31 results on '"Cecchi, F."'
Search Results
2. P1243Comparison of long-term clinical course and outcome of MYBPC3 - versus MYH7 - related hypertrophic cardiomyopathy
3. 1473Microvascular coronary disease and myocardial fibrosis within the spectrum of hypertrophic cardiomyopathy: a histopathologic study
4. P4235Telemedicine cardiovascular screening program in low-income settings by smartphone based technology
5. P2594Prevalence of cardiac amyloidosis by age-class in patients presenting with hypertrophic cardiomyopathy
6. 479Age-specific prevalence of cardiac structural alterations in a large consecutive cohort of athletes by pre-participation screening
7. P3167Extra long term follow up of the original tuscany cohort of patients with hypertrophic cardiomyopathy
8. 145Clinical course and significance of hypertrophic cardiomyopathy without left ventricular hypertrophy
9. P3545Efficacy and safety of dysopiramide in patients with obstructive hypertrophic cardiomyopathy
10. P5504Diagnostic yield of 7-days versus 21-days recordings by using a new wearable wireless continuous ambulatory ECG recorder
11. P4506Genetic basis of pediatric sarcomeric hypertrophic cardiomyopathy: impact on long term outcome
12. P2316Outcome of septal reduction therapies for obstructive hypertrophic cardiomyopathy in a high-flow referral centre with moderate volume procedural programmes
13. P4497Accuracy of LGE-CMR compared with histometric quantification of myocardial fibrosis in transplanted hearts of end-stage HCM
14. 124Predictive value of classic sudden death risk factors in pediatric-onset hypertrophic cardiomyopathy
15. P818Transcatheter ablation for atrial fibrillation in patients with hypertrophic cardiomyopathy: long-term results and clinical outcomes
16. Outcome of hypertrophic cardiomyopathy associated with sarcomere protein gene mutations: impact of the implantable cardioverter-defibrillator
17. A novel desmoplakin dominant mutation responsible for Carvajal/Naxos syndrome identified by exome sequencing
18. Genetic causes of cardiomyopathies identified by Whole Exome Sequencing
19. Prevalence and clinical correlates of QT prolongation in patients with hypertrophic cardiomyopathy
20. Myocardial bridging and sudden death in hypertrophic cardiomyopathy: Salome drops another veil
21. What do tachycardiomyopathy belong to?: reply
22. The new European definition of cardiomyopathies: which space for muscle dystrophies?: reply
23. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases
24. ECG-based screening: not only for athletes
25. Syncope and ventricular arrhythmias in hypertrophic cardiomyopathy are not related to the derangement of coronary microvascular function
26. Right ventricular infarction: Clinical, hemodynamic, mono- and two-dimensional echocardiographic features.
27. The need for European Registries in inherited cardiomyopathies.
28. Syncope and ventricular arrhythmias in hypertrophic cardiomyopathy are not related to the derangement of coronary microvascular function
29. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).
30. Left ventricular hypertrophy in Fabry disease: a practical approach to diagnosis.
31. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.
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