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Page 1
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
Sander T, Windemuth C, Schulz H, Saar K, Gennaro E, Bianchi A, Zara F, Bulteau C, Kaminska A, Ville D, Cieuta C, Prud'homme JF, Dulac O, Bate L, Gardiner RM, de Haan GJ, Janssen GA, Witte J, Halley DJ, Lindhout D, Wienker TF, Janz D; European Consortium on the Genetics of Idiopathic Generalized Epilepsy. Sander T, et al. Among authors: ville d. Am J Med Genet. 2002 Aug 8;114(6):673-8. doi: 10.1002/ajmg.10645. Am J Med Genet. 2002. PMID: 12210286
Electroclinical features and phenotypic differences in adenylosuccinate lyase deficiency: Long-term follow-up of seven patients from four families and appraisal of the literature.
Cutillo G, Masnada S, Lesca G, Ville D, Accorsi P, Giordano L, Pichiecchio A, Valente M, Borrelli P, Ferraro OE, Veggiotti P. Cutillo G, et al. Among authors: ville d. Epilepsia Open. 2024 Feb;9(1):106-121. doi: 10.1002/epi4.12837. Epub 2023 Nov 27. Epilepsia Open. 2024. PMID: 37842880 Free PMC article.
Genome search for susceptibility loci of common idiopathic generalised epilepsies.
Sander T, Schulz H, Saar K, Gennaro E, Riggio MC, Bianchi A, Zara F, Luna D, Bulteau C, Kaminska A, Ville D, Cieuta C, Picard F, Prud'homme JF, Bate L, Sundquist A, Gardiner RM, Janssen GA, de Haan GJ, Kasteleijn-Nolst-Trenité DG, Bader A, Lindhout D, Riess O, Wienker TF, Janz D, Reis A. Sander T, et al. Among authors: ville d. Hum Mol Genet. 2000 Jun 12;9(10):1465-72. doi: 10.1093/hmg/9.10.1465. Hum Mol Genet. 2000. PMID: 10888596
Functional imaging in the work-up of childhood epilepsy.
Hertz-Pannier L, Chiron C, Véra P, Van de Morteele PF, Kaminska A, Bourgeois M, Hollo A, Ville D, Cieuta C, Dulac O, Brunelle F, LeBihan D. Hertz-Pannier L, et al. Among authors: ville d. Childs Nerv Syst. 2001 Apr;17(4-5):223-8. doi: 10.1007/s003810000390. Childs Nerv Syst. 2001. PMID: 11398941 Review.
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures.
Windemuth C, Schulz H, Saar K, Gennaro E, Bianchi A, Zara F, Bulteau C, Kaminska A, Ville D, Cieuta C, Nabbout-Tarantino R, Prud'homme JF, Dulac O, Bate L, Gardiner RM, Lindhout D, Wienker TF, Janz D, Sander T; European Consortium on the Genetics of Idiopathic Generalized Epilepsy. Windemuth C, et al. Among authors: ville d. Epilepsy Res. 2002 Sep;51(1-2):23-9. doi: 10.1016/s0920-1211(02)00097-9. Epilepsy Res. 2002. PMID: 12350381
[Epilepsy in chromosome aberrations].
Bahi-Buisson N, Ville D, Eisermann M, Plouin P, Kaminska A, Chiron C. Bahi-Buisson N, et al. Among authors: ville d. Arch Pediatr. 2005 Apr;12(4):449-58. doi: 10.1016/j.arcped.2004.12.016. Arch Pediatr. 2005. PMID: 15808438 Review. French.
Early pattern of epilepsy in the ring chromosome 20 syndrome.
Ville D, Kaminska A, Bahi-Buisson N, Biraben A, Plouin P, Telvi L, Dulac O, Chiron C. Ville D, et al. Epilepsia. 2006 Mar;47(3):543-9. doi: 10.1111/j.1528-1167.2006.00465.x. Epilepsia. 2006. PMID: 16529619 Free article.
421 results