"Epilepsy, Rolandic" 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.
An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and dysarthria. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)
Concept/Terms
Epilepsy, Rolandic- Epilepsy, Rolandic
- Epilepsies, Rolandic
- Rolandic Epilepsies
- Rolandic Epilepsy
- Sylvian Epilepsy
- Epilepsy, Sylvian
- Rolands Epilepsy
- Epilepsy, Rolands
Benign Rolandic Epilepsy- Benign Rolandic Epilepsy
- Epilepsy, Benign Rolandic
- Rolandic Epilepsy, Benign
- BECTS
- Epilepsy, Centrotemporal
- Centrotemporal Epilepsies
- Centrotemporal Epilepsy
- Epilepsies, Centrotemporal
- Benign Epilepsy With Centrotemporal Spikes
- Benign Rolandic Epilepsy of Childhood
- Centralopathic Epilepsy
- Centralopathic Epilepsies
- Epilepsies, Centralopathic
- Epilepsy, Centralopathic
- BCECTS
- Benign Childhood Epilepsy With Centro-Temporal Spikes
- Benign Childhood Epilepsy With Centro Temporal Spikes
Below are MeSH descriptors whose meaning is more general than "Epilepsy, Rolandic".
Below are MeSH descriptors whose meaning is more specific than "Epilepsy, Rolandic".
This graph shows the total number of publications written about "Epilepsy, Rolandic" by people in Harvard Catalyst Profiles by year, and whether "Epilepsy, Rolandic" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2001 | 2 | 0 | 2 |
2004 | 0 | 1 | 1 |
2007 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2011 | 3 | 0 | 3 |
2015 | 2 | 0 | 2 |
2017 | 2 | 0 | 2 |
2019 | 4 | 0 | 4 |
2020 | 4 | 0 | 4 |
2021 | 4 | 0 | 4 |
2022 | 2 | 0 | 2 |
2023 | 3 | 0 | 3 |
Below are the most recent publications written about "Epilepsy, Rolandic" by people in Profiles.
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Atypical functional connectivity hierarchy in Rolandic epilepsy. Commun Biol. 2023 07 10; 6(1):704.
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Decreased thalamocortical connectivity in resolved Rolandic epilepsy. Clin Neurophysiol. 2023 09; 153:21-27.
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Children with Rolandic epilepsy have micro- and macrostructural abnormalities in white matter constituting networks necessary for language function. Epilepsy Behav. 2023 Jul; 144:109254.
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Transient, developmental functional and structural connectivity abnormalities in the thalamocortical motor network in Rolandic epilepsy. Neuroimage Clin. 2022; 35:103102.
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Source EEG reveals that Rolandic epilepsy is a regional epileptic encephalopathy. Neuroimage Clin. 2022; 33:102956.
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Influence of epileptogenic region on brain structural changes in Rolandic epilepsy. Brain Imaging Behav. 2022 Feb; 16(1):424-434.
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Measuring the effects of sleep on epileptogenicity with multifrequency entropy. Clin Neurophysiol. 2021 09; 132(9):2012-2018.
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Delayed brain development of Rolandic epilepsy profiled by deep learning-based neuroanatomic imaging. Eur Radiol. 2021 Dec; 31(12):9628-9637.
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Anti-seizure medication correlated changes of cortical morphology in childhood epilepsy with centrotemporal spikes. Epilepsy Res. 2021 07; 173:106621.
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Persistent abnormalities in Rolandic thalamocortical white matter circuits in childhood epilepsy with centrotemporal spikes. Epilepsia. 2020 11; 61(11):2500-2508.