المؤلفون: Møller, Rikke S, Weber, Yvonne G, Klitten, Laura L, Trucks, Holger, Muhle, Hiltrud, Kunz, Wolfram S, Mefford, Heather C, Franke, Andre, Kautza, Monika, Wolf, Peter, Dennig, Dieter, Schreiber, Stefan, Rückert, Ina-Maria, Wichmann, H-Erich, Ernst, Jan P, Schurmann, Claudia, Grabe, Hans J, Tommerup, Niels, Stephani, Ulrich, Lerche, Holger, Hjalgrim, Helle, Helbig, Ingo, Sander, Thomas

المصدر: Møller , R S , Weber , Y G , Klitten , L L , Trucks , H , Muhle , H , Kunz , W S , Mefford , H C , Franke , A , Kautza , M , Wolf , P , Dennig , D , Schreiber , S , Rückert , I-M , Wichmann , H-E , Ernst , J P , Schurmann , C , Grabe , H J , Tommerup , N , Stephani , U , Lerche , H , Hjalgrim , H , Helbig , I , Sander , T & ....

مصطلحات موضوعية: Adult, Age of Onset, Anticonvulsants, Case-Control Studies, Cell Adhesion Molecules, Neuronal, DNA Copy Number Variations, Electroencephalography, Epilepsy, Generalized, Exons, Family, Female, Fructose, Gene Deletion, Genotype, Humans, Infant, Male, Microarray Analysis, Middle Aged, Nerve Tissue Proteins, Neuropsychological Tests, Odds Ratio, Pedigree, Triazines, Valproic Acid

الإتاحة: https://doi.org/10.1111/epi.12078Test
https://curis.ku.dk/portal/da/publications/exondisrupting-deletions-of-nrxn1-in-idiopathicTest-generalized-epilepsy(0a401632-41f9-4d2d-8c00-8b34369b7ca9).html

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 ....

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

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/8a0c0fe6-8b99-428b-a630-fa94af64e271Test

الإتاحة: https://doi.org/10.1111/j.1528-1167.2011.03379.xTest
https://portal.findresearcher.sdu.dk/da/publications/8a0c0fe6-8b99-428b-a630-fa94af64e271Test

المؤلفون: de Kovel, Carolien G F, Trucks, Holger, Helbig, Ingo, Mefford, Heather C, Baker, Carl, Leu, Costin, Kluck, Christian, Muhle, Hiltrud, von Spiczak, Sarah, Ostertag, Philipp, Obermeier, Tanja, Kleefuss-Lie, Ailing A, Hallmann, Kerstin, Steffens, Michael, Gaus, Verena, Klein, Karl M, Hamer, Hajo M, Rosenow, Felix, Brilstra, Eva H, Trenité, Dorothée Kasteleijn-Nolst, Swinkels, Marielle E M, Weber, Yvonne G, Unterberger, Iris, Zimprich, Fritz, Urak, Lydia, Feucht, Martha, Fuchs, Karoline, Møller, Rikke S, Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Rückert, Ina-Maria, Wichmann, Heinz-Erich, Franke, Andre, Schreiber, Stefan, Nürnberg, Peter, Elger, Christian E, Lerche, Holger, Stephani, Ulrich, Koeleman, Bobby P C, Lindhout, Dick, Eichler, Evan E, Sander, Thomas

المصدر: de Kovel , C G F , Trucks , H , Helbig , I , Mefford , H C , Baker , C , Leu , C , Kluck , C , Muhle , H , von Spiczak , S , Ostertag , P , Obermeier , T , Kleefuss-Lie , A A , Hallmann , K , Steffens , M , Gaus , V , Klein , K M , Hamer , H M , Rosenow , F , Brilstra , E H , Trenité , D K-N , Swinkels , M E M , Weber , Y ....

مصطلحات موضوعية: Adolescent, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 15, Pair 16, Cohort Studies, Epilepsy, Generalized, Female, Genetic Predisposition to Disease, Humans, Male, Pedigree, Young Adult

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/1c598aa3-9bb8-4acb-9795-a3eff304b0d4Test

الإتاحة: https://doi.org/10.1093/brain/awp262Test
https://portal.findresearcher.sdu.dk/da/publications/1c598aa3-9bb8-4acb-9795-a3eff304b0d4Test

المؤلفون: de Kovel, Carolien G F, Trucks, Holger, Helbig, Ingo, Mefford, Heather C, Baker, Carl, Leu, Costin, Kluck, Christian, Muhle, Hiltrud, von Spiczak, Sarah, Ostertag, Philipp, Obermeier, Tanja, Kleefuss-Lie, Ailing A, Hallmann, Kerstin, Steffens, Michael, Gaus, Verena, Klein, Karl M, Hamer, Hajo M, Rosenow, Felix, Brilstra, Eva H, Trenité, Dorothée Kasteleijn-Nolst, Swinkels, Marielle E M, Weber, Yvonne G, Unterberger, Iris, Zimprich, Fritz, Urak, Lydia, Feucht, Martha, Fuchs, Karoline, Møller, Rikke S, Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Rückert, Ina-Maria, Wichmann, Heinz-Erich, Franke, Andre, Schreiber, Stefan, Nürnberg, Peter, Elger, Christian E, Lerche, Holger, Stephani, Ulrich, Koeleman, Bobby P C, Lindhout, Dick, Eichler, Evan E, Sander, Thomas

المصدر: de Kovel , C G F , Trucks , H , Helbig , I , Mefford , H C , Baker , C , Leu , C , Kluck , C , Muhle , H , von Spiczak , S , Ostertag , P , Obermeier , T , Kleefuss-Lie , A A , Hallmann , K , Steffens , M , Gaus , V , Klein , K M , Hamer , H M , Rosenow , F , Brilstra , E H , Trenité , D K-N , Swinkels , M E M , Weber , Y ....

مصطلحات موضوعية: Adolescent, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 15, Pair 16, Cohort Studies, Epilepsy, Generalized, Female, Genetic Predisposition to Disease, Humans, Male, Pedigree, Young Adult

الإتاحة: https://doi.org/10.1093/brain/awp262Test
https://curis.ku.dk/portal/da/publications/recurrent-microdeletions-at-15q112-and-16p1311-predispose-to-idiopathicTest-generalized-epilepsies(717fad95-f2ca-466b-89ca-dd8257644da2).html