Zobrazeno 1 - 5
of 5
pro vyhledávání: '"E. V. Horolets"'
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 6, Iss 1, Pp 42-47 (2016)
Aim. To study purine metabolism and lipid peroxidation in patients with acute myocardial infarction with ST segment elevation (STEMI) in dependence on severity of acute heart failure (AHF). To evaluate effects of thrombolytic therapy on purine metabo
Externí odkaz:
https://doaj.org/article/b02e6bfec6194c7392472374de545bf4
Publikováno v:
Racionalʹnaâ Farmakoterapiâ v Kardiologii, Vol 6, Iss 1, Pp 42-47 (2016)
Aim. To study purine metabolism and lipid peroxidation in patients with acute myocardial infarction with ST segment elevation (STEMI) in dependence on severity of acute heart failure (AHF). To evaluate effects of thrombolytic therapy on purine metabo
Autor:
N A Koziolova, Alexey Nikitin, Dzhaiani Na, Evgeniya V. Akatova, K A Blagodatskih, A N Brovkin, E. G. Volkova, O. I. Boyeva, S. V Shlyk, S N Tereschenko, A. S. Galyavich, AA Pushkov, V. O. Konstantinov, Baklanova Tn, E V Horolets, A V Yagoda, Nosikov Vv, Glezer Mg, Evdokimova Ma, D A Zateyshchikov
Publikováno v:
Journal of Clinical Practice. 4:4-11
The aim of this study was to investigate an association of polymorphic markers G(-308)A of TNF gene and Thr26Asn of LTA gene with the frequency of poor outcomes in patients with the history of acute coronary syndrome.Methods. A total of 1145 patients
Autor:
I. O. Guz, L. O. Minushkina, O. Yu. Aseycheva, S. V. Shlyk, Talyzin Pa, K. A. Blagodatskikh, E. V. Akanova, Sidorenko Ba, Dzhaiani Na, V. S. Osmolovskaya, Nosikov Vv, M. P. Margaryan, A. A. Pushkov, A. S. Galyavich, Evdokimova Ma, Zakirova Vb, Baklanova Tn, Chudakova Da, Alexandr Yagoda, Glezer Mg, O. P. Donetskaya, Alexey Nikitin, N. A. Koziolova, D. A. Zeteyshchikov, V. O. Konstantinov, Brovkin An, E. V. Horolets, S. N. Tereschenko, O. I. Boyeva, Yu. V. Agapkina, E. G. Volkova
Publikováno v:
Russian Journal of Genetics. 47:1234-1239
The polymorphic markers Ala455Val of the THBD gene and Arg353Gln of the F7 gene were tested for association with the frequency of unfavorable outcomes in patients with a history of acute ischemic heart disease. The study involved 1145 patients hospit
Autor:
Dankovtseva En, Alexandr Yagoda, O. Yu. Aseycheva, Reznichenko Ne, Kochkina Ms, I. O. Guz, A. A. Pushkov, V. S. Osmolovskaya, Nosikov Vv, Sidorenko Ba, M. P. Margaryan, Talyzin Pa, Dzhaiani Na, Yu. V. Agapkina, S. V. Shlyk, Glezer Mg, E. V. Horolets, E. G. Volkova, Zakirova Vb, S. N. Tereschenko, D. A. Zateyshchikov, L. O. Minushkina, O. I. Boyeva, Brovkin An, Evdokimova Ma, A. N. Timofeyeva, N. A. Koziolova, V. O. Konstantinov, Selezneva Nd, L. I. Katelnitskaya, Akatova Ev, Chumakova Os, Baklanova Tn, I. V. Timofeeva, O. P. Donetskaya, Krasil'nikova Es, Alexey Nikitin, A. S. Galyavich
Publikováno v:
Molecular Biology. 44:541-545
Associations of polymorphisms of genes FGB G(−455)A and PROC C(−1654)T with the frequency of poor outcomes in patients with the history of acute coronary syndrome (ACS) were studied in the Russian population. A total of 1145 patients admitted to