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604 results on '"Arbustini, Eloisa"'

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1. The contribution of amyloid deposition in the aortic valve to calcification and aortic stenosis.

3. Management of Adults With Anomalous Aortic Origin of the Coronary Arteries: State-of-the-Art Review

5. The new 2023 ESC guidelines for the management of cardiomyopathies: a guiding path for cardiologist decisions

6. Impediments to Heart Transplantation in Adults With MELASMT-TL1:m.3243A>G Cardiomyopathy

12. Rationale and design of the CV-PREVITAL study: an Italian multiple cohort randomised controlled trial investigating innovative digital strategies in primary cardiovascular prevention

13. Acute necrotizing eosinophilic myocarditis presenting with cardiogenic shock after mRNA booster dose for COVID-19: Case report and review of literature

14. Broncho-alveolar inflammation in COVID-19 patients: a correlation with clinical outcome

15. Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny.

16. Mitochondrial DNA Variant Discovery and Evaluation in Human Cardiomyopathies through Next-Generation Sequencing

18. Spontaneous coronary artery dissection: an unpredictable event

23. European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

26. Prevalence and Complications of Aberrant Subclavian Artery in Patients With Heritable and Nonheritable Arteriopathies

28. 42 SEASON VARIABILITY IN ATHEROSCLEROSIS COMPOSITION: INSIGHTS FROM 1848 NON-CULPRIT CORONARY PLQUES

29. Pathologic Findings at Risk Reducing Surgery in BRCA and Non-BRCA Mutation Carriers: A Single-Center Experience

30. Fifteen-Year Surveillance of LTR Receiving Pre-Emptive Therapy for CMV Infection: Prevention of CMV Disease and Incidence of CLAD

31. Genetics and clinics: together to diagnose cardiomyopathies

33. Impediments to Heart Transplantation in Adults With MELAS:m.3243A>G Cardiomyopathy

34. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension Developed by the task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS). Endorsed by the International Society for Heart and Lung Transplantation (ISHLT) and the European Reference Network on rare respiratory diseases (ERN-LUNG)

35. TCT-237 Clinical Effectiveness of Functional Assessment of Non-Culprit Coronary Lesions Using an Optical Coherence Tomography Computational Algorithm: A CLIMA Post-Hoc Analysis

37. International External Validation Study of the 2014 European Society of Cardiology Guidelines on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (EVIDENCE-HCM)

39. Optical coherence tomography-derived lipid core burden index and clinical outcomes: results from the CLIMA registry.

40. causes muscular dystrophy and arrhythmia by affecting protein trafficking

42. Optical coherence tomography-derived lipid core burden index and clinical outcomes: results from the CLIMA registry

46. Evaluation of Oxidative Stress and Metabolic Profile in a Preclinical Kidney Transplantation Model According to Different Preservation Modalities

47. Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

48. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy.

49. Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics

50. Genetic Basis of Myocarditis: Myth or Reality?

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