36 results on '"Mauriello, Alfredo"'
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2. Prevalence and clinical significance of right ventricular pulmonary arterial uncoupling in cardiac amyloidosis
3. Echocardiography in Cardiac Arrest: Incremental Diagnostic and Prognostic Role during Resuscitation Care.
4. Migration of long-sensing vector implantable loop recorder unmasked by remote monitoring in patient with unexplained syncope.
5. The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies
6. Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia
7. The Lipid-Lowering Efficacy of a Nutraceutical Combination Including Leucoselect Phytosome, Red Yeast Rice, Policosanol and Folic Acid in Dyslipidaemia Patients: Real-World Insights
8. Enhancing ST-Elevation Myocardial Infarction Diagnosis and Management: The Integral Role of Echocardiography in Patients Rushed to the Cardiac Catheterization Laboratory
9. Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network
10. Advanced Heart Failure in Special Population—Pediatric Age
11. Effects of Heart Failure Therapies on Atrial Fibrillation: Biological and Clinical Perspectives.
12. Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from Italian Neuro-Cardiology Network
13. Pharmacogenomics of Cardiovascular Drugs for Atherothrombotic, Thromboembolic and Atherosclerotic Risk
14. Arrhythmogenic Left Ventricular Cardiomyopathy: From Diagnosis to Risk Management.
15. Anti-Inflammatory and Anticancer Effects of Anticoagulant Therapy in Patients with Malignancy
16. Syncope without prodromes during fever in type 1‐induced BrS patient: Looks can be deceiving
17. Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes
18. Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies
19. “Narrow-Wide-Narrow” QRS Complex Tachycardia—Beware the Smartwatch Monsters
20. The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases
21. Multimodality Imaging in Arrhythmogenic Left Ventricular Cardiomyopathy
22. Coronary Embolism in Patient with Prosthetic Aortic Valve: Looks Can Be Deceiving.
23. Thoracic Aortic Dilation: Implications for Physical Activity and Sport Participation
24. Multimodality Imaging in Cardiomyopathies with Hypertrophic Phenotypes
25. 589 External validation of the increased wall thickness score for the diagnosis of cardiac amyloidosis
26. 585 Natural history of left ventricular hypertrophy in infants of diabetic mothers
27. Syncope without prodromes during fever in type 1‐induced BrSpatient: Looks can be deceiving
28. Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome
29. The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies
30. Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia
31. Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes
32. The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases
33. Multimodality Imaging in Arrhythmogenic Left Ventricular Cardiomyopathy
34. Multimodality Imaging in Cardiomyopathies with Hypertrophic Phenotypes
35. Prevalence and Cardiovascular Outcomes of Left Ventricular Hypertrabeculation in Children.
36. [Clinical and genetic manifestations of left ventricular non-compaction in children].
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