552 results on '"Giudicessi, John R."'
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2. Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank Study
3. A multi-omics atlas of sex-specific differences in obstructive hypertrophic cardiomyopathy
4. The impact of mavacamten dosing on wall thickness regression: an insight from longer term follow-up based on genetic profile
5. Arrhythmic manifestations and outcomes of definite and probable cardiac sarcoidosis
6. Imaging of Cardiac Sarcoidosis: An Update and Future Aspects
7. Sudden cardiac arrest occurring in temporal proximity to consumption of energy drinks
8. Temporal Association Between Vaping and Risk of Cardiac Events
9. Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathy
10. Novel risk predictor of arrhythmias for patients with potassium channel–related congenital long QT syndrome
11. Unexplained sudden cardiac arrest and sudden cardiac death in the young: What is killing these young people when nothing is found?
12. Frequency of and outcomes associated with nonadherence to guideline-based recommendations for an implantable cardioverter-defibrillator in patients with congenital long QT syndrome
13. Arrhythmic prognosis according to left ventricular systolic dysfunction severity in cardiac sarcoidosis
14. Precision therapy in congenital long QT syndrome
15. Genetic mechanisms underlying arrhythmogenic mitral valve prolapse: Current and future perspectives
16. An International Multicenter Evaluation of Type 5 Long QT Syndrome
17. Injectable contraceptive Depo-Provera induces erratic beating patterns in patient-specific induced pluripotent stem cell–derived cardiomyocytes with long QT syndrome type 2
18. Functional characterization and identification of a therapeutic for a novel SCN5A-F1760C variant causing type 3 long QT syndrome refractory to all guideline-directed therapies
19. Spectrum and prevalence of side effects and complications with guideline-directed therapies for congenital long QT syndrome
20. Characterization of N-terminal RYR2 variants outside CPVT1 hotspot regions using patient iPSCs reveal pathogenesis and therapeutic potential
21. Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant
22. Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemic
23. A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome
24. Role of chronic continuous intravenous lidocaine in the clinical management of patients with malignant type 3 long QT syndrome
25. Histone Modifications and miRNA Perturbations Contribute to Transcriptional Dysregulation of Hypertrophy in Obstructive Hypertrophic Cardiomyopathy
26. Artificial Intelligence-Enabled Electrocardiography to Screen Patients with Dilated Cardiomyopathy
27. Cardiac Toxicity of Chloroquine or Hydroxychloroquine in Patients With COVID-19: A Systematic Review and Meta-regression Analysis
28. Abstract 15101: Return-to-Work for Patients in High-Risk Professions Diagnosed With a Sudden Death-Predisposing Genetic Heart Disease
29. Congenital Long-QT Syndrome: From Genetics to Clinical Management
30. Genetic Architecture, Pathophysiology, and Clinical Management of Brugada Syndrome
31. Catecholaminergic Polymorphic Ventricular Tachycardia
32. Purkinje system hyperexcitability and ventricular arrhythmia risk in type 3 long QT syndrome
33. Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit
34. Urgent Guidance for Navigating and Circumventing the QTc-Prolonging and Torsadogenic Potential of Possible Pharmacotherapies for Coronavirus Disease 19 (COVID-19)
35. Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign
36. State of Gene Therapy for Monogenic Cardiovascular Diseases
37. Incidence of Newly Recognized Atrial Fibrillation in Patients with Obstructive Hypertrophic Cardiomyopathy Treated with Mavacamten
38. A Multi-Omics Atlas of Sex-Specific Differences in Obstructive Hypertrophic Cardiomyopathy
39. Prognostic Value of Multiplexed Assays of Variant Effect and Automated Patch-clamping forKCNH2-LQTS Risk Stratification
40. Return to work for patients in high-risk professions diagnosed with a sudden cardiac death–predisposing genetic heart disease
41. Exercise testing oversights underlie missed and delayed diagnosis of catecholaminergic polymorphic ventricular tachycardia in young sudden cardiac arrest survivors
42. A Clinical Diagnostic Test for Calcium Release Deficiency Syndrome.
43. Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young
44. Artificial intelligence-enhanced electrocardiogram for arrhythmogenic right ventricular cardiomyopathy detection
45. Role of genetic heart disease in sentinel sudden cardiac arrest survivors across the age spectrum
46. The genetic architecture of long QT syndrome: A critical reappraisal
47. Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant
48. Risk Factors for Sudden Cardiac Arrest and Ventricular Arrhythmias in Arrhythmogenic Mitral Valve Prolapse Syndrome
49. Cardiac Sarcoidosis Mimickers: Genetic Testing in Undifferentiated Inflammatory Cardiomyopathies
50. Fatal Cardiac Arrhythmias During Electronic Gaming in Patients With Genetically Mediated Heart Diseases
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