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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies.
Lal D, Ruppert AK, Trucks H, Schulz H, de Kovel CG, Kasteleijn-Nolst Trenité D, Sonsma AC, Koeleman BP, Lindhout D, Weber YG, Lerche H, Kapser C, Schankin CJ, Kunz WS, Surges R, Elger CE, Gaus V, Schmitz B, Helbig I, Muhle H, Stephani U, Klein KM, Rosenow F, Neubauer BA, Reinthaler EM, Zimprich F, Feucht M, Møller RS, Hjalgrim H, De Jonghe P, Suls A, Lieb W, Franke A, Strauch K, Gieger C, Schurmann C, Schminke U, Nürnberg P; EPICURE Consortium; Sander T. Lal D, et al. Among authors: neubauer ba. PLoS Genet. 2015 May 7;11(5):e1005226. doi: 10.1371/journal.pgen.1005226. eCollection 2015 May. PLoS Genet. 2015. PMID: 25950944 Free PMC article.
Neuroborreliosis and isolated trochlear palsy.
Müller D, Neubauer BA, Waltz S, Stephani U. Müller D, et al. Among authors: neubauer ba. Eur J Paediatr Neurol. 1998;2(5):275-6. doi: 10.1016/s1090-3798(98)80042-1. Eur J Paediatr Neurol. 1998. PMID: 10726831
Genetics of photosensitivity (photoparoxysmal response): a review.
Stephani U, Tauer U, Koeleman B, Pinto D, Neubauer BA, Lindhout D. Stephani U, et al. Among authors: neubauer ba. Epilepsia. 2004;45 Suppl 1:19-23. doi: 10.1111/j.0013-9580.2004.451008.x. Epilepsia. 2004. PMID: 14706040 Free article. Review.
Photosensitivity: genetics and clinical significance.
Neubauer BA, Waltz S, Grothe M, Hahn A, Tuxhorn I, Sander T, Kurlemann G, Stephani U. Neubauer BA, et al. Adv Neurol. 2005;95:217-26. Adv Neurol. 2005. PMID: 15508925 No abstract available.
142 results