 Epilepsies, Myoclonic
"Epilepsies, Myoclonic" 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 clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic.
| Descriptor ID |
D004831
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| MeSH Number(s) |
C10.228.140.490.375.130 C10.228.140.490.493.063
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| Concept/Terms |
Epilepsies, Myoclonic- Epilepsies, Myoclonic
- Epilepsy, Myoclonic
- Myoclonic Epilepsies
- Myoclonic Seizure Disorder
- Myoclonic Seizure Disorders
- Seizure Disorder, Myoclonic
- Seizure Disorders, Myoclonic
- Myoclonic Epilepsy
- Epilepsy, Myoclonus
- Myoclonus Epilepsies
- Myoclonus Epilepsy
Early Childhood Epilepsy, Myoclonic- Early Childhood Epilepsy, Myoclonic
- Myoclonic Epilepsy, Early Childhood
- Epilepsy, Myoclonic, Early Childhood
- Early Childhood, Myoclonic Epilepsy
- Epilepsy, Early Childhood, Myoclonic
Epilepsy, Myoclonic, Infantile- Epilepsy, Myoclonic, Infantile
- Myoclonic Epilepsy, Infantile
- Epilepsies, Infantile Myoclonic
- Epilepsy, Infantile Myoclonic
- Infantile Myoclonic Epilepsies
- Infantile Myoclonic Epilepsy
- Myoclonic Epilepsies, Infantile
Symptomatic Myoclonic Epilepsy- Symptomatic Myoclonic Epilepsy
- Epilepsies, Symptomatic Myoclonic
- Epilepsy, Symptomatic Myoclonic
- Myoclonic Epilepsies, Symptomatic
- Myoclonic Epilepsy, Symptomatic
- Symptomatic Myoclonic Epilepsies
Idiopathic Myoclonic Epilepsy- Idiopathic Myoclonic Epilepsy
- Epilepsies, Idiopathic Myoclonic
- Epilepsy, Idiopathic Myoclonic
- Idiopathic Myoclonic Epilepsies
- Myoclonic Epilepsies, Idiopathic
- Myoclonic Epilepsy, Idiopathic
- Cryptogenic Myoclonic Epilepsy
- Cryptogenic Myoclonic Epilepsies
- Epilepsies, Cryptogenic Myoclonic
- Epilepsy, Cryptogenic Myoclonic
- Myoclonic Epilepsies, Cryptogenic
- Myoclonic Epilepsy, Cryptogenic
Myoclonic Absence Epilepsy- Myoclonic Absence Epilepsy
- Absence Epilepsies, Myoclonic
- Absence Epilepsy, Myoclonic
- Epilepsies, Myoclonic Absence
- Epilepsy, Myoclonic Absence
- Myoclonic Absence Epilepsies
Myoclonic Astatic Epilepsy- Myoclonic Astatic Epilepsy
- Astatic Epilepsies, Myoclonic
- Astatic Epilepsy, Myoclonic
- Epilepsies, Myoclonic Astatic
- Epilepsy, Myoclonic Astatic
- Myoclonic Astatic Epilepsies
Myoclonic Encephalopathy- Myoclonic Encephalopathy
- Encephalopathies, Myoclonic
- Myoclonic Encephalopathies
- Encephalopathy, Myoclonic
Benign Infantile Myoclonic Epilepsy- Benign Infantile Myoclonic Epilepsy
- Myoclonic Epilepsy, Benign Infantile
- Myoclonic Epilepsy, Infantile, Benign
- Epilepsy, Myoclonic, Infantile, Benign
Epilepsy, Myoclonic, Infantile, Severe- Epilepsy, Myoclonic, Infantile, Severe
- Infantile Severe Myoclonic Epilepsy
- Myoclonic Epilepsy, Infantile, Severe
- Myoclonic Epilepsy, Severe, Of Infancy
- Severe Infantile Myoclonic Epilepsy
- Severe Myoclonic Epilepsy, Infantile
- Severe Myoclonic Epilepsy Of Infancy
- Dravet Syndrome
- Dravet Syndromes
- Doose Syndrome
- Myoclonic Epilepsy, Severe Infantile
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Below are MeSH descriptors whose meaning is more general than "Epilepsies, Myoclonic".
Below are MeSH descriptors whose meaning is more specific than "Epilepsies, Myoclonic".
This graph shows the total number of publications written about "Epilepsies, Myoclonic" by people in this website by year, and whether "Epilepsies, Myoclonic" 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 |
|---|
| 2015 | 1 | 0 | 1 | | 2017 | 5 | 0 | 5 | | 2018 | 5 | 0 | 5 | | 2019 | 3 | 0 | 3 | | 2020 | 4 | 0 | 4 | | 2021 | 4 | 0 | 4 | | 2022 | 5 | 0 | 5 | | 2023 | 1 | 0 | 1 | | 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Epilepsies, Myoclonic" by people in Profiles.
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Sullivan J, Wirrell E, Knupp KG, Chen D, Flamini R, Zafar M, Ventola P, Avenda?o J, Wang F, Parkerson KA, Ticho B. Adaptive functioning and neurodevelopment in patients with Dravet syndrome: 12-month interim analysis of the BUTTERFLY observational study. Epilepsy Behav. 2024 Feb; 151:109604.
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Perry MS, Scheffer IE, Sullivan J, Brunklaus A, Boronat S, Wheless JW, Laux L, Patel AD, Roberts CM, Dlugos D, Holder D, Knupp KG, Lallas M, Phillips S, Segal E, Smeyers P, Lal D, Wirrell E, Zuberi S, Br?nger T, Wojnaroski M, Maru B, O'Donnell P, Morton M, James E, Vila MC, Huang N, Gofshteyn JS, Rico S. Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study. Epilepsia. 2024 Feb; 65(2):322-337.
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Bishop KI, Isquith PK, Gioia GA, Knupp KG, Scheffer IE, Nabbout R, Specchio N, Sullivan J, Auvin S, Helen Cross J, Guerrini R, Farfel G, Galer BS, Gammaitoni AR. Fenfluramine treatment is associated with improvement in everyday executive function in preschool-aged children (<5 years) with Dravet syndrome: A critical period for early neurodevelopment. Epilepsy Behav. 2023 01; 138:108994.
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Sullivan J, Wirrell E, Knupp KG, Chen D, Zafar M, Flamini R, Stutely J, Brathwaite C, Ventola P, Avenda?o J, Parkerson KA, Wyant N, Ticho B. Interim results of adaptive functioning and neurodevelopment in BUTTERFLY - An observational study of children and adolescents with Dravet syndrome. Epilepsy Behav. 2022 12; 137(Pt A):108955.
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Lopez JC, Pare JR, Blackmer AB, Orth LE. Treatment-Refractory Dravet Syndrome: Considerations for Novel Medications. J Pediatr Health Care. 2022 Sep-Oct; 36(5):479-488.
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Wirrell EC, Hood V, Knupp KG, Meskis MA, Nabbout R, Scheffer IE, Wilmshurst J, Sullivan J. International consensus on diagnosis and management of Dravet syndrome. Epilepsia. 2022 07; 63(7):1761-1777.
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Hood V, Berg AT, Knupp KG, Koh S, Laux L, Meskis MA, Zulfiqar-Ali Q, Perry MS, Scheffer IE, Sullivan J, Wirrell E, Andrade DM. COVID-19 vaccine in patients with Dravet syndrome: Observations and real-world experiences. Epilepsia. 2022 07; 63(7):1778-1786.
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Andrade DM, Berg AT, Hood V, Knupp KG, Koh S, Laux L, Meskis MA, Miller I, Perry MS, Scheffer IE, Sullivan J, Villas N, Wirrell E. Dravet syndrome: A quick transition guide for the adult neurologist. Epilepsy Res. 2021 Nov; 177:106743.
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Isom LL, Knupp KG. Dravet Syndrome: Novel Approaches for the Most Common Genetic Epilepsy. Neurotherapeutics. 2021 07; 18(3):1524-1534.
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Gil-Nagel A, Sullivan J, Ceulemans B, Wirrell E, Devinsky O, Nabbout R, Knupp KG, Scott Perry M, Polster T, Davis R, Lock M, Cortes RM, Gammaiton AR, Farfel G, Galer BS, Agarwal A. Treatment with fenfluramine in patients with Dravet syndrome has no long-term effects on weight and growth. Epilepsy Behav. 2021 09; 122:108212.
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