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Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants.
Thompson-Lake DGY, Liegeois FJ, Braden RO, Jackson GD, Turner SJ, Morison L, Hildebrand M, Scheffer IE, Morgan AT. Thompson-Lake DGY, et al. Among authors: jackson gd. Neurol Genet. 2024 Feb 26;10(2):e200129. doi: 10.1212/NXG.0000000000200129. eCollection 2024 Apr. Neurol Genet. 2024. PMID: 38715655 Free PMC article.
Longitudinal study of MRS metabolites in Rasmussen encephalitis.
Wellard RM, Briellmann RS, Wilson JC, Kalnins RM, Anderson DP, Federico P, Fabinyi GC, Scheffer IE, Harvey AS, Jackson GD. Wellard RM, et al. Among authors: jackson gd. Brain. 2004 Jun;127(Pt 6):1302-12. doi: 10.1093/brain/awh157. Epub 2004 Apr 6. Brain. 2004. PMID: 15069020
Thalamic atrophy in childhood absence epilepsy.
Chan CH, Briellmann RS, Pell GS, Scheffer IE, Abbott DF, Jackson GD. Chan CH, et al. Among authors: jackson gd. Epilepsia. 2006 Feb;47(2):399-405. doi: 10.1111/j.1528-1167.2006.00435.x. Epilepsia. 2006. PMID: 16499767 Free article.
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
340 results