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Issue | Title | |
Vol 14, No 2 (2022) | Epilepsy syndromes: the 2022 ILAE definition and classification | Abstract similar documents |
D. V. Blinov | ||
"... Until recently, no classification of epileptic syndromes officially approved by the International ..." | ||
Vol 14, No 2 (2022) | Clinical case of distal arthrogryposis in combination with epilepsy due to an unbalanced translocation | Abstract similar documents |
T. V. Kozhanova, S. S. Zhilina, T. I. Meshсheryakova, N. P. Prokopyeva, A. G. Prityko, N. N. Zavadenko | ||
"... with Freeman–Sheldon syndrome had no mutations in genes associated with distal arthrogryposis. Chromosomal ..." | ||
Vol 14, No 1 (2022) | Idiopathic and symptomatic forms of genetic epilepsy | Abstract similar documents |
A. G. Malov | ||
"... epilepsies (e.g., Dravet syndrome) as well as symptomatic epilepsies due to other genetically ..." | ||
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 | ||
"... Lennox–Gastaut syndrome is an epileptic encephalopathy with onset in childhood. The classical ..." | ||
Vol 13, No 4 (2021) | Short-term and long-term changes in seizure frequency and neurocognitive status in pediatric patients after surgery for mixed neuronal-glial brain tumors | Abstract similar documents |
L. A. Gorlova, O. O. Shmeleva, E. V. Fedorov, A. V. Kim, Yu. V. Dinikina, W. A. Khachatryan, K. A. Samochernykh | ||
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