139 results on '"Serio, Alessandra"'
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2. The new 2023 ESC guidelines for the management of cardiomyopathies: a guiding path for cardiologist decisions
3. Classification of cardiomyopathies
4. Prevalence and Complications of Aberrant Subclavian Artery in Patients With Heritable and Nonheritable Arteriopathies
5. Genetics and clinics: together to diagnose cardiomyopathies
6. Impediments to Heart Transplantation in Adults With MELAS:m.3243A>G Cardiomyopathy
7. Aortic root 3D parametric morphological model from 2D-echo images
8. ‘Precision and personalized medicine,’ a dream that comes true?
9. Diagnostic Work-Up and Risk Stratification in X-Linked Dilated Cardiomyopathies Caused by Dystrophin Defects
10. Prognostic relevance of the echocardiographic assessment of right ventricular function in patients with idiopathic pulmonary arterial hypertension
11. When Should Cardiologists Suspect Anderson-Fabry Disease?
12. Atlas of the clinical genetics of human dilated cardiomyopathy
13. Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies
14. Diagnostic Criteria of Left Ventricular Dysfunction in Patients With Myotonic Dystrophy Type 1
15. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers
16. Response of the right ventricle to acute pulmonary vasodilation predicts the outcome in patients with advanced heart failure and pulmonary hypertension
17. Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2)
18. Myths to debunk: the non-compacted myocardium
19. Hereditary muscle diseases and the heart: the cardiologist’s perspective
20. Regional abnormalities of myocardial deformation in patients with hypertrophic cardiomyopathy: correlations with delayed enhancement in cardiac magnetic resonance
21. POST-TRANSPLANT OUTCOME OF DILATED CARDIOMYOPATHY CAUSED BY DYSTROPHIN GENE DEFECTS: P-152
22. Long-term left ventricular reverse remodelling with cardiac resynchronization therapy: results from the CARE-HF trial
23. Effects of nebivolol in elderly heart failure patients with or without systolic left ventricular dysfunction: results of the SENIORS echocardiographic substudy
24. Interventricular and intraventricular dyssynchrony are common in heart failure patients, regardless of QRS duration
25. Reply
26. Cardio-Oncology
27. Genetic causes of dilated cardiomyopathy
28. Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty Clinics
29. Left Ventricular Noncompaction
30. MUTATIONS IN SMOOTH MUSCLE AORTIC ALPHA-ACTIN GENE ARE ASSOCIATED WITH FAMILIAL THORACIC AORTIC ANEURYSM AND DISSECTION
31. Atlas of the clinical genetics of human dilated cardiomyopathy
32. Atlas of the clinical genetics of human dilated cardiomyopathy
33. The MOGE(S) Classification of Cardiomyopathy for Clinicians
34. Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A
35. Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy
36. Prevalence of J-Point Elevation in Families With Sudden Arrhythmic Death Syndrome
37. Transcriptomic and proteomic analysis in the cardiovascular setting: unravelling the disease?
38. Rationale and design of a trial evaluating the effects of losartan vs. nebivolol vs. the association of both on the progression of aortic root dilation in Marfan syndrome with FBN1 gene mutations
39. Abstract 4877: Clinical Phenotypes and Outcome of 101 LMNA Gene Mutation Carriers
40. Hemodynamic changes before acute heart failure episodes in patients with advanced systolic left ventricular dysfunction
41. Increased expression of peripheral benzodiazepine receptors on leukocytes in silent myocardial ischemia
42. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
43. Cardio-Oncology: The Carney Complex Type I.
44. Baseline echocardiographic characteristics of heart failure patients enrolled in a large European multicentre trial (CArdiac REsynchronisation Heart Failure study)
45. P4-95: Minute ventilation and patient’s activity may predict acute heart failure events in CRT patients
46. Clinical Phenotypes and Outcome of 101 LMNA Gene Mutation Carriers
47. POST-TRANSPLANT OUTCOME OF DILATED CARDIOMYOPATHY CAUSED BY DYSTROPHIN GENE DEFECTS
48. High Risk of Cardiac Events in Hypertrophic Cardiomyopathy Patients With Double/Compound Heterozigosity
49. Phenotype heterogeneity in a consecutive series of genotyped patients diagnosed with hypertrophic cardiomyopathy
50. Corrigendum to: ‘Effects of nebivolol in elderly heart failure patients with or without systolic left ventricular dysfunction: results of the SENIORS echocardiographic substudy’.
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