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243 results

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Page 1
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
Berkovic SF, Serratosa JM, Phillips HA, Xiong L, Andermann E, Díaz-Otero F, Gómez-Garre P, Martín M, Fernández-Bullido Y, Andermann F, Lopes-Cendes I, Dubeau F, Desbiens R, Scheffer IE, Wallace RH, Mulley JC, Pandolfo M. Berkovic SF, et al. Among authors: andermann e, andermann f. Epilepsia. 2004 Sep;45(9):1054-60. doi: 10.1111/j.0013-9580.2004.30502.x. Epilepsia. 2004. PMID: 15329069 Free article.
Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
Dibbens LM, de Vries B, Donatello S, Heron SE, Hodgson BL, Chintawar S, Crompton DE, Hughes JN, Bellows ST, Klein KM, Callenbach PM, Corbett MA, Gardner AE, Kivity S, Iona X, Regan BM, Weller CM, Crimmins D, O'Brien TJ, Guerrero-López R, Mulley JC, Dubeau F, Licchetta L, Bisulli F, Cossette P, Thomas PQ, Gecz J, Serratosa J, Brouwer OF, Andermann F, Andermann E, van den Maagdenberg AM, Pandolfo M, Berkovic SF, Scheffer IE. Dibbens LM, et al. Among authors: andermann e, andermann f. Nat Genet. 2013 May;45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31. Nat Genet. 2013. PMID: 23542697
Progressive myoclonus epilepsies: clinical and genetic aspects.
Berkovic SF, Cochius J, Andermann E, Andermann F. Berkovic SF, et al. Among authors: andermann e, andermann f. Epilepsia. 1993;34 Suppl 3:S19-30. doi: 10.1111/j.1528-1167.1993.tb06256.x. Epilepsia. 1993. PMID: 8500430 Review.
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
Singh R, Andermann E, Whitehouse WP, Harvey AS, Keene DL, Seni MH, Crossland KM, Andermann F, Berkovic SF, Scheffer IE. Singh R, et al. Among authors: andermann e, andermann f. Epilepsia. 2001 Jul;42(7):837-44. doi: 10.1046/j.1528-1157.2001.042007837.x. Epilepsia. 2001. PMID: 11488881 Free article.
Outcome of surgical treatment in familial mesial temporal lobe epilepsy.
Kobayashi E, D'Agostino MD, Lopes-Cendes I, Andermann E, Dubeau F, Guerreiro CA, Schenka AA, Queiroz LS, Olivier A, Cendes F, Andermann F. Kobayashi E, et al. Among authors: andermann e, andermann f. Epilepsia. 2003 Aug;44(8):1080-4. doi: 10.1046/j.1528-1157.2003.06503.x. Epilepsia. 2003. PMID: 12887440 Free article.
Biparental inheritance in idiopathic generalized epilepsy.
Jansen AC, Andermann E, Andermann F. Jansen AC, et al. Among authors: andermann e, andermann f. Epilepsia. 2004 Oct;45(10):1294-5. doi: 10.1111/j.0013-9580.2004.22004.x. Epilepsia. 2004. PMID: 15461686 Free article. No abstract available.
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis.
Al-Asmi A, Jansen AC, Badhwar A, Dubeau F, Tampieri D, Shustik C, Mercho S, Savard G, Dobson-Stone C, Monaco AP, Andermann F, Andermann E. Al-Asmi A, et al. Among authors: andermann e, andermann f. Epilepsia. 2005 Aug;46(8):1256-63. doi: 10.1111/j.1528-1167.2005.65804.x. Epilepsia. 2005. PMID: 16060937 Free article.
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis.
Berkovic SF, Dibbens LM, Oshlack A, Silver JD, Katerelos M, Vears DF, Lüllmann-Rauch R, Blanz J, Zhang KW, Stankovich J, Kalnins RM, Dowling JP, Andermann E, Andermann F, Faldini E, D'Hooge R, Vadlamudi L, Macdonell RA, Hodgson BL, Bayly MA, Savige J, Mulley JC, Smyth GK, Power DA, Saftig P, Bahlo M. Berkovic SF, et al. Among authors: andermann e, andermann f. Am J Hum Genet. 2008 Mar;82(3):673-84. doi: 10.1016/j.ajhg.2007.12.019. Epub 2008 Feb 28. Am J Hum Genet. 2008. PMID: 18308289 Free PMC article.
243 results