Epilepsy phenotype in individuals with chromosomal duplication encompassing FGF12

- Willemsen, Marjolein H., Goel, Himanshu, Verhoeven, Judith S., Braakman, Hilde M. H., de Leeuw, Nicole, Freeth, Alison, Minassian, Berge A.

Gabapentin modulates HCN4 channel voltage-dependence

- Tae, Han-Shen, Smith, Kelly M., Petrou, Steven, Reid, Christopher A., Phillips, A. Marie, Boyle, Kieran A., Li, Melody, Forster, Ian C., Hatch, Robert J., Richardson, Robert, Hughes, David I., Graham, Brett A.

Quantitative EEG analysis of the maturational changes associated with childhood absence epilepsy

- Rosso, O. A., Hyslop, Wendy, Gerlach, Richard Helmut, Smith, R. L. L., Rostas, John Andrew, Hunter, Mick

Astrocytes: a central element in neurological diseases

- Pekny, Milos, Pekna, Marcela, Messing, Albee, Steinhäuser, Christian, Lee, Jin-Moo, Parpura, Vladimir, Hol, Elly M., Sofroniew, Michael V., Verkhratsky, Alexei

Cardiovascular fitness and later risk of epilepsy: a Swedish population-based cohort study

- Nyberg, Jenny, Åberg, Maria A. I., Toren, K., Nilsson, Michael, Ben-Menachem, H., Kuhn, H. G.

Individual resilience as a strategy to counter employment barriers for people with epilepsy in Zimbabwe

- Mugumbate, Jacob, Gray, Mel

The role of social workers in the social management of epilepsy in Africa

- Mugumbate, Jacob, Riphagenn, Harmiena, Gathara, Rosemary

Disability, employment, and social justice: employment experiences of people with epilepsy in Harare, Zimbabwe

- Mugumbate, Jacob

Evidence for type-specific DNA methylation patterns in epilepsy: a discordant monozygotic twin approach

- Mohandas, Namitha, Loke, Yuk Jing, Hopkins, Stephanie, Mackenzie, Lisa, Bennett, Carmen, Berkovic, Samuel F., Vadlamudi, Lata, Craig, Jeffery M.

Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy

- Kamien, Benjamin, Harraway, James, Lundie, Ben, Smallhorne, Lex, Gibbs, Vicki, Heath, Anna, Fullerton, Janice M.

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families

- Hynes, Kim, Tarpey, Patrick, Haan, Eric, Turner, Gillian, Christodoulou, John, Leonard, Helen, Gill, Deepak, Stratton, Michael R., Gecz, Jozef, Scheffer, Ingrid E., Dibbens, Leanne M., Bayly, Marta A., Berkovic, Samuel F., Smith, Raffaella, Al Raisi, Zahyia, Turner, Samantha J., Brown, Natasha J., Desai, Tarishi D.

Efficacy and safety of cannabidivarin treatment of epilepsy in girls with Rett syndrome: A phase 1 clinical trial

- Hurley, Ellen N., Ellaway, Carolyn J., Johnson, Alexandra M., Truong, Linda, Gordon, Rebecca, Galettis, Peter, Martin, Jennifer H., Lawson, John A.

Burden of epilepsy: a prevalence-based cost of illness study of direct, indirect and intangible costs for epilepsy

- Gao, Lan, Xia, Li, Pan, Song-Qing, Xiong, Tao, Li, Shu-Chuen

Psychometric properties of Chinese language Liverpool Seizure Severity Scale 2.0 (LSSS 2.0) and status and determinants of seizure severity for patients with epilepsy in China

- Gao, Lan, Xia, Li, Pan, Song-Qing, Xiong, Tao, Li, Shu-Chuen

Reliability and validity of QOLIE-10 in measuring health-related quality of life (HRQoL) in Chinese epilepsy patients

- Gao, Lan, Xia, Li, Pan, Song-Qing, Xiong, Tao, Li, Shu-Chuen

Validation of a Chinese version of the quality of well-being scale-self-administered (QWB-SA) in patients with epilepsy

- Gao, Lan, Xia, Li, Pan, Song-Qing, Xiong, Tao, Li, Shu-Chuen

Validation of the Chinese version of the NUCOG cognitive screening tool in patients with epilepsy, dementia and other neurological disorders

- Gao, Lan, Li, Shu-Chuen, Xia, Li, Pan, Songqing, Velakoulis, Dennis, Walterfang, Mark

Health-related quality of life and willingness to pay per quality-adjusted life-year threshold-a study in patients with epilepsy in China

- Gao, Lan, Xia, Li, Pan, Song-Qing, Xiong, Tao, Li, Shu-Chuen

Temozolomide and seizure outcomes in a randomized clinical trial of elderly glioblastoma patients

- Climans, Seth A., Brandes, Alba A., Phillips, Claire, Roa, Wilson, Wick, Wolfgang, Winch, Chad, Mason, Warren P., Cairncross, J. Gregory, Ding, Keyue, Fay, Michael, Laperriere, Normand, Menten, Johan, Nishikawa, Ryo, O'Callaghan, Christopher J., Perry, James R.

Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic-atonic seizures

- Carvill, Gemma L., McMahon, Jacinta M., Mecarelli, Oriano, Smith, Robert L., Leventer, Richard J., Møller, Rikke S., Nikanorova, Marina, Dimova, Petia, Jordanova, Albena, Petrou, Steven, Helbig, Ingo, Striano, Pasquale, Schneider, Amy, Zemel, Matthew, Myers, Candace T., Saykally, Julia, Nguyen, John, Robbiano, Angela, Zara, Frederico, Specchio, Nicola