Grinton BE - Search Results

1

The non-neurologists' view on epilepsy syndromes classification.

Vears DF, Grinton BE. Vears DF, et al. Among authors: grinton be. Epileptic Disord. 2006 Jun;8(2):160-1. Epileptic Disord. 2006. PMID: 16793580 No abstract available.

2

Liquid serial dilution is inferior to solid media for isolation of cultures representative of the phylum-level diversity of soil bacteria.

Schoenborn L, Yates PS, Grinton BE, Hugenholtz P, Janssen PH. Schoenborn L, et al. Among authors: grinton be. Appl Environ Microbiol. 2004 Jul;70(7):4363-6. doi: 10.1128/AEM.70.7.4363-4366.2004. Appl Environ Microbiol. 2004. PMID: 15240320 Free PMC article.

3

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.

Crompton DE, Scheffer IE, Taylor I, Cook MJ, McKelvie PA, Vears DF, Lawrence KM, McMahon JM, Grinton BE, McIntosh AM, Berkovic SF. Crompton DE, et al. Among authors: grinton be. Brain. 2010 Nov;133(11):3221-31. doi: 10.1093/brain/awq251. Epub 2010 Sep 23. Brain. 2010. PMID: 20864493

4

Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.

Mulley JC, Scheffer IE, Desai T, Bayly MA, Grinton BE, Vears DF, Berkovic SF, Dibbens LM. Mulley JC, et al. Among authors: grinton be. Epilepsia. 2011 Oct;52(10):e139-42. doi: 10.1111/j.1528-1167.2011.03188.x. Epub 2011 Jul 21. Epilepsia. 2011. PMID: 21777232 Free article.

5

Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.

Vears DF, Tsai MH, Sadleir LG, Grinton BE, Lillywhite LM, Carney PW, Harvey AS, Berkovic SF, Scheffer IE. Vears DF, et al. Among authors: grinton be. Epilepsia. 2012 Feb;53(2):319-24. doi: 10.1111/j.1528-1167.2011.03368.x. Epub 2012 Jan 5. Epilepsia. 2012. PMID: 22220564 Free article.

6

Genetic epilepsy with febrile seizures plus: Refining the spectrum.

Zhang YH, Burgess R, Malone JP, Glubb GC, Helbig KL, Vadlamudi L, Kivity S, Afawi Z, Bleasel A, Grattan-Smith P, Grinton BE, Bellows ST, Vears DF, Damiano JA, Goldberg-Stern H, Korczyn AD, Dibbens LM, Ruzzo EK, Hildebrand MS, Berkovic SF, Scheffer IE. Zhang YH, et al. Among authors: grinton be. Neurology. 2017 Sep 19;89(12):1210-1219. doi: 10.1212/WNL.0000000000004384. Epub 2017 Aug 25. Neurology. 2017. PMID: 28842445

7

Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.

Wallace RH, Hodgson BL, Grinton BE, Gardiner RM, Robinson R, Rodriguez-Casero V, Sadleir L, Morgan J, Harkin LA, Dibbens LM, Yamamoto T, Andermann E, Mulley JC, Berkovic SF, Scheffer IE. Wallace RH, et al. Among authors: grinton be. Neurology. 2003 Sep 23;61(6):765-9. doi: 10.1212/01.wnl.0000086379.71183.78. Neurology. 2003. PMID: 14504318

8

The health-related quality of life of childhood epilepsy syndromes.

Sabaz M, Cairns DR, Bleasel AF, Lawson JA, Grinton B, Scheffer IE, Bye AM. Sabaz M, et al. J Paediatr Child Health. 2003 Dec;39(9):690-6. doi: 10.1046/j.1440-1754.2003.00270.x. J Paediatr Child Health. 2003. PMID: 14629502

9

Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.

Richards MC, Heron SE, Spendlove HE, Scheffer IE, Grinton B, Berkovic SF, Mulley JC, Davy A. Richards MC, et al. J Med Genet. 2004 Mar;41(3):e35. doi: 10.1136/jmg.2003.013938. J Med Genet. 2004. PMID: 14985406 Free PMC article. No abstract available.

10

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.

Berkovic SF, Heron SE, Giordano L, Marini C, Guerrini R, Kaplan RE, Gambardella A, Steinlein OK, Grinton BE, Dean JT, Bordo L, Hodgson BL, Yamamoto T, Mulley JC, Zara F, Scheffer IE. Berkovic SF, et al. Among authors: grinton be. Ann Neurol. 2004 Apr;55(4):550-7. doi: 10.1002/ana.20029. Ann Neurol. 2004. PMID: 15048894

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