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1. Lipoprotein (a) as a marker of hereditary lipid metabolism disorders in patients with early manifestation of coronary artery disease

2. The levels of certain circulating microRNAs in hypertrophic cardiomyopathy are associated with echocardiographic parameters

3. A rare variant in the TTR gene (p.E112K) is associated with systemic amyloidosis and a new symptom – skin hyperemia in response to ethanol intake: family segregation analysis, literature review, and a clinical case. Case report

4. Molecular cardiology: from decoding the genetic nature and mechanisms of the diseases development to the introduction into the clinic

5. Practical guidelines for the diagnosis and treatment of transthyretin amyloid cardiomyopathy (ATTR-CM or transthyretin cardiac amyloidosis)

6. Pitavastatin: focus on safety and drug interactions

7. A clinical case of hypertrophic cardiomyopathy and family hyperlipidemia

9. Left ventricular global function index and peculiarities of daily blood pressure profile in patients with arterial hypertension

10. Prevalence of hereditary factors in different age groups in patients with acute coronary syndrome

11. Cardiology: genetics’ time

12. Switching of Oral Anticoagulation Therapy After PCI in Patients With Atrial Fibrillation: The RE-DUAL PCI Trial Subanalysis

13. Ticagrelor in patients with diabetes and stable coronary artery disease with a history of previous percutaneous coronary intervention (THEMIS-PCI): a phase 3, placebo-controlled, randomised trial

14. An intuitive risk factors search algorithm: usage of the Bayesian network technique in personalized medicine

15. Association of the CYBA, PPARGC1A, PPARG3, and PPARD gene variants with coronary artery disease and metabolic risk factors of coronary atherosclerosis in a Russian population

16. Advanced age, low left atrial appendage velocity, and Factor V promoter sequence variation as predictors of left atrial thrombosis in patients with nonvalvular atrial fibrillation

17. A Novel Hypoxia-Inducible Factor-Prolyl Hydroxylase Inhibitor (GSK1278863) for Anemia in CKD: A 28-Day, Phase 2A Randomized Trial

18. Association of CYP2D6 and ADRB1 genes with hypotensive and antichronotropic action of betaxolol in patients with arterial hypertension

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