Olga Favorova
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Explore the profile of Olga Favorova including associated specialties, affiliations and a list of published articles.
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27
Citations
292
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Recent Articles
1.
Kiselev I, Kulakova O, Baturina O, Kabilov M, Boyko A, Favorova O
Mult Scler Relat Disord
. 2024 Oct;
91:105910.
PMID: 39369632
Background: Relapsing-remitting multiple sclerosis (RRMS) is a most common form of multiple sclerosis in which periods of neurological worsening are followed by periods of clinical remission. RRMS relapses are caused...
2.
Matveeva N, Kiselev I, Baulina N, Semina E, Kakotkin V, Agapov M, et al.
Front Aging Neurosci
. 2023 Nov;
15:1287322.
PMID: 37927339
The severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) and the сoronavirus disease 2019 (COVID-19) have become a global health threat. At the height of the pandemic, major efforts were focused...
3.
Kiselev I, Kozin M, Baulina N, Pisklova M, Danilova L, Zotov A, et al.
Int J Mol Sci
. 2022 Dec;
23(23).
PMID: 36499607
Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease; its pathogenesis is still being intensively studied to explain the reasons for the significant genetic and phenotypic heterogeneity of the...
4.
Pisklova M, Osmak G, Favorova O
Biochemistry (Mosc)
. 2022 Sep;
87(8):832-838.
PMID: 36171647
Hypertrophic cardiomyopathy (HCM) is a hereditary heart disease caused by mutations in the sarcomere genes, which is accompanied by myocardial fibrosis leading to progressive heart failure and arrhythmias. Recent studies...
5.
Titov B, Matveeva N, Kulakova O, Baulina N, Bazyleva E, Kheymets G, et al.
Genes (Basel)
. 2022 Sep;
13(9).
PMID: 36140820
Vasovagal syncope (VVS) is the most common cause of sudden loss of consciousness. VVS results from cerebral hypoperfusion, due to abnormal autonomic control of blood circulation, leading to arterial hypotension....
6.
Baulina N, Kiselev I, Kozin M, Kabaeva A, Boyko A, Favorova O
Gene
. 2022 Jun;
836:146676.
PMID: 35714798
The role of miRNAs, small non-coding regulatory RNAs, in the molecular mechanisms of multiple sclerosis (MS) development has been intensively studied. MiRNAs tend to be clustered within imprinted regions, and...
7.
Baulina N, Pisklova M, Kiselev I, Chumakova O, Zateyshchikov D, Favorova O
Int J Mol Sci
. 2022 Apr;
23(7).
PMID: 35409153
Hypertrophic cardiomyopathy (HCM) is the most common inherited myocardial disease with significant genetic and phenotypic heterogeneity. To search for novel biomarkers, which could increase the accuracy of HCM diagnosis and...
8.
Kiselev I, Danilova L, Baulina N, Baturina O, Kabilov M, Boyko A, et al.
Mult Scler Relat Disord
. 2022 Mar;
60:103714.
PMID: 35245816
Multiple sclerosis (MS) is a chronic autoimmune and degenerative disease of the central nervous system, which develops in genetically predisposed individuals upon exposure to environmental influences. Environmental triggers of MS,...
9.
Kozin M, Kiselev I, Baulina N, Kabaeva A, Pavlova G, Boyko A, et al.
Mult Scler Relat Disord
. 2021 Dec;
58:103469.
PMID: 34954650
The presence of brain/spinal white matter lesions typical for multiple sclerosis (MS) in asymptomatic individuals is known as 'radiologically isolated syndrome' (RIS). Taking into account that RIS patients are at...
10.
Osmak G, Baulina N, Kiselev I, Favorova O
Genes (Basel)
. 2021 Dec;
12(12).
PMID: 34946964
Hypertrophic cardiomyopathy (HCM) is the most common hereditary heart disease. The wide spread of high-throughput sequencing casts doubt on its monogenic nature, suggesting the presence of mechanisms of HCM development...