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[Surgical treatment of cerebral aneurysms in the Russian Federation]

Publikováno v: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko. 82(6)

The objective of this study was to evaluate the results of surgical treatment of cerebral aneurysms in the Russian Federation.We analyzed performance indicators in neurosurgical departments of regional and federal health institutions of the Russian F

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58a43758747411e20801fa8b58f26903
https://pubmed.ncbi.nlm.nih.gov/30721212

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[Results of implementation of a 'Complex of measures to improve medical care for patients with stroke in the Russian Federation']

Autor: Shetova Im, E. P. Kakorina, V. V. Krylov, E. G. Kamkin, E. L. Boiko, B. G. Alekyan, Skvortsova Vi, V. G. Dashyan, G. E. Ivanova, Shamalov Na

Publikováno v: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 118(4)

Vascular diseases of the brain and heart are the main cause of death and disability of the population of the Russian Federation. The social and economic burden of acute cerebral circulation disorders necessitated the development of a national program

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8b41df63572e6a81f5651d224fac05d
https://pubmed.ncbi.nlm.nih.gov/29863686

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Comparative analysis of associations between polymorphic variants of the F2, F5, GP1BA, and ACE genes and the risk of developing stroke in Russian and Ukrainian populations

Autor: E. A. Bondarenko, T. V. Tupitsyna, D. V. Shul’zhenko, S. A. Kravchenko, P. A. Slominsky, Shetova Im, L. A. Livshits, Svetlana A. Limborska, Skvortsova Vi, P. F. Tatarskyy, S. M. Kuznetsova, Shamalov Na

Publikováno v: Molecular Genetics, Microbiology and Virology. 28:8-14

We performed comparative analysis of associations between the F2 gene G20210A polymorphism, the F5 gene G1691A polymorphism, the GP1BA gene -5T/C polymorphism, the ACE gene insertion/deletion (I/D) polymorphism and the risk of developing stroke in tw

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7c1de5dc1a36a1e5e2cb2738a6c1faca
https://doi.org/10.3103/s0891416813010072

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Association between Polymorphisms in the Phosphodiesterase 4D (PDE4D) Gene and the Development of Cerebral Stroke in Patients in the Moscow Population

Autor: E. A. Bondarenko, P. A. Slominskii, D. Yu. Timofeev, Skvortsova Vi, Shetova Im, N. A. Shamalov, S. A. Limborskaya

Publikováno v: Neuroscience and Behavioral Physiology. 42:838-841

Two polymorphisms in the PDE4D gene – SNP41 (rs152312) and SNP87 (rs2910829), encoding phosphodiesterase 4D – were studied in patients during the acute period of stroke (n = 577) and a control cohort (n = 270). Significant differences between the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f2c9787088654424d2413d5c1075c473
https://doi.org/10.1007/s11055-012-9645-4

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Association of polymophisms of renin-angiotensin and hemostasis system genes with ischemic stroke in Russians from central Russia

Autor: Skvortsova Vi, P. A. Slominskii, N. A. Shamalov, Bondarenko Ev, S. A. Limborskaya, T. V. Nasedkina, Alexander V. Chudinov, Shetova Im, Alexander V. Kulikov, Alexander S. Zasedatelev, A. Yu. Ikonnikova, Yu. P. Lysov, M. A. Usacheva

Publikováno v: Molecular Biology. 46:192-199

The allele and genotype frequencies of 14 SNPs of renin-angiotensin (REN, AGT, AGTR1, AGTR2, BKR2, and ADRB2) and hemostasis (FGB, F2, F5, F7, ITGB3, SERPINE1, MTHFR) system genes, as well as of the ACE insertion-deletion polymorphism, were analyzed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7e0165d720246468a64db882d424be27
https://doi.org/10.1134/s0026893312010232

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Analysis of acute ischemic stroke DNA markers in Russian and Moldavian populations

Autor: E. A. Bondarenko, Svetlana A. Limborska, P. A. Slominsky, N. I. Barbacar, L. Lysyi, Skvortsova Vi, G. S. Kurochkin, E. I. Mocan, Shetova Im, N. A. Shamalov, S. S. Protopop

Publikováno v: Russian Journal of Genetics. 47:1240-1247

Polymorphisms c.202G > A of prothrombin F2 gene, c.1691G > A of coagulation factor V F5 gene, c.675delinsG of plasminogen activator 1 gene, and (−5)T > C Kozak gene of thrombocytic receptor were studied in the Russian and Moldavian ethnic groups. W

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eab8edf40db060c72312249ee95c5c20
https://doi.org/10.1134/s1022795411100048

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Analysis of polymorphic variants of PDE4D gene in patients with acute stroke from Moldavian population

Autor: Skvortsova Vi, T. V. Tupitsyna, E. I. Mocan, N. A. Shamalov, A. Yu. Botsina, Shetova Im, N. I. Barbacar, Svetlana A. Limborska, E. A. Bondarenko, P. A. Slominskii

Publikováno v: Molecular Genetics, Microbiology and Virology. 26:50-53

The risk of the development of ischemic stroke is caused by both genetic predisposition and environmental factors. In recent investigations, the DeCode group discovered polymorphisms in the phosphodiesterase 4D (PDE4D) gene associated with the risk o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7e048dc323cdd2c87ddb6ee31f05ccdc
https://doi.org/10.3103/s0891416811020030

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Polymorphic variants of ALOX5AP gene and the risk of acute stroke development in the Russian population

Autor: E. A. Bondarenko, P. A. Slominsky, Shetova Im, Skvortsova Vi, D. Yu. Timofeev, Svetlana A. Limborska

Publikováno v: Russian Journal of Genetics. 47:500-503

The role of variants of the gene encoding arachidonate 5-lipoxygenase-activating protein (ALOX5AP) as possible susceptibility factors for acute stroke were examinated. Two ALOX5AP gene polymorphisms (SG13S114 (rs10507391) and SG13S32 (rs9551963)), wh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::882cf32fed01116a97fd5d8741d5e3f4
https://doi.org/10.1134/s102279541104003x

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Role of polymorphic variants of gene of inducible NO synthase NOS2 in brain infarction in patients with acute ischemic stroke

Autor: A. Yu. Botsina, P. A. Slominskii, E. A. Bondarenko, S. A. Limborskaya, Skvortsova Vi, T. V. Tupitsyna, Shetova Im

Publikováno v: Molecular Genetics, Microbiology and Virology. 25:89-94

Cerebrovascular diseases, including stroke, are an important problem in public health. Stroke development depends on external factors and the individual genetic specificity of the patient. Excessive NO production by inducible NO synthase (iNOS) damag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5845ee63963c926148fbec66a2d39d22
https://doi.org/10.3103/s0891416810030018

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Phosphodiesterase 4D (PDE4D) gene polymorphism in patients with acute stroke from Moscow

Autor: E. A. Bondarenko, N. A. Shamalov, Skvortsova Vi, S. A. Limborska, A. Yu. Botsina, Shetova Im, T. V. Tupitsina, P. A. Slominsky

Publikováno v: Scopus-Elsevier

Two PDE4D gene polymorphisms [SNP41 (rs152312 and SNP87 (rs2910829)] were studied in patients with acute stroke (n = 577) and in control sample (n = 270). Significant differences in the genotype and allele frequency distribution were found between th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e9822927c8fdab37c6ff6384c04f8f9
https://doi.org/10.1134/s1022795410060189

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