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| Issue | Title | |
| Vol 12, No 3 (2020) | New-Onset Refractory Status Epilepticus (NORSE): literature review and clinical case description | Abstract similar documents |
| S. G. Burd, M. B. Mironov, E. R. Moizykevich, Yu. V. Rubleva, M. A. Bogomazova, А. V. Yurchenko, T. M. Krasilshchikova, A. Yu. Suvorov, A. V. Lebedeva, R. T. Tairova | ||
| "... В статье представлены дефиниции первичного рефрактерного эпилептического статуса (NORSE-синдром ..." | ||
| Vol 8, No 4 (2016) | NEW OPPORTUNITIES PHARMACOTHERAPY PATIENTS WITH REFRACTORY EPILEPSY | Abstract similar documents |
| P. N. Vlasov | ||
| "... – 46,2% и височной – 44,2% локализацией эпилептического очага. Большинству пациентов (71,2%) перампанел ..." | ||
| Vol 14, No 1 (2022) | Epilepsy in Norrie disease | Abstract similar documents |
| V. A. Aysina, О. V. Kozhevnikova, О. V. Osipova, A. V. Lashkova | ||
| "... Рассмотрены представления о болезни Норри с позиции неврологии и клинический случай рефрактерной ..." | ||
| Vol 8, No 1 (2016) | EFFECT OF KETOGENIC DIET ON COGNITIVE AND MOTOR FUNCTIONS IN CHILDREN WITH DRUG-RESISTANT EPILEPSY | Abstract similar documents |
| E. G. Lukyanova, S. O. Ayvazyan, K. V. Osipova, T. N. Sorvacheva, E. A. Pyreva | ||
| "... возрасте, вызывая так называемую эпилептическую энцефалопатию, приводящую к регрессу когнитивных ..." | ||
| Vol 14, No 3 (2022) | Diagnostics and age-related evolution of Lennox–Gastaut syndrome. Management in diverse patient age periods | Abstract similar documents |
| E. D. Belousova, S. G. Burd, N. A. Ermolenko, K. Yu. Mukhin | ||
| "... известна классическая триада критериев диагноза: 1) наличие разнообразных типов рефрактерных эпилептических ..." | ||
| Vol 16, No 4 (2024) | DEPDC5 mutations in familial epilepsy syndrome: genetic insights and therapeutic approaches | Abstract PDF (Eng) similar documents |
| M. K.C. Diallo, S. Mukesh, L. Kapil, R. Singla, D. Tar, S. N. Tammineedi, E. Singer, H. Chhayani, K. Arumaithurai, U. K. Patel, R. Arora | ||
| "... -10 и pleckstrin) представляет собой группу эпилептических расстройств, вызванных мутациями в гене DEPDC5, который ..." | ||
| 1 - 6 of 6 Items | ||
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