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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, pp. 3160-3178, 141, (11), ISSN 1460-2156,
[Article]

Lemke, Johannes R. and Geider, Kirsten and Helbig, Katherine L. and Heyne, Henrike O. and Schütz, Hannah and Hentschel, Julia and Courage, Carolina and Depienne, Christel and Nava, Caroline and Heron, Delphine and Møller, Rikke S. and Hjalgrim, Helle and Lal, Dennis and Neubauer, Bernd A. and Nürnberg, Peter and Thiele, Holger and Kurlemann, Gerhard and Arnold, Georgianne L. and Bhambhani, Vikas and Bartholdi, Deborah and Pedurupillay, Christeen Ramane J. and Misceo, Doriana and Frengen, Eirik and Strømme, Petter and Dlugos, Dennis J. and Doherty, Emily S. and Bijlsma, Emilia K. and Ruivenkamp, Claudia A. and Hoffer, Mariette J. V. and Goldstein, Amy and Rajan, Deepa S. and Narayanan, Vinodh and Ramsey, Keri and Belnap, Newell and Schrauwen, Isabelle and Richholt, Ryan and Koeleman, Bobby P. C. and Sá, Joaquim and Mendonça, Carla and de Kovel, Carolien G. F. and Weckhuysen, Sarah and Hardies, Katia and De Jonghe, Peter and De Meirleir, Linda and Milh, Mathieu and Badens, Catherine and Lebrun, Marine and Busa, Tiffany and Francannet, Christine and Piton, Amélie and Riesch, Erik and Biskup, Saskia and Vogt, Heinrich and Dorn, Thomas and Helbig, Ingo and Michaud, Jacques L. and Laube, Bodo and Syrbe, Steffen (2016):
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
In: Neurology, pp. 2171-8, 86, (23), ISSN 1526-632X,
[Article]

This list was generated on Sat Nov 16 01:13:23 2019 CET.