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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 12, No 1 (2020) | Epilepsy in Sturge-Weber syndrome: a literature review and description of a clinical case | Abstract similar documents |
| N. I. Shova, V. A. Mikhailov, S. A. Korovina, D. V. Alekseeva | ||
| "... The Struge-Weber syndrome is the third most common neurodermal disease after neurofibromatosis ..." | ||
| Vol 12, No 1S (2020) | What’s hidden behind Lennox-Gastaut syndrome? | Abstract similar documents |
| E. D. Belousova | ||
| "... A number of epileptologists often diagnose Lennox-Gastaut syndrome, while others almost never do ..." | ||
| 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 | ||
| "... for patients with Helsmoortel-van der Aa syndrome (OMIM: # 615873). Mutations in the ADNP gene are the genetic ..." | ||
| 1 - 4 of 4 Items | ||
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