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Quoted phrase not found in phrase index: "Developmental and epileptic encephalopathy, 32"
Page 1
Efficacy and tolerability of fenfluramine in patients with Dravet syndrome: A systematic review and meta-analysis.
Sharawat IK, Panda PK, Kasinathan A, Panda P, Dawman L, Joshi K. Sharawat IK, et al. Seizure. 2021 Feb;85:119-126. doi: 10.1016/j.seizure.2020.12.016. Epub 2021 Jan 11. Seizure. 2021. PMID: 33461030 Free article.
BACKGROUND: Dravet syndrome (DS) is an infantile-onset developmental and epileptic encephalopathy syndrome with limited treatment options. ...Fenfluramine was found to be more efficacious than placebo, in terms of mean convulsive and total seizure frequency r …
BACKGROUND: Dravet syndrome (DS) is an infantile-onset developmental and epileptic encephalopathy syndrome with limited …
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 c …
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 epilep …
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 …
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. ...Individual cas …
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 …
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 …
Efficacy and Safety of Adjunctive Cannabidiol in Patients with Lennox-Gastaut Syndrome: A Systematic Review and Meta-Analysis.
Lattanzi S, Brigo F, Cagnetti C, Trinka E, Silvestrini M. Lattanzi S, et al. CNS Drugs. 2018 Oct;32(10):905-916. doi: 10.1007/s40263-018-0558-9. CNS Drugs. 2018. PMID: 30132269
BACKGROUND: Lennox-Gastaut syndrome (LGS) is a severe developmental epileptic encephalopathy, and available interventions fail to control seizures in most patients. ...
BACKGROUND: Lennox-Gastaut syndrome (LGS) is a severe developmental epileptic encephalopathy, and available interventio …
Neurodevelopmental outcomes in preterm or low birth weight infants with germinal matrix-intraventricular hemorrhage: a meta-analysis.
Zhou M, Wang S, Zhang T, Duan S, Wang H. Zhou M, et al. Pediatr Res. 2024 Feb;95(3):625-633. doi: 10.1038/s41390-023-02877-8. Epub 2023 Nov 7. Pediatr Res. 2024. PMID: 37935882 Free PMC article.
METHODS: Four databases were searched for observational studies that were qualified using the Newcastle-Ottawa Scale. RESULTS: 37 studies involving 32,370 children were included. Compared to children without IVH, children with mild IVH had higher incidences of neurodevelop …
METHODS: Four databases were searched for observational studies that were qualified using the Newcastle-Ottawa Scale. RESULTS: 37 studies in …
Customized multigene panels in epilepsy: the best things come in small packages.
Pellacani S, Dosi C, Valvo G, Moro F, Mero S, Sicca F, Santorelli FM. Pellacani S, et al. Neurogenetics. 2020 Jan;21(1):1-18. doi: 10.1007/s10048-019-00598-x. Epub 2019 Dec 13. Neurogenetics. 2020. PMID: 31834528
Our analyses suggest that the usefulness and diagnostic power of customized gene panels for epilepsy may be greatest when these panels are confined to rationally selected, relatively small, pools of genes, and applied in more carefully selected epilepsy patients (th …
Our analyses suggest that the usefulness and diagnostic power of customized gene panels for epilepsy may be greatest when these panel …
12 results