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1. Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy

2. Correction to: Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy

3. Abstract 4144360: Neurohormonal therapies at baseline and follow-up and survival in patients with wild-type transthyretin cardiac amyloidosis

4. Clinical and Prognostic Implications of Right Ventricular Uptake on Bone Scintigraphy in Transthyretin Amyloid Cardiomyopathy

6. Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms

7. Incidence and predictors of sudden death in patients with cardiac amyloidosis.

10. Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis: Insights From THAOS

11. Temporal implementation of a regional referral pathway in transthyretin cardiac amyloidosis: Emilia-Romagna experience.

12. Characterization and natural history of different phenotypes in hereditary transthyretin amyloidosis: 40-year experience at a single Italian referral center

13. Familial Cardiac Amyloidoses

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

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

18. Tc-99m labelled bone scintigraphy in suspected cardiac amyloidosis

19. Diagnostic pathways to wild‐type transthyretin amyloid cardiomyopathy: a multicentre network study

20. Screening approaches to cardiac amyloidosis in different clinical settings: Current practice and future perspectives

21. 172 CLINICAL AND PROGNOSTIC IMPLICATIONS OF RV UPTAKE WITH RADIONUCLIDE SCINTIGRAPHY IN TRANSTHYRETIN CARDIAC AMYLOIDOSIS

23. 826 NEW THERAPEUTIC PERSPECTIVES IN CARDIAC AMYLOIDOSIS

25. Systemic embolism in amyloid transthyretin cardiomyopathy

28. 172 Two mutations, one patient: which phenotype?

29. 334 Hereditary transthyretin amyloidosis: main features and profiles of different clinical phenotypes

30. 199 Lower aortic valve calcium scores by computed tomography scan. A potential new red flag of concomitant cardiac amyloidosis in patients with severe aortic stenosis

31. 351 Prevalence and prognostic significance of RV uptake (biventricular uptake) at planar scintigraphy in patients with ATTR cardiac amyloidosis

32. Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis

37. Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis : Insights From THAOS

38. Role of gender in transthyretin-related amyloidosis: an international perspective based on the Transthyretin Amyloid Outcomes Survey (THAOS)

39. Current patterns of beta‐blocker prescription in cardiac amyloidosis: an Italian nationwide survey

41. Phenotypic profile of Ile68Leu transthyretin amyloidosis: an underdiagnosed cause of heart failure

42. Role of gender in transthyretin-related amyloidosis: an international perspective based on the Transthyretin Amyloid Outcomes Survey (THAOS)

43. Carpal tunnel syndrome in cardiac amyloidosis: implications for early diagnosis and prognostic role across the spectrum of aetiologies

45. Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths

46. The Authors Reply

48. La cardiomiopatia amiloidotica correlata alla transtiretina: Alla ricerca del trattamento eziologico

49. Atrial fibrillation in amyloidotic cardiomyopathy: prevalence, incidence, risk factors and prognostic role

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