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6. Gold Glyconanoparticles Combined with 91–99 Peptide of the Bacterial Toxin, Listeriolysin O, Are Efficient Immunotherapies in Experimental Bladder Tumors

9. Poster session: Dobutamine stress echo

11. 549 High prevalence of intracardiac thrombi in cardiac amyloidosis.

15. Histological Typing in Patients With Cardiac Amyloidosis: JACC Review Topic of the Week.

16. Biallelic Loss of Function Variants in Myocardial Zonula Adherens Protein Gene (MYZAP) Cause a Severe Recessive Form of Dilated Cardiomyopathy.

17. Feasibility and safety of left bundle branch area pacing in cardiac amyloidosis. A single center experience.

18. Predictors and outcomes of pacemaker implantation in patients with cardiac amyloidosis.

19. Testing a vaccine candidate against Hepatitis C virus designed by combinatorial optimization.

21. Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain.

22. Racial Differences in Atrial Fibrillation Management Between White Patients and Black Patients in Transthyretin Cardiac Amyloid.

23. Frequency of hereditary transthyretin amyloidosis among elderly patients with transthyretin cardiomyopathy.

24. Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms.

25. Fluorescence labeling of mitochondria in living cells by the cationic photosensitizer ZnTM2,3PyPz, and the possible roles of redox processes and pseudobase formation in facilitating dye uptake.

26. Systemic embolism in amyloid transthyretin cardiomyopathy.

27. Gold Glyconanoparticles Combined with 91-99 Peptide of the Bacterial Toxin, Listeriolysin O, Are Efficient Immunotherapies in Experimental Bladder Tumors.

28. First computational design using lambda-superstrings and in vivo validation of SARS-CoV-2 vaccine.

29. Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy.

30. Early Preventive Treatment With Enalapril Improves Cardiac Function and Delays Mortality in Mice With Arrhythmogenic Right Ventricular Cardiomyopathy Type 5.

31. Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases.

32. Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.

33. Transthyretin amyloid cardiomyopathy.

34. Clinical profile and outcome of cardiac amyloidosis in a Spanish referral center.

35. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis.

36. Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmogenic right ventricular cardiomyopathy type 5.

37. Multiparametric Echocardiography Scores for the Diagnosis of Cardiac Amyloidosis.

38. Dopamine beta-hydroxylase and its genetic variants in human health and disease.

39. Prevalence of Cardiac Amyloidosis in Patients with Carpal Tunnel Syndrome.

40. Correction to: Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data.

41. High Prevalence of Intracardiac Thrombi in Cardiac Amyloidosis.

42. A single nucleotide polymorphism in dopamine beta hydroxylase (rs6271(C>T)) is over-represented in inflammatory bowel disease patients and reduces circulating enzyme.

43. Homozygosity for the SCN10A Polymorphism rs6795970 Is Associated With Hypoalgesic Inflammatory Bowel Disease Phenotype.

44. A new staging system for cardiac transthyretin amyloidosis.

45. Diagnostic performance of T 1 and T 2 mapping to detect intramyocardial hemorrhage in reperfused ST-segment elevation myocardial infarction (STEMI) patients.

46. Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.

47. Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis.

48. Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data.

49. Automated Extracellular Volume Fraction Mapping Provides Insights Into the Pathophysiology of Left Ventricular Remodeling Post-Reperfused ST-Elevation Myocardial Infarction.

50. Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease.

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