169 results on '"Zumhagen, Sven"'
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2. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
3. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome
4. Long-term follow-up of subcutaneous ICD systems in patients with hypertrophic cardiomyopathy: a single-center experience
5. Limitations in S-ICD therapy: reasons for system explantation
6. Safety of Endomyocardial Biopsy in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy: A Study Analyzing 161 Diagnostic Procedures
7. Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking
8. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
9. Pairwise Feature Interactions to Predict Arrhythmic Risk of Brugada Syndrome
10. Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype
11. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
12. Inherited long QT syndrome: Clinical manifestation, genetic diagnostics, and therapy
13. Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder
14. Genes Causing Inherited Forms of Cardiomyopathies: A Current Compendium
15. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
16. Was darf ein ICD-Träger und was nicht?
17. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
18. Totally Subcutaneous Implantable Cardioverter Defibrillator with an Alternative, Right Parasternal, Electrode Placement
19. Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: A long-term follow-up
20. Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances
21. Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K + Channel) Channel Function
22. Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography
23. A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction
24. (Tpeak − Tend)/QRS and (Tpeak − Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply
25. Sodium permeable and “hypersensitive” TREK ‐1 channels cause ventricular tachycardia
26. Corneal Densitometry as a Novel Technique for Monitoring Amiodarone Therapy
27. Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs
28. Intraoperative Defibrillation Testing of Subcutaneous Implantable Cardioverter‐Defibrillator Systems—A Simple Issue?
29. Tpeak–Tendinterval and Tpeak–Tend/QT ratio in patients with Brugada syndrome
30. Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia
31. Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction
32. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
33. Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography.
34. Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking
35. Long-term follow-up of subcutaneous ICD systems in patients with hypertrophic cardiomyopathy: a single-center experience
36. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2
37. High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature
38. Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndrome.
39. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
40. Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes
41. Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
42. A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of Brugada or Long QT Syndrome
43. Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia.
44. Angeborenes Langes QT-Syndrom
45. A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
46. Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel
47. Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances
48. Totally Subcutaneous Implantable Cardioverter Defibrillator with an Alternative, Right Parasternal, Electrode Placement
49. Faculty Opinions recommendation of Patient-specific induced pluripotent stem-cell models for long-QT syndrome.
50. Faculty Opinions recommendation of An entirely subcutaneous implantable cardioverter-defibrillator.
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