When left-hemisphere reading is compromised: Comparing reading ability in participants after left cerebral hemispherectomy and participants with developmental dyslexia.

Katzir T, Christodoulou JA, de Bode S. When left-hemisphere reading is compromised: Comparing reading ability in participants after left cerebral hemispherectomy and participants with developmental dyslexia. Epilepsia. 2016;57(10):1602-1609. DOI: 10.1111/epi.13507. PubMed PMID: 27573872.

Incidence and outcome of epilepsy syndromes with onset in the first year of life: A retrospective population-based study.

Gaily E, Lommi M, Lapatto R, Lehesjoki A-E. Incidence and outcome of epilepsy syndromes with onset in the first year of life: A retrospective population-based study. Epilepsia. 2016;57(10):1594-1601. DOI: 10.1111/epi.13514. PubMed PMID: 27574005.

Sudden unexpected death in epilepsy: epidemiology, mechanisms, and prevention.

Devinsky O, Hesdorffer DC, Thurman DJ, Lhatoo S, Richerson G. Sudden unexpected death in epilepsy: epidemiology, mechanisms, and prevention. Lancet Neurol. 2016;15(10):1075-88. DOI: 10.1016/S1474-4422(16)30158-2. PubMed PMID: 27571159.

Quantifying antiepileptic drug effects using intrinsic excitability measures.

Meisel C, Plenz D, Schulze-Bonhage A, Reichmann H. Quantifying antiepileptic drug effects using intrinsic excitability measures. Epilepsia. 2016;57(11):e210-e215. DOI: 10.1111/epi.13517. PubMed PMID: 27562603.

Depression and genetic causal attribution of epilepsy in multiplex epilepsy families.

Sorge ST, Hesdorffer DC, Phelan JC, Winawer MR, Shostak S, Goldsmith J, et al. Depression and genetic causal attribution of epilepsy in multiplex epilepsy families. Epilepsia. 2016;57(10):1643-1650. DOI: 10.1111/epi.13500. PubMed PMID: 27558297.

The spectrum of epilepsy and electroencephalographic abnormalities due to SHANK3 loss-of-function mutations.

Holder JL, Quach MM. The spectrum of epilepsy and electroencephalographic abnormalities due to SHANK3 loss-of-function mutations. Epilepsia. 2016;57(10):1651-1659. DOI: 10.1111/epi.13506. PubMed PMID: 27554343.

Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review.

Anagnostou M-E, Ng YS, Taylor RW, McFarland R. Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review. Epilepsia. 2016;57(10):1531-1545. DOI: 10.1111/epi.13508. PubMed PMID: 27554452.

Association of HLA genotypes with phenobarbital hypersensitivity in children.

Manuyakorn W, Mahasirimongkol S, Likkasittipan P, Kamchaisatian W, Wattanapokayakit S, Inunchot W, et al. Association of HLA genotypes with phenobarbital hypersensitivity in children. Epilepsia. 2016;57(10):1610-1616. DOI: 10.1111/epi.13509. PubMed PMID: 27554620.

Comparative effectiveness of levetiracetam, valproate and carbamazepine among elderly patients with newly diagnosed epilepsy: subgroup analysis of the randomized, unblinded KOMET study.

Pohlmann-Eden B, Marson AG, Noack-Rink M, Ramirez F, Tofighy A, Werhahn KJ, et al. Comparative effectiveness of levetiracetam, valproate and carbamazepine among elderly patients with newly diagnosed epilepsy: subgroup analysis of the randomized, unblinded KOMET study. Bmc Neurol. 2016;16(1):149. DOI: 10.1186/s12883-016-0663-7. PubMed PMID: 27552848.

Complications of subdural and depth electrodes in 269 patients undergoing 317 procedures for invasive monitoring in epilepsy.

Schmidt RF, Wu C, Lang MJ, Soni P, Williams KA, Boorman DW, et al. Complications of subdural and depth electrodes in 269 patients undergoing 317 procedures for invasive monitoring in epilepsy. Epilepsia. 2016;57(10):1697-1708. DOI: 10.1111/epi.13503. PubMed PMID: 27549686.