Zobrazeno 1 - 10
of 18
pro vyhledávání: '"E. A. Kantimirova"'
Autor:
K. D. Lysova, I. K. Kuznetsov, A. I. Paramonova, A. A. Usoltseva, E. A. Kantimirova, N. A. Shnayder, D. V. Dmitrenko
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 16, Iss 1, Pp 77-87 (2024)
Background. Сognitive impairment is one of the major epilepsy-related comorbidities. Upon long-term disease course, a decline in cognitive functions occurs in about 70–80% of cases. Juvenile myoclonic epilepsy (JME) is one of the most common forms
Externí odkaz:
https://doaj.org/article/f5de541ffb7946879b52e93f0d5f105a
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 14, Iss 1, Pp 74-90 (2022)
Investigation of autoimmune epilepsy (AIE) has been attracting increasingly more attention due to discovery of neuronal antibodies and improved understanding of the mechanisms related to such immune-mediated syndromes. The review is aimed at autoimmu
Externí odkaz:
https://doaj.org/article/13d94ab2d12347e78df2c169074adfc2
Autor:
E. A. Kantimirova, N. A. Shnaider, M. M. Petrova, I. G. Strotskaya, N. E. Dutova, O. V. Alekseeva, E. A. Shapovalova
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 7, Iss 4, Pp 18-22 (2016)
Arnold-Chiari malformation (ACM) is a group of congenital hindbrain malformations affecting the structural relationships between the cerebellum, brain stem, top cervical spinal cord, and bones of the skull base. In clinical practice, ACM types 0 and
Externí odkaz:
https://doaj.org/article/908367d7b29f417fb27df5d74eb34945
Autor:
N. A. Shnayder, D. V. Dmitrenko, Yu. B. Govorina, E. A. Kantimirova, O. V. Alekseeva, A. A. Molgachev, A. A. Makarkin
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 7, Iss 3, Pp 40-45 (2015)
Subcortical laminar heterotopia (double cortex syndrome) is an orphan disease with an incidence of 1 to 200,000 people in the population. The cause of the disease is mutation of the gene DCX (synonyms: DBCN, XLIS) in chromosome Xq22.3-q23. The type o
Externí odkaz:
https://doaj.org/article/f091b0f00a9e42749e917dfda5c5174c
Publikováno v:
Нервно-мышечные болезни, Vol 5, Iss 2, Pp 10-15 (2015)
Current article provides an overview of the results of epidemiological studies of chronic inflammatory demyelinating polyneuropathy (CIDP) in Russia and abroad. It is shown that the prevalence of CIDP is different in countries, due to the use of diff
Externí odkaz:
https://doaj.org/article/2d191f966b3a4997886b1ecf9271a7d1
Autor:
T. E. Popova, N. A. Shnayder, M. M. Petrova, T. Ya. Nikolaeva, E. A. Kantimirova, N. V. Isaeva, V. A. Shnayder, Yu. S. Panina, A. V. Dyuzhakova, S. K. Dyuzhakov
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 7, Iss 2, Pp 28-34 (2015)
Herpesviruses can directly affect the structure of the nervous system, resulting in encephalitis, and also induce immune-mediated disorders of the peripheral nervous system as sensory-predominant chronic inflammatory demyelinating polyneuropathy (CID
Externí odkaz:
https://doaj.org/article/355bc6b5ea8847ed87884b0eaecdd986
Autor:
E. V. Glushchenko, N. A. Shnayder, E. A. Kantimirova, E. A. Kozulina, M. I. Voevoda, V. N. Maksimov, A. A. Allakhverdyan
Publikováno v:
Нервно-мышечные болезни, Vol 0, Iss 1, Pp 41-52 (2015)
Hereditary neuropathy Charcot-Marie-Tooth (CMT) is the most common form of hereditary polyneuropathies. Goal of the study was the development of evidence-based diagnostic and treatment algorithms using patients with CMT (for example, in Krasnoyarsk T
Externí odkaz:
https://doaj.org/article/792fc9f9904e465688e44e0160b6f455
Publikováno v:
Нервно-мышечные болезни, Vol 0, Iss 3, Pp 22-26 (2015)
This article provides an overview of the Russian and foreign studies on paraneoplastic opsoсlonus-myoclonus syndrome. Opsoclonus is characterized by involuntary, arrhythmic, chaotic, multi-directional saccades with horizontal, vertical and torsional
Externí odkaz:
https://doaj.org/article/e1dfb12eeaaa4be9a30a11386a4bbe08
Autor:
I. G. Strotskaya, E. A. Shapovalova, E. A. Kantimirova, N. E. Dutova, M. M. Petrova, N. A. Shnaider, O. V. Alekseeva
Publikováno v:
Nevrologiâ, Nejropsihiatriâ, Psihosomatika, Vol 7, Iss 4, Pp 18-22 (2016)
Arnold-Chiari malformation (ACM) is a group of congenital hindbrain malformations affecting the structural relationships between the cerebellum, brain stem, top cervical spinal cord, and bones of the skull base. In clinical practice, ACM types 0 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2922cbe62aeede27dc2ad60645b7a01c
https://doi.org/10.14412/2074-2711-2015-4-18-22
https://doi.org/10.14412/2074-2711-2015-4-18-22
Autor:
D. V. Dmitrenko, S.A. Shevchenko, S. I. Goncharova, A.V. Duzackova, Natalia Shnayder, E. A. Kantimirova, T. E. Popova
Publikováno v:
Siberian Medical Review. :15-25
Disorders of physical activity in patients with Charcot-Marie-Tooth disease (CMT) can cause disease progression and decreasing time of disability, however, is treatable through regular physical activity. For keeping the physical activity of the patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::235684e458554ce61f7b45d0a392ddec
https://doi.org/10.20333/25000136-2015-2-15-25
https://doi.org/10.20333/25000136-2015-2-15-25