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Number of items: 2.


Marini, Carla and Porro, Alessandro and Rastetter, Agnès and Dalle, Carine and Rivolta, Ilaria and Bauer, Daniel and Oegema, Renske and Nava, Caroline and Parrini, Elena and Mei, Davide and Mercer, Catherine and Dhamija, Radhika and Chambers, Chelsea and Coubes, Christine and Thévenon, Julien and Kuentz, Paul and Julia, Sophie and Pasquier, Laurent and Dubourg, Christèle and Carré, Wilfrid and Rosati, Anna and Melani, Federico and Pisano, Tiziana and Giardino, Maria and Innes, A Micheil and Alembik, Yves and Scheidecker, Sophie and Santos, Manuela and Figueiroa, Sonia and Garrido, Cristina and Fusco, Carlo and Frattini, Daniele and Spagnoli, Carlotta and Binda, Anna and Granata, Tiziana and Ragona, Francesca and Freri, Elena and Franceschetti, Silvana and Canafoglia, Laura and Castellotti, Barbara and Gellera, Cinzia and Milanesi, Raffaella and Mancardi, Maria Margherita and Clark, Damien R. and Kok, Fernando and Helbig, Katherine L. and Ichikawa, Shoji and Sadler, Laurie and Neupauerová, Jana and Laššuthova, Petra and Šterbová, Katalin and Laridon, Annick and Brilstra, Eva and Koeleman, Bobby and Lemke, Johannes R. and Zara, Federico and Striano, Pasquale and Soblet, Julie and Smits, Guillaume and Deconinck, Nicolas and Barbuti, Andrea and DiFrancesco, Dario and LeGuern, Eric and Guerrini, Renzo and Santoro, Bina and Hamacher, Kay and Thiel, Gerhard and Moroni, Anna and DiFrancesco, Jacopo C. and Depienne, Christel (2018):
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond.
In: Brain : a journal of neurology, 141 (11), pp. 3160-3178, ISSN 1460-2156,


Platzer, Konrad and Yuan, Hongjie and Schütz, Hannah and Winschel, Alexander and Chen, Wenjuan and Hu, Chun and Kusumoto, Hirofumi and Heyne, Henrike O. and Helbig, Katherine L. and Tang, Sha and Willing, Marcia C. and Tinkle, Brad T. and Adams, Darius J. and Depienne, Christel and Keren, Boris and Mignot, Cyril and Frengen, Eirik and Strømme, Petter and Biskup, Saskia and Döcker, Dennis and Strom, Tim M. and Mefford, Heather C. and Myers, Candace T. and Muir, Alison M. and LaCroix, Amy and Sadleir, Lynette and Scheffer, Ingrid E. and Brilstra, Eva and van Haelst, Mieke M. and van der Smagt, Jasper J. and Bok, Levinus A. and Møller, Rikke S. and Jensen, Uffe B. and Millichap, John J. and Berg, Anne T. and Goldberg, Ethan M. and De Bie, Isabelle and Fox, Stephanie and Major, Philippe and Jones, Julie R. and Zackai, Elaine H. and Abou Jamra, Rami and Rolfs, Arndt and Leventer, Richard J. and Lawson, John A. and Roscioli, Tony and Jansen, Floor E. and Ranza, Emmanuelle and Korff, Christian M. and Lehesjoki, Anna-Elina and Courage, Carolina and Linnankivi, Tarja and Smith, Douglas R. and Stanley, Christine and Mintz, Mark and McKnight, Dianalee and Decker, Amy and Tan, Wen-Hann and Tarnopolsky, Mark A. and Brady, Lauren I. and Wolff, Markus and Dondit, Lutz and Pedro, Helio F. and Parisotto, Sarah E. and Jones, Kelly L. and Patel, Anup D. and Franz, David N. and Vanzo, Rena and Marco, Elysa and Ranells, Judith D. and Di Donato, Nataliya and Dobyns, William B. and Laube, Bodo and Traynelis, Stephen F. and Lemke, Johannes R. (2017):
GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
In: Journal of medical genetics, 54 (7), pp. 460-470, ISSN 1468-6244,

This list was generated on Sat May 23 01:40:53 2020 CEST.