4-aminopyridine has been researched along with Epilepsies, Myoclonic in 2 studies
Epilepsies, Myoclonic: 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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lévesque, M | 1 |
Salami, P | 1 |
Behr, C | 1 |
Avoli, M | 1 |
Liautard, C | 1 |
Scalmani, P | 1 |
Carriero, G | 1 |
de Curtis, M | 1 |
Franceschetti, S | 1 |
Mantegazza, M | 1 |
2 other studies available for 4-aminopyridine and Epilepsies, Myoclonic
Article | Year |
---|---|
Temporal lobe epileptiform activity following systemic administration of 4-aminopyridine in rats.
Topics: 4-Aminopyridine; Animals; Behavior, Animal; CA3 Region, Hippocampal; Electrodes, Implanted; Electroe | 2013 |
Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndrome.
Topics: 4-Aminopyridine; Age Factors; Animals; Animals, Newborn; Bicuculline; Cerebral Cortex; Disease Model | 2013 |