611 results on '"Postema, Pieter G"'
Search Results
2. The Dutch Idiopathic Ventricular Fibrillation Registry: progress report on the quest to identify the unidentifiable
3. A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand
4. Stereotactic arrhythmia radioablation (STAR)—A systematic review and meta-analysis of prospective trials on behalf of the STOPSTORM.eu consortium
5. A bizarre electrocardiogram with a fruitful recovery
6. Ventricular arrhythmias after atrial fibrillation electrical cardioversion: A multicenter study
7. Comparing adolescent- and adult-onset unexplained cardiac arrest: Results from the Dutch Idiopathic VF Registry
8. Predicting postinfarct ventricular tachycardia by integrating cardiac MRI and advanced computational reentrant pathway analysis
9. Optimizing ventricular tachycardia ablation through imaging-based assessment of arrhythmic substrate: A comprehensive review and roadmap for the future
10. Development, validation and long-term evaluation of a liquid chromatography-tandem mass spectrometry method for simultaneous quantification of amiodarone, desethylamiodarone and mexiletine in human plasma and serum
11. Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
12. Sex and ethnic differences in unrecognized myocardial infarctions: Observations on recognition and preventive therapies from the multiethnic population-based HELIUS cohort
13. Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome
14. Refining critical structure contouring in STereotactic Arrhythmia Radioablation (STAR): Benchmark results and consensus guidelines from the STOPSTORM.eu consortium
15. Stereotactic arrhythmia radioablation: A multicenter pre-post intervention safety evaluation of the implantable cardioverter-defibrillator function
16. Provocation testing in congenital long QT syndrome: A practical guide
17. Novelties in Brugada Syndrome: Complex Genetics, Risk Stratification, and Catheter Ablation
18. Malignant Purkinje ectopy induced by sodium channel blockers
19. Standardizing the Cardiac Radioablation Targeting Workflow: Enabling Semi-Automated Angulation and Segmentation of the Heart According to the American Heart Association Segmented Model
20. A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.
21. Congenital Long QT Syndrome
22. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
23. Echocardiographic deformation imaging unmasks global and regional mechanical dysfunction in patients with idiopathic ventricular fibrillation: A multicenter case-control study
24. A Rare Noncoding Enhancer Variant in SCN5AContributes to the High Prevalence of Brugada Syndrome in Thailand
25. Fractionated Epicardial Electrograms: Implication for Mechanism of the Brugada Pattern
26. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
27. Age, Sex and Racial Differences in Cardiac Repolarization and Arrhythmogenesis
28. SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes
29. Cardiac radioablation—A systematic review
30. Improving long QT syndrome diagnosis by a polynomial-based T-wave morphology characterization
31. Chapter 7 - ECG findings of isolated long QT syndrome 1
32. Chapter 6 - Drug-induced Torsades de Pointes and other forms of “acquired LQTS”
33. Comparing adolescent- and adult-onset unexplained cardiac arrest: Results from the Dutch Idiopathic VF Registry
34. Comparing adolescent- and adult-onset unexplained cardiac arrest:Results from the Dutch Idiopathic VF Registry
35. The Dutch Idiopathic Ventricular Fibrillation Registry: progress report on the quest to identify the unidentifiable
36. Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy
37. Sex and ethnic differences in unrecognized myocardial infarctions:Observations on recognition and preventive therapies from the multiethnic population-based HELIUS cohort
38. Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome
39. Idiopathic Ventricular Fibrillation and Early Repolarization
40. Inherited Arrhythmias: Brugada Syndrome and Early Repolarisation Syndrome
41. Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients
42. Fever-related arrhythmic events in the multicenter Survey on Arrhythmic Events in Brugada Syndrome
43. The effect of revascularization of a chronic total coronary occlusion on electrocardiographic variables. A sub-study of the EXPLORE trial
44. Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)
45. STereotactic Arrhythmia Radioablation (STAR): the Standardized Treatment and Outcome Platform for Stereotactic Therapy Of Re-entrant tachycardia by a Multidisciplinary consortium (STOPSTORM.eu) and review of current patterns of STAR practice in Europe
46. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
47. A rare non-coding enhancer variant in SCN5A contributes to the high prevalence of Brugada syndrome in Thailand
48. The Genetic Basis of Apparently Idiopathic Ventricular Fibrillation – a Retrospective Overview
49. Pushing prognostic boundaries in Brugada syndrome: Trying to predict the unpredictable
50. Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families
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