273 results on '"Rampazzo, Alessandra"'
Search Results
2. Animal Models and Molecular Pathogenesis of Arrhythmogenic Cardiomyopathy Associated with Pathogenic Variants in Intercalated Disc Genes
3. Clinical profile and long-term follow-up of a cohort of patients with desmoplakin cardiomyopathy
4. Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathy
5. Abstract 13516: Natural History, Penotypes and Clinical Outcomes in Desmin Related Arrhythmogenic Cardiomyopathy
6. A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy
7. Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical Stimuli
8. Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases
9. Arrhythmogenic Ventricular Cardiomyopathy Associated With Fibromuscular Dysplasia of Ostial Right Main Coronary Artery
10. Homozygous Desmocollin-2 Mutations and Arrhythmogenic Cardiomyopathy
11. Advances in Genetics: Dominant Forms
12. Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing
13. Desmin Mutations and Arrhythmogenic Right Ventricular Cardiomyopathy
14. Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients
15. Arrhythmogenic cardiomyopathy: a disease of intercalated discs
16. Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations
17. Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
18. Recent Advances in CRISPR/Cas9-Based Genome Editing Tools for Cardiac Diseases
19. Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy
20. Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy
21. A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life
22. Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies
23. Comparison of Clinical Features of Arrhythmogenic Right Ventricular Cardiomyopathy in Men Versus Women
24. Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria
25. ‘Hot phase’ clinical presentation in arrhythmogenic cardiomyopathy
26. Arrhythmogenic Cardiomyopathy
27. Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria
28. Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy
29. Regulatory mutations in transforming growth factor-β3 gene involved in arrhythmogenic right ventricular cardiomyopathy
30. Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. (Report)
31. Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
32. Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology
33. Pathogenic Potential of Hic1-Expressing Cardiac Stromal Progenitors
34. Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities
35. Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies
36. Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations
37. 'Hot phase' clinical presentation in arrhythmogenic cardiomyopathy.
38. Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical Stimuli
39. Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: Early diagnosis of asymptomatic carriers
40. Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro
41. Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy
42. Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy
43. Acciaio come paglia, Louis I. Kahn : il caso dell'Indian Institute of Management di Ahmedabad
44. Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43
45. A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signalling and miRNA dysregulation
46. Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy
47. A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43
48. Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy
49. Wnt/β-catenin pathway in arrhythmogenic cardiomyopathy
50. A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signalling and miRNA dysregulation.
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