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| Issue | Title | |
| 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 | ||
| "... Aim. To consolidate literature data and to demonstrate rare hereditary neurogenetic syndromes ..." | ||
| Vol 8, No 4 (2016) | EPILEPSY MANIFESTATIONS IN PATIENTS WITH MALFORMATIONS OF THE CORPUS CALLOSUM | Abstract similar documents |
| O. A. Milovanova, E. R. Moyzykevich, G. G. Avakian, Y. Yu. Tarakanova | ||
| "... of the example of two disembriogenetic syndromes (Aicardi syndrome and Pierre-Robin syndrome). These hereditary ..." | ||
| Vol 9, No 1 (2017) | ILAE CLASSIFICATION OF THE EPILEPSIES: THE 2017 REVISION AND UPDATE | Abstract similar documents |
| G. N. Avakyan, D. V. Blinov, A. V. Lebedeva, S. G. Burd, G. G. Avakyan | ||
| "... syndrome. An etiologic diagnosis should be considered at each step along the diagnostic pathway ..." | ||
| Vol 11, No 3 (2019) | Recommendations of the Russian League Against Epilepsy (RLAE) on the use of magnetic resonance imaging in the diagnosis of epilepsy | Abstract similar documents |
| G. N. Avakyan, D. V. Blinov, A. A. Alikhanov, E. M. Perepelova, V. A. Perepelov, S. G. Burd, A. V. Lebedeva, G. G. Avakyan | ||
| 1 - 4 of 4 Items | ||
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