Grinton B - Search Results

1

Recognition and epileptology of protracted CLN3 disease.

Cameron JM, Damiano JA, Grinton B, Carney PW, McKelvie P, Silbert P, Lawn N, Scheffer IE, Oliver KL, Hildebrand MS, Berkovic SF. Cameron JM, et al. Among authors: grinton b. Epilepsia. 2023 Jul;64(7):1833-1841. doi: 10.1111/epi.17616. Epub 2023 Apr 27. Epilepsia. 2023. PMID: 37039534 Free PMC article.

2

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

3

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. Among authors: grinton b. 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

4

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. Among authors: grinton b. 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.

5

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. Ann Neurol. 2004 Apr;55(4):550-7. doi: 10.1002/ana.20029. Ann Neurol. 2004. PMID: 15048894

6

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF. Marini C, et al. Epilepsia. 2004 May;45(5):467-78. doi: 10.1111/j.0013-9580.2004.46803.x. Epilepsia. 2004. PMID: 15101828 Free article.

7

Familial clustering of seizure types within the idiopathic generalized epilepsies.

Winawer MR, Marini C, Grinton BE, Rabinowitz D, Berkovic SF, Scheffer IE, Ottman R. Winawer MR, et al. Among authors: grinton be. Neurology. 2005 Aug 23;65(4):523-8. doi: 10.1212/01.wnl.0000172920.34994.63. Neurology. 2005. PMID: 16116110 Free PMC article.

8

Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.

Scheffer IE, Harkin LA, Grinton BE, Dibbens LM, Turner SJ, Zielinski MA, Xu R, Jackson G, Adams J, Connellan M, Petrou S, Wellard RM, Briellmann RS, Wallace RH, Mulley JC, Berkovic SF. Scheffer IE, et al. Brain. 2007 Jan;130(Pt 1):100-9. doi: 10.1093/brain/awl272. Epub 2006 Oct 4. Brain. 2007. PMID: 17020904

9

Invited comments on the Shostak and Ottman review.

Grinton BE, Scheffer IE, Berkovic SF. Grinton BE, et al. Epilepsia. 2006 Oct;47(10):1751-2; author reply 1755-6. doi: 10.1111/j.1528-1167.2006.00885_6.x. Epilepsia. 2006. PMID: 17054705 Free article. No abstract available.

10

SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.

Herlenius E, Heron SE, Grinton BE, Keay D, Scheffer IE, Mulley JC, Berkovic SF. Herlenius E, et al. Epilepsia. 2007 Jun;48(6):1138-42. doi: 10.1111/j.1528-1167.2007.01049.x. Epub 2007 Mar 26. Epilepsia. 2007. PMID: 17386050 Free article.

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