Výsledky vyhledávání - "Kapser, Claudia"

No Evidence For A Brd2 Promoter Hypermethylation Inblood Leukocytes Of Europeans With Juvenile Myoclonic Epilepsy

Juvenile myoclonic epilepsy (JME) is a common syndrome of genetic generalized epilepsies (GGEs). Linkage and association studies suggest that the gene encoding the bromodomain-containing protein 2 (BRD2) may increase risk of JME. The present methylat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=r39c86a4b39b::d1e8478beea9773dafe4e11f462b448a
https://aperta.ulakbim.gov.tr/record/69915

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Investigation of GRIN2A in common epilepsy phenotypes

Autor: 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

Publikováno v: 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

Recently, mutations and deletions in the GRIN2A gene have been identified to predispose to benign and severe idiopathic focal epilepsies (IFE), revealing a higher incidence of GRIN2A alterations among the more severe phenotypes. This study aimed to e

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

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