| Nome |
# |
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Facciamo il punto: miocardio non compatto, file e2913fdf-368c-f688-e053-3705fe0a67e0
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4.216
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Cardioprotective factors against myocardial infarction selected in vivo from an AAV secretome library, file 83471447-ebfe-4bbf-b843-55233129c309
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320
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Cardiac fluid dynamics meets deformation imaging, file e2913fdb-d621-f688-e053-3705fe0a67e0
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185
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AAV-mediated in vivo functional selection of tissue-protective factors against ischaemia, file e2913fd9-9d68-f688-e053-3705fe0a67e0
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158
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Left Ventricular Response to Cardiac Resynchronization Therapy: Insights From Hemodynamic Forces Computed by Speckle Tracking, file e2913fdc-9bab-f688-e053-3705fe0a67e0
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145
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MiR-320a as a Potential Novel Circulating Biomarker of Arrhythmogenic CardioMyopathy, file e2913fdb-ef20-f688-e053-3705fe0a67e0
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133
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Chapter 5: Genetics of Dilated Cardiomyopathy: Current Knowledge and Future Perspectives, file e2913fdd-055e-f688-e053-3705fe0a67e0
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113
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Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy, file e2913fdf-8687-f688-e053-3705fe0a67e0
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112
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Myocarditis: Which Role for Genetics?, file e2913fde-b7f6-f688-e053-3705fe0a67e0
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85
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Prevalence and evolution of right ventricular dysfunction among different genetic backgrounds in dilated cardiomyopathy, file e2913fde-bd7a-f688-e053-3705fe0a67e0
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84
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Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy, file b94d515a-becd-4903-a261-cc573898540d
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81
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Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies, file b0e9a5c9-c8eb-4279-af3f-4c444ec2a703
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65
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Echocardiographic evaluation of centenarians in Trieste, file e2913fdf-7633-f688-e053-3705fe0a67e0
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64
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Lymphocytic Myocarditis: A Genetically Predisposed Disease?, file e2913fdf-62b6-f688-e053-3705fe0a67e0
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59
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Evolving trends in epidemiology and natural history of cardiac amyloidosis: 30-year experience from a tertiary referral center for cardiomyopathies, file 1851ed4a-89b8-4429-b25f-013ca26d3d91
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38
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SARS-CoV-2, myocardial injury and inflammation: insights from a large clinical and autopsy study, file e2913fde-a162-f688-e053-3705fe0a67e0
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36
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Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator, file 47fefdc4-dfdb-41dd-b894-af07fed403a5
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34
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Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases, file f50b394e-f924-4aae-bfa0-1467e26e95e2
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32
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Preserved skeletal muscle mitochondrial function, redox state, inflammation and mass in obese mice with chronic heart failure, file e2913fdd-b5cc-f688-e053-3705fe0a67e0
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22
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Arrhythmic risk stratification in non-ischaemic dilated cardiomyopathy, file 5bc133c7-5edb-4d19-bfd9-853bb4b88c75
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19
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Cardiology of the future: xenotransplantation with porcine heart, file 6be161cb-fa8d-4550-9ce0-2c22e6c987f0
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19
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n-3 PUFA-Enriched Diet Preserves Skeletal Muscle Mitochondrial Function and Redox State and Prevents Muscle Mass Loss in Mice with Chronic Heart Failure, file 5cca230e-f29c-4ff0-a7e3-9c055bbde8d4
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18
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Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation, file fb87c15d-f57c-4bfc-a69f-c0979cd112e1
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15
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Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies, file ba1aa3f1-88f3-4e0e-bdd9-b28b4f952923
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13
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Role of the Electrocardiogram in Differentiating Genetically Determined Dilated Cardiomyopathy from Athlete's Heart, file 7c298ae7-036f-4ec9-b110-2608b4672470
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11
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Prognostic value of echocardiographic evaluation of cardiac mechanics in patients with aortic stenosis and preserved left ventricular ejection fraction, file 8e17c83e-91ed-4fd3-b543-2195c6b4a263
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11
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Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy, file e2913fdd-3ddc-f688-e053-3705fe0a67e0
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11
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Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy, file fb51c173-2e58-4db6-8025-638ad59f7921
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10
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Il Registro Regionale delle Morti Cardiache Improvvise in età giovanile del Friuli Venezia Giulia. Protocolli operativi e risultati di un progetto multidisciplinare, file 747bf26a-7312-47e0-81ac-7de423771d01
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8
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The Arrhythmic Phenotype in Cardiomyopathy, file a0ecd932-c448-4841-8195-c4af7833cee4
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7
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Cardiac Magnetic Resonance Feature-Tracking Identifies Preclinical Abnormalities in Hypertrophic Cardiomyopathy Sarcomere Gene Mutation Carriers, file 17de9db9-06be-47ac-9a3d-a351f656cc41
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5
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Sport and Exercise in Genotype positive (+) Phenotype negative (-) Individuals. Current Dilemmas and Future Perspectives, file 4c52c468-d0a2-44e4-b1a2-5d25df871406
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5
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Lymphocytic Myocarditis: A Genetically Predisposed Disease?, file e2913fdd-f221-f688-e053-3705fe0a67e0
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5
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Prognostic value of echocardiographic evaluation of cardiac mechanics in patients with aortic stenosis and preserved left ventricular ejection fraction, file 41491617-08a3-4728-8139-259d5d138009
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4
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Terapia di modulazione della contrattilità cardiaca: basi molecolari e razionale per l’impiego in modelli di insufficienza cardiaca sistolica e diastolica, file 46718475-1a60-4ffd-b22f-b96063e5492b
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4
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Echocardiographic evaluation of centenarians in Trieste, file e2913fdd-a3e8-f688-e053-3705fe0a67e0
|
4
|
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SARS-CoV-2, myocardial injury and inflammation: insights from a large clinical and autopsy study, file e2913fde-8f41-f688-e053-3705fe0a67e0
|
4
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Heart failure with reduced ejection fraction and monogenic dilated cardiomyopathy: distinct diseases? Insights from randomized controlled trials, file 0ecf19ce-cbe9-4151-be88-5bf0c5830c62
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3
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Sport and Exercise in Genotype positive (+) Phenotype negative (-) Individuals. Current Dilemmas and Future Perspectives, file 23bbf54a-cdfa-4cbc-9af3-10c1738afecb
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3
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Role of the Electrocardiogram in Differentiating Genetically Determined Dilated Cardiomyopathy from Athlete's Heart, file 7a37629f-0417-4176-a3da-be4a8ade9fda
|
3
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Cardioprotective factors against myocardial infarction selected in vivo from an AAV secretome library, file ad589799-a87e-4f08-8667-9cd81ee6710d
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3
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Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy, file e2913fdc-79b3-f688-e053-3705fe0a67e0
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3
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Inquadramento e gestione delle cardiomiopatie: il protocollo della Cardiologia di Trieste, file e2913fde-058c-f688-e053-3705fe0a67e0
|
3
|
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Association of Titin Variations with Late-Onset Dilated Cardiomyopathy, file e2913fdf-80d6-f688-e053-3705fe0a67e0
|
3
|
|
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases, file ec2fcf49-9fc6-4a68-a941-ba6e89e85358
|
3
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Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants, file 3d021a52-c487-40cf-8075-edcb557a4d58
|
2
|
|
Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular Cardiomyopathies, file 9cef1d5c-a603-46b6-b153-e2667a78d84b
|
2
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In Vivo Functional Selection Identifies Cardiotrophin-1 as a Cardiac Engraftment Factor for Mesenchymal Stromal Cells, file e2913fdb-db4c-f688-e053-3705fe0a67e0
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2
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Facciamo il punto: miocardio non compatto, file e2913fdd-91ce-f688-e053-3705fe0a67e0
|
2
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Toward standardization of echocardiography for the evaluation of left ventricular function in adult rodents: a position paper of the ESC Working Group on Myocardial Function, file e2913fde-0bbb-f688-e053-3705fe0a67e0
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2
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High prevalence of subtle systolic and diastolic dysfunction in genotype-positive phenotype-negative relatives of dilated cardiomyopathy patients, file e2913fde-106e-f688-e053-3705fe0a67e0
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2
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Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants, file 17e14e42-f82f-4e37-b132-6f54a90a6ccd
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1
|
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Acute heart failure: mechanisms and pre-clinical models-a Scientific Statement of the ESC Working Group on Myocardial Function, file 22c2d0d5-6fbe-4196-a1c2-bee59b84f259
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1
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Lamin A/C Cardiomyopathy: Cutting Edge to Personalized Medicine, file e2913fdb-c309-f688-e053-3705fe0a67e0
|
1
|
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Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy, file e2913fdc-b406-f688-e053-3705fe0a67e0
|
1
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Cardiomyopathies in children: Classification, diagnosis and treatment, file e2913fde-9485-f688-e053-3705fe0a67e0
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1
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Prevalence and evolution of right ventricular dysfunction among different genetic backgrounds in dilated cardiomyopathy, file e2913fde-b55e-f688-e053-3705fe0a67e0
|
1
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| Totale |
6.197 |