المؤلفون: Hoffmann, Judith M., Elger, Christian E., Kleefuss-Lie, Ailing A.

المصدر: In Seizure: European Journal of Epilepsy 2010 19(4):217-221

المؤلفون: Hoffmann, Judith M., Elger, Christian E., Kleefuss-Lie, Ailing A.

المصدر: In Epilepsy Research December 2009 87(2-3):144-147

المؤلفون: Hoffmann, Judith M., Elger, Christian E., Kleefuss-Lie, Ailing A.

المصدر: In Epilepsy and Behavior 2008 13(4):634-636

المؤلفون: Reinthaler, Eva M., Lal, Dennis, Lebon, Sebastien, Hildebrand, Michael S., Dahl, Hans-Henrik M., Regan, Brigid M., Feucht, Martha, Steinböck, Hannelore, Neophytou, Birgit, Ronen, Gabriel M., Roche, Laurian, Gruber-Sedlmayr, Ursula, Geldner, Julia, Haberlandt, Edda, Hoffmann, Per, Herms, Stefan, Gieger, Christian, Waldenberger, Melanie, Franke, Andre, Wittig, Michael, Schoch, Susanne, Becker, Albert J., Hahn, Andreas, Männik, Katrin, Toliat, Mohammad R., Winterer, Georg, Lerche, Holger, Nürnberg, Peter, Mefford, Heather, Scheffer, Ingrid E., Berkovic, Samuel F., Beckmann, Jacques S., Sander, Thomas, Jacquemont, Sebastien, Reymond, Alexandre, Zimprich, Fritz, Neubauer, Bernd A., Neubauer, Bernd, Mörzinger, Martina, Suls, Arvid, Weckhuysen, Sarah, Claes, Lieve, Deprez, Liesbet, Smets, Katrien, Van Dyck, Tine, Deconinck, Tine, De Jonghe, Peter, Møller, Rikke S., Klitten, Laura L., Hjalgrim, Helle, Campus, Kiel, Helbig, Ingo, Muhle, Hiltrud, Ostertag, Philipp, von Spiczak, Sarah, Stephani, Ulrich, Trucks, Holger, Elger, Christian E., Kleefuß-Lie, Ailing A., Kunz, Wolfram S., Surges, Rainer, Gaus, Verena, Janz, Dieter, Schmitz, Bettina, Rosenow, Felix, Klein, Karl Martin, Reif, Philipp S., Oertel, Wolfgang H., Hamer, Hajo M., Becker, Felicitas, Weber, Yvonne, Koeleman, Bobby P.C., de Kovel, Carolien, Lindhout, Dick, Ameil, Agnès, Andrieux, Joris, Bouquillon, Sonia, Boute, Odile, de Flandre, Jeanne, Cuisset, Jean Marie, Cuvellier, Jean-Christophe, Salengro, Roger, David, Albert, de Vries, Bert, Delrue, Marie-Ange, Doco-Fenzy, Martine, Fernandez, Bridget A., Heron, Delphine, Keren, Boris, Lebel, Robert, Leheup, Bruno, Lewis, Suzanne, Mencarelli, Maria Antonietta, Mignot, Cyril, Minet, Jean-Claude, Moerman, Alexandre, Morice-Picard, Fanny, Mucciolo, Mafalda, Ounap, Katrin, Pasquier, Laurent, Petit, Florence, Ragona, Francesca, Rajcan-Separovic, Evica, Renieri, Alessandra, Rieubland, Claudine, Sanlaville, Damien, Sarrazin, Elisabeth, Shen, Yiping, van Haelst, Mieke, Silfhout, Anneke Vulto-van

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_______805::e74c7afdb66a96703aaca984fd8659ca
http://doc.rero.ch/record/291490/files/ddu306.pdf

المؤلفون: Lal, Dennis, Steinbrücker, Sandra, Schubert, Julian, Sander, Thomas, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Thiele, Holger, Krause, Roland, Lehesjoki, Anna Elina, Nürnberg, Peter, Palotie, Aarno, Neubauer, Bernd A., Muhle, Hiltrud, Stephani, Ulrich, Helbig, Ingo, Becker, Albert J., Schoch, Susanne, Hansen, Jörg, Dorn, Thomas, Hohl, Christin, Lüscher, Nicole, von Spiczak, Sarah, Lemke, Johannes R., Zimprich, Fritz, Feucht, Martha, Suls, Arvid, Weckhuysen, Sarah, Claes, Lieve, Deprez, Liesbet, Smets, Katrien, Dyck, Tine Van, Deconinck, Tine, De Jonghe, Peter, Møller, Rikke S., Klitten, Laura L., Hjalgrim, Helle, Campus, Kiel, Ostertag, Philipp, Trucks, Hol ger, Elger, Christian E., Kleefuß-Lie, Ailing A., Kunz, Wolfram S., Surges, Rainer, Gaus, Verena, Janz, Dieter, Schmitz, Bettina, Klein, Karl Martin, Reif, Philipp S., Oertel, Wolfgang H., Hamer, Hajo M., Rosenow, Felix, Kapser, Claudia, Schankin, Christoph J., Koeleman, Bobby P C, de Kovel, Carolien, Lindhout, Dick, Reinthaler, Eva M., Steinboeck, Hannelore, Neo-phytou, Birgit, Geldner, Julia, Gruber-Sedlmayr, Ursula, Haberlandt, Edda, Ronen, Gabriel M., Altmueller, Janine, Nuernberg, Peter, Neubauer, Bernd, Sirén, Auli

المساهمون: Neuroscience Center, Research Programs Unit, Department of Medical and Clinical Genetics, Anna-Elina Lehesjoki / Principal Investigator, Research Programme for Molecular Neurology, Medicum, Institute for Molecular Medicine Finland, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders, Suls, Arvid, Weckhuysen, Sarah, Claes, Godelieve, Deprez, Liesbet, Smets, Katrien, Van Dyck, Tine, Deconinck, Tine, De Jonghe, Peter, Epicure Consortium, EuroEPINOMICS-CoGIE Consortium

المصدر: Epilepsy Research
Epilepsy Research, 115, 95. Elsevier
Epilepsy research
Lal, D, Steinbrücker, S, Schubert, J, Sander, T, Becker, F, Weber, Y, Lerche, H, Thiele, H, Krause, R, Lehesjoki, A-E, Nürnberg, P, Palotie, A, Neubauer, B A, Muhle, H, Stephani, U, Helbig, I, Becker, A J, Schoch, S, Hansen, J, Dorn, T, Hohl, C, Lüscher, N, von Spiczak, S, Lemke, J R, EPICURE Consortium, Møller, R S, Line Klitten, L & Hjalgrim, H 2015, ' Investigation of GRIN2A in common epilepsy phenotypes ', Epilepsy Research, vol. 115, pp. 95-99 . https://doi.org/10.1016/j.eplepsyres.2015.05.010

مصطلحات موضوعية: Pathology, Idiopathic generalized epilepsy, DEPDC5, Genotyping Techniques, CHILDHOOD, Bioinformatics, GRIN2A, 3124 Neurology and psychiatry, Cohort Studies, Epilepsy, 0302 clinical medicine, Databases, Genetic, Medicine, Copy-number variation, TERMINOLOGY, Non-U.S. Gov't, Temporal lobe epilepsy, FOCAL EPILEPSIES, Exome sequencing, Sanger sequencing, 0303 health sciences, Research Support, Non-U.S. Gov't, Phenotype, Neurology, symbols, Epilepsy, Generalized, medicine.medical_specialty, DNA Copy Number Variations, DISORDERS, Clinical Neurology, Research Support, Receptors, N-Methyl-D-Aspartate, CLASSIFICATION, Juvenile Absence Epilepsy, 03 medical and health sciences, symbols.namesake, Journal Article, Humans, Biology, 030304 developmental biology, business.industry, MUTATIONS, Copy number variation, 3112 Neurosciences, INCLUDING GRIN2A, medicine.disease, DELETIONS, Epilepsy, Absence, Epilepsy, Temporal Lobe, Epilepsy syndromes, Mutation, SEIZURES, Neurology (clinical), Human medicine, business, 030217 neurology & neurosurgery

وصف الملف: image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40230a95e916659f604965c70b8b6b8e
https://dspace.library.uu.nl/handle/1874/335854

المؤلفون: Becker, Felicitas, Reid, Christopher A., Hallmann, Kerstin, Tae, Han‐Shen, Phillips, A. Marie, Teodorescu, Georgeta, Weber, Yvonne G., Kleefuss‐Lie, Ailing, Elger, Christian, Perez‐Reyes, Edward, Petrou, Steven, Kunz, Wolfram S., Lerche, Holger, Maljevic, Snezana

المصدر: Epilepsia Open; 2017, Vol. 2 Issue 3, p334-342, 9p

مصطلحات موضوعية: EPILEPSY, HYPERPOLARIZATION (Cytology), TEMPORAL lobe epilepsy

المؤلفون: 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

المصدر: Leu, C, de Kovel, C G F, Zara, F, Striano, P, Pezzella, M, Robbiano, A, Bianchi, A, Bisulli, F, Coppola, A, Giallonardo, A T, Beccaria, F, Trenité, D K-N, Lindhout, D, Gaus, V, Schmitz, B, Janz, D, Weber, Y G, Becker, F, Lerche, H, Kleefuss-Lie, A A, Hallman, K, Kunz, W S, Elger, C E, Muhle, H, Stephani, U, Møller, R S, Hjalgrim, H, Mullen, S, Scheffer, I E, Berkovic, S F, Everett, K V, Gardiner, M R, Marini, C, Guerrini, R, Lehesjoki, A-E, Siren, A, Nabbout, R, Baulac, S, Leguern, E, Serratosa, J M, Rosenow, F, Feucht, M, Unterberger, I, Covanis, A, Suls, A, Weckhuysen, S, Kaneva, R, Caglayan, H, Turkdogan, D, Baykan, B & EPICURE Consortium 2012, ' Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies ', Epilepsia, vol. 53, no. 2, pp. 308-318 . https://doi.org/10.1111/j.1528-1167.2011.03379.x

مصطلحات موضوعية: Male, Chromosomes, Human, Pair 13, Genotype, Genetic Linkage, Chromosome Mapping, Pedigree, Phenotype, Genetic Loci, Chromosomes, Human, Pair 2, Humans, Epilepsy, Generalized, Family, Female, Genetic Predisposition to Disease, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3062::ebe6d81bc13280125f07c577bc67a736
https://portal.findresearcher.sdu.dk/da/publications/8a0c0fe6-8b99-428b-a630-fa94af64e271

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