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	21.	SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations. [electronic resource] by Usluer, Sunay Salar, Seda Arslan, Mutluay Yiş, Uluç Kara, Bülent Tektürk, Pınar Baykan, Betül Meral, Cihan Türkdoğan, Dilşad Bebek, Nerses Yalçın Çapan, Özlem Gündoğdu Eken, Aslı Çağlayan, S Hande Producer: 20170213 In: Seizure vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures. [electronic resource] by Yalçin, Ozlem Baykan, Betül Ağan, Kadriye Yapici, Zuhal Yalçin, Destina Dizdarer, Gülşen Türkdoğan, Dilşad Ozkara, Ciğdem Unalp, Aycan Uludüz, Derya Gül, Günay Kuşcu, Demet Ayta, Semih Tutkavul, Kemal Comu, Sinan Tatli, Burak Meral, Cihan Bebek, Nerses Cağlayan, Server Hande Producer: 20110714 In: Epilepsia vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	PRRT2 mutations are the major cause of benign familial infantile seizures. [electronic resource] by Schubert, Julian Paravidino, Roberta Becker, Felicitas Berger, Andrea Bebek, Nerses Bianchi, Amedeo Brockmann, Knut Capovilla, Giuseppe Dalla Bernardina, Bernardo Fukuyama, Yukio Hoffmann, Georg F Jurkat-Rott, Karin Anttonen, Anna-Kaisa Kurlemann, Gerhard Lehesjoki, Anna-Elina Lehmann-Horn, Frank Mastrangelo, Massimo Mause, Ulrike Müller, Stephan Neubauer, Bernd Püst, Burkhard Rating, Dietz Robbiano, Angela Ruf, Susanne Schroeder, Christopher Seidel, Andreas Specchio, Nicola Stephani, Ulrich Striano, Pasquale Teichler, Jens Turkdogan, Dilsad Vigevano, Federico Viri, Maurizio Bauer, Peter Zara, Federico Lerche, Holger Weber, Yvonne G Producer: 20130705 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. [electronic resource] by Leu, Costin de Kovel, Carolien G F Zara, Federico Striano, Pasquale Pezzella, Marianna Robbiano, Angela Bianchi, Amedeo Bisulli, Francesca Coppola, Antonietta Giallonardo, Anna Teresa Beccaria, Francesca Trenité, Dorothée Kasteleijn-Nolst Lindhout, Dick Gaus, Verena Schmitz, Bettina Janz, Dieter Weber, Yvonne G Becker, Felicitas Lerche, Holger Kleefuss-Lie, Ailing A Hallman, Kerstin Kunz, Wolfram S Elger, Christian E Muhle, Hiltrud Stephani, Ulrich Møller, Rikke S Hjalgrim, Helle Mullen, Saul Scheffer, Ingrid E Berkovic, Samuel F Everett, Kate V Gardiner, Mark R Marini, Carla Guerrini, Renzo Lehesjoki, Anna-Elina Siren, Auli Nabbout, Rima Baulac, Stephanie Leguern, Eric Serratosa, Jose M Rosenow, Felix Feucht, Martha Unterberger, Iris Covanis, Athanasios Suls, Arvid Weckhuysen, Sarah Kaneva, Radka Caglayan, Hande Turkdogan, Dilsad Baykan, Betul Bebek, Nerses Ozbek, Ugur Hempelmann, Anne Schulz, Herbert Rüschendorf, Franz Trucks, Holger Nürnberg, Peter Avanzini, Giuliano Koeleman, Bobby P C Sander, Thomas Producer: 20120309 In: Epilepsia vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)