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| Issue | Title | |
| Vol 16, No 2 (2024) | Atypical course of severe myoclonic epilepsy of infancy (Dravet syndrome) | Abstract PDF (Eng) similar documents |
| B. A. Abusueva, M. D. Shanavazova, М. A. Askevova, V. S. Khalilov, M. Yu. Bobylova | ||
| "... Представлен клинический пример пациента с синдромом Драве, вызванным мутацией в гене SCN ..." | ||
| Vol 10, No 3 (2018) | Sudden unexpected death in genetic epileptic encephalopathies: a role of neurocardiac genes | Abstract similar documents |
| E. D. Belousova, M. A. Shkolnikova | ||
| "... » гены ответственны за функции ионных каналов – натриевых, калиевых и др. Так, при синдроме Драве ..." | ||
| Vol 12, No 1S (2020) | Genetic epilepsy with febrile seizures plus (GEFS+) | Abstract similar documents |
| A. A. Sharkov | ||
| "... в генах SCN1B, SCN1A, GABRG2, GABRD, SCN9A, STX1B, HCN1 и др.), так и хромосомные перестройки. Близнецовые ..." | ||
| Vol 14, No 1 (2022) | Idiopathic and symptomatic forms of genetic epilepsy | Abstract similar documents |
| A. G. Malov | ||
| "... группами, обусловленными данной этиологией, являются моногенные эпилепсии (например, синдром Драве ..." | ||
| Vol 15, No 2 (2023) | Third generation antiepileptic drugs: mechanism of action, pharmacokinetics, interaction and use in childhood | Abstract similar documents |
| Z. G. Tadtaeva, A. N. Galustyan, O. A. Gromova, I. S. Sardaryan | ||
| "... приступов, а также при специфических эпилептических синдромах (синдром Леннокса–Гасто, синдром Драве ..." | ||
| 1 - 5 of 5 Items | ||
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