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

Year Number of Results
1993 1
2003 1
2006 1
2010 1
2014 1
2018 2
2020 5
2021 2
2022 1
2023 4
2024 1

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16 results

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Page 1
West syndrome: a comprehensive review.
Pavone P, Polizzi A, Marino SD, Corsello G, Falsaperla R, Marino S, Ruggieri M. Pavone P, et al. Neurol Sci. 2020 Dec;41(12):3547-3562. doi: 10.1007/s10072-020-04600-5. Epub 2020 Aug 22. Neurol Sci. 2020. PMID: 32827285 Free PMC article. Review.
Since its first clinical description (on his son) by William James West (1793-1848) in 1841, and the definition of the classical triad of (1) infantile spasms; (2) hypsarrhythmia, and (3) developmental arrest or regression as "West syndrome", new and relevant advances have …
Since its first clinical description (on his son) by William James West (1793-1848) in 1841, and the definition of the classical triad of (1 …
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 …
The Glycosylphosphatidylinositol biosynthesis pathway in human diseases.
Wu T, Yin F, Guang S, He F, Yang L, Peng J. Wu T, et al. Orphanet J Rare Dis. 2020 May 28;15(1):129. doi: 10.1186/s13023-020-01401-z. Orphanet J Rare Dis. 2020. PMID: 32466763 Free PMC article. Review.
Glycosylphosphatidylinositol biosynthesis defects cause rare genetic disorders characterised by developmental delay/intellectual disability, seizures, dysmorphic features, and diverse congenital anomalies associated with a wide range of additional features (hypotonia, hear …
Glycosylphosphatidylinositol biosynthesis defects cause rare genetic disorders characterised by developmental delay/intellectual disa …
Caring electronically for young outpatients who have epilepsy.
Oppenheimer J, Leviton A, Chiujdea M, Antonetty A, Ojo OW, Garcia S, Weas S, Fleegler EW, Chan E, Loddenkemper T. Oppenheimer J, et al. Epilepsy Behav. 2018 Oct;87:226-232. doi: 10.1016/j.yebeh.2018.06.018. Epub 2018 Sep 7. Epilepsy Behav. 2018. PMID: 30197227 Review.
PURPOSE: The purpose of this study was to review electronic tools that might improve the delivery of epilepsy care, reduce medical care costs, and empower families to improve self-management capability. METHOD: We reviewed the epilepsy-specific literature about self …
PURPOSE: The purpose of this study was to review electronic tools that might improve the delivery of epilepsy care, reduce medical ca …
Phenotypic and molecular spectrum of pyridoxamine-5'-phosphate oxidase deficiency: A scoping review of 87 cases of pyridoxamine-5'-phosphate oxidase deficiency.
Alghamdi M, Bashiri FA, Abdelhakim M, Adly N, Jamjoom DZ, Sumaily KM, Alghanem B, Arold ST. Alghamdi M, et al. Clin Genet. 2021 Jan;99(1):99-110. doi: 10.1111/cge.13843. Epub 2020 Sep 16. Clin Genet. 2021. PMID: 32888189 Free PMC article. Review.
Pyridoxamine-5'-phosphate oxidase (PNPO) deficiency is an autosomal recessive pyridoxal 5'-phosphate (PLP)-vitamin-responsive epileptic encephalopathy. The emerging feature of PNPO deficiency is the occurrence of refractory seizures in the first year of life. ...In …
Pyridoxamine-5'-phosphate oxidase (PNPO) deficiency is an autosomal recessive pyridoxal 5'-phosphate (PLP)-vitamin-responsive epileptic …
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. ...The developmental his …
PURPOSE: The top citation article reflects the developmental milestone of a given field. The purpose of this bibliometric analysis wa …
Early surgical approaches in pediatric epilepsy - a systematic review and meta-analysis.
Frank NA, Greuter L, Guzman R, Soleman J. Frank NA, et al. Childs Nerv Syst. 2023 Mar;39(3):677-688. doi: 10.1007/s00381-022-05699-x. Epub 2022 Oct 11. Childs Nerv Syst. 2023. PMID: 36219224 Review.
The aim of this systematic review and meta-analysis is to analyze the potential benefit of early epilepsy surgery in children concerning primarily seizure and developmental outcome. ...Favorable outcome for the VNS cohort was seen in 52%, 65% in the early and 45.1% …
The aim of this systematic review and meta-analysis is to analyze the potential benefit of early epilepsy surgery in children concern …
Dyke-Davidoff-Masson Syndrome: Main clinical and radiological findings- systematic literature review.
Rondão MBA, Hsu BRRHS, Centeno RS, de Aguiar PHP. Rondão MBA, et al. Seizure. 2023 Aug;110:58-68. doi: 10.1016/j.seizure.2023.04.020. Epub 2023 Jun 3. Seizure. 2023. PMID: 37327751 Review.
RESULTS: The mean age of the patients was 19.44 (0-83 years), and the majority were male (55.32%). The most common types of epileptic seizures were generalised tonic-clonic seizures (31 cases), focal impaired awareness seizures (20 cases), focal motor seizures (13 cases), …
RESULTS: The mean age of the patients was 19.44 (0-83 years), and the majority were male (55.32%). The most common types of epileptic …
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review.
André MV, Cacciagli P, Cano A, Vaugier L, Roussel M, Girard N, Chabrol B, Villard L, Milh M. André MV, et al. Arch Pediatr. 2021 Jan;28(1):87-92. doi: 10.1016/j.arcped.2020.10.015. Epub 2020 Dec 17. Arch Pediatr. 2021. PMID: 33342683 Review.
We describe the clinical, electroencephalography (EEG), and developmental features of a patient with developmental and epileptic encephalopathy due to a homozygous pathogenic variation of mitochondrial glutamate/H(+) symporter SLC25A22. ...We confirm i …
We describe the clinical, electroencephalography (EEG), and developmental features of a patient with developmental and epil …
Current state of hemispherectomy and callosotomy for pediatric refractory epilepsy in Denmark.
De Knegt VE, Børresen ML, Knudsen M, Thomsen KM, Uldall PV, Jakobsen AV, Hoei-Hansen CE. De Knegt VE, et al. Brain Dev. 2024 Mar;46(3):142-148. doi: 10.1016/j.braindev.2023.11.009. Epub 2023 Dec 3. Brain Dev. 2024. PMID: 38044196 Review.
Median IQ/developmental quotient (IQ/DQ) was low preoperatively (44.0 [IQR: 40.0-55.0]) and remained unchanged postoperatively (IQ change: 0.0 [IQR: -10.0-+4.0]). ...CONCLUSION: Hemispherectomy and callosotomy result in a substantial reduction in seizure frequency and ASM …
Median IQ/developmental quotient (IQ/DQ) was low preoperatively (44.0 [IQR: 40.0-55.0]) and remained unchanged postoperatively (IQ ch …
16 results