Scheffer IE - Search Results

1

Focal epilepsy in SCN1A-mutation carrying patients: is there a role for epilepsy surgery?

Vezyroglou A, Varadkar S, Bast T, Hirsch E, Strobl K, Harvey AS; Epilepsy Surgery in SCN1A Study Group; Scheffer IE, Sisodiya SM, Cross JH. Vezyroglou A, et al. Among authors: scheffer ie. Dev Med Child Neurol. 2020 Nov;62(11):1331-1335. doi: 10.1111/dmcn.14588. Epub 2020 Jun 15. Dev Med Child Neurol. 2020. PMID: 32538476 Free article.

2

Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation.

Scheffer IE, Jones L, Pozzebon M, Howell RA, Saling MM, Berkovic SF. Scheffer IE, et al. Ann Neurol. 1995 Oct;38(4):633-42. doi: 10.1002/ana.410380412. Ann Neurol. 1995. PMID: 7574460

3

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.

Scheffer IE, Berkovic SF. Scheffer IE, et al. Brain. 1997 Mar;120 ( Pt 3):479-90. doi: 10.1093/brain/120.3.479. Brain. 1997. PMID: 9126059

4

Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variation.

Hayman M, Scheffer IE, Chinvarun Y, Berlangieri SU, Berkovic SF. Hayman M, et al. Among authors: scheffer ie. Neurology. 1997 Oct;49(4):969-75. doi: 10.1212/wnl.49.4.969. Neurology. 1997. PMID: 9339675

5

Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2.

Scheffer IE, Phillips HA, O'Brien CE, Saling MM, Wrennall JA, Wallace RH, Mulley JC, Berkovic SF. Scheffer IE, et al. Ann Neurol. 1998 Dec;44(6):890-9. doi: 10.1002/ana.410440607. Ann Neurol. 1998. PMID: 9851433

6

Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.

Singh R, Scheffer IE, Crossland K, Berkovic SF. Singh R, et al. Among authors: scheffer ie. Ann Neurol. 1999 Jan;45(1):75-81. doi: 10.1002/1531-8249(199901)45:1<75::aid-art13>3.0.co;2-w. Ann Neurol. 1999. PMID: 9894880

7

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.

8

Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.

Wallace RH, Scheffer IE, Parasivam G, Barnett S, Wallace GB, Sutherland GR, Berkovic SF, Mulley JC. Wallace RH, et al. Among authors: scheffer ie. Neurology. 2002 May 14;58(9):1426-9. doi: 10.1212/wnl.58.9.1426. Neurology. 2002. PMID: 12011299

9

X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX.

Scheffer IE, Wallace RH, Phillips FL, Hewson P, Reardon K, Parasivam G, Stromme P, Berkovic SF, Gecz J, Mulley JC. Scheffer IE, et al. Neurology. 2002 Aug 13;59(3):348-56. doi: 10.1212/wnl.59.3.348. Neurology. 2002. PMID: 12177367

10

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.

Marini C, Harkin LA, Wallace RH, Mulley JC, Scheffer IE, Berkovic SF. Marini C, et al. Among authors: scheffer ie. Brain. 2003 Jan;126(Pt 1):230-40. doi: 10.1093/brain/awg018. Brain. 2003. PMID: 12477709

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