261 results on '"Amin, Ahmad S."'
Search Results
2. A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand
3. Importance of exercise stress testing in evaluation of unexplained cardiac arrest survivor
4. Catheter Ablation for Ventricular Tachycardia in Patients With Desmoplakin Cardiomyopathy
5. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
6. Novelties in Brugada Syndrome: Complex Genetics, Risk Stratification, and Catheter Ablation
7. Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy
8. Clinical applicability of artificial intelligence for patients with an inherited heart disease: A scoping review
9. Cardiac Repolarization in Health and Disease
10. Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?
11. Echocardiographic deformation imaging unmasks global and regional mechanical dysfunction in patients with idiopathic ventricular fibrillation: A multicenter case-control study
12. Improving electrocardiogram-based detection of rare genetic heart disease using transfer learning: An application to phospholamban p.Arg14del mutation carriers
13. Computer versus cardiologist: Is a machine learning algorithm able to outperform an expert in diagnosing a phospholamban p.Arg14del mutation on the electrocardiogram?
14. Catheter Ablation for Ventricular Tachycardia in Patients With Desmoplakin Cardiomyopathy
15. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
16. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand
17. Diagnosis of Brugada Syndrome With a Sodium- Channel-Blocker Test: Who Should Be Tested? Who Should Not?
18. Tropomyosin–troponin complex in inherited cardiomyopathies
19. A rare non-coding enhancer variant in SCN5A contributes to the high prevalence of Brugada syndrome in Thailand
20. Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review
21. Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy
22. Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families
23. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies
24. Use, misuse, and pitfalls of the drug challenge test in the diagnosis of the Brugada syndrome
25. The future of sudden cardiac death research
26. An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome
27. Variant Location Is a Novel Risk Factor for Individuals with Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant
28. Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy
29. Variant Location Is a Novel Risk Factor for Individuals with Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant
30. Genetic Control of Potassium Channels
31. Penetrance and Prognosis of MYH7Variant-Associated Cardiomyopathies
32. Inheritable Potassium Channel Diseases
33. Contributors
34. Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant
35. Multimodality Screening For (Peri)Myocarditis In Newly Diagnosed Idiopathic Inflammatory Myopathies: A Cross-Sectional Study
36. Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy
37. 'An Apple a day keeps the doctor away': How the use of commercial algorithmic devices influences the cardiologist -patient interactions during diagnosis
38. KBTBD13 is a novel cardiomyopathy gene
39. RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling
40. Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy
41. Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
42. KBTBD13 is a novel cardiomyopathy gene
43. PO-631-03 DEEP LEARNING FOR THE IDENTIFICATION OF PATIENTS WITH A HIGH RISK FOR IDIOPATHIC VENTRICULAR FIBRILLATION
44. PO-629-03 IN-DEPTH ANALYSIS OF THE SCN5A LOCUS HIGHLIGHTS DISTINCT GENETIC ARCHITECTURES FOR BRUGADA SYNDROME IN DIFFERENT ANCESTRIES AND IDENTIFIES A NOVEL RARE ENHANCER VARIANT ASSOCIATED WITH DISEASE IN SOUTHEAST ASIAN PATIENTS
45. European Reference Network for rare, low prevalence, or complex diseases of the heart (ERN GUARD-Heart): 5 year anniversary
46. 50 - Inheritable Potassium Channel Diseases
47. PO-06-091 GENE-SPECIFIC PLAKOPHILIN-2 FAMILY SCREENING FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY
48. Clinical applicability of artificial intelligence for patients with an inherited heart disease: a scoping review
49. Genetic screening in acquired long QT syndrome? CAUTION: proceed carefully
50. Cardiac ion channels in health and disease
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