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Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes.
Rudolf G, de Bellescize J, de Saint Martin A, Arzimanoglou A, Valenti Hirsch MP, Labalme A, Boulay C, Simonet T, Boland A, Deleuze JF, Nitschké P, Ollivier E, Sanlaville D, Hirsch E, Chelly J, Lesca G. Rudolf G, et al. Eur J Paediatr Neurol. 2020 Jul;27:104-110. doi: 10.1016/j.ejpn.2020.05.003. Epub 2020 May 29. Eur J Paediatr Neurol. 2020. PMID: 32600977
Isolated paroxysmal arousals as focal epilepsy.
Valenti MP, Froelich S, Rudolf G, Thibault A, Chassagnon S, Arzimanoglou A, Hirsch E. Valenti MP, et al. Among authors: rudolf g. Epileptic Disord. 2006 Mar;8(1):45-52. Epileptic Disord. 2006. PMID: 16567325 Free article.
Landau-Kleffner syndrome is not an eponymic badge of ignorance.
Hirsch E, Valenti MP, Rudolf G, Seegmuller C, de Saint Martin A, Maquet P, Wioland N, Metz-Lutz MN, Marescaux C, Arzimanoglou A. Hirsch E, et al. Among authors: rudolf g. Epilepsy Res. 2006 Aug;70 Suppl 1:S239-47. doi: 10.1016/j.eplepsyres.2006.02.010. Epub 2006 Jun 27. Epilepsy Res. 2006. PMID: 16806832 Review.
Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfall.
Carelle-Calmels N, Girard-Lemaire F, Guérin E, Bieth E, Rudolf G, Biancalana V, Pecheur H, Demil H, Schneider T, de Saint-Martin A, Caron O, Legrain M, Gaston V, Flori E. Carelle-Calmels N, et al. Among authors: rudolf g. Eur J Med Genet. 2008 Nov-Dec;51(6):547-57. doi: 10.1016/j.ejmg.2008.07.003. Epub 2008 Jul 22. Eur J Med Genet. 2008. PMID: 18692163
296 results