Zobrazeno 1 - 10
of 30
pro vyhledávání: '"E. S. Il'ina"'
Autor:
M. Yu. Bobylova, V. S. Kakaulina, E. S. Il’ina, I. V. Nekrasova, N. L. Pechatnikova, S. V. Mikhaylova, M. B. Mironov, K. Yu. Mironov
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 9, Iss 2, Pp 39-46 (2017)
Dystonic hyperkinesias in children of early childhood may beinvolved in the structure of many syndromes that have differentetiological factors, prognosis, and treatment. This review presentsvarious clinical types of dystonias: benign idiopathic forms
Externí odkaz:
https://doaj.org/article/c1516c10273e4865ab72b5a2e5b2acad
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
Autor:
M. Yu. Bobylova, K. Yu. Mukhin, I. V. Ivanova, I. V. Nekrasova, O. A. Pylaeva, N. Yu. Borovikova, E. S. Il’ina
Publikováno v:
Русский журнал детской неврологии, Vol 11, Iss 1, Pp 23-28 (2016)
Examinations were made in 11 female patients aged 3 to 23 years with Rett syndrome and typical mutation in the MECP2 gene, who had been followed up from 2006 to 2015. The investigators evaluated neurological and psychic status (systematically) and pe
Externí odkaz:
https://doaj.org/article/b467a58d0aed40b5a56fa277475f0762
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:
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
Autor:
A A, Kholin, N N, Zavadenko, I D, Fedonyuk, A V, Antonets, K Yu, Mukhin, A G, Malov, M I, Vshivkov, G V, Anisimov, E S, Il'ina
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 119(7. Vyp. 2)
To study clinical and neurophysiological data of early infantile epileptic encephalopathy type 14 caused by KCNT1 mutations.For the period 2017 to 2019, 3 non-relative girls with clinical characteristics of epilepsy of infancy with migrating focal se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d2f3f26d5ffe58f00d53ad1b63fd13d
https://pubmed.ncbi.nlm.nih.gov/31532594
https://pubmed.ncbi.nlm.nih.gov/31532594
Publikováno v:
Epilepsy & Behavior. 101:106743
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59461217d6468d5dfd3b8b132b8c61fa
https://doi.org/10.1016/j.yebeh.2019.08.018
https://doi.org/10.1016/j.yebeh.2019.08.018
Autor:
L. M. Kolpakchi, V S Khalilov, N. N. Zavadenko, E S Il'ina, A. A. Kholin, I. D. Fedonyuk, E. S. Kosyakova
Publikováno v:
Neuroscience and Behavioral Physiology. 44:765-771
A total of 722 patients (374 men and 348 women, aged from three months to 57 years) were treated with topiramate during the period 2002–2012. Epilepsy was diagnosed and antiepileptic treatment was evaluated using follow-up video-EEG monitoring. Top
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::465277d5afb71e772355c1200eee1787
https://doi.org/10.1007/s11055-014-9981-7
https://doi.org/10.1007/s11055-014-9981-7
Publikováno v:
Klinicheskaia meditsina. 93(10)
Brugada syndrome is a commonest cause of malignant disorders of cardiac rhythm associated with sudden death. It is diagnosed based on characteristic ECG signs and ventricular arrhythmia. This paper reports a 49 year-old patient with long-standing lat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ba0f9c4894afe3162d17db07b1c27e5a
https://pubmed.ncbi.nlm.nih.gov/26964470
https://pubmed.ncbi.nlm.nih.gov/26964470