"Epileptic Syndromes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
EPILEPTIC SEIZURES that are of similar type and age of onset and have other similar features (e.g., clinical course, EEG findings, genetic association and neuropathology).
| Descriptor ID |
D000073376
|
| MeSH Number(s) |
C10.228.140.490.493
|
| Concept/Terms |
Epileptic Syndromes- Epileptic Syndromes
- Epileptic Syndrome
- Epilepsy Syndromes
- Epilepsy Syndrome
- Syndromic Epilepsies
- Epilepsies, Syndromic
- Epilepsy, Syndromic
- Syndromic Epilepsy
|
Below are MeSH descriptors whose meaning is more general than "Epileptic Syndromes".
Below are MeSH descriptors whose meaning is more specific than "Epileptic Syndromes".
This graph shows the total number of publications written about "Epileptic Syndromes" by people in this website by year, and whether "Epileptic Syndromes" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 1 | 1 | 2 |
| 2023 | 2 | 0 | 2 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Epileptic Syndromes" by people in Profiles.
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Comparative analysis of patients with new onset refractory status epilepticus preceded by fever (febrile infection-related epilepsy syndrome) versus without prior fever: An interim analysis. Epilepsia. 2024 Jun; 65(6):e87-e96.
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Pediatric epilepsy syndromes with associated developmental impairment. Dev Med Child Neurol. 2024 Jun; 66(6):691-701.
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Letter on: 3D figure of epilepsy syndromes. Epilepsia Open. 2023 09; 8(3):1202-1204.
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Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany. Epilepsia. 2021 10; 62(10):2518-2527.
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Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey. Mol Genet Genomic Med. 2021 07; 9(7):e1665.