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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1982 2
1983 7
1984 6
1986 3
1987 2
1988 5
1989 5
1990 2
1991 13
1992 7
1993 15
1994 11
1995 14
1996 9
1997 14
1998 17
1999 18
2000 29
2001 19
2002 15
2003 20
2004 21
2005 16
2006 21
2007 29
2008 20
2009 24
2010 37
2011 17
2012 32
2013 37
2014 28
2015 25
2016 19
2017 27
2018 23
2019 30
2020 23
2021 31
2022 33
2023 24
2024 8

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709 results

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Page 1
Somatic mosaicism in focal epilepsies.
Gooley S, Perucca P, Tubb C, Hildebrand MS, Berkovic SF. Gooley S, et al. Among authors: berkovic sf. Curr Opin Neurol. 2024 Apr 1;37(2):105-114. doi: 10.1097/WCO.0000000000001244. Epub 2024 Jan 18. Curr Opin Neurol. 2024. PMID: 38235675 Review.
Exploring individual fixel-based white matter abnormalities in epilepsy.
Mito R, Pedersen M, Pardoe H, Parker D, Smith RE, Cameron J, Scheffer IE, Berkovic SF, Vaughan DN, Jackson GD. Mito R, et al. Among authors: berkovic sf. Brain Commun. 2023 Dec 22;6(1):fcad352. doi: 10.1093/braincomms/fcad352. eCollection 2024. Brain Commun. 2023. PMID: 38187877 Free PMC article.
Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort study.
Nightscales R, Chen Z, Barnard S, Auvrez C, Tao G, Sivathamboo S, Bennett C, Rychkova M, D'Souza W, Berkovic SF, Nicolo JP, O'Brien TJ, Perucca P, Scheffer IE, Kwan P. Nightscales R, et al. Among authors: berkovic sf. Epilepsia Open. 2024 Apr;9(2):602-612. doi: 10.1002/epi4.12894. Epub 2024 Jan 24. Epilepsia Open. 2024. PMID: 38135919 Free PMC article.
Are Germline Mosaic TSC1/2 Variants Present in Controls? Implications for Diagnosis.
Ye Z, Lin S, Zhao X, Wallis M, Gao X, Sun L, Wu J, Duan J, Yao Y, Li L, Chen L, Cao D, Hu Z, Zhang VW, Berkovic SF, Scheffer IE, Liao J, Hildebrand MS. Ye Z, et al. Among authors: berkovic sf. Pediatr Neurol. 2024 Jan;150:37-39. doi: 10.1016/j.pediatrneurol.2023.10.008. Epub 2023 Oct 22. Pediatr Neurol. 2024. PMID: 37951160 Free article. No abstract available.
Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature.
LaFlamme CW, Rastin C, Sengupta S, Pennington HE, Russ-Hall SJ, Schneider AL, Bonkowski ES, Almanza Fuerte EP, Galey M, Goffena J, Gibson SB, Allan TJ, Nyaga DM, Lieffering N, Hebbar M, Walker EV, Darnell D, Olsen SR, Kolekar P, Djekidel N, Rosikiewicz W, McConkey H, Kerkhof J, Levy MA, Relator R, Lev D, Lerman-Sagie T, Park KL, Alders M, Cappuccio G, Chatron N, Demain L, Genevieve D, Lesca G, Roscioli T, Sanlaville D, Tedder ML, Hubshman MW, Ketkar S, Dai H, Worley KC, Rosenfeld JA, Chao HT; Undiagnosed Diseases Network; Neale G, Carvill GL; University of Washington Center for Rare Disease Research; Wang Z, Berkovic SF, Sadleir LG, Miller DE, Scheffer IE, Sadikovic B, Mefford HC. LaFlamme CW, et al. Among authors: berkovic sf. medRxiv [Preprint]. 2023 Oct 12:2023.10.11.23296741. doi: 10.1101/2023.10.11.23296741. medRxiv. 2023. PMID: 37873138 Free PMC article. Preprint.
Neuropsychological function in psychosis of epilepsy.
Allebone J, Kanaan RA, Rayner G, Maller J, O'Brien TJ, Mullen SA, Cook M, Adams SJ, Vogrin S, Vaughan DN, Kwan P, Berkovic SF, D'Souza WJ, Jackson G, Velakoulis D, Wilson SJ. Allebone J, et al. Among authors: berkovic sf. Epilepsy Res. 2023 Oct;196:107222. doi: 10.1016/j.eplepsyres.2023.107222. Epub 2023 Sep 15. Epilepsy Res. 2023. PMID: 37717505 Free article.
709 results