 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
|
| MeSH Number(s) |
C10.228.140.490.375.130 C10.228.140.490.493.063
|
| 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
|
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 | 6 | 0 | 6 | | 2019 | 3 | 0 | 3 | | 2020 | 4 | 0 | 4 | | 2021 | 4 | 0 | 4 | | 2022 | 3 | 0 | 3 |
To return to the timeline, click here.
Below are the most recent publications written about "Epilepsies, Myoclonic" by people in Profiles.
-
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.
-
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.
-
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.
-
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.
-
Isom LL, Knupp KG. Dravet Syndrome: Novel Approaches for the Most Common Genetic Epilepsy. Neurotherapeutics. 2021 07; 18(3):1524-1534.
-
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.
-
Van Nuland A, Ivanenko A, Meskis MA, Villas N, Knupp KG, Berg AT. Sleep in Dravet syndrome: A parent-driven survey. Seizure. 2021 Feb; 85:102-110.
-
Joshi C, Nickels K, Demarest S, Eltze C, Cross JH, Wirrell E. Results of an international Delphi consensus in epilepsy with myoclonic atonic seizures/ Doose syndrome. Seizure. 2021 Feb; 85:12-18.
-
Nickels K, Kossoff EH, Eschbach K, Joshi C. Epilepsy with myoclonic-atonic seizures (Doose syndrome): Clarification of diagnosis and treatment options through a large retrospective multicenter cohort. Epilepsia. 2021 01; 62(1):120-127.
-
Berg AT, Gaebler-Spira D, Wilkening G, Zelko F, Knupp K, Dixon-Salazar T, Villas N, Meskis MA, Harwell V, Thompson T, Sims S, Nesbitt G. Nonseizure consequences of Dravet syndrome, KCNQ2-DEE, KCNB1-DEE, Lennox-Gastaut syndrome, ESES: A functional framework. Epilepsy Behav. 2020 10; 111:107287.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|