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3. Cancelled STEMI patients: what happen to them?

6. A second update on mapping the human genetic architecture of COVID-19

7. Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death

8. Classic and genetic cardiovascular risk burden and case-fatality from SARS-CoV-2 virus infection. The CARGENCORS study

9. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

11. Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

13. Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy

14. Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome

15. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6)

16. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

17. Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes

22. Genetic risk score for risk stratification of patients positive for SARS-CoV-2 virus. The CARGENCORS study

23. Novel genes and sex differences in COVID-19 severity

24. Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A

25. Brugada Syndrome in Women: What Do We Know After 30 Years?

28. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

29. Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation

30. Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy

31. Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies

32. Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later

40. Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

41. Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation

42. The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope

43. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome .

44. Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

45. Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

48. Atenolol is not effective in reducing ventricular arrhythmia severity on exercise stress test in patients with catecholaminergic polymorphic ventricular tachycardia

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