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1. Clinical Management of Brugada Syndrome: Commentary From the Experts

6. Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

7. From gene-discovery to gene-Tailored clinical management: 25 years of research in channelopathies and cardiomyopathies

10. Acute Myocarditis Associated With Desmosomal Gene Variants

11. Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder

12. Rationale and design of the HeartLogic French Cohort Study: Remote monitoring of heart failure patients implanted with a cardiac defibrillator enabled with the HeartLogic algorithm

14. Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation

16. Evaluation of a multisensory algorithm to prevent acute decompensation of heart failure in patients implanted with a cardioverter defibrillator: rationale and design

17. Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features

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

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

20. SCN5A mutation type and a genetic risk score associate variably with brugada syndrome phenotype in SCN5A families

21. 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)

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

24. Effects of alirocumab on cardiovascular and metabolic outcomes after acute coronary syndrome in patients with or without diabetes: a prespecified analysis of the ODYSSEY OUTCOMES randomised controlled trial

26. Fast Track hERG phenotyping to evaluate the pathogenicity of KCNH2 genetic variants

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

28. 2020 APHRS/HRS Expert Consensus Statement on the Investigation of Decedents with Sudden Unexplained Death and Patients with Sudden Cardiac Arrest, and of Their Families

33. SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.

35. Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine

36. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

38. Authorization for athletes with a cardiomyopathy to participate in competitive or recreational sport: study of concordance within a panel of expert

40. The added value of contrast-enhanced cardiac magnetic resonance to predict positive genetic testing in clinically suspected Lamin A/C cardiomyopathy

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

45. GENECHOC study: genetic markers of arrhythmic risk in heart failure

46. Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome

48. Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

49. The added value of contrast-enhanced cardiac magnetic resonance to predict positive genetic testing in clinically suspected Lamin A/C cardiomyopathy

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