222 results on '"Eckhardt, Lee L."'
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2. 2023 ACC/AHA/ACCP/HRS Guideline for the Diagnosis and Management of Atrial Fibrillation: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines
3. Clinical Management of Brugada Syndrome: Commentary From the Experts
4. Top stories on the study of inherited arrhythmias using iPSCs
5. An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia
6. Caveolin-3 and Caveolae regulate ventricular repolarization
7. Inward Rectifier Potassium Channels (Kir2.x) and Caveolin-3 Domain–Specific Interaction
8. Cardiac potassium inward rectifier Kir2: Review of structure, regulation, pharmacology, and arrhythmogenesis
9. Shared Decision-Making in Cardiac Electrophysiology Procedures and Arrhythmia Management
10. A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants
11. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population
12. Most myopathic lamin variants aggregate: a functional genomics approach for assessing variants of uncertain significance
13. Into a Fluoroless Future: an Appraisal of Fluoroscopy-Free Techniques in Clinical Cardiac Electrophysiology
14. Management of Congenital Long-QT Syndrome: Commentary From the Experts
15. Inappropriate sinus tachycardia
16. Contributors
17. Genetic Loss of IK1 Causes Adrenergic-induced Phase 3 Early Afterdepolarizations and Polymorphic and Bi-directional Ventricular Tachycardia
18. Genetic Loss of IK1 Causes Adrenergic-Induced Phase 3 Early Afterdepolariz ations and Polymorphic and Bidirectional Ventricular Tachycardia
19. Lifestyle and Risk Factor Modification for Reduction of Atrial Fibrillation: A Scientific Statement From the American Heart Association
20. Elucidation of ALG10B as a Novel Long-QT Syndrome–Susceptibility Gene
21. Structural-functional characterization of KCNJ2 variants associated with ventricular arrhythmic syndrome phenotypes
22. Shocking Aspects of Nonconductive Plastics: Electrophysiologic Implications of Plasticizers
23. Challenges and innovation: Disease modeling using human-induced pluripotent stem cell-derived cardiomyocytes
24. How Functional Genomics Can Keep Pace With VUS Identification
25. Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes
26. Arrhythmogenesis and Prolonged Repolarization From Synthetic Opioids: Finally Sorted?
27. Machine Learning Algorithm Predicts Cardiac Resynchronization Therapy Outcomes: Lessons From the COMPANION Trial
28. Abstract 15976: CPVT Arrhythmic Phenotype in KCNJ2-R67Q KI Mouse With Decreased Repolarization Reserve and Increased Triggered Activity
29. Injectable loop recorder implantation in an ambulatory setting by advanced practice providers: Analysis of outcomes
30. Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome
31. Machine Learning in CRT Outcomes
32. The Changing Complexities of Opioid-Related Sudden Death.
33. Abstract 9103: Electrophysiological Arrhythmia Characterization of a Stress-Induced Idiopathic VF IPS-CMs Using Fluorescent Optical Mapping
34. Proteomic Analysis of the Functional Inward Rectifier Potassium Channel (Kir) 2.1 Reveals Several Novel Phosphorylation Sites
35. Evaluation for Myocarditis in Competitive Student Athletes Recovering From Coronavirus Disease 2019 With Cardiac Magnetic Resonance Imaging
36. Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell–Derived Cardiomyocytes
37. Chapter 40 - Inappropriate sinus tachycardia
38. KCNJ2 mutations in arrhythmia patients referred for LQT testing: A mutation T305A with novel effect on rectification properties
39. Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and [I.sub.Kr]
40. An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms ofCASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia
41. Genetic Loss of I K1 Causes Adrenergic-Induced Phase 3 Early Afterdepolariz ations and Polymorphic and Bidirectional Ventricular Tachycardia
42. Cryoablation for AVNRT: Importance of Ablation Endpoint Criteria
43. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population
44. Induced cardiac progenitor cells repopulate decellularized mouse heart scaffolds and differentiate to generate cardiac tissue
45. Protein trafficking abnormalities: a new mechanism in drug-induced long QT syndrome
46. Inward Rectifier Potassium Channels (Kir2.x) and Caveolin-3 Domain-Specific Interaction: Implications for Purkinje Cell-Dependent Ventricular Arrhythmias
47. Replacing Hardware With “Viralware”
48. Caveolin-3 Microdomain: Arrhythmia Implications for Potassium Inward Rectifier and Cardiac Sodium Channel
49. Abstract 17137: Unmasking Pathological Mechanisms of Long QT Syndrome KCNH2 H70R Variant Using Human iPSC-Cardiomyocytes
50. P‐Wave Amplitude and PR Changes in Patients With Inappropriate Sinus Tachycardia: Findings Supportive of a Central Mechanism
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