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Browsing by Author Chympoy, K.A.
Showing results 1 to 9 of 9
Issue Date | Title | Author(s) |
2016 | ASSOCIATION OF MARKERS OF THE SYSTEM OF FIBRINOLYSIS OF THE BLOOD PLASMA WITH А/С POLYMORPHISM OF DIOI AND PR0197LEU OF GPX1 GENES IN PATIENTS WITH NONVIRAL CHRONIC HEPATITIS AND LIVER CIRRHOSIS | Chympoy, K.A.; Buriak, O.G.; Pavlyukovich, N.D. |
2014 | Association of the Pro197Leu polymorphism of the glutathione peroxidase 1 gene and markers of endothelium function in patients with chronic, diffuse liver diseases. Genomic influence on the «clinical phenotype» of chronic, diffuse liver diseases | Pashkovska, N.V.; Chympoy, K.A.; Pankiv, I.V. |
2015 | Effect of DIO1 and GPX1 gene polymorphism on the functional condition of the endothelium in patients with chronic diffuse liver disease | Chympoy, K.A.; Pashkovska, N.V.; Olinyk, O.Ju.; Teleki, Ja.M. |
2014 | Effect of GPX1 gene polymorphism distribution on the indices of cellular adhesion and functional condition of the endothelium in patients with chronic diffuse liver diseases | Chympoy, K.A.; Pashkovska, N.V. |
2014 | Genetic determinism of the functional condition of the endothelium in patients with chronic diffuse liver disease and disoders of thyroid homeostasis | Chympoy, K.A.; Pashkovska, N.V.; Garasdyuk, O.I.; Pavlyukovich, N.D. |
2012 | Parameters of thyroid homeostasis in patients with chronic diffuse liver diseases depending on type 1 deiodinase gene polymorphism | Chympoy, K.A.; Palibroda, N.; Moskaliuk, I. |
2015 | PATHOGENETIC SUBSTANTIATION OF USING SELENIUM-CONTAINING DRUGS FOR THE CORRECT DISORDERS OF THE BLOOD PLASMA FIBRINOLYTIC SYSTEM IN PATIENTS WITH CHRONIC DIFFUSE LIVER DISEASES AND EUTHYROID SYNDROME PATHOLOGY | Chympoy, K.A.; Pashkovska, N.V.; Pankiv, V.I. |
2014 | Pathogenetic substantiation to correct disorders of the blood plasma fibrinolytic system in patients with chronic diffuse liverdiseases and disorders of thyroid homeostasis | Chympoy, K.A.; Pashkovska, N.V.; Fediv, O.I.; Pavlibroda, N.M. |
2015 | Peculitaries of indeces of endothelial function in patients with metabolic syndrome depending on Pro197Leu polymorphism of the GPX1 gene | Abramova, N.O.; Pashkovska, N.V.; Chympoy, K.A. |