Zobrazeno 1 - 10
of 19
pro vyhledávání: '"S L Timerbaeva"'
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 9, Iss 4, Pp 37-41 (2017)
Neurological syndromes caused by production of antibodies toglutamic acid decarboxylase (GAD65) are a relatively new areaof modern clinical neurology, which is of great theoretical andpractical interest. High titer of identified antibodies is a not a
Externí odkaz:
https://doaj.org/article/9eee343c9a3645ff9127376993c836d1
Autor:
M. Yu. Krasnov, S. L. Timerbaeva, N. Yu. Abramycheva, M. S. Stepanova, Yu. A. Shpilyukova, M. V. Ershova
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 10, Iss 2, Pp 52-56 (2017)
DYT6 is a recently described autosomal dominant form of primarydystonia with early onset of symptoms caused by mutationsin THAP1 gene in chromosome 8. The incidence of this formin various populations is extremely variable and ranges from 1%to 25%. Kn
Externí odkaz:
https://doaj.org/article/ce4bef34a2e94799b55f130e87f35e9d
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 6, Iss 4, Pp 4-9 (2017)
Primary blepharospasm (BS) is one of most frequent forms offocal dystonia characterized by excessive involuntary eye closure.Pathophysiology of primary BS remains obscure. The purposeof this study: to determine changes of the cerebral gray mattervolu
Externí odkaz:
https://doaj.org/article/a834d26415d44d108cb9f0bb93948cd8
Autor:
S. L. Timerbaeva
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 6, Iss 2, Pp 48-54 (2017)
Presented is a detailed analysis of different modern neuroimagingtechnologies used for studying pathophysiological mechanismsand morpho-physiological substrate of primary focal dystonia.Main attention is paid to functional MRI and voxel-basedmorphome
Externí odkaz:
https://doaj.org/article/b9c4c41fbd9042c29f5016e6a7c43c19
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 7, Iss 2, Pp 55-62 (2017)
Dystonia is one of the most common movement disorders withgreat medical, social and economic importance. Genetics playssignificant role in the development of different, and mainly primary,forms of dystonia. At present the range of hereditary dystonic
Externí odkaz:
https://doaj.org/article/ec6af381f9d64026951ef91e97d23f6b
Publikováno v:
Human Physiology. 42:874-878
Neurological disorders associated with glutamic acid decarboxylase (GAD65) antibodies represent a relatively new field of research in the modern clinical neurology and are of great theoretical and practical interest. High titer of anti-GAD65 antibodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c515d40129b548f0a585be2e655f4993
https://doi.org/10.1134/s0362119716080089
https://doi.org/10.1134/s0362119716080089
Autor:
V. V. Ustinova, S. L. Timerbaeva, V.E. Kunetsky, Sergey N. Illarioshkin, M. S. Stepanova, N. Yu. Abramycheva, Ya.I. Alekseev, E. Yu. Fedotova, S. A. Klyushnikov
Publikováno v:
Современные технологии в медицине.
Цель исследования оценка эффективности разработанной нами диагностической панели, основанной на технологиях секвенирования следующе
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b88839e8e0f50f0cb03d992b00f9c2c2
http://cyberleninka.ru/article/n/an-original-target-genetic-panel-to-diagnose-neurodegenerative-diseases-on-the-basis-of-next-generation-sequencing-first-experience
http://cyberleninka.ru/article/n/an-original-target-genetic-panel-to-diagnose-neurodegenerative-diseases-on-the-basis-of-next-generation-sequencing-first-experience
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 115(5)
The analysis of the results of treatment of the Russian patient population in the frame of international, multicenter, non-interventional study of CD, the primary purpose of which was to determine the response rate to therapy with BTA at the peak of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae9bbb9b2455a4ba9aad80c337afa3f4
https://pubmed.ncbi.nlm.nih.gov/26356161
https://pubmed.ncbi.nlm.nih.gov/26356161
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 75:1558-1561
Objective: To study the efficacy, safety, and incidence of BtxA antibody formation with repeated treatments with BtxA in post-stroke upper limb muscle spasticity. Methods: The study was a prospective open label trial. Patients with established post-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79526add1e8a00f97748e0a3f5e8b73e
https://doi.org/10.1136/jnnp.2003.035139
https://doi.org/10.1136/jnnp.2003.035139
Autor:
M. S. Stepanova, A. A. Moroz, N. Yu. Abramycheva, Sergei N. Illarioshkin, R. N. Konovalov, S. L. Timerbaeva
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 117:75
Cerebral autosomal dominant arteriopathy with subcortical infarctions and leucoencephalopathy (CADASIL) is an inherited CNS disease, which is caused by mutations in the NOTCH3 gene. Selective disorders of small vessels underlie the disease pathogenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8641c9eca8d65f66177b09209619d72
https://doi.org/10.17116/jnevro20171174175-80
https://doi.org/10.17116/jnevro20171174175-80