Auflistung Universitätsbibliographie nach Autor "Hedrich, Ulrike B. S."

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Auflistung Universitätsbibliographie nach Autor "Hedrich, Ulrike B. S."

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  • 4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy
    Hedrich, Ulrike B. S.; Lauxmann, Stephan; Wolff, Markus; Synofzik, Matthis; Bast, Thomas; Binelli, Adrian; Serratosa, Jose M.; Martinez-Ulloa, Pedro; Allen, Nicholas M.; King, Mary D.; Gorman, Kathleen M.; Ben Zeev, Bruria; Tzadok, Michal; Wong-Kisiel, Lily; Marjanovic, Dragan; Rubboli, Guido; Sisodiya, Sanjay M.; Lutz, Florian; Ashraf, Harshad Pannikkaveettil; Torge, Kirsten; Yan, Pu; Bosselmann, Christian; Schwarz, Niklas; Fudali, Monika; Lerche, Holger (2021)
  • A Recurrent Mutation in KCNA2 as a Novel Cause of Hereditary Spastic Paraplegia and Ataxia
    Helbig, Katherine L.; Hedrich, Ulrike B. S.; Shinde, Deepali N.; Krey, Ilona; Teichmann, Anne-Christin; Hentschel, Julia; Schubert, Julian; Chamberlin, Adam C.; Huether, Robert; Lu, Hsiao-Mei; Alcaraz, Wendy A.; Tang, Sha; Jungbluth, Chelsy; Dugan, Sarah L.; Vainionpaa, Leena; Karle, Kathrin N.; Synofzik, Matthis; Lehesjoki, Anna-Elina; Helbig, Ingo; Lerche, Holger; Lemke, Johannes R.; Schöls, Ludger; Schüle-Freyer, Rebecca (2016)
  • An SCN2A mutation in a family with infantile seizures from Madagascar reveals an increased subthreshold Na+ current
    Lauxmann, Stephan; Boutry-Kryza, Nadia; Rivier, Clotilde; Mueller, Stephan; Hedrich, Ulrike B. S.; Maljevic, Snezana; Szepetowski, Pierre; Lerche, Holger; Lesca, Gaetan (2013)
  • Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies
    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.; Moller, Rikke S.; Lerche, Holger; Rubboli, Guido (2017)
  • De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
    Syrbe, Steffen; Hedrich, Ulrike B. S.; Riesch, Erik; Djemie, Tania; Mueller, Stephan; Moller, Rikke S.; Maher, Bridget; Hernandez-Hernandez, Laura; Synofzik, Matthis; Caglayan, Hande S.; Arslan, Mutluay; Serratosa, Jose M.; Nothnagel, Michael; May, Patrick; Krause, Roland; Loeffler, Heidrun; Detert, Katja; Dorn, Thomas; Vogt, Heinrich; Kraemer, Guenter; Schoels, 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; Zuechner, Stephan; Palotie, Aarno; Suls, Arvid; De Jonghe, Peter; Helbig, Ingo; Biskup, Saskia; Wolff, Markus; Maljevic, Snezana; Schule, Rebecca; Sisodiya, Sanjay M.; Weckhuysen, Sarah; Lerche, Holger; Lemke, Johannes R. (2015)
  • De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias
    Helbig, Katherine L.; Lauerer, Robert J.; Bahr, Jacqueline C.; Souza, Ivana A.; Myers, Candace T.; Uysal, Betuel; Schwarz, Niklas; Gandini, Maria A.; Huang, Sun; Keren, Boris; Mignot, Cyril; Afenjar, Alexandra; de Villemeur, Thierry Billette; Heron, Delphine; Nava, Caroline; Valence, Stephanie; Buratti, Julien; Fagerberg, Christina R.; Soerensen, Kristina P.; Kibaek, Maria; Kamsteeg, Erik-Jan; Koolen, David A.; Gunning, Boudewijn; Schelhaas, H. Jurgen; Kruer, Michael C.; Fox, Jordana; Bakhtiari, Somayeh; Jarrar, Randa; Padilla-Lopez, Sergio; Lindstrom, Kristin; Jin, Sheng Chih; Zeng, Xue; Bilguvar, Kaya; Papavasileiou, Antigone; Xin, Qinghe; Zhu, Changlian; Boysen, Katja; Vairo, Filippo; Lanpher, Brendan C.; Klee, Eric W.; Tillema, Jan-Mendelt; Payne, Eric T.; Cousin, Margot A.; Kruisselbrink, Teresa M.; Wick, Myra J.; Baker, Joshua; Haan, Eric; Smith, Nicholas; Corbett, Mark A.; MacLennan, Alastair H.; Gecz, Jozef; Biskup, Saskia; Goldmann, Eva; Rodan, Lance H.; Kichula, Elizabeth; Segal, Eric; Jackson, Kelly E.; Asamoah, Alexander; Dimmock, David; McCarrier, Julie; Botto, Lorenzo D.; Filloux, Francis; Tvrdik, Tatiana; Cascino, Gregory D.; Klingerman, Sherry; Neumann, Catherine; Wang, Raymond; Jacobsen, Jessie C.; Nolan, Melinda A.; Snell, Russell G.; Lehnert, Klaus; Sadleir, Lynette G.; Anderlid, Britt-Marie; Kvarnung, Malin; Guerrini, Renzo; Friez, Michael J.; Lyons, Michael J.; Leonhard, Jennifer; Kringlen, Gabriel; Casas, Kari; El Achkar, Christelle M.; Smith, Lacey A.; Rotenberg, Alexander; Poduri, Annapurna; Sanchis-Juan, Alba; Carss, Keren J.; Rankin, Julia; Zeman, Adam; Raymond, F. Lucy; Blyth, Moira; Kerr, Bronwyn; Ruiz, Karla; Urquhart, Jill; Hughes, Imelda; Banka, Siddharth; Hedrich, Ulrike B. S.; Scheffer, Ingrid E.; Helbig, Ingo; Zamponi, Gerald W.; Lerche, Holger; Mefford, Heather C. (2018)
  • Dravet Variant SCN1A(A1783V) Impairs Interneuron Firing Predominantly by Altered Channel Activation
    Layer, Nikolas; Sonnenberg, Lukas; Gonzalez, Emilio Pardo; Benda, Jan; Hedrich, Ulrike B. S.; Lerche, Holger; Koch, Henner; Wuttke, Thomas, V (2021)
  • Early-onset familial hemiplegic migraine due to a novel SCN1A mutation
    Fan, Chunxiang; Wolking, Stefan; Lehmann-Horn, Frank; Hedrich, Ulrike B. S.; Freilinger, Tobias; Lerche, Holger; Borck, Guntram; Kubisch, Christian; Jurkat-Rott, Karin (2016)
  • Endogenous but not sensory-driven activity controls migration, morphogenesis and survival of adult-born juxtaglomerular neurons in the mouse olfactory bulb
    Li, Kaizhen; Figarella, Katherine; Su, Xin; Kovalchuk, Yury; Gorzolka, Jessika; Neher, Jonas J.; Mojtahedi, Nima; Casadei, Nicolas; Hedrich, Ulrike B. S.; Garaschuk, Olga (2023)
  • Epileptogenese und Konsequenzen für die Therapie
    Hedrich, Ulrike B. S.; Koch, Henner; Becker, Albert; Lerche, Holger (2019)
  • Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
    Wolff, Markus; Johannesen, Katrine M.; Hedrich, Ulrike B. S.; Masnada, Silvia; Rubboli, Guido; Gardella, Elena; Lesca, Gaetan; Ville, Dorothee; Milh, Mathieu; Villard, Laurent; Afenjar, Alexandra; Chantot-Bastaraud, Sandra; Mignot, Cyril; Lardennois, Caroline; Nava, Caroline; Schwarz, Niklas; Gerard, Marion; Perrin, Laurence; Doummar, Diane; Auvin, Stephane; Miranda, Maria J.; Hempel, Maja; Brilstra, Eva; Knoers, Nine; Verbeek, Nienke; van Kempen, Marjan; Braun, Kees P.; Mancini, Grazia; Biskup, Saskia; Hoertnagel, Konstanze; Doecker, Miriam; Bast, Thomas; Loddenkemper, Tobias; Wong-Kisiel, Lily; Baumeister, Friedrich M.; Fazeli, Walid; Striano, Pasquale; Dilena, Robertino; Fontana, Elena; Zara, Federico; Kurlemann, Gerhard; Klepper, Joerg; Thoene, Jess G.; Arndt, Daniel H.; Deconinck, Nicolas; Schmitt-Mechelke, Thomas; Maier, Oliver; Muhle, Hiltrud; Wical, Beverly; Finetti, Claudio; Brueckner, Reinhard; Pietz, Joachim; Golla, Guenther; Jillella, Dinesh; Linnet, Karen M.; Charles, Perrine; Moog, Ute; Oiglane-Shlik, Eve; Mantovani, John F.; Park, Kristen; Deprez, Marie; Lederer, Damien; Mary, Sandrine; Scalais, Emmanuel; Selim, Laila; Van Coster, Rudy; Lagae, Lieven; Nikanorova, Marina; Hjalgrim, Helle; Korenke, G. Christoph; Trivisano, Marina; Specchio, Nicola; Ceulemans, Berten; Dorn, Thomas; Helbig, Katherine L.; Hardies, Katia; Stamberger, Hannah; de Jonghe, Peter; Weckhuysen, Sarah; Lemke, Johannes R.; Kraegeloh-Mann, Ingeborg; Helbig, Ingo; Kluger, Gerhard; Lerche, Holger; Moller, Rikke S. (2017)
  • GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers
    Li, Dong; Yuan, Hongjie; Ortiz-Gonzalez, Xilma R.; Marsh, Eric D.; Tian, Lifeng; McCormick, Elizabeth M.; Kosobucki, Gabrielle J.; Chen, Wenjuan; Schulien, Anthony J.; Chiavacci, Rosetta; Tankovic, Anel; Naase, Claudia; Brueckner, Frieder; Hu, Chun; Kusumoto, Hirofumi; Hedrich, Ulrike B. S.; Elsen, Gina; Aizenman, Elias; Lemke, Johannes R.; Hakonarson, Hakon; Traynelis, Stephen F.; Falk, Marni J.; von Stülpnagel-Steinbeis, Celina; Hörtnagel, Konstanze (2016)
  • 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)
  • 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 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)
  • Ionenkanalerkrankungen des Gehirns – monogene Epilepsien
    Maljevic, S.; Hedrich, U. B. S.; Lerche, H. (2013)
  • iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis
    Schoendorf, David C.; Aureli, Massimo; McAllister, Fiona E.; Hindley, Christopher J.; Mayer, Florian; Schmid, Benjamin; Sardi, S. Pablo; Valsecchi, Manuela; Hoffmann, Susanna; Schwarz, Lukas Kristoffer; Hedrich, Ulrike; Berg, Daniela; Shihabuddin, Lamya S.; Hu, Jing; Pruszak, Jan; Gygi, Steven P.; Sonnino, Sandro; Gasser, Thomas; Deleidi, Michela (2014)
  • KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine
    Mueller, Peter; Takacs, Danielle S.; Hedrich, Ulrike B. S.; Coorg, Rohini; Masters, Laura; Glinton, Kevin E.; Dai, Hongzheng; Cokley, Jon A.; Riviello, James J.; Lerche, Holger; Cooper, Edward C. (2023)
  • KCNC1-related disorders: new de novo variants expand the phenotypic spectrum
    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. (2019)