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Page 1
Genetics of febrile seizure subtypes and syndromes: a twin study.
Eckhaus J, Lawrence KM, Helbig I, Bui M, Vadlamudi L, Hopper JL, Scheffer IE, Berkovic SF. Eckhaus J, et al. Among authors: helbig i. Epilepsy Res. 2013 Jul;105(1-2):103-9. doi: 10.1016/j.eplepsyres.2013.02.011. Epub 2013 Mar 21. Epilepsy Res. 2013. PMID: 23522981
Investigation of GRIN2A in common epilepsy phenotypes.
Lal D, Steinbrücker S, Schubert J, Sander T, Becker F, Weber Y, Lerche H, Thiele H, Krause R, Lehesjoki AE, Nürnberg P, Palotie A, Neubauer BA, Muhle H, Stephani U, Helbig I, Becker AJ, Schoch S, Hansen J, Dorn T, Hohl C, Lüscher N; Epicure consortium; EuroEPINOMICS-CoGIE consortium; von Spiczak S, Lemke JR. Lal D, et al. Among authors: helbig i. Epilepsy Res. 2015 Sep;115:95-9. doi: 10.1016/j.eplepsyres.2015.05.010. Epub 2015 Jun 2. Epilepsy Res. 2015. PMID: 26220384
Primer Part 1-The building blocks of epilepsy genetics.
Helbig I, Heinzen EL, Mefford HC; ILAE Genetics Commission. Helbig I, et al. Epilepsia. 2016 Jun;57(6):861-8. doi: 10.1111/epi.13381. Epub 2016 May 25. Epilepsia. 2016. PMID: 27226047 Free article. Review.
Early mortality in SCN8A-related epilepsies.
Johannesen KM, Gardella E, Scheffer I, Howell K, Smith DM, Helbig I, Møller RS, Rubboli G. Johannesen KM, et al. Among authors: helbig i. Epilepsy Res. 2018 Jul;143:79-81. doi: 10.1016/j.eplepsyres.2018.04.008. Epub 2018 Apr 13. Epilepsy Res. 2018. PMID: 29677576
Current practice in diagnostic genetic testing of the epilepsies.
Krey I, Platzer K, Esterhuizen A, Berkovic SF, Helbig I, Hildebrand MS, Lerche H, Lowenstein D, Møller RS, Poduri A, Sadleir L, Sisodiya SM, Weckhuysen S, Wilmshurst JM, Weber Y, Lemke JR, Berkovic SF, Cross JH, Helbig I, Lerche H, Lowenstein D, Mefford HC, Perucca P, Tan NC, Caglayan H, Helbig K, Singh G, Weber Y, Weckhuysen S. Krey I, et al. Among authors: helbig i, helbig k. Epileptic Disord. 2022 Oct 1;24(5):765-786. doi: 10.1684/epd.2022.1448. Epileptic Disord. 2022. PMID: 35830287 Free PMC article.
300 results