Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Olga Sysoeva"'
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Background Rett syndrome (RS) is a rare neurodevelopmental disorder characterized by mutations in the MECP2 gene. Patients with RS have severe motor abnormalities and are often unable to walk, use hands and speak. The preservation of percept
Externí odkaz:
https://doaj.org/article/bc875e7dcc9d44588b5542c5ff840ae9
Autor:
Olga Sysoeva, Vladimir Maximenko, Alexander Kuc, Victoria Voinova, Olga Martynova, Alexander Hramov
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Spontaneous EEG contains important information about neuronal network properties that is valuable for understanding different neurological and psychiatric conditions. Rett syndrome (RTT) is a rare neurodevelopmental disorder, caused by mutat
Externí odkaz:
https://doaj.org/article/4e07347952724d05b424ac7f4f7a2f74
Publikováno v:
Frontiers in Neuroinformatics, Vol 18 (2024)
IntroductionMental disorders are a significant concern in contemporary society, with a pressing need to identify biological markers. Long-range temporal correlations (LRTC) of brain rhythms have been widespread in clinical cohort studies, especially
Externí odkaz:
https://doaj.org/article/1c1f73062a024be59ca4cf4dd926aeb3
Publikováno v:
PLoS ONE, Vol 18, Iss 8, p e0289964 (2023)
Our study describes the effects of sensory tetanization on neurophysiological and behavioral measures in humans linking cellular studies of long-term potentiation with high-level brain processes. Rapid (every 75ms) presentation of pure tone (1020 Hz,
Externí odkaz:
https://doaj.org/article/77a09a4d679c4734a8ff007809397d45
Autor:
Gurgen Soghoyan, Alexander Ledovsky, Maxim Nekrashevich, Olga Martynova, Irina Polikanova, Galina Portnova, Anna Rebreikina, Olga Sysoeva, Maxim Sharaev
Publikováno v:
Frontiers in Neuroinformatics, Vol 15 (2021)
Independent Component Analysis (ICA) is a conventional approach to exclude non-brain signals such as eye movements and muscle artifacts from electroencephalography (EEG). A rejection of independent components (ICs) is usually performed in semiautomat
Externí odkaz:
https://doaj.org/article/9d25f5e1329440c78e8fc7e2d97a4dd4
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10, p 5308 (2021)
Rett syndrome (RTT) is a rare neurodevelopmental disorder that is usually caused by mutations of the MECP2 gene. Patients with RTT suffer from severe deficits in motor, perceptual and cognitive domains. Electroencephalogram (EEG) has provided useful
Externí odkaz:
https://doaj.org/article/e0f8a3bf783b496e966ef29ef7e26dbe
Autor:
Semen Kurkin, Nikita Smirnov, Elena Pitsik, Muhammad Salman Kabir, Olga Martynova, Olga Sysoeva, Galina Portnova, Alexander Hramov
Publikováno v:
The European Physical Journal Special Topics. 232:683-693
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bf72bd48f860556dfd14ed9fff07ee4
https://doi.org/10.1140/epjs/s11734-022-00717-0
https://doi.org/10.1140/epjs/s11734-022-00717-0
Autor:
Olga Sysoeva, Vladimir Maximenko, Alexander Kuc, Victoria Voinova, Olga Martynova, Alexander Hramov
Spontaneous EEG contains important information about neuronal network properties that is valuable for understanding different neurological and psychiatric conditions. Rett syndrome (RTT) is a rare neurodevelopmental disorder, caused by mutation in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd5af17dd82d2da4b75947958cc4af45
https://doi.org/10.21203/rs.3.rs-2273718/v1
https://doi.org/10.21203/rs.3.rs-2273718/v1
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 12; Pages: 1973
Rett syndrome (RTT), a severe neurodevelopmental disorder caused by MECP2 gene abnormalities, is characterized by atypical EEG activity, and its detailed examination is lacking. We combined the comparison of one-time eyes open EEG resting state activ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b00e5bbb342e6f2721a48421c16d94d