; Feucht, Martha; Francis, Ben; Franke, Andre; French, Jacqueline A.; Freytag, Saskia; Gaus, Verena; Geller, Eric B.; Gieger, Christian; Glauser, Tracy; Glynn, Simon; Goldstein, David B.; Gui, Hongsheng; Guo, Youling; Haas, Kevin F.; Hakonarson, Hakon; Hallmann, Kerstin; Haut, Sheryl; Heinzen, Erin L.; Helbig, Ingo; Hengsbach, Christian; Hjalgrim, Helle; Iacomino, Michele; Ingason, Andres; Jamnadas-Khoda, Jennifer; Johnson, Michael R.; Kalviainen, Reetta; Kantanen, Anne-Mari; Kasperaviciute, Dalia; Trenite, Dorothee Kasteleijn-Nolst; Kirsch, Heidi E.; Knowlton, Robert C.; Koeleman, Bobby P. C.; Krause, Roland; Krenn, Martin; Kunz, Wolfram S.; Kuzniecky, Ruben; Kwan, Patrick; Lal, Dennis; Lau, Yu-Lung; Lehesjoki, Anna-Elina; Lerche, Holger; Leu, Costin; Lieb, Wolfgang; Lindhout, Dick; Lo, Warren D.; Lopes-Cendes, Iscia; Lowenstein, Daniel H.; Malovini, Alberto; Marson, Anthony G.; Mayer, Thomas; McCormack, Mark; Mills, James L.; Mirza, Nasir; Moerzinger, Martina; Moller, Rikke S.; Molloy, Anne M.; Muhle, Hiltrud; Newton, Mark; Ng, Ping-Wing; Noethen, Markus M.; Nuernberg, Peter; O'Brien, Terence J.; Oliver, Karen L.; Palotie, Aarno (2018)
  • Gentherapien für Epilepsie: Klinische Studien sind auf dem Weg
    Mueller, Peter; Lerche, Holger (2023)
  • GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
    Striano, P.; Weber, Y. G.; Toliat, M. R.; Schubert, J.; Leu, C.; Chaimana, R.; Baulac, S.; Guerrero, R.; LeGuern, E.; Lehesjoki, A. -E.; Polvi, A.; Robbiano, A.; Serratosa, J. M.; Guerrini, R.; Nuernberg, P.; Sander, T.; Zara, F.; Lerche, H.; Marini, C. (2012)
  • Heritability of Magnetoencephalography Phenotypes Among Patients With Genetic Generalized Epilepsy and Their Siblings
    Stier, Christina; Elshahabi, Adham; Li Hegner, Yiwen; Kotikalapudi, Raviteja; Marquetand, Justus; Braun, Christoph; Lerche, Holger; Focke, Niels K. (2021)
  • Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies
    Perez-Palma, Eduardo; Helbig, Ingo; Klein, Karl Martin; Anttila, Verneri; Horn, Heiko; Reinthaler, Eva Maria; Gormley, Padhraig; Ganna, Andrea; Byrnes, Andrea; Pernhorst, Katharina; Toliat, Mohammad R.; Saarentaus, Elmo; Howrigan, Daniel P.; Hoffman, Per; Miquel, Juan Francisco; De Ferrari, Giancarlo V.; Nuernberg, Peter; Lerche, Holger; Zimprich, Fritz; Neubauer, Bern A.; Becker, Albert J.; Rosenow, Felix; Perucca, Emilio; Zara, Federico; Weber, Yvonne G.; Lal, Dennis (2017)
  • Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
    Park, Joohyun; Tucci, Arianna; Cipriani, Valentina; Demidov, German; Rocca, Clarissa; Senderek, Jan; Butryn, Michaela; Velic, Ana; Lam, Tanya; Galanaki, Evangelia; Cali, Elisa; Vestito, Letizia; Maroofian, Reza; Deininger, Natalie; Rautenberg, Maren; Admard, Jakob; Hahn, Gesa-Astrid; Bartels, Claudius; van Os, Nienke J. H.; Horvath, Rita; Chinnery, Patrick F.; Tiet, May Yung; Hewamadduma, Channa; Hadjivassiliou, Marios; Tofaris, George K.; Wood, Nicholas W.; Hayer, Stefanie N.; Bender, Friedemann; Menden, Benita; Cordts, Isabell; Klein, Katrin; Huu Phuc Nguyen; Krauss, Joachim K.; Blahak, Christian; Strom, Tim M.; Sturm, Marc; van de Warrenburg, Bart; Lerche, Holger; Macek, Boris; Synofzik, Matthis; Ossowski, Stephan; Timmann, Dagmar; Wolf, Marc E.; Smedley, Damian; Riess, Olaf; Schoels, Ludger; Houlden, Henry; Haack, Tobias B.; Hengel, Holger (2022)
  • Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
    Blumcke, I.; Spreafico, R.; Haaker, G.; Coras, R.; Kobow, K.; Bien, C. G.; Pfaefflin, M.; Elger, C.; Widman, G.; Schramm, J.; Becker, A.; Braun, K. P.; Leijten, F.; Baayen, J. C.; Aronica, E.; Chassoux, F.; Hamer, H.; Stefan, H.; Roessler, K.; Thom, M.; Walker, M. C.; Sisodiya, S. M.; Duncan, J. S.; McEvoy, A. W.; Pieper, T.; Holthausen, H.; Kudernatsch, M.; Meencke, H. J.; Kahane, P.; Schulze-Bonhage, A.; Zentner, J.; Heiland, D. H.; Urbach, H.; Steinhoff, B. J.; Bast, T.; Tassi, L.; Lo Russo, G.; Ozkara, C.; Oz, B.; Krsek, P.; Vogelgesang, S.; Runge, U.; Lerche, H.; Weber, Y.; Honavar, M.; Pimentel, J.; Arzimanoglou, A.; Ulate-Campos, A.; Noachtar, S.; Hartl, E.; Schijns, O.; Guerrini, R.; Barba, C.; Jacques, T. S.; Cross, J. H.; Feucht, M.; Muehlebner, A.; Grunwald, T.; Trinka, E.; Winkler, P. A.; Gil-Nagel, A.; Delgado, R. Toledano; Mayer, T.; Lutz, M.; Zountsas, B.; Garganis, K.; Rosenow, F.; Hermsen, A.; von Oertzen, T. J.; Diepgen, T. L.; Avanzini, G. (2017)
  • Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy
    Kudin, Alexei P.; Baron, Gregor; Zsurka, Gabor; Hampel, Kevin G.; Elger, Christian E.; Grote, Alexander; Weber, Yvonne; Lerche, Holger; Thiele, Holger; Nuernberg, Peter; Schulz, Herbert; Ruppert, Ann-Kathrin; Sander, Thomas; Cheng, Qing; Arner, Elias S. J.; Schomburg, Lutz; Seeher, Sandra; Fradejas-Villar, Noelia; Schweizer, Ulrich; Kunz, Wolfram S. (2017)
  • Human Cerebrospinal fluid promotes long-term neuronal viability and network function in human neocortical organotypic brain slice cultures
    Schwarz, Niklas; Hedrich, Ulrike B. S.; Schwarz, Hannah; Harshad, P. A.; Dammeier, Nele; Auffenberg, Eva; Bedogni, Francesco; Honegger, Juergen B.; Lerche, Holger; Wuttke, Thomas V.; Koch, Henner (2017)
  • Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
    Auffenberg, Eva; Hedrich, Ulrike B. S.; Barbieri, Raffaella; Miely, Daniela; Groschup, Bernhard; Wuttke, Thomas, V; Vogel, Niklas; Luehrs, Philipp; Zanardi, Ilaria; Bertelli, Sara; Spielmann, Nadine; Gailus-Durner, Valerie; Fuchs, Helmut; de Angelis, Martin Hrabe; Pusch, Michael; Dichgans, Martin; Lerche, Holger; Gavazzo, Paola; Plesnila, Nikolaus; Freilinger, Tobias (2021)
  • Ictal Electroencephalographic Characteristics of Nodding Syndrome: A Comparative Case-Series from South Sudan, Tanzania, and Uganda
    Mazumder, Rajarshi; Lagoro, David Kitara; Nariai, Hiroki; Danieli, Alberto; Eliashiv, Dawn; Engel, Jerome, Jr.; Dalla Bernardina, Bernardo; Kegele, Josua; Lerche, Holger; Sejvar, James; Matuja, William; Schmutzhard, Erich; Bonanni, Paolo; De Polo, Gianni; Wagner, Thomas; Winkler, Andrea Sylvia (2022)
  • Idiopathic-generalized epilepsy shows profound white matter diffusiontensor imaging alterations
    Focke, Niels K.; Diederich, Christine; Helms, Gunther; Nitsche, Michael A.; Lerche, Holger; Paulus, Walter (2014)
  • Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature
    Wolking, Stefan; Schaeffeler, Elke; Lerche, Holger; Schwab, Matthias; Nies, Anne T. (2015)
  • Impaired Action Potential Initiation in GABAergic Interneurons Causes Hyperexcitable Networks in an Epileptic Mouse Model Carrying a Human Na(V)1.1 Mutation
    Hedrich, Ulrike B. S.; Liautard, Camille; Kirschenbaum, Daniel; Pofahl, Martin; Lavigne, Jennifer; Liu, Yuanyuan; Theiss, Stephan; Slotta, Johannes; Escayg, Andrew; Dihne, Marcel; Beck, Heinz; Mantegazza, Massimo; Lerche, Holger (2014)
  • In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment
    Rosa, Filip; Dhingra, Ashutosh; Uysal, Betuel; Mendis, G. Dulini C.; Loeffler, Heidi; Elsen, Gina; Mueller, Stephan; Schwarz, Niklas; Castillo-Lizardo, Melissa; Cuddy, Claire; Becker, Felicitas; Heutink, Peter; Reid, Christopher A.; Petrou, Steven; Lerche, Holger; Maljevic, Snezana (2020)
  • In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders
    Bayraktar, Erva; Liu, Yuanyuan; Sonnenberg, Lukas; Hedrich, Ulrike B. S.; Sara, Yildirim; Eltokhi, Ahmed; Lyu, Hang; Lerche, Holger; Wuttke, Thomas V.; Lauxmann, Stephan (2023)
  • In vitro neuronal network activity as a new functional diagnostic system to detect effects of Cerebrospinal fluid from autoimmune encephalitis patients
    Koch, Henner; Niturad, Cristina E.; Theiss, Stephan; Bien, Christian G.; Elger, Christian; Wandinger, Klaus-Peter; Vincent, Angela; Malter, Michael; Kortvelyessy, Peter; Lerche, Holger; Dihne, Marcel (2019)