Zobrazeno 1 - 10
of 155
pro vyhledávání: '"I. A. Zavalishin"'
Autor:
S. N. Kulikova, A. V. Peresedova, M. V. Krotenkova, V. V. Bryukhov, O. V. Trifonova, I. A. Zavalishin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 8, Iss 1, Pp 22-29 (2017)
Motor disorders are a frequent syndrome in multiple sclerosis(MS), leading to severe disability, possibly associated with inefficiencyof adaptive mechanisms, probably because of widespreadstructural changes. Hand palsy with fine motor skillsdamage in
Externí odkaz:
https://doaj.org/article/25b50f1e1191419da5fea662a0faa4b5
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 7, Iss 3, Pp 47-54 (2017)
Magnetic resonance imaging (MRI) is one of the main methodsof multiple sclerosis (MS) diagnostic, differential diagnostic anddisease course monitoring. Conventional MRI techniques havelow sensitivity in the assessment of diffuse damage of normalappea
Externí odkaz:
https://doaj.org/article/962ec86f0e2c42628c26001512b0e64d
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 7, Iss 3, Pp 55-59 (2017)
The article contains recent literature data concerning vascularaspects of multiple sclerosis (MS). The review provides a summaryof three vascular abnormalities described in MS which includeincreased risk of developing ischaemic stroke, widespread dec
Externí odkaz:
https://doaj.org/article/bdcdf414dfd24af68c82470cfbaf347c
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 4, Iss 4, Pp 51-55 (2017)
A pseudo-tumoral course of multiple sclerosis is very rare. In the paper, a morphologically confirmed case of multiple sclerosis with a pseudo-tumoral course is described. A radiation treatment (because of a misdiagnosis of cerebral tumor) resulted i
Externí odkaz:
https://doaj.org/article/9a002aef2b0144e68938b31f897c0a77
Autor:
D. D. Eliseeva, I. A. Zavalishin, S. N. Bykovskaya, T. N. Fedorova, E. N. Karandashov, O. A. Trunova
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 5, Iss 2, Pp 9-13 (2017)
In the maintenance of immunological tolerance a recently discoveredpopulation of regulatory T-cells CD4+CD25+Foxp3+(Treg) plays an important role. These cells have potential in suppressingpathologic immune response observed in variousautoimmune disea
Externí odkaz:
https://doaj.org/article/ad78b3b5dfa446e7b0e5f607eae08cd7
Autor:
A. V. Peresedova, I. A. Zavalishin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 3, Iss 1, Pp 43-47 (2017)
Etiology of multiple sclerosis has both genetic and environmental components. The current conception is that multiple sclerosis pathogenesis comprises an initial inflammatory phase, followed by a phase of demyelination and last, a neurodegenerativeph
Externí odkaz:
https://doaj.org/article/a7b7ac182ff0452bb1d09a9f0d6117e7
Autor:
I. A. Zavalishin, A. V. Peresedova, N. I. Stoida, L. Sh. Askarova, M. N. Zakharova, L. S. Adarcheva, A. S. Niyazbekova, O. V. Trifonova, O. Yu. Rebrova, D. D. Eliseeva
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 3, Iss 3, Pp 21-24 (2017)
In the paper, the results of 1-year treatment with avonex, a newimmunomodulator from the group of interferons b, in 34patients with relapsing remitting multiple sclerosis have beenreported. In the treated patients it was shown significantdecrease of
Externí odkaz:
https://doaj.org/article/ac79783f88614576aabee6bcaf726629
Autor:
A. V. Peresedova, I. A. Zavalishin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 6, Iss 1, Pp 57-63 (2017)
Creutzfeldt-Jakob disease and others human prion diseases arefatal neurodegenerative conditions. Etiologic classificationincludes sporadic, hereditary and acquired forms.Conformational change of the normal (cellular) form of prionprotein (PrPc) to a
Externí odkaz:
https://doaj.org/article/b9548b2fc2d9481b911bebb94777c3ef
Autor:
A. V. Peresedova, N. I. Stoida, L. Sh. Askarova, M. N. Zakharova, L. S. Adarcheva, A. S. Niyazbekova, O. V. Trifonova, O. Yu. Rebrova, I. A. Zavalishin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 4, Iss 3, Pp 20-24 (2017)
Results of the two-year treatment with avonex of 34 patients withrelapsing remitting multiple sclerosis are summarized. This studyprovides evidence for the significant decrease in activity of thepathological process in patients treated with avonex, w
Externí odkaz:
https://doaj.org/article/c3b00f3b895e43589ac090bf7bbe7949
Autor:
A. V. Peresedova, N. I. Stoida, V. V. Gnezdizky, R. N. Konоvаlоv, O. S. Kоrеpina, I. A. Zavalishin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 5, Iss 4, Pp 52-56 (2017)
Creutzfeldt-Jakob disease (CJD) is a form of human prion diseases,fatal neurodegenerative conditions. They can be etiologicallydivided into sporadic, hereditary and acquired forms.Conformational change of the normal (cellular) form of prionprotein (P
Externí odkaz:
https://doaj.org/article/f787db629b1f45c68349ff2ae05b906a