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JUVENILE MYOCLONIC EPILEPSY: FOCUS ON THE USE OF TOPIRAMATE (LITERATURE REVIEW AND OWN DATA)
Juvenile myoclonic epilepsy (JME) is an inherited genetic syndrome within the group of idiopathic generalized epilepsies (IGE). The disease is characterized by an adolescence-onset with massive myoclonic seizures often combined with generalized convulsive seizures and absence seizures and by typical...
Wedi'i Gadw mewn:
| Prif Awduron: | , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Russo |
| Cyhoeddwyd: |
ABV-press
2017-08-01
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| Cyfres: | Russkij Žurnal Detskoj Nevrologii |
| Pynciau: | |
| Mynediad Ar-lein: | https://rjdn.abvpress.ru/jour/article/view/208 |
| Tagiau: |
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