 Epilepsy
"Epilepsy" 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.
A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)
| Descriptor ID |
D004827
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| MeSH Number(s) |
C10.228.140.490
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| Concept/Terms |
Epilepsy- Epilepsy
- Epilepsies
- Seizure Disorder
- Seizure Disorders
- Seizures, Epileptic
- Epileptic Seizures
- Epileptic Seizure
- Seizure, Epileptic
Single Seizure- Single Seizure
- Seizure, Single
- Seizures, Single
- Single Seizures
Epilepsy, Cryptogenic- Epilepsy, Cryptogenic
- Cryptogenic Epilepsies
- Cryptogenic Epilepsy
- Epilepsies, Cryptogenic
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Below are MeSH descriptors whose meaning is more general than "Epilepsy".
Below are MeSH descriptors whose meaning is more specific than "Epilepsy".
This graph shows the total number of publications written about "Epilepsy" by people in this website by year, and whether "Epilepsy" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 | | 2015 | 2 | 0 | 2 | | 2016 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 1 | 2 | | 2022 | 1 | 0 | 1 | | 2023 | 2 | 0 | 2 |
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Below are the most recent publications written about "Epilepsy" by people in Profiles.
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Potic A, Perrier S, Radovic T, Gavrilovic S, Ostojic J, Tran LT, Thiffault I, Pastinen T, Schiffmann R, Bernard G. Hypomyelination caused by a novel homozygous pathogenic variant in FOLR1: complete clinical and radiological recovery with oral folinic acid therapy and review of the literature. Orphanet J Rare Dis. 2023 Jul 13; 18(1):187.
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Thompson L, Sullivan DK, Varghese K, Abdelmoity A, Malik M, Abdelmoity A, Hall A. Factors Associated With Growth in Patients Treated With the Classic Ketogenic Diet for Drug-Resistant Epilepsy. Pediatr Neurol. 2023 09; 146:110-115.
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Bakula DM, Junger KW, Guilfoyle SM, Mara CA, Modi AC. Key predictors of the need for a family-focused pediatric epilepsy adherence intervention. Epilepsia. 2022 08; 63(8):2120-2129.
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Abdelmoity SA, Abdelmoity AA, Riordan SM, Kaufman C, Le Pichon JB, Abdelmoity A. The efficacy and tolerability of auto-stimulation-VNS in children with Lennox-Gastaut syndrome. Seizure. 2021 Mar; 86:168-174.
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Bakula DM, Wetter SE, Peugh JL, Modi AC. A Longitudinal Assessment of Parenting Stress in Parents of Children with New-Onset Epilepsy. J Pediatr Psychol. 2021 01 20; 46(1):91-99.
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Gali K, Joshi S, Hueneke S, Katzenbach A, Radecki L, Calabrese T, Fletcher L, Trandafir C, Wilson C, Goyal M, Wusthoff CJ, Le Pichon JB, Corvalan R, Golson A, Hardy J, Smith M, Cook E, Bonkowsky JL. Barriers, access and management of paediatric epilepsy with telehealth. J Telemed Telecare. 2022 Apr; 28(3):213-223.
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Khalid R, Ilyas M, Abdelmoity A. The Case of a Twitchy Tongue: An Uncommon Presentation of a Common Childhood Epilepsy. J Pediatr. 2020 01; 216:240-240.e1.
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Thiffault I, Farrow E, Smith L, Lowry J, Zellmer L, Black B, Abdelmoity A, Miller N, Soden S, Saunders C. PCDH19-related epileptic encephalopathy in a male mosaic for a truncating variant. Am J Med Genet A. 2016 06; 170(6):1585-9.
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Thiffault I, Speca DJ, Austin DC, Cobb MM, Eum KS, Safina NP, Grote L, Farrow EG, Miller N, Soden S, Kingsmore SF, Trimmer JS, Saunders CJ, Sack JT. A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization. J Gen Physiol. 2015 Nov; 146(5):399-410.
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Saunders C, Smith L, Wibrand F, Ravn K, Bross P, Thiffault I, Christensen M, Atherton A, Farrow E, Miller N, Kingsmore SF, Ostergaard E. CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduria. Am J Hum Genet. 2015 Feb 05; 96(2):258-65.
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