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| Issue | Title | |
| Vol 3, No 4 (2011) | KABUKI SYNDROME WITH EPILEPSY: CLINICAL CASE | Abstract similar documents |
| N. Yu. Borovikova, K. S. Borovikov, K. Yu. Mukhin, M. B. Mironov | ||
| "... Kabuki syndrome is rare genetic disorder. Patients with this syndrome are phenotypically similar ..." | ||
| 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 5, No 2 (2013) | FEJERMAN SYNDROME (BENIGN NONEPILEPTIC MYOCLONUS OF INFANCY) | Abstract similar documents |
| M. B. Mironov, V. Iu. Nogovitsyn, M. O. Abramov, E. A. Dobrovskaya, N. E. Kvaskova, K. Yu. Mukhin | ||
| "... Abstract: Fejerman syndrome (benign nonepileptic myoclonus of infancy) is a rare nonepileptic ..." | ||
| Vol 5, No 3 (2013) | CLINICAL AND ELECTROENCEPHALOGRAPHIC SEMIOLOGY OF MYOCLONIC-ATONIC SEIZURES | Abstract similar documents |
| M. B. Mironov, K. Yu. Mukhin, T. M. Krasilschikova, A. F. Dolinina, A. S. Petrukhin | ||
| "... .2% of the patients. Lennox-Gastaut syndrome was revealed in 23.6% of cases. Onset of epilepsy with MAS varied widely ..." | ||
| 1 - 4 of 4 Items | ||
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