Zobrazeno 1 - 10
of 754
pro vyhledávání: '"A S, Kotov"'
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 16, Iss 0, Pp 38-43 (2024)
Neuromyelitis optica spectrum disorders (NMOSD) are a group of chronic autoimmune diseases of the central nervous system with a relapsing course. Unfortunately, the symptoms of exacerbation cannot always be completely stopped, and in addition to moto
Externí odkaz:
https://doaj.org/article/d7e00b27bcbb406ca1f7bda67f31d7b1
Clinical polymorphism of myelitis in neurologic practice. Lecture with description of clinical cases
Autor:
A. A. Kondratov, A. S. Kotov
Publikováno v:
Русский журнал детской неврологии, Vol 19, Iss 2, Pp 33-48 (2024)
Among rather rare but extremely interesting and important conditions, myelitis stands apart due to its complexity and diversity of clinical manifestations. In this article, in addition to the well-known data on this group of diseases, we present the
Externí odkaz:
https://doaj.org/article/09adb95669da4394a7789bf548a567a6
Autor:
A. Sh. Latypov, E. V. Proskurina, S. V. Kotov, O. P. Sidorova, I. A. Vasilenko, D. V. Kassina, A. S. Kotov
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 4, Pp 53-57 (2024)
MERRF syndrome (myoclonic epilepsy ragged red fibres) belongs to the group of primary mitochondrial diseases and is characterized by a combination of myoclonic epilepsy and the phenomenon of ragged red fibres on muscle biopsy. The aim of this work is
Externí odkaz:
https://doaj.org/article/7029547030f64eaab67c392e81e882f7
Autor:
A. A. Kondratov, A. S. Kotov
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 4, Pp 44-48 (2024)
For more than two hundred years after its discovery, nitric oxide (I) has been widely used in medicine as an anesthetic, in the car industry as an engine performance enhancer, in the food industry as a preservative, and, unfortunately, among young pe
Externí odkaz:
https://doaj.org/article/fb30f2111f7a41d296565354213e7c8e
Autor:
A. A. Ershova, A. S. Kotov
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 2-3, Pp 45-51 (2023)
Leukodystrophies are genetically determined diseases characterised by primary damage to the white matter of the central nervous system, irrespective of the genetic defect and structural component involved. This paper classification is presented based
Externí odkaz:
https://doaj.org/article/beea818c30c4424fa52dbffa6c073190
Autor:
Sergey V. Kotov, Maria M. Shcherbakova, Valentina A. Zenina, Elena V. Isakova, Alexey S. Kotov
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 17, Iss 3, Pp 13-20 (2023)
Introduction. Various speech disorders that lead to impaired communication occur in 3050% of ischemic stroke (IS) survivors. Although most attention is traditionally paid to aphasia, speech disorders also include the following: dysarthria, dysphonia
Externí odkaz:
https://doaj.org/article/3557673a78d74dcfb0be3826e2a8ac20
Publikováno v:
Русский журнал детской неврологии, Vol 19, Iss 1 (2024)
Wernicke encephalopathy is a neuropsychiatric syndrome characterized by three main symptoms: oculomotor disturbances, cerebellar ataxia, and psychiatric disturbances. The condition is associated with a high mortality and morbidity rate. Wernicke ence
Externí odkaz:
https://doaj.org/article/36ef9c0f79b346c3bdd3546c372195d9
Autor:
E. A. Sandu, A. S. Kotov
Publikováno v:
Русский журнал детской неврологии, Vol 19, Iss 1 (2024)
Background. Remission in general sense means disappearance of signs and symptoms of the disease. The risk of recurrence of seizures is usually evaluated only in terms of the risk of a second unprovoked seizure after the first one or the risk of recur
Externí odkaz:
https://doaj.org/article/0ce2f20f780a421494956835e4c37e4a
Autor:
V. E. Avdeeva, A. S. Kotov
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 1, Pp 10-21 (2023)
Acute disseminated encephalomyelitis is an acute autoimmune demyelinating disease that manifests as a widespread polyfocal asymmetric lesions of the central nervous system and, in some cases, optic nerves with the formation of corresponding neurologi
Externí odkaz:
https://doaj.org/article/8f8e47a93dc746029e9edd781e427df7
Autor:
A. S. Kotov, K. V. Firsov
Publikováno v:
Русский журнал детской неврологии, Vol 17, Iss 4, Pp 63-70 (2023)
Mitochondrial dysfunction mainly affects organs with high metabolic demand, primarily the brain. Epilepsy is a common phenotypic sign of both syndromic and non-syndromic mitochondrial diseases. Epilepsy in mitochondrial diseases is poorly treatable a
Externí odkaz:
https://doaj.org/article/a3e68cc9994a4fb88666c4940ec1cf71