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569 results on '"Tadros, Rafik"'

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1. Distinct Substrates of Idiopathic Ventricular Fibrillation Revealed by Arrhythmia Characteristics on Implantable Cardioverter-Defibrillator

3. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS Substudy

4. Long-term Outcomes with Spinal versus General Anesthesia for Hip Fracture Surgery: A Randomized Trial

5. Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

6. Identification and in-silico characterization of splice-site variants from a large cardiogenetic national registry

8. The Prevalence and Characteristics of Arrhythmic Mitral Valve Prolapse in Patients With Unexplained Cardiac Arrest

10. An International Multicenter Evaluation of Type 5 Long QT Syndrome

12. Rationale and Design of the Randomized Bayesian Multicenter COME-TAVI Trial in Patients With a New Onset Left Bundle Branch Block

13. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation

14. Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci

16. Integration of 3D nuclear imaging in 3D mapping system for ventricular tachycardia ablation in patients with implanted devices: Perfusion/voltage retrospective assessment of scar location

17. Acute Myocarditis Associated With Desmosomal Gene Variants

18. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

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

22. Safety of the oral factor XIa inhibitor asundexian compared with apixaban in patients with atrial fibrillation (PACIFIC-AF): a multicentre, randomised, double-blind, double-dummy, dose-finding phase 2 study

24. Return of Results Policies for Genomic Research: Current Practices and the Hearts in Rhythm Organization (HiRO) Approach

25. Overcoming Access Challenges to Treat Arrhythmias in Patients with Congenital Heart Disease Using Robotic Magnetic-Guided Catheter Ablation.

26. Innovative approaches to atrial fibrillation prediction: should polygenic scores and machine learning be implemented in clinical practice?

27. Deep Learning–Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome

30. Engaging patients as partners in a multicentre trial of spinal versus general anaesthesia for older adults

31. Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe

32. Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe

33. Pulmonary Vein Stenosis After Atrial Fibrillation Ablation: Insights From the ADVICE Trial

34. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand

36. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

37. A Clinical Diagnostic Test for Calcium Release Deficiency Syndrome.

38. Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe

39. A Genotype-phenotype Taxonomy of Hypertrophic Cardiomyopathy

40. A rare non-coding enhancer variant in SCN5A contributes to the high prevalence of Brugada syndrome in Thailand

41. Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy

42. Sudden cardiac death risk stratification in heritable cardiomyopathies: phenotype-based to genotype-based risk scores.

43. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

44. Blinded Randomized Trial of Anticoagulation to Prevent Ischemic Stroke and Neurocognitive Impairment in Atrial Fibrillation (BRAIN-AF): Methods and Design

45. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

46. Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia

47. Challenge and Impact of Quinidine Access in Sudden Death Syndromes: A National Experience

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

50. Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER)

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