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

Year Number of Results
1979 1
1995 1
2001 1
2002 1
2008 1
2010 1
2011 1
2014 2
2015 2
2016 2
2018 2
2019 2
2020 2
2021 5
2022 2
2023 3

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Page 1
Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
D'Antonio F, Pagani G, Familiari A, Khalil A, Sagies TL, Malinger G, Leibovitz Z, Garel C, Moutard ML, Pilu G, Bhide A, Acharya G, Leombroni M, Manzoli L, Papageorghiou A, Prefumo F. D'Antonio F, et al. Pediatrics. 2016 Sep;138(3):e20160445. doi: 10.1542/peds.2016-0445. Pediatrics. 2016. PMID: 27581855 Review.
Gross and fine motor control were abnormal in 4.40% (95% CI, 0.6-11.3) and 10.98% (95% CI, 4.1-20.6) of the cases, respectively, whereas 6.80% (95% CI, 1.7-14.9) presented with epilepsy. Abnormal cognitive status occurred in 15.16% (95% CI, 6.9-25.9) of cases. ...Fine moto …
Gross and fine motor control were abnormal in 4.40% (95% CI, 0.6-11.3) and 10.98% (95% CI, 4.1-20.6) of the cases, respectively, whereas 6.8 …
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 2 …
SEARCH METHODS: For the latest update we searched the Cochrane Epilepsy Group's Specialised Register (23 May 2017), the Cochra …
Neurological aspects of human glycosylation disorders.
Freeze HH, Eklund EA, Ng BG, Patterson MC. Freeze HH, et al. Annu Rev Neurosci. 2015 Jul 8;38:105-25. doi: 10.1146/annurev-neuro-071714-034019. Epub 2015 Apr 2. Annu Rev Neurosci. 2015. PMID: 25840006 Free PMC article. Review.
Most of these disorders impact the central and/or peripheral nervous systems. Patients typically have developmental delays/intellectual disabilities, hypotonia, seizures, neuropathy, and metabolic abnormalities in multiple organ systems. ...
Most of these disorders impact the central and/or peripheral nervous systems. Patients typically have developmental delays/intellectu …
Capturing seizures in clinical trials of antiseizure medications for KCNQ2-DEE.
Millichap JJ, Harden CL, Dlugos DJ, French JA, Butterfield NN, Grayson C, Aycardi E, Pimstone SN. Millichap JJ, et al. Epilepsia Open. 2021 Jan 29;6(1):38-44. doi: 10.1002/epi4.12466. eCollection 2021 Mar. Epilepsia Open. 2021. PMID: 33681646 Free PMC article. Review.
Literature review of patients with KCNQ2 developmental and epileptic encephalopathy (KCNQ2-DEE) reveals, based on 16 reports including 139 patients, a clinical phenotype that includes age- and disease-specific stereotyped seizures. ...Therefore, we propose th …
Literature review of patients with KCNQ2 developmental and epileptic encephalopathy (KCNQ2-DEE) reveals, based on 16 re …
Epilepsy Surgery is a Viable Treatment for Lennox Gastaut Syndrome.
Keator CG. Keator CG. Semin Pediatr Neurol. 2021 Jul;38:100894. doi: 10.1016/j.spen.2021.100894. Epub 2021 May 11. Semin Pediatr Neurol. 2021. PMID: 34183143 Review.
Lennox Gastaut Syndrome (LGS) is a severe developmental epileptic encephalopathy with onset in childhood characterized by multiple seizure types and characteristic electroencephalogram findings. ...Epilepsy surgery can reduce seizure burden, in some ca …
Lennox Gastaut Syndrome (LGS) is a severe developmental epileptic encephalopathy with onset in childhood characterized …
Epilepsy-related clinical characteristics and mortality: a systematic review and meta-analysis.
Nevalainen O, Ansakorpi H, Simola M, Raitanen J, Isojärvi J, Artama M, Auvinen A. Nevalainen O, et al. Neurology. 2014 Nov 18;83(21):1968-77. doi: 10.1212/WNL.0000000000001005. Epub 2014 Oct 22. Neurology. 2014. PMID: 25339211 Review.
RESULTS: Pooled mortality was threefold (relative risk 3.33, 95% confidence interval 2.83-3.92) in 38 epilepsy cohorts including 165,879 patients (79.6% from Nordic countries). ...CONCLUSION: Excess mortality was highly related to the etiology of epilepsy in …
RESULTS: Pooled mortality was threefold (relative risk 3.33, 95% confidence interval 2.83-3.92) in 38 epilepsy cohorts includi …
Genetic Testing in Children with Epilepsy: Report of a Single-Center Experience.
Lee S, Karp N, Zapata-Aldana E, Sadikovic B, Yang P, Balci TB, Prasad AN. Lee S, et al. Can J Neurol Sci. 2021 Mar;48(2):233-244. doi: 10.1017/cjn.2020.167. Epub 2020 Aug 3. Can J Neurol Sci. 2021. PMID: 32741404 Review.
BACKGROUND: Retrospective observational study to determine diagnostic yield and utility of genetic testing in children with epilepsy attending the Epilepsy Clinic at Children's Hospital, London, Ontario, Canada. ...RESULTS: In total, 105 children (52.38 …
BACKGROUND: Retrospective observational study to determine diagnostic yield and utility of genetic testing in children with epilepsy …
Epilepsy and genetic malformations of the cerebral cortex.
Guerrini R, Carrozzo R. Guerrini R, et al. Am J Med Genet. 2001 Summer;106(2):160-73. doi: 10.1002/ajmg.1569. Am J Med Genet. 2001. PMID: 11579436 Review.
Malformations of the cerebral cortex are an important cause of developmental disabilities and epilepsy. Here we review those malformations for which a genetic basis has been elucidated or is suspected and the types of associated epilepsy. Schizencephaly (clef …
Malformations of the cerebral cortex are an important cause of developmental disabilities and epilepsy. Here we review those m …
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. ...RES …
BACKGROUND: KCNQ2 related disorders comprise both benign seizure disorders and early onset epileptic encephalopathies. Especia …
The neuroimaging spectrum of SLC13A5 related developmental and epileptic encephalopathy.
Whitney R, Choi E, Jones KC. Whitney R, et al. Seizure. 2023 Mar;106:8-13. doi: 10.1016/j.seizure.2023.01.014. Epub 2023 Jan 23. Seizure. 2023. PMID: 36701889 Review.
BACKGROUND: SLC13A5 related developmental and epileptic encephalopathy (DEE) is an autosomal recessive condition characterized by neonatal seizures, fever sensitivity, status epilepticus, developmental delay and tooth anomalies. ...White matter abnorma …
BACKGROUND: SLC13A5 related developmental and epileptic encephalopathy (DEE) is an autosomal recessive condition charac …
23 results