Berkovic SF - Search Results

1

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.

Cavalleri GL, Weale ME, Shianna KV, Singh R, Lynch JM, Grinton B, Szoeke C, Murphy K, Kinirons P, O'Rourke D, Ge D, Depondt C, Claeys KG, Pandolfo M, Gumbs C, Walley N, McNamara J, Mulley JC, Linney KN, Sheffield LJ, Radtke RA, Tate SK, Chissoe SL, Gibson RA, Hosford D, Stanton A, Graves TD, Hanna MG, Eriksson K, Kantanen AM, Kalviainen R, O'Brien TJ, Sander JW, Duncan JS, Scheffer IE, Berkovic SF, Wood NW, Doherty CP, Delanty N, Sisodiya SM, Goldstein DB. Cavalleri GL, et al. Among authors: berkovic sf. Lancet Neurol. 2007 Nov;6(11):970-80. doi: 10.1016/S1474-4422(07)70247-8. Lancet Neurol. 2007. PMID: 17913586

2

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Steinlein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, Scheffer IE, Berkovic SF. Steinlein OK, et al. Among authors: berkovic sf. Nat Genet. 1995 Oct;11(2):201-3. doi: 10.1038/ng1095-201. Nat Genet. 1995. PMID: 7550350

3

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. Among authors: berkovic sf. Ann Neurol. 1995 Oct;38(4):633-42. doi: 10.1002/ana.410380412. Ann Neurol. 1995. PMID: 7574460

4

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2.

Phillips HA, Scheffer IE, Berkovic SF, Hollway GE, Sutherland GR, Mulley JC. Phillips HA, et al. Among authors: berkovic sf. Nat Genet. 1995 May;10(1):117-8. doi: 10.1038/ng0595-117. Nat Genet. 1995. PMID: 7647781

5

Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20.

Berkovic SF, Kennerson ML, Howell RA, Scheffer IE, Hwang PA, Nicholson GA. Berkovic SF, et al. Arch Neurol. 1994 Nov;51(11):1125-8. doi: 10.1001/archneur.1994.00540230063014. Arch Neurol. 1994. PMID: 7980108

6

Optimizing the diagnosis of hippocampal sclerosis using MR imaging.

Jackson GD, Berkovic SF, Duncan JS, Connelly A. Jackson GD, et al. Among authors: berkovic sf. AJNR Am J Neuroradiol. 1993 May-Jun;14(3):753-62. AJNR Am J Neuroradiol. 1993. PMID: 8517369 Free PMC article.

7

Plasmapheresis in Rasmussen's encephalitis.

Andrews PI, Dichter MA, Berkovic SF, Newton MR, McNamara JO. Andrews PI, et al. Among authors: berkovic sf. Neurology. 1996 Jan;46(1):242-6. doi: 10.1212/wnl.46.1.242. Neurology. 1996. PMID: 8559385

8

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.

Wallace RH, Berkovic SF, Howell RA, Sutherland GR, Mulley JC. Wallace RH, et al. Among authors: berkovic sf. J Med Genet. 1996 Apr;33(4):308-12. doi: 10.1136/jmg.33.4.308. J Med Genet. 1996. PMID: 8730286 Free PMC article.

9

The first gene for an idiopathic epilepsy: a fruitful collaboration of Australian clinical research and molecular genetics.

Berkovic SF, Mulley JC. Berkovic SF, et al. Aust N Z J Med. 1996 Apr;26(2):154-6. doi: 10.1111/j.1445-5994.1996.tb00877.x. Aust N Z J Med. 1996. PMID: 8744611 Review. No abstract available.

10

Familial temporal lobe epilepsy: a common disorder identified in twins.

Berkovic SF, McIntosh A, Howell RA, Mitchell A, Sheffield LJ, Hopper JL. Berkovic SF, et al. Ann Neurol. 1996 Aug;40(2):227-35. doi: 10.1002/ana.410400214. Ann Neurol. 1996. PMID: 8773604

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