Auflistung Universitätsbibliographie nach Autor "Maljevic, Snezana"

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Auflistung Universitätsbibliographie nach Autor "Maljevic, Snezana"

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  • A conserved threonine in the S1-S2 loop of K(V)7.2 and K(V)7.3 channels regulates voltage-dependent activation
    Fuell, Yvonne; Seebohm, Guiscard; Lerche, Holger; Maljevic, Snezana (2013)
  • A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
    Muona, Mikko; Berkovic, Samuel F.; Dibbens, Leanne M.; Oliver, Karen L.; Maljevic, Snezana; Bayly, Marta A.; Joensuu, Tarja; Canafoglia, Laura; Franceschetti, Silvana; Michelucci, Roberto; Markkinen, Salla; Heron, Sarah E.; Hildebrand, Michael S.; Andermann, Eva; Andermann, Frederick; Gambardella, Antonio; Tinuper, Paolo; Licchetta, Laura; Scheffer, Ingrid E.; Criscuolo, Chiara; Filla, Alessandro; Ferlazzo, Edoardo; Ahmad, Jamil; Ahmad, Adeel; Baykan, Betul; Said, Edith; Topcu, Meral; Riguzzi, Patrizia; King, Mary D.; Ozkara, Cigdem; Andrade, Danielle M.; Engelsen, Bernt A.; Crespel, Arielle; Lindenau, Matthias; Lohmann, Ebba; Saletti, Veronica; Massano, Joao; Privitera, Michael; Espay, Alberto J.; Kauffmann, Birgit; Duchowny, Michael; Moller, Rikke S.; Straussberg, Rachel; Afawi, Zaid; Ben-Zeev, Bruria; Samocha, Kaitlin E.; Daly, Mark J.; Petrou, Steven; Lerche, Holger; Palotie, Aarno; Lehesjoki, Anna-Elina (2015)
  • 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)
  • Characterization of the GABRB2-Associated Neurodevelopmental Disorders
    el Achkar, Christelle M.; Harrer, Merle; Smith, Lacey; Kelly, McKenna; Iqbal, Sumaiya; Maljevic, Snezana; Niturad, Cristina E.; Vissers, Lisenka E. L. M.; Poduri, Annapurna; Yang, Edward; Lal, Dennis; Lerche, Holger; Moller, Rikke S.; Olson, Heather E. (2021)
  • 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)
  • Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy
    Corbett, Mark A.; Bellows, Susannah T.; Li, Melody; Carroll, Renee; Micallef, Silvana; Carvill, Gemma L.; Myers, Candace T.; Howell, Katherine B.; Maljevic, Snezana; Lerche, Holger; Gazina, Elena V.; Mefford, Heather C.; Bahlo, Melanie; Berkovic, Samuel F.; Petrou, Steven; Scheffer, Ingrid E.; Gecz, Jozef (2016)
  • Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy
    Orhan, Goekce; Bock, Merle; Schepers, Dorien; Ilina, Elena I.; Reichel, Stephanie Nadine; Loeffler, Heidi; Jezutkovic, Nicole; Weckhuysen, Sarah; Mandelstam, Simone; Suls, Arvid; Danker, Timm; Guenther, Elke; Scheffer, Ingrid E.; De Jonghe, Peter; Lerche, Holger; Maljevic, Snezana (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)
  • Ionenkanalerkrankungen des Gehirns – monogene Epilepsien
    Maljevic, S.; Hedrich, U. B. S.; Lerche, H. (2013)
  • Mechanismen genetischer Epilepsien
    Hedrich, Ulrike; Maljevic, Snezana; Lerche, Holger (2013)
  • Mutations in GABRB3. From febrile seizures to epileptic encephalopathies
    Moller, 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; de Bellescize, Julitta; 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; von Spiczak, Sarah; Hopkins, Sarah; Dubbs, Holly; Mang, Yuan; Mukhin, Konstantin; Holthausen, Hans; van Gassen, Koen L.; Dahl, Hans A.; Tommerup, Niels; Mefford, Heather C.; Rubboli, Guido; Guerrini, Renzo; Lemke, Johannes R.; Lerche, Holger; Muhle, Hiltrud; Maljevic, Snezana (2017)
  • Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia
    Schwarz, N.; Hahn, A.; Bast, T.; Mueller, S.; Loeffler, H.; Maljevic, S.; Gaily, E.; Prehl, I.; Biskup, S.; Joensuu, T.; Lehesjoki, A. -E.; Neubauer, B. A.; Lerche, H.; Hedrich, U. B. S. (2016)
  • Myoclonus Epilepsy and Ataxia due to KCNC1 Mutation : Analysis of 20 Cases and K plus Channel Properties
    Oliver, Karen L.; Franceschetti, Silvana; Milligan, Carol J.; Muona, Mikko; Mandelstam, Simone A.; Canafoglia, Laura; Boguszewska-Chachulska, Anna M.; Korczyn, Amos D.; Bisulli, Francesca; Di Bonaventura, Carlo; Ragona, Francesca; Michelucci, Roberto; Ben-Zeev, Bruria; Straussberg, Rachel; Panzica, Ferruccio; Massano, Joao; Friedman, Daniel; Crespel, Arielle; Engelsen, Bernt A.; Andermann, Frederick; Andermann, Eva; Spodar, Krystyna; Lasek-Bal, Anetta; Riguzzi, Patrizia; Pasini, Elena; Tinuper, Paolo; Licchetta, Laura; Gardella, Elena; Lindenau, Matthias; Wulf, Annette; Moller, Rikke S.; Benninger, Felix; Afawi, Zaid; Rubboli, Guido; Reid, Christopher A.; Maljevic, Snezana; Lerche, Holger; Lehesjoki, Anna-Elina; Petrou, Steven; Berkovic, Samuel F. (2017)
  • 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)
  • Potassium channel genes and benign familial neonatal epilepsy
    Maljevic, Snezana; Lerche, Holger (2014)
  • Potassium channels: a review of broadening therapeutic possibilities for neurological diseases
    Maljevic, Snezana; Lerche, Holger (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)
  • Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features
    Niturad, Cristina Elena; Lev, Dorit; Kalscheuer, Vera M.; Charzewska, Agnieszka; Schubert, Julian; Lerman-Sagie, Tally; Kroes, Hester Y.; Oegema, Renske; Traverso, Monica; Specchio, Nicola; Lassota, Maria; Chelly, Jamel; Bennett-Back, Odeya; Carmi, Nirit; Koffler-Brill, Tal; Iacomino, Michele; Trivisano, Marina; Capovilla, Giuseppe; Striano, Pasquale; Nawara, Magdalena; Rzonca, Sylwia; Fischer, Ute; Bienek, Melanie; Jensen, Corinna; Hu, Hao; Thiele, Holger; Altmuller, Janine; Krause, Roland; May, Patrick; Becker, Felicitas; Balling, Rudi; Biskup, Saskia; Haas, Stefan A.; Nuernberg, Peter; van Gassen, Koen L. I.; Lerche, Holger; Zara, Federico; Maljevic, Snezana; Leshinsky-Silver, Esther (2017)
  • SRF modulates seizure occurrence, activity induced gene transcription and hippocampal circuit reorganization in the mouse pilocarpine epilepsy model
    Loesing, Pascal; Niturad, Cristina Elena; Harrer, Merle; zu Reckendorf, Christopher Meyer; Schatz, Theresa; Sinske, Daniela; Lerche, Holger; Maljevic, Snezana; Knoell, Bernd (2017)
  • Zebrafish Bioassay-Guided Microfractionation Identifies Anticonvulsant Steroid Glycosides from the Philippine Medicinal Plant Solanum torvum
    Challal, Soura; Buenafe, Olivia E. M.; Queiroz, Emerson F.; Maljevic, Snezana; Marcourt, Laurence; Bock, Merle; Kloeti, Werner; Dayrit, Fabian M.; Harvey, Alan L.; Lerche, Holger; Esguerra, Camila V.; de Witte, Peter A. M.; Wolfender, Jean-Luc; Crawford, Alexander D. (2014)