Zobrazeno 1 - 10
of 18
pro vyhledávání: '"I D, Fedonyuk"'
Autor:
A. L. Kurenkov, L. M. Kuzenkova, B. I. Bursagova, V. V. Chernikov, O. V. Agranovich, L. G. Khachatryan, V. M. Kenis, V. A. Zherebtsova, M. N. Sarzhina, N. D. Odinaeva, A. R. Artemenko, G. A. Popova, E. A. Moroshek, E. E. Tabe, A. A. Nezhelskaya, A. A. Maksimenko, L. Ya. Akhadova, M. V. Indereikin, N. V. Duibanova, L. V. Tikhonova, A. V. Sapogovskiy, Z. M. Gadzhialieva, A. V. Grigorieva, V. S. Perminov, I. D. Fedonyuk, L. M. Kolpakchi, A. Yu. Kursakova, N. A. Tsurina
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 2, Pp 117-125 (2022)
Botulinum therapy for cerebral palsy (CP) is considered not only as one of the effective approaches for the treatment of increased muscle tone and spasticity, but also as a method of excessive salivation correction. The article presents an overview o
Externí odkaz:
https://doaj.org/article/9d0b5cf529ef41c19d59bbf356c0c69c
Autor:
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
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 11, Iss 4, Pp 321-334 (2020)
Objective: to analyse the clinical and neurophysiological data from a case of early infantile epileptic encephalopathy type 16 in a child with homozygous mutation in TBC1D24 gene.Material and methods. Female child M. aged 1 year and 2 months, with id
Externí odkaz:
https://doaj.org/article/523b59da7fd948b0b5de1941641f0d9f
Autor:
A. A. Kholin, N. N. Zavadenko, L. M. Kolpakchi, I. D. Fedonyuk, A. S. Papikyan, А. N. Zavadenko, E. S. Ilina
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 11, Iss 2, Pp 164-174 (2019)
Objective. Study the clinical and neurophysiological evolution of early infantile epileptic encephalopathy type 4 (EIEE4) caused by a STXBP1 gene mutation.Material and methods. During 2016-2019, we conducted dynamic observation and treatment of a gir
Externí odkaz:
https://doaj.org/article/9693fc1805a84005a893f6009843e1da
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 9, Iss 2, Pp 21-28 (2017)
Electrical status epilepticus during slow-wave sleep (ESES) is an EEG pattern of continuous (85-100%) diffuse epileptiform activity in the sleep EEG. The morphology of the epileptiform complexes is identical to benign epileptiform discharges of child
Externí odkaz:
https://doaj.org/article/090ea7f13f864f49b9cebf03474d7d89
Autor:
A. A. Kholin, N. N. Zavadenko, E. S. Il'ina, I. D. Fedonyuk, L. M. Kolpakchi, V. S. Khalilov, E. S. Kosyakova
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 5, Iss 3, Pp 34-40 (2016)
Abstract: the aim of the study was to analyst the efficiency and safety of topiramate in children and adult epileptic populations depending on the patient’s age and forms of epilepsy. 597 epileptic patients receiving topiramate (302 males, 295 fema
Externí odkaz:
https://doaj.org/article/adf616170a8a4155b3131ac3a1a43c66
Publikováno v:
Русский журнал детской неврологии, Vol 9, Iss 1, Pp 5-22 (2015)
The authors had properly analyzed 28 clinical cases of epilepsy aggravation on levetiracetam therapy in pediatric patients receiving levetiracetam (n = 183). Risk of aggravation was 15,3 % (n = 28), including aggravation of epileptic status in 3,3 %
Externí odkaz:
https://doaj.org/article/e720625c04df4a738f2703036c29705a
Autor:
G. V. Anisimov, E S Il'ina, M. I. Vshivkov, A A Kholin, N. N. Zavadenko, K. Yu. Mukhin, A. G. Malov, A. V. Antonets, I. D. Fedonyuk
Publikováno v:
Neuroscience and Behavioral Physiology. 50:534-540
Objectives. To study the clinical and electroencephalographic characteristics of early infantile epileptic encephalopathy (EIEE) type 14, due to mutations in the KCNT1 gene. Materials and methods. Over the period 2017–2019, three unrelated girls (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bd02bb2e305635d7ac60cf5e69dd531
https://doi.org/10.1007/s11055-020-00933-y
https://doi.org/10.1007/s11055-020-00933-y
Autor:
G. Sh. Khondkarian, E. A. Kholina, I. D. Fedonyuk, E. S. Il`ina, T.V. Kozhanova, N. N. Zavadenko, A A Kholin, O. P. Dovelman
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 11, Iss 4, Pp 321-334 (2020)
Objective: to analyse the clinical and neurophysiological data from a case of early infantile epileptic encephalopathy type 16 in a child with homozygous mutation in TBC1D24 gene. Material and methods . Female child M. aged 1 year and 2 months, with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df766546dcbe78c243731e958f4df820
https://doi.org/10.17749/2077-8333.2019.11.4.321-334
https://doi.org/10.17749/2077-8333.2019.11.4.321-334
Autor:
N. N. Zavadenko, А. N. Zavadenko, L. M. Kolpakchi, A. S. Papikyan, E S Il'ina, I. D. Fedonyuk, A A Kholin
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 11, Iss 2, Pp 164-174 (2019)
Objective . Study the clinical and neurophysiological evolution of early infantile epileptic encephalopathy type 4 (EIEE4) caused by a STXBP1 gene mutation. Material and methods. During 2016-2019, we conducted dynamic observation and treatment of a g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0abb9ef7ec7ed304659f253d00da45ad
https://www.epilepsia.su/jour/article/view/476
https://www.epilepsia.su/jour/article/view/476
Autor:
I. D. Fedonyuk, I. F. Stetsenko, V V Ilinsky, E. I. Surkova, Elena Grigorievna Okuneva, A. A. Kholin, Nikolay Plotnikov, Olesia Igorevna Klimchuk, Natalia Vladimirovna Baryshnikova, Anna Krasnenko, Anastasiya Aleksandrovna Kozina, E S Il'ina
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Background Epilepsy with intellectual disability limited to females (Epileptic encephalopathy, early infantile, 9; EIEE9) is a rare early infantile epileptic encephalopathy characterized by an unusual X-linked inheritance: females with heterozygous m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d15f916bd54d5a16ae162e510fdb865a
https://doi.org/10.1186/s12881-020-01119-6
https://doi.org/10.1186/s12881-020-01119-6