All Stories

  1. Which scale is best to assess the risk of upper gastrointestinal bleeding in patients with stable coronary artery disease in the Russian population?
  2. Predictive value of left ventricular global function index in patients with aortic stenosis
  3. Clinical and Genetic Landscape Hypertrophic Cardiomyopathy on a Russian Single-Center Cohort Study
  4. Cardiology 2023: the time of genetics
  5. Assessment and modification of cardiovascular risk in non-cardiac surgery. Clinical guidelines 2023
  6. Results of a pilot clinical trial of the safety and efficacy of an original glycoprotein IIb/IIIa receptor inhibitor in acute coronary syndrome
  7. Lipoprotein (a) as a marker of hereditary lipid metabolism disorders in patients with early manifestation of coronary artery disease
  8. 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
  9. The levels of certain circulating microRNAs in hypertrophic cardiomyopathy are associated with echocardiographic parameters
  10. Mortality among kidney transplant recipients with SARS-CoV-2: a systematic review and meta-analysis of cohorts and clinical registries
  11. Mortality in kidney transplant recipients: a systematic review and meta-analysis of cohorts and clinical registries
  12. Novel Genes Involved in Hypertrophic Cardiomyopathy: Data of Transcriptome and Methylome Profiling
  13. Overlapping Phenotype of Adult-Onset ALPK3-Cardiomyopathy in the Setting of Two Novel Variants
  14. A survey of physician opinions in Russia in the field of pharmacogenetics of cardiovascular disease
  15. Left ventricular global function index and peculiarities of daily blood pressure profile in patients with arterial hypertension
  16. Molecular cardiology: from decoding the genetic nature and mechanisms of the diseases development to the introduction into the clinic
  17. Practical guidelines for the diagnosis and treatment of transthyretin amyloid cardiomyopathy (ATTR-CM or transthyretin cardiac amyloidosis)
  18. Prospects for Using Chromatography–Mass Spectrometry for the Determination of Lipids in Clinical Cardiolipidology
  19. Circulating miR-499a-5p Is a Potential Biomarker of MYH7—Associated Hypertrophic Cardiomyopathy
  20. Сonsensus statement of Russian experts on the prevention, diagnosis and treatment of cardiotoxicity of anticancer therapy
  21. Left ventricular global function index as a predictor of adverse cardiovascular events in patients with acute coronary syndrome
  22. Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy
  23. Visit-to-visit blood pressure variability in patients after acute coronary syndrome
  24. Changes in plasma sphingolipid levels against the background of lipid-lowering therapy in patients with premature atherosclerosis
  25. Pitavastatin: focus on safety and drug interactions
  26. Prevalence of hereditary factors in different age groups in patients with acute coronary syndrome
  27. Risk Stratification after an Acute Coronary Syndrome: Significance of Antithrombotic Therapy
  28. Using the ORACLE Risk Score to Assess Hemorrhagic Risk in Patients with Acute Coronary Syndrome and Atrial Fibrillation
  29. RESULTS OF MULTICENTER MONITORING OF HEMOSTASIS PARAMETERS IN PATIENTS WITH COVID-19
  30. Bleeding risk scales in patients with acute coronary syndrome: place of the ORACUL scale
  31. Can left ventricular global function index be a novel marker of unfavorable outcome in patients with acute coronary syndrome
  32. Contribution of electrocardiography to the diagnosis of cardiomyopathies and athletic heart syndrome
  33. Inherited thrombophilia and venous thromboembolism: testing rules in clinical practice
  34. Changes in the management of patients with acute coronary syndrome – have the disease outcomes changed?
  35. The Risk of Developing Ischemic Stroke in Patients After Exacerbation of Ischemic Heart Disease
  36. Recommendations of the Eurasian Arrhythmology Association (EURA) for the diagnosis and treatment of patients with arrhythmias and conduction disorders during the COVID-19 pandemic
  37. CYP2C9 and VKORC1 genotyping for the quality of long-standing warfarin treatment in Russian patients
  38. Bleeding rate and diagnostic value of different hemorrhagic risk scores in certain clinical groups of patients with acute coronary syndrome
  39. Cardiology: genetics’ time
  40. Lipidome features in patients with different probability of family hypercholesterolemia
  41. External validation of the ORACLE bleeding risk score using the database of the RECORD 3 registry
  42. Outcomes in Newly Diagnosed Atrial Fibrillation and History of Acute Coronary Syndromes: Insights from GARFIELD-AF
  43. Switching of Oral Anticoagulation Therapy After PCI in Patients With Atrial Fibrillation
  44. Place of Prasugrel, P2Y12 receptor antagonist, in an early invasive treatment of patients with acute coronary syndrome (according to the results of multicenter randomized controlled trial ISAR-REACT 5)
  45. A clinical case of hypertrophic cardiomyopathy and family hyperlipidemia
  46. Ticagrelor in Patients with Stable Coronary Disease and Diabetes
  47. 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
  48. Participation of Sphingolipids in the Pathogenesis of Atherosclerosis
  49. Predictors of NOAC versus VKA use for stroke prevention in patients with newly diagnosed atrial fibrillation: Results from GARFIELD-AF
  50. VISIT-TO-VISIT BLOOD PRESSURE VARIABILITY AND RISK OF ALL-CAUSE DEATH
  51. Analysis of Outcomes in Ischemic vs Nonischemic Cardiomyopathy in Patients With Atrial Fibrillation
  52. Influence of Microvascular Disease on Cardiovascular Events in Type 2 Diabetes
  53. Bleeding risk factors in patients with acute coronary syndrome: data from observational studies ORACUL II
  54. Physicians' guideline adherence is associated with long‐term heart failure mortality in outpatients with heart failure with reduced ejection fraction: the QUALIFY international registry
  55. Rationale, Design, and Baseline Characteristics of THEMIS: Effect of Ticagrelor on Health Outcomes in Diabetes Mellitus Patients Intervention Study
  56. Management and 1‐Year Outcomes of Patients With Newly Diagnosed Atrial Fibrillation and Chronic Kidney Disease: Results From the Prospective GARFIELD‐AF Registry
  57. Early Risks of Death, Stroke/Systemic Embolism, and Major Bleeding in Patients With Newly Diagnosed Atrial Fibrillation
  58. Psychosomatic Disorders in Patients with Pulmonary Hypertension: Impact on Treatment Adherence
  59. Characteristics and Management of Patients with Venous Thromboembolism: The GARFIELD-VTE Registry
  60. Risk Profile and 1-Year Outcome of Newly Diagnosed Atrial Fibrillation in Japan ― Insights From GARFIELD-AF ―
  61. Polymorphism of TNF gene in acute coronary syndrome patients: data from the registries ORACLE I and ORACLE II
  62. Targeted sequencing in patients with clinically diagnosed hereditary lipid metabolism disorder and acute coronary syndrome
  63. Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry
  64. Treatment patterns in anticoagulant therapy in patients with newly diagnosed atrial fibrillation in Belgium: results from the GARFIELD-AF registry
  65. Empagliflozin and Kidney Function Decline in Patients with Type 2 Diabetes: A Slope Analysis from the EMPA-REG OUTCOME Trial
  66. Rivaroxaban for Thromboprophylaxis after Hospitalization for Medical Illness
  67. Screening of familial hypercholesterolemia among patients in age under 40 years old exposed by duplex scanning of carotid arteries, by the local registry data
  68. Polymorphism of ANXA2 gene may accelerate vulnerability and calcinosis in patients with coronary atherosclerosis
  69. IL-10 GENE POLYMORPHISM AND STROKE RISK IN PATIENTS WITH CORONARY ARTERY DISEASE
  70. STRATEGY TO MINIMIZE THE BLEEDING RISKS IN PATIENTS WITH ATRIAL FIBRILLATION WHO RECEIVE COMBINED ANTITHROMBOTIC THERAPY AFTER PERCUTANEOUS CORONARY INTERVENTION
  71. Empagliflozin in women with type 2 diabetes and cardiovascular disease – an analysis of EMPA-REG OUTCOME®
  72. Emergency care of patients receiving non-vitamin K antagonist oral anticoagulants
  73. GENETIC MARKERS OF MYOCARDIAL FIBROSIS: OPPORTUNITY TO PREDICT ADVERSE OUTCOMES IN AORTIC STENOSIS
  74. IS IT SAFE TO SWITCH OAC IN PATIENTS WITH ATRIAL FIBRILLATION UNDERGOING PERCUTANEOUS CORONARY INTERVENTION? RESULTS FROM A RE-DUAL PCI SUBANALYSIS
  75. Risk factors for death, stroke, and bleeding in 28,628 patients from the GARFIELD-AF registry: Rationale for comprehensive management of atrial fibrillation
  76. Empagliflozin and Clinical Outcomes in Patients With Type 2 Diabetes Mellitus, Established Cardiovascular Disease, and Chronic Kidney Disease
  77. Family History of Cardiovascular Disease in Patients With Early Development of Acute Coronary Syndrome
  78. Possibilities of molecular biopsy in differential diagnosis of pulmonary arterial hypertension: case description and literature review
  79. Risk of Stroke After Exacerbation of Ischemic Heart Disease: Data of 3‑Years Follow-up
  80. Rivaroxaban with or without aspirin in patients with stable coronary artery disease: an international, randomised, double-blind, placebo-controlled trial
  81. Rivaroxaban with or without aspirin in patients with stable peripheral or carotid artery disease: an international, randomised, double-blind, placebo-controlled trial
  82. Characteristics of patients with atrial fibrillation prescribed antiplatelet monotherapy compared with those on anticoagulants: insights from the GARFIELD-AF registry
  83. Improved risk stratification of patients with atrial fibrillation: an integrated GARFIELD-AF tool for the prediction of mortality, stroke and bleed in patients with and without anticoagulation
  84. International trends in clinical characteristics and oral anticoagulation treatment for patients with atrial fibrillation: Results from the GARFIELD-AF, ORBIT-AF I, and ORBIT-AF II registries
  85. Rivaroxaban with or without Aspirin in Stable Cardiovascular Disease
  86. [PP.30.09] KIF6 GENE POLYMORPHISM IS ASSOCIATED WITH ARTERIAL RESISTANCE AND ATHEROSCLEROSIS IN PATIENTS WITH HYPERTENSION
  87. Impact of Spontaneous Extracranial Bleeding Events on Health State Utility in Patients with Atrial Fibrillation: Results from the ENGAGE AF‐TIMI 48 Trial
  88. Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease
  89. Cardiovascular Efficacy and Safety of Bococizumab in High-Risk Patients
  90. Empagliflozin and Cerebrovascular Events in Patients With Type 2 Diabetes Mellitus at High Cardiovascular Risk
  91. Edoxaban for the Prevention of Thromboembolism in Patients With Atrial Fibrillation and Bioprosthetic Valves
  92. Impact of gender on event rates at 1 year in patients with newly diagnosed non-valvular atrial fibrillation: contemporary perspective from the GARFIELD-AF registry
  93. Empagliflozin and Cardiovascular Outcomes in Asian Patients With Type 2 Diabetes and Established Cardiovascular Disease ― Results From EMPA-REG OUTCOME® ―
  94. OUP accepted manuscript
  95. OUP accepted manuscript
  96. GENETIC POLYMORPHISM OF THE INFLAMMATORY CYTOKINE GENES AND ARTERIAL WALL PROPERTIES IN HYPERTENSIVE PATIENTS
  97. PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
  98. Stroke and Mortality Risk in Patients With Various Patterns of Atrial Fibrillation
  99. Evolving quality standards for large-scale registries: the GARFIELD-AF experience
  100. Vitamin K antagonist control in patients with atrial fibrillation in Asia compared with other regions of the world: Real-world data from the GARFIELD-AF registry
  101. Quality of Vitamin K Antagonist Control and 1-Year Outcomes in Patients with Atrial Fibrillation: A Global Perspective from the GARFIELD-AF Registry
  102. Evolving antithrombotic treatment patterns for patients with newly diagnosed atrial fibrillation
  103. Multiple coronary fistulae into left ventricle as a rare cause of myocardial ischemia
  104. [PP.07.21] PARG GENE POLYMORPHISM IS ASSOCIATED THE DEVELOPMENT OF LEFT VENTRICULAR HYPERTROPHY IN ARTERIAL HYPERTENSION
  105. Outcomes With Edoxaban Versus Warfarin in Patients With Previous Cerebrovascular Events
  106. Empagliflozin and Progression of Kidney Disease in Type 2 Diabetes
  107. Two-year outcomes of patients with newly diagnosed atrial fibrillation: results from GARFIELD-AF
  108. A Novel Hypoxia-Inducible Factor−Prolyl Hydroxylase Inhibitor (GSK1278863) for Anemia in CKD: A 28-Day, Phase 2A Randomized Trial
  109. Comparison of international normalized ratio audit parameters in patients enrolled in GARFIELD-AF and treated with vitamin K antagonists
  110. Cardioversion of Atrial Fibrillation in ENGAGE AF-TIMI 48
  111. The use of optimal partitionings for multiparameter data analysis in clinical trials
  112. Cause of Death and Predictors of All‐Cause Mortality in Anticoagulated Patients With Nonvalvular Atrial Fibrillation: Data From ROCKET AF
  113. Percutaneous Coronary Intervention in Patients With Acute Myocardial Infarction With ST-Segment Elevation After Prehospital Thrombolysis
  114. Using Necrosis Biomarkers for the Early Diagnosis of Myocardial Infarction in Modern Conditions
  115. Heart failure outcomes with empagliflozin in patients with type 2 diabetes at high cardiovascular risk: results of the EMPA-REG OUTCOME®trial
  116. Early Systolic Dysfunction of Left Ventricular Myocardium Is Reflected On Electrocardiogram of Patients With Aortic Stenosis
  117. Genetic Features of Factors of Inflammation and Fibrosis – Possible Common Pathway of Formation of Predisposition to Atrial Fibrillation and Chronic Obstructive Pulmonary Disease
  118. MOLECULAR-GENETIC FACTORS, ASSOCIATED WITH AORTIC STENOSIS DEVELOPMENT
  119. Atrial Fibrillation in Patients With Chronic Obstructive Pulmonary Disease Is Associated With Polymorphism of Interleukin 6 Gene
  120. GENETIC POLYMORPHISM OF INFLAMMATORY FACTORS IS ASSOCIATED WITH THROMBOEMBOLIC COMPLICATIONS OF ATRIAL FIBRILLATION
  121. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes
  122. THE REVOLUTION, WE HAVE ALMOST OVERSLEPT
  123. Biomarkers in Heart Failure: Apelin Level Is not Associated With Presence and Severity of the Disease
  124. Does Sex Affect Anticoagulant Use for Stroke Prevention in Nonvalvular Atrial Fibrillation?: The Prospective Global Anticoagulant Registry in the FIELD-Atrial Fibrillation
  125. Late Silent Stent Abscess
  126. Chronic Thromboembolic Pulmonary Hypertension
  127. Current Aspects of Fibrinolysis
  128. Сhronic Thromboembolic Pulmonary Hypertension
  129. Effect of Darapladib on Major Coronary Events After an Acute Coronary Syndrome
  130. Cerebrovascular Events in 21 105 Patients With Atrial Fibrillation Randomized to Edoxaban Versus Warfarin
  131. An intuitive risk factors search algorithm: usage of the Bayesian network technique in personalized medicine
  132. Laboratory Monitoring of the Efficacy and Safety of Anticoagulants
  133. Degenerative Aortic Stenosis: Prediction of Poor Prognosis by 2D Left Ventricular Longitudinal Strain in Non-Operated Patients
  134. Dabigatran in Prevention of Stroke in Atrial Fibrillation: Three Years of Clinical Application
  135. Varespladib and Cardiovascular Events in Patients With an Acute Coronary Syndrome
  136. Edoxaban versus Warfarin in Patients with Atrial Fibrillation
  137. Prasugrel versus Clopidogrel for Acute Coronary Syndromes without Revascularization
  138. ISSUES OF ANTICOAGULANT TREATMENT MANAGEMENT
  139. WARFARIN IN PATIENTS WITH CARDIOEMBOLIC STROKE
  140. Polymorphic markers Ala455Val of the THBD gene and Arg353Gln of the F7 gene and genetic association with unfavorable outcomes of coronary atherosclerosis in patients with a history of acute ischemic heart disease
  141. Rationale, design, and results from RENO-DEFEND 1: A randomized, dose-finding study of the selective A1 adenosine antagonist SLV320 in patients hospitalized with acute heart failure
  142. 602 ASSOCIATION OF POLYMORPHIC MARKERS C3386A OF HMGCR GENE AND G(-198)A OF FDFT1 GENE WITH CORONARY ARTERY DISEASE
  143. 611 DEVELOPMENT OF GENDER PRESPECIFIED PREDICTION MODEL BASED ON BAYESIAN BELIEVE NETWORKS METHOD FOR RISK ESTIMATION AFTER ACUTE CORONARY SYNDROME
  144. 869 DEVELOPMENT OF GENDER PRESPECIFIED PREDICTIVE MODEL BASED ON BAYESIAN BELIEVE NETWORKS METHOD FOR UNFAVOURABLE OUTCOMES AFTER ACUTE CORONARY SYNDROME
  145. 634 GENDER DEPENDENT ASSOCIATION BETWEEN KIF6 POLYMORPHISM AND RISK OF UNFAVORABLE OUTCOME IN PATIENTS SURVIVED ACUTE CORONARY SYNDROME
  146. 639 POLYMORPHIC MARKERS OF THBD AND PROC GENES AND GENETIC PREDISPOSITION TO UNFAVOURABLE OUTCOMES IN PATIENTS AFTER ACUTE CORONARY SYNDROME
  147. Ispol'zovanie rozuvastatina v lechenii bol'nykh gruppy riska sosudistykh oslozhneniy ateroskleroza.
  148. PECULIAR PROPERTIES OF ANTITHROMBOTIC THERAPY IN PATIENTS WITH ARTERIAL HYPERTENSION. IS IT POSSIBLE TO DO THE TREATMENT SAFE?
  149. Rolofylline, an Adenosine A1−Receptor Antagonist, in Acute Heart Failure
  150. The polymorphisms G(−174)C in IL6 gene and G(−1082)A in IL10 gene are associated with poor outcomes in patients with acute coronary syndrome
  151. Rimonabant for prevention of cardiovascular events (CRESCENDO): a randomised, multicentre, placebo-controlled trial
  152. Association of the polymorphic markers G(−455)A in the FGB gene and C(−1654)T in the PROC gene with hereditary predisposition to unfavourable outcome in patients with history of acute coronary syndrome
  153. MS217 ASSOCIATION OF THE CHOLESTEROL ESTER TRANSFER PROTEIN GENE (CETP) WITH CORONARY ARTERY DISEASE
  154. MS216 IL6 AND IL10 GENES ARE ASSOCIATED WITH UNFAVOURABLE OUTCOMES IN PATIENTS WITH ACUTE CORONARY SYNDROME
  155. 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
  156. 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
  157. Design and Rationale of the PROTECT Study: A Placebo-controlled Randomized Study of the Selective A1 Adenosine Receptor Antagonist Rolofylline for Patients Hospitalized With Acute Decompensated Heart Failure and Volume Overload to Assess Treatment Effe...
  158. THE MODERN ASPECTS OF CLOPIDOGREL USE
  159. Ticagrelor versus Clopidogrel in Patients with Acute Coronary Syndromes
  160. Chronic Thromboembolic Pulmonary Hypertension
  161. The PROTECT Pilot Study: A Randomized, Placebo-Controlled, Dose-Finding Study of the Adenosine A1 Receptor Antagonist Rolofylline in Patients With Acute Heart Failure and Renal Impairment
  162. Ivabradine for patients with stable coronary artery disease and left-ventricular systolic dysfunction (BEAUTIFUL): a randomised, double-blind, placebo-controlled trial
  163. Safety and Efficacy of Outpatient Nesiritide in Patients With Advanced Heart Failure
  164. The BEAUTIFUL Study: Randomized Trial of Ivabradine in Patients with Stable Coronary Artery Disease and Left Ventricular Systolic Dysfunction – Baseline Characteristics of the Study Population
  165. Association of GNB3 gene C825T polymorphism with coronary heart disease
  166. Association of CYP2D6 and ADRB1 genes with hypotensive and antichronotropic action of betaxolol in patients with arterial hypertension
  167. Comparison of Fondaparinux and Enoxaparin in Acute Coronary Syndromes
  168. Mo-P6:387 Genetic predisposition to early onset of coronary artery disease in Russian patients
  169. Mo-P6:455 Genetic predisposition to unfavourable outcomes in patients with unstable angina
  170. W03-P-008 Genetic basis of inherited predisposition to coronary artery disease
  171. Association of Polymorphic Marker A1/A2 of Gene ITGB3 with Coronary Artery Disease and Myocardial Infarction
  172. Association of Polymorphic Marker G(–455)A of Gene FGB with Coronary Artery Disease
  173. ASSOCIATION OF THE POLYMORPHIC MARKERS OF MTHFR, EDN1, CYP11B2, PPARA AND PPARG2 GENES WITH THE SEVERITY OF ESSENTIAL HYPERTENSION
  174. Anticoagulant properties of the endothelium studied by the standard venous occlusion test