Zobrazeno 1 - 10
of 18
pro vyhledávání: '"V. S., Khalilov"'
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 16, Iss 2, Pp 130-136 (2024)
A clinical observation of a patient with Dravet syndrome caused by SCN1A gene mutation is presented. Dravet syndrome is a severe epileptic encephalopathy that occurs in early childhood, accompanied by seizure polymorphism, drug-resistant course and s
Externí odkaz:
https://doaj.org/article/19fb025abb994b6b8df9a5072ab49787
Autor:
V. S. Khalilov, A. N. Kislyakov, A. A. Kholin, U. A. Kukota, N. A. Medvedeva, A. S. Shapovalov, A. E. Druy
Publikováno v:
Русский журнал детской неврологии, Vol 19, Iss 2, Pp 64-71 (2024)
Diffuse leptomeningeal glioneuronal tumor was introduced into the World Health Organization classification of central nervous system tumors in 2016. According to the actual World Health Organization classification of central nervous system tumors eme
Externí odkaz:
https://doaj.org/article/dfea64631e4c4f06ae2c35b96c178dfb
Publikováno v:
Русский журнал детской неврологии, Vol 13, Iss 4, Pp 23-39 (2019)
Background. It has been suggested that the part of the cryptogenic epilepsies is a consequence of minor-foci disorders of cortical architectonics, the diagnosis of which is not always possible due to the unavailability of MR-scanners with high magnet
Externí odkaz:
https://doaj.org/article/eeeb6d21f26b45a69c0c19afed76c96d
Autor:
V. S. Khalilov, A. N. Kislyakov, N. A. Medvedeva, A. V. Sadykova, D. N. Kopachev, А. A. Kholin
Publikováno v:
Diagnostic radiology and radiotherapy. 13:88-96
A new form of morphologically and molecularly distinguishable epileptogenic neoplasia with characteristic microscopic findings and a distinct DNA methylation signature as well as frequent genetic anomalies, was revealed in 2017; the tumor was called
Autor:
V. S. Khalilov, A. N. Kislyakov, A. A. Kholin, Kh. S. Gazdieva, K. I. Panova, N. N. Zavadenko, K. Kobow
Publikováno v:
Diagnostic radiology and radiotherapy. 13:21-29
Gangliogliomas are known to be rare and mainly slow-growing benign primary central nervous system tumors, most frequently occurring in children and young adults. They are the most common epilepsy-associated tumors, which frequent location is the temp
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:
V. S. Khalilov, A. A. Kholin, A. N. Kislyakov, B. R. Bakaeva, N. A. Medvedeva, K. I. Panova, N. N. Zavadenko
Publikováno v:
Neuroscience and Behavioral Physiology. 52:362-367
Publikováno v:
Diagnostic radiology and radiotherapy. 12:93-100
Recently, in the scientist community of specialists dealing with structural epilepsy, it has been noticed an increasing interest in a special form of cortical development disorder not to be included in the ILAE Classification of the epilepsies the 20
Autor:
N N Zavadenko, A A Kholin, N A Medvedeva, B R Bakaeva, K I Panova, A N Kislyakov, V S Khalilov
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 121(6)
On the example of the diagnosis of the structural basis of focal epilepsy in an adult patient, the possibilities of a multimodal and interdisciplinary approach to diagnosis, combining the latest methods of neuroimaging with the results of neurophysio
Autor:
V. S. Khalilov, A. A. Kholin, N. A. Medvedeva, I. G. Vasiliev, I. V. Rasskazchikova, A. N. Kislyakov, R. R. Ismailova, N. N. Zavadenko
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 5, Pp 103-112 (2016)
Fifty-six out of 79 pediatric patients with supratentorial brain tumors were noted to have symptomatic epilepsy. Dysembryoplastic neuroepithelial tumors (DNET), diffuse astrocytomas (DA), and gangliogliomas (GG) were the most epileptogenic tumors. Se