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2,894 results

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Page 1
Nuclear localization of a novel human syntaxin 1B isoform.
Pereira S, Massacrier A, Roll P, Vérine A, Etienne-Grimaldi MC, Poitelon Y, Robaglia-Schlupp A, Jamali S, Roeckel-Trevisiol N, Royer B, Pontarotti P, Lévêque C, Seagar M, Lévy N, Cau P, Szepetowski P. Pereira S, et al. Gene. 2008 Nov 1;423(2):160-71. doi: 10.1016/j.gene.2008.07.010. Epub 2008 Jul 17. Gene. 2008. PMID: 18691641
SRPX2 mutations in disorders of language cortex and cognition.
Roll P, Rudolf G, Pereira S, Royer B, Scheffer IE, Massacrier A, Valenti MP, Roeckel-Trevisiol N, Jamali S, Beclin C, Seegmuller C, Metz-Lutz MN, Lemainque A, Delepine M, Caloustian C, de Saint Martin A, Bruneau N, Depétris D, Mattéi MG, Flori E, Robaglia-Schlupp A, Lévy N, Neubauer BA, Ravid R, Marescaux C, Berkovic SF, Hirsch E, Lathrop M, Cau P, Szepetowski P. Roll P, et al. Among authors: pereira s. Hum Mol Genet. 2006 Apr 1;15(7):1195-207. doi: 10.1093/hmg/ddl035. Epub 2006 Feb 23. Hum Mol Genet. 2006. PMID: 16497722
Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex.
Jamali S, Bartolomei F, Robaglia-Schlupp A, Massacrier A, Peragut JC, Régis J, Dufour H, Ravid R, Roll P, Pereira S, Royer B, Roeckel-Trevisiol N, Fontaine M, Guye M, Boucraut J, Chauvel P, Cau P, Szepetowski P. Jamali S, et al. Among authors: pereira s. Brain. 2006 Mar;129(Pt 3):625-41. doi: 10.1093/brain/awl001. Epub 2006 Jan 6. Brain. 2006. PMID: 16399808
Epilepsy and deletions at chromosome 2q24.
Pereira S, Vieira JP, Cau P, Genton P, Szepetowski P. Pereira S, et al. Am J Med Genet A. 2006 Jun 15;140(12):1354-5. doi: 10.1002/ajmg.a.31299. Am J Med Genet A. 2006. PMID: 16700054 Free article. No abstract available.
2,894 results