KRAUSE, ROLAND

KRAUSE, ROLAND  

100013 - Dipartimento di Giurisprudenza  

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Alterations in the alfa(2) gamma ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies 1-gen-2017 Santolini, Ines; Celli, Roberta; Cannella, Milena; Imbriglio, Tiziana; Guiducci, Michela; Parisi, Pasquale; Schubert, Julian; Iacomino, Michele; Zara, Federico; Lerche, Holger; Moyanova, Slavianka; Ngomba, Richard Teke; van Luijtelaar, Gilles; Battaglia, Giuseppe; Bruno, Valeria; Striano, Pasquale; Nicoletti, Ferdinando; Palotie, Aarno; Folkhälsan, Anna-Elina Lehesjoki; Ruppert, Ann-Kathrin; Siren, Auli; Koeleman, Bobby; Lal, Dennis; Becker, Felicitas; Caglayan, Hande; Hjalgrim, Helle; Muhle, Hiltrud; Thiele, Holger; Helbig, Ingo; Altmuller, Janine; Jabbari, Kamel; Everett, Kate; May, Patrick; Nurnberg, Peter; Møller, Rikke; Nabbout, Rima; Krause, Roland; Balling, Rudi; Baulac, Stephanie; Sander, Thomas; Kunz, Wolfram; Weber, Yvonne; Bianchi, Amedeo; La Neve, Angela; Coppola, Antonietta; Striano, Salvatore; Capovilla, Giuseppe; Ferlazzo, Edoardo; Bagnasco, Irene; Ferretti, Alessandro; Di Bonaventura, Carlo; Vari, Maria Stella; Pinto, Francesca; Bisulli, Francesca; Tinuper, Paolo; Minetti, Carlo; Belcastro, Vincenzo; Giordano, Lucio; Gambardella, Antonio
CHD2 variants are a risk factor for photosensitivity in epilepsy 1-gen-2015 Galizia, Elizabeth C; Myers, Candace T; Leu, Costin; de Kovel, Carolien G. F; Afrikanova, Tatiana; Cordero Maldonado, Maria Lorena; Martins, Teresa G; Jacmin, Maxime; Drury, Suzanne; Krishna Chinthapalli, V; Muhle, Hiltrud; Pendziwiat, Manuela; Sander, Thomas; Ruppert, Ann Kathrin; Møller, Rikke S; Thiele, Holger; Krause, Roland; Schubert, Julian; Lehesjoki, Anna Elina; Nürnberg, Peter; Lerche, Holger; Palotie, Aarno; Coppola, Antonietta; Striano, Salvatore; Gaudio, Luigi Del; Boustred, Christopher; Schneider, Amy L; Lench, Nicholas; Jocic Jakubi, Bosanka; Covanis, Athanasios; Capovilla, Giuseppe; Veggiotti, Pierangelo; Piccioli, Marta; Parisi, Pasquale; Cantonetti, Laura; Sadleir, Lynette G; Mullen, Saul A; Berkovic, Samuel F; Stephani, Ulrich; Helbig, Ingo; Crawford, Alexander D; Esguerra, Camila V; Kasteleijn Nolst Trenité, Dorothee G. A; Koeleman, Bobby P. C; Mefford, Heather C; Scheffer, Ingrid E; Sisodiya, Sanjay M.
De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy 1-gen-2015 Syrbe, Steffen; Hedrich, Ulrike B. S.; Riesch, Erik; Djémié, Tania; Müller, Stephan; Møller, Rikke S.; Maher, Bridget; Hernandez Hernandez, Laura; Synofzik, Matthis; Caglayan, Hande S.; Arslan, Mutluay; Serratosa, José M.; Nothnagel, Michael; May, Patrick; Krause, Roland; Löffler, Heidrun; Detert, Katja; Dorn, Thomas; Vogt, Heinrich; Krämer, Günter; Schöls, 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; Züchner, Stephan; Palotie, Aarno; Suls, Arvid; De Jonghe, Peter; Helbig, Ingo; Biskup, Saskia; Wolff, Markus; Maljevic, Snezana; Schüle, Rebecca; Sisodiya, Sanjay M.; Weckhuysen, Sarah; Lerche, Holger; Lemke, Johannes R.
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam 1-gen-2022 Campbell, Ciarán; Mccormack, Mark; Patel, Sonn; Stapleton, Caragh; Bobbili, Dheeraj; Krause, Roland; Depondt, Chantal; Sills, Graeme J; Koeleman, Bobby P; Striano, Pasquale; Zara, Federico; Sander, Josemir W; Lerche, Holger; Kunz, Wolfram S; Stefansson, Kari; Stefansson, Hreinn; Doherty, Colin P; Heinzen, Erin L; Scheffer, Ingrid E; Goldstein, David B; O'Brien, Terence; Cotter, David; Berkovic, Samuel F; Sisodiya, Sanjay M; Delanty, Norman; Cavalleri, Gianpiero L
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features 1-gen-2017 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; Altmã¼ller, Janine; Krause, Roland; May, Patrick; Becker, Felicitas; Balling, Rudi; Biskup, Saskia; Haas, Stefan A.; Nã¼rnberg, Peter; van Gassen, Koen L. I; Lerche, Holger; Zara, Federico; Maljevic, Snezana; Leshinsky-Silver, Esther
Rare gene deletions in genetic generalized and Rolandic epilepsies 1-gen-2018 Jabbari, K.; Bobbili, D. R.; Lal, D.; Reinthaler, E. M.; Schubert, J.; Wolking, S.; Sinha, V.; Motameny, S.; Thiele, H.; Kawalia, A.; Altmuller, J.; Toliat, M. R.; Kraaij, R.; van Rooij, J.; Uitterlinden, A. G.; Arfan Ikram, M.; Zara, F.; Lehesjoki, A. -E.; Krause, R.; Zimprich, F.; Sander, T.; Neubauer, B. A.; May, P.; Lerche, H.; Nurnberg, P.