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| Issue | Title | |
| Vol 12, No 1S (2020) | Juvenile Myoclonic Epilepsy. Update | Abstract similar documents |
| I. V. Volkov, O. K. Volkova | ||
| Vol 11, No 4 (2019) | Significance of exome sequencing for diagnosis of epilepsy in children | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko | ||
| Vol 12, No 1 (2020) | Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko | ||
| Vol 11, No 4 (2019) | Is it possible to predict the treatment efficacy in adult patients with focal epilepsy? | Abstract similar documents |
| K. V. Firsov, M. G. Amirhanyan, A. S. Kotov | ||
| Vol 12, No 1 (2020) | Childhood autism associated with neurological manifestations and corpus callosum hypoplasia: literature review and clinical cases | Abstract similar documents |
| O. A. Komissarova, O. A. Milovanova, G. G. Avakyan, S. V. Bugriy | ||
| Vol 11, No 4 (2019) | The use of intraoperative ultrasound in patients with focal cortical dysplasia: preliminary observations | Abstract similar documents |
| A. A. Sufianov, S. V. Mirhaydarov, Yu. A. Yakimov, O. M. Klimenko, A. A. Skripnikov, S. Z. Stefanov, O. N. Sadykova, R. S. Talybov, R. A. Sufianov | ||
| Vol 11, No 4 (2019) | Early infantile epileptic encephalopathy type 16: the new clinical and genetic variant of TBC1D24 gene mutation | Abstract similar documents |
| A. A. Kholin, I. D. Fedonyuk, O. P. Dovelman, N. N. Zavadenko, T. V. Kozhanova, E. A. Kholina, G. Sh. Khondkarian, E. S. Il`ina | ||
| 1 - 7 of 7 Items | ||
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