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243 results

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Page 1
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.
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.
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.
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.
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
Marini C, Scheffer IE, Nabbout R, Mei D, Cox K, Dibbens LM, McMahon JM, Iona X, Carpintero RS, Elia M, Cilio MR, Specchio N, Giordano L, Striano P, Gennaro E, Cross JH, Kivity S, Neufeld MY, Afawi Z, Andermann E, Keene D, Dulac O, Zara F, Berkovic SF, Guerrini R, Mulley JC. Marini C, et al. Among authors: andermann e. Epilepsia. 2009 Jul;50(7):1670-8. doi: 10.1111/j.1528-1167.2009.02013.x. Epub 2009 Mar 12. Epilepsia. 2009. PMID: 19400878 Free article.
A life in epilepsy.
Andermann E, Andermann F. Andermann E, et al. Among authors: andermann f. Epilepsia. 2010 Feb;51 Suppl 1:101-3. doi: 10.1111/j.1528-1167.2009.02462.x. Epilepsia. 2010. PMID: 20331732 Free article. No abstract available.
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
Mulley JC, Hodgson B, McMahon JM, Iona X, Bellows S, Mullen SA, Farrell K, Mackay M, Sadleir L, Bleasel A, Gill D, Webster R, Wirrell EC, Harbord M, Sisodiya S, Andermann E, Kivity S, Berkovic SF, Scheffer IE, Dibbens LM. Mulley JC, et al. Among authors: andermann e. Epilepsia. 2013 Sep;54(9):e122-6. doi: 10.1111/epi.12323. Epub 2013 Jul 29. Epilepsia. 2013. PMID: 23895530 Free article.
243 results