Scheffer IE - Search Results

1

Classification as autonomic versus sensory seizures.

Fisher RS, Cross H, D'Souza C, French JA, Haut S, Higurashi N, Hirsch E, Jansen FE, Peltola J, Moshe SL, Perucca E, Lagae L, Roulet-Perez E, Schulze-Bonhage A, Scheffer IE, Somerville E, Sperling MR, Wiebe S, Yacubian EM, Zuberi S. Fisher RS, et al. Among authors: scheffer ie. Epilepsia. 2019 Sep;60(9):2003-2005. doi: 10.1111/epi.16308. Epub 2019 Jul 29. Epilepsia. 2019. PMID: 31353460 No abstract available.

2

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: scheffer ie. Epilepsia. 2001 Jul;42(7):837-44. doi: 10.1046/j.1528-1157.2001.042007837.x. Epilepsia. 2001. PMID: 11488881 Free article.

3

Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy.

McLellan A, Phillips HA, Rittey C, Kirkpatrick M, Mulley JC, Goudie D, Stephenson JB, Tolmie J, Scheffer IE, Berkovic SF, Zuberi SM. McLellan A, et al. Among authors: scheffer ie. Epilepsia. 2003 Apr;44(4):613-7. doi: 10.1046/j.1528-1157.2003.20102.x. Epilepsia. 2003. PMID: 12681012 Free article.

4

Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).

Scheffer IE, Harkin LA, Dibbens LM, Mulley JC, Berkovic SF. Scheffer IE, et al. Epilepsia. 2005;46 Suppl 10:41-7. doi: 10.1111/j.1528-1167.2005.00358.x. Epilepsia. 2005. PMID: 16359471 Free article. Review. No abstract available.

5

Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration.

Vadlamudi L, Kjeldsen MJ, Corey LA, Solaas MH, Friis ML, Pellock JM, Nakken KO, Milne RL, Scheffer IE, Harvey AS, Hopper JL, Berkovic SF. Vadlamudi L, et al. Among authors: scheffer ie. Epilepsia. 2006 Mar;47(3):550-5. doi: 10.1111/j.1528-1167.2006.00466.x. Epilepsia. 2006. PMID: 16529620 Free article.

6

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.

Berkovic SF, Harkin L, McMahon JM, Pelekanos JT, Zuberi SM, Wirrell EC, Gill DS, Iona X, Mulley JC, Scheffer IE. Berkovic SF, et al. Among authors: scheffer ie. Lancet Neurol. 2006 Jun;5(6):488-92. doi: 10.1016/S1474-4422(06)70446-X. Lancet Neurol. 2006. PMID: 16713920

7

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults.

Jansen FE, Sadleir LG, Harkin LA, Vadlamudi L, McMahon JM, Mulley JC, Scheffer IE, Berkovic SF. Jansen FE, et al. Among authors: scheffer ie. Neurology. 2006 Dec 26;67(12):2224-6. doi: 10.1212/01.wnl.0000249312.73155.7d. Neurology. 2006. PMID: 17190949

8

Gene expression analysis in absence epilepsy using a monozygotic twin design.

Helbig I, Matigian NA, Vadlamudi L, Lawrence KM, Bayly MA, Bain SM, Diyagama D, Scheffer IE, Mulley JC, Holloway AJ, Dibbens LM, Berkovic SF, Hayward NK. Helbig I, et al. Among authors: scheffer ie. Epilepsia. 2008 Sep;49(9):1546-54. doi: 10.1111/j.1528-1167.2008.01630.x. Epub 2008 Apr 24. Epilepsia. 2008. PMID: 18435749 Free article.

9

Classification and clinical features of absence epilepsies: how evidence leads to changing concepts.

Scheffer IE, Berg AT. Scheffer IE, et al. Epilepsia. 2008 Dec;49(12):2140-1. doi: 10.1111/j.1528-1167.2008.01904.x. Epilepsia. 2008. PMID: 19049570 Free article. No abstract available.

10

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

Scheffer IE, Zhang YH, Jansen FE, Dibbens L. Scheffer IE, et al. Brain Dev. 2009 May;31(5):394-400. doi: 10.1016/j.braindev.2009.01.001. Epub 2009 Feb 8. Brain Dev. 2009. PMID: 19203856 Review.

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