Zobrazeno 1 - 10
of 134
pro vyhledávání: '"O O, Favorova"'
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 16, Iss 0, Pp 31-37 (2024)
Objective: to look for differences in the transcriptome profiles in mononuclear blood cells of a group of patients with radiologically isolated syndrome (RIS) who developed symptoms of multiple sclerosis (MS) in the following three years of observati
Externí odkaz:
https://doaj.org/article/6bdaa64ad8d5454b8e560ec2c05dfa07
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 15, Iss 0, Pp 4-7 (2023)
Multiple sclerosis (MS) is an autoimmune inflammatory neurodegenerative disease of the central nervous system. The disease is characterized by a heterogeneous clinical course, which is reflected in the fact that there are various types, such as relap
Externí odkaz:
https://doaj.org/article/6c07ed75f7ed4b208a4bb6dbd46eea88
Autor:
M. S. Kozin, N. M. Baulina, I. S. Kiselev, A. R. Kabaeva, A. N. Boyko, O. O. Favorova, O. G. Kulakova
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 1S, Pp 16-20 (2022)
Radiologically isolated syndrome (RIS) is a nosological form in which magnetic resonance imaging (MRI) reveals lesions of the white matter of the brain and/or spinal cord characteristic of multiple sclerosis (MS) in individuals in the absence of clin
Externí odkaz:
https://doaj.org/article/06f80ebfb28c49adb4c9ef8ae6c1378c
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 2, Pp 64-70 (2022)
The role of miRNAs – small, regulatory, noncoding RNAs – in the multiple sclerosis (MS) development is being intensively investigated. Previously, we the first who observed a significant increase in the expression of 26 microRNA genes localized i
Externí odkaz:
https://doaj.org/article/2bedd7e22fac44d69ecd61231d03d4dc
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 12, Iss 1S, Pp 15-19 (2020)
Multiple sclerosis (MS) is a severe chronic CNS disease characterized by autoimmune inflammation, demyelination, and neurodegeneration. The interaction of mitochondrial and nuclear genomes is shown to be important in the formation of a predisposition
Externí odkaz:
https://doaj.org/article/6510d07371b54f42adcb06fc9f0cd469
Autor:
I. S. Kiselev, M. S. Kozin, N. M. Baulina, G. V. Pavlova, A. N. Boyko, O. G. Kulakova, O. O. Favorova
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 12, Iss 1S, Pp 4-8 (2020)
Multiple sclerosis (MS) is a chronic autoimmune disease, in the pathogenesis of which the concurrence of demyelination of central nervous system (CNS) axons and neurodegeneration plays a role and which is accompanied by progressive neurological dysfu
Externí odkaz:
https://doaj.org/article/fcfb9645bb0b42aba1e6c92494bb83d4
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 11, Iss 3, Pp 43-46 (2019)
Mitochondrial DNA (mtDNA) polymorphism makes a certain contribution to the formation of a genetic risk of multiple sclerosis (MS).Objective: to analyze the frequency of mtDNA variants in patients with MS and control individuals in the Russian populat
Externí odkaz:
https://doaj.org/article/0ce80cee909d4ed28d771f7110420ed6
Autor:
I V Zhirov, N M Baulina, S N Nasonova, G Zh Osmak, N A Matveyeva, D R Mindzaev, O O Favorova, S N Tereshchenko
Publikováno v:
Терапевтический архив, Vol 91, Iss 9, Pp 62-67 (2019)
It is known that micro RNAs are an important regulatory element in the pathogenesis of many diseases, including cardiovascular diseases. Different levels of expression of these molecules in various pathologies makes miRNA a potential diagnostic and p
Externí odkaz:
https://doaj.org/article/ddf45f82f1564ba2ad8f2a1eaf2e8b1b
Autor:
O. V. Sapelnikov, A. A. Kulikov, O. O. Favorova, N. A. Matveeva, D. I. Cherkashin, O. A. Nikolaeva, R. S. Akchurin
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 15, Iss 3, Pp 407-415 (2019)
Atrial fibrillation (AF) is one of the most common arrhythmia that occurs in patients with cardiovascular diseases. Congenital forms of AF are quite rare. Many studies have shown that genetic, epigenetic and transcription factors may play an importan
Externí odkaz:
https://doaj.org/article/9799b609f6684ec2acbcd43e4aa95e01
Publikováno v:
Терапевтический архив, Vol 90, Iss 9, Pp 115-122 (2018)
Family hyperaldosteronism type I (glucocorticoids-remediable hyperaldosteronism) is a rare form of symptomatic arterial hypertension (AH), which often leads to the development of cerebrovascular complications. The disease is caused by the formation o
Externí odkaz:
https://doaj.org/article/250ab1fe8f404337b9a5a924492f1f14