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Quoted phrase not found in phrase index: "Developmental and epileptic encephalopathy, 82"
Page 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 …
Peri-Insular Hemispherotomy: A Systematic Review and Institutional Experience.
Yates CF, Malone S, Riney K, Shah U, Wood MJ. Yates CF, et al. Pediatr Neurosurg. 2023;58(1):18-28. doi: 10.1159/000529098. Epub 2023 Jan 13. Pediatr Neurosurg. 2023. PMID: 36693334 Free PMC article.
RESULTS: Systematic review of the literature identified 393 patients from 13 eligible studies. Engel class 1 outcomes occurred in 82.4% of patients, while 8.6% developed post-operative hydrocephalus. Hydrocephalus was most common in the youngest patient cohorts. Develop
RESULTS: Systematic review of the literature identified 393 patients from 13 eligible studies. Engel class 1 outcomes occurred in 82. …
Minimally invasive procedures for hypothalamic hamartoma-related epilepsy: a systematic review and meta-analysis.
Iranmehr A, Dabbagh Ohadi MA, Chavoshi M, Jahanbakhshi A, Slavin KV. Iranmehr A, et al. Neurosurg Focus. 2022 Oct;53(4):E8. doi: 10.3171/2022.7.FOCUS22296. Neurosurg Focus. 2022. PMID: 36183177
OBJECTIVE: Hypothalamic hamartoma (HH) is a rare, nonmalignant, heterotopic developmental malformation that consists of a mixture of normal neurons and glial cells. ...The authors defined seizure freedom as Engel class I or International League Against Epilepsy clas …
OBJECTIVE: Hypothalamic hamartoma (HH) is a rare, nonmalignant, heterotopic developmental malformation that consists of a mixture of …
Clinical presentation, natural history, and outcomes for infantile intracranial cavernous malformations: case series and systematic review of the literature.
Goyal A, Fernandes-Torres J, Flemming KD, Williams LN, Daniels DJ. Goyal A, et al. Childs Nerv Syst. 2023 Jun;39(6):1545-1554. doi: 10.1007/s00381-023-05903-6. Epub 2023 Mar 14. Childs Nerv Syst. 2023. PMID: 36917267 Review.
INTRODUCTION: Intracranial cavernous malformations (CMs) are rare vascular malformations of the central nervous system in children. Infantile patients, being a developmentally vulnerable age group, pose a special challenge for management of these lesions. ...A total of 77% …
INTRODUCTION: Intracranial cavernous malformations (CMs) are rare vascular malformations of the central nervous system in children. Infantil …
Efficacy and safety of fenfluramine in patients with Dravet syndrome: A meta-analysis.
Zhang L, Li W, Wang C. Zhang L, et al. Acta Neurol Scand. 2021 Apr;143(4):339-348. doi: 10.1111/ane.13387. Epub 2020 Dec 17. Acta Neurol Scand. 2021. PMID: 33336426
BACKGROUND: Dravet syndrome (DS) is a severe, drug-resistant, developmental epileptic encephalopathy. Despite multiple anti-epileptic drug regimens, the syndrome remains poorly controlled and nearly half of patients still experience at least four tonic …
BACKGROUND: Dravet syndrome (DS) is a severe, drug-resistant, developmental epileptic encephalopathy. Despite multiple …
Comparison of neurodevelopmental, educational and adult socioeconomic outcomes in offspring of women with and without epilepsy: A systematic review and meta-analysis.
Mazzone PP, Hogg KM, Weir CJ, Stephen J, Bhattacharya S, Richer S, Chin RFM. Mazzone PP, et al. Seizure. 2024 Apr;117:213-221. doi: 10.1016/j.seizure.2024.02.014. Epub 2024 Feb 29. Seizure. 2024. PMID: 38484631 Free article.
BACKGROUND: Adequate pre-pregnancy counselling and education planning are essential to improve outcomes for offspring of women with epilepsy (OWWE). The current systematic review and meta-analysis aimed to compare outcomes for OWWE and offspring of women without epileps
BACKGROUND: Adequate pre-pregnancy counselling and education planning are essential to improve outcomes for offspring of women with epile
A meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations.
Chang X, Wu Y, Zhou J, Meng H, Zhang W, Guo J. Chang X, et al. Medicine (Baltimore). 2020 Jan;99(5):e18634. doi: 10.1097/MD.0000000000018634. Medicine (Baltimore). 2020. PMID: 32000367 Free PMC article.
The most common clinical features of Leigh syndrome included elevated blood and/or cerebrospinal fluid (CSF) levels of lactate (72%), developmental retardation (57%), hypotonia (42%), followed by respiratory dysfunction (34%), epileptic seizures (33%), poor feeding …
The most common clinical features of Leigh syndrome included elevated blood and/or cerebrospinal fluid (CSF) levels of lactate (72%), dev
Predictors of seizure outcomes in children with tuberous sclerosis complex and intractable epilepsy undergoing resective epilepsy surgery: an individual participant data meta-analysis.
Fallah A, Guyatt GH, Snead OC 3rd, Ebrahim S, Ibrahim GM, Mansouri A, Reddy D, Walter SD, Kulkarni AV, Bhandari M, Banfield L, Bhatnagar N, Liang S, Teutonico F, Liao J, Rutka JT. Fallah A, et al. PLoS One. 2013;8(2):e53565. doi: 10.1371/journal.pone.0053565. Epub 2013 Feb 6. PLoS One. 2013. PMID: 23405072 Free PMC article. Review.
OBJECTIVE: To perform a systematic review and individual participant data meta-analysis to identify preoperative factors associated with a good seizure outcome in children with Tuberous Sclerosis Complex undergoing resective epilepsy surgery. DATA SOURCES: Electronic datab …
OBJECTIVE: To perform a systematic review and individual participant data meta-analysis to identify preoperative factors associated with a g …