640 results on '"Campuzano, Oscar"'
Search Results
2. Interpreting the actionable clinical role of rare variants associated with short QT syndrome
3. Sudden Arrhythmic Death Syndrome and Ventricular Tachycardia in Children
4. Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
5. Role of microRNAs in arrhythmogenic cardiomyopathy: translation as biomarkers into clinical practice
6. Postmortem diagnosis of Takotsubo syndrome on autoptic findings: is it reliable? A systematic review
7. Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
8. Short QT Syndrome: Update on Genetic Basis
9. Natural History of MYH7-Related Dilated Cardiomyopathy
10. Post-mortem toxicology analysis in a young sudden cardiac death cohort
11. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
12. Rare variants in genes encoding structural myocyte contribute to a thickened ventricular septum in sudden death population without ventricular alterations
13. Circulating circRNA as biomarkers for dilated cardiomyopathy etiology
14. Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins
15. Sudden unexplained death in young people: A family matter
16. Brugada Syndrome
17. Long-term prognosis of women with Brugada syndrome and electrophysiological study
18. Lafora Disease Is an Inherited Metabolic Cardiomyopathy
19. Role of miRNA–mRNA Interactome in Pathophysiology of Arrhythmogenic Cardiomyopathy.
20. A narrative review of inherited arrhythmogenic syndromes in young population: role of genetic diagnosis in exercise recommendations.
21. Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
22. Genetic variants of uncertain significance: How to match scientific rigour and standard of proof in sudden cardiac death?
23. Peripheral microRNA panels to guide the diagnosis of familial cardiomyopathy
24. Plasma microrna expression profile for reduced ejection fraction in dilated cardiomyopathy
25. Genetic analysis, in silico prediction, and family segregation in long QT syndrome
26. Update on Genes Associated with Arrhythmogenic Cardiomyopathy
27. Chapter 11 - The electrocardiographic spectrum of the long QT syndrome in pediatric patients
28. Electroanatomic and Pathologic Right Ventricular Outflow Tract Abnormalities in Patients With Brugada Syndrome
29. The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe.
30. Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?
31. Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.
32. Editorial: Genetics of sudden unexplained death in children and young adults: state of the art, testing and implications for translational research, public health and forensic pathology
33. Molecular autopsy in a cohort of infants died suddenly at rest
34. Present Status of Brugada Syndrome: JACC State-of-the-Art Review
35. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
36. Sudden cardiac death of arrhythmic origin: Value of post-mortem genetic analysis
37. Brugada Syndrome
38. Genetic analysis in post-mortem samples with micro-ischemic alterations
39. A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia
40. Deporte y síndromes arritmogénicos hereditarios.
41. Genetic basis of dilated cardiomyopathy
42. Plasma microRNAs as biomarkers for Lamin A/C-related dilated cardiomyopathy
43. Sex differences in long QT syndrome
44. LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation
45. Characterization of cardiac involvement in children with LMNA-related muscular dystrophy
46. Editorial: Genetics of sudden unexplained death in children and young adults: state of the art, testing and implications for translational research, public health and forensic pathology
47. Proteomic identification of putative biomarkers for early detection of sudden cardiac death in a family with a LMNA gene mutation causing dilated cardiomyopathy
48. Ventricular Tachycardiac and Sudden Arrhythmic Death
49. Negative Autopsy in Infant and Juvenile Population: Role of Cardiac Arrhythmias
50. Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death
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