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

Year Number of Results
1995 1
2002 1
2006 1
2007 2
2008 1
2011 6
2014 1
2015 1
2018 1
2019 1
2020 3
2021 2
2022 3
2023 5
2024 1

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Page 1
The etiologic classification of epilepsy.
Shorvon SD. Shorvon SD. Epilepsia. 2011 Jun;52(6):1052-7. doi: 10.1111/j.1528-1167.2011.03041.x. Epub 2011 Mar 30. Epilepsia. 2011. PMID: 21449936 Free article. Review.
The etiology of epilepsy is a major determinant of clinical course and prognosis, yet the current classifications of epilepsy do not list etiology in any detail. ...A commentary addressing the following points is included: problems associated with assigning causatio …
The etiology of epilepsy is a major determinant of clinical course and prognosis, yet the current classifications of epilepsy …
Early-Life Epilepsies.
Akiyama LF, Saneto RP. Akiyama LF, et al. Pediatr Ann. 2023 Oct;52(10):e381-e387. doi: 10.3928/19382359-20230829-01. Epub 2023 Oct 1. Pediatr Ann. 2023. PMID: 37820708 Review.
Here, we review the self-limited epilepsy syndromes and developmental and epileptic encephalopathies that begin in the neonatal-infantile period with an emphasis on genetic etiology and the shifting landscape of treatment options based on genetic findi …
Here, we review the self-limited epilepsy syndromes and developmental and epileptic encephalopathies that begin …
Drug management for acute tonic-clonic convulsions including convulsive status epilepticus in children.
McTague A, Martland T, Appleton R. McTague A, et al. Cochrane Database Syst Rev. 2018 Jan 10;1(1):CD001905. doi: 10.1002/14651858.CD001905.pub3. Cochrane Database Syst Rev. 2018. PMID: 29320603 Free PMC article. Review.
SEARCH METHODS: For the latest update we searched the Cochrane Epilepsy Group's Specialised Register (23 May 2017), the Cochrane Central Register of Controlled Trials (CENTRAL) via the Cochrane Register of Studies Online (CRSO, 23 May 2017), MEDLINE (Ovid, 1946 to 23 May 2 …
SEARCH METHODS: For the latest update we searched the Cochrane Epilepsy Group's Specialised Register (23 May 2017), the Cochrane Cent …
[Developmental and epileptic encephalopathy 85 caused by SMC1A gene truncating variation: 4 cases report and literature review].
Ye YZ, Duan J, Hu ZQ, Cao DZ, Liao JX, Chen L. Ye YZ, et al. Zhonghua Er Ke Za Zhi. 2022 Jun 2;60(6):583-587. doi: 10.3760/cma.j.cn112140-20211126-00994. Zhonghua Er Ke Za Zhi. 2022. PMID: 35658367 Review. Chinese.
Objective: To summarize the clinical phenotype of patients with developmental and epileptic encephalopathy 85 caused by SMC1A gene truncating variation. ...Related literatures up to October 2021 with the key words "SMC1A" "Developmental and epilepti …
Objective: To summarize the clinical phenotype of patients with developmental and epileptic encephalopathy 85 caused by …
The core Dravet syndrome phenotype.
Dravet C. Dravet C. Epilepsia. 2011 Apr;52 Suppl 2:3-9. doi: 10.1111/j.1528-1167.2011.02994.x. Epilepsia. 2011. PMID: 21463272 Free article. Review.
Later on, multiple seizure types, mainly myoclonic, atypical absences, and focal seizures appear, as well as a slowing of developmental and cognitive skills, and the appearance of behavioral disorders. ...All seizure types are pharmacoresistent, but a trend toward less sev …
Later on, multiple seizure types, mainly myoclonic, atypical absences, and focal seizures appear, as well as a slowing of developmental …
The influence of disease course and surgery on quality of life in children with focal cortical dysplasia and long-term epilepsy-associated tumours: A systematic review and meta-analysis.
Vasilica AM, Winsor A, Chari A, Scott R, Baldeweg T, Tisdall M. Vasilica AM, et al. Epilepsy Res. 2023 May;192:107132. doi: 10.1016/j.eplepsyres.2023.107132. Epub 2023 Mar 30. Epilepsy Res. 2023. PMID: 37023554 Free article. Review.
INTRODUCTION: Carefully selected patients with lesional epilepsy, including focal cortical dysplasia (FCD) and long-term epilepsy-associated tumours (LEAT), can benefit from epilepsy surgery. ...Age at epilepsy surgery, type of surgery and epilepsy …
INTRODUCTION: Carefully selected patients with lesional epilepsy, including focal cortical dysplasia (FCD) and long-term epilepsy …
Antiepileptic therapy approaches in KCNQ2 related epilepsy: A systematic review.
Kuersten M, Tacke M, Gerstl L, Hoelz H, Stülpnagel CV, Borggraefe I. Kuersten M, et al. Eur J Med Genet. 2020 Jan;63(1):103628. doi: 10.1016/j.ejmg.2019.02.001. Epub 2019 Feb 14. Eur J Med Genet. 2020. PMID: 30771507 Review.
BACKGROUND: KCNQ2 related disorders comprise both benign seizure disorders and early onset epileptic encephalopathies. Especially within the latter group, patients suffer from refractory seizures to standard antiepileptic drugs and developmental delay. ...Bas …
BACKGROUND: KCNQ2 related disorders comprise both benign seizure disorders and early onset epileptic encephalopathies. Especia …
In vitro evaluation suggests fenfluramine and norfenfluramine are unlikely to act as perpetrators of drug interactions.
Martin P, Czerwiński M, Limaye PB, Ogilvie BW, Smith S, Boyd B. Martin P, et al. Pharmacol Res Perspect. 2022 Jun;10(3):e00959. doi: 10.1002/prp2.959. Pharmacol Res Perspect. 2022. PMID: 35599347 Free PMC article. Review.
Studies support the safety and efficacy of fenfluramine (FFA) as an antiseizure medication (ASM) in Dravet syndrome, Lennox-Gastaut syndrome, or CDKL5 deficiency disorder, all pharmacoresistant developmental and epileptic encephalopathies. However, drug-drug …
Studies support the safety and efficacy of fenfluramine (FFA) as an antiseizure medication (ASM) in Dravet syndrome, Lennox-Gastaut syndrome …
The 100 most-cited manuscripts in epilepsy epigenetics: a bibliometric analysis.
Fan L, Liu L, Rao X, Wang X, Luo H, Gan J. Fan L, et al. Childs Nerv Syst. 2023 Nov;39(11):3111-3122. doi: 10.1007/s00381-023-06032-w. Epub 2023 Jun 20. Childs Nerv Syst. 2023. PMID: 37340273 Free PMC article. Review.
PURPOSE: The top citation article reflects the developmental milestone of a given field. The purpose of this bibliometric analysis was to identify and assess the 100 most-cited (T100) articles on the epigenetics mechanism of epilepsy. ...CONCLUSIONS: The research on …
PURPOSE: The top citation article reflects the developmental milestone of a given field. The purpose of this bibliometric analysis wa …
Molecular mechanisms of cognitive and behavioral comorbidities of epilepsy in children.
Brooks-Kayal A. Brooks-Kayal A. Epilepsia. 2011 Jan;52 Suppl 1(Suppl 1):13-20. doi: 10.1111/j.1528-1167.2010.02906.x. Epilepsia. 2011. PMID: 21214535 Free PMC article. Review.
Intellectual and developmental disabilities (IDDs) such as autistic spectrum disorders (ASDs) and epilepsies are heterogeneous disorders that have diverse etiologies and pathophysiologies. ...Increased understanding of the common genetic, molecular, and cellular mechanisms …
Intellectual and developmental disabilities (IDDs) such as autistic spectrum disorders (ASDs) and epilepsies are heterogeneous disord …
25 results