671 results on '"Sarquella-Brugada, Georgia"'
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2. Cardiac channelopathies in pediatrics: a genetic update
3. Spanish catheter ablation registry. 23rd official report of the Heart Rhythm Association of the Spanish Society of Cardiology (2023)
4. An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia
5. Sudden Arrhythmic Death Syndrome and Ventricular Tachycardia in Children
6. Loss of sodium current caused by a Brugada syndrome–associated variant is determined by patient-specific genetic background
7. Spanish catheter ablation registry. 22nd official report of the Heart Rhythm Association of the Spanish Society of Cardiology (2022)
8. Registro español de ablación con catéter. XXII informe oficial de la Asociación del Ritmo Cardiaco de la Sociedad Española de Cardiología (2022)
9. Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT Syndrome
10. Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
11. Role of microRNAs in arrhythmogenic cardiomyopathy: translation as biomarkers into clinical practice
12. Postmortem diagnosis of Takotsubo syndrome on autoptic findings: is it reliable? A systematic review
13. Clinical Management of Brugada Syndrome: Commentary From the Experts
14. Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
15. Short QT Syndrome: Update on Genetic Basis
16. Evaluation of age at symptom onset, proband status, and sex as predictors of disease severity in pediatric catecholaminergic polymorphic ventricular tachycardia
17. Plasma idebenone monitoring in Friedreich’s ataxia patients during a long-term follow-up
18. Ventricular Repolarization Parameters and Coronary Involvement in Kawasaki Disease
19. Circulating circRNA as biomarkers for dilated cardiomyopathy etiology
20. Usefulness of SCT in detecting clinical reasoning deficits among pediatric professionals
21. Long-term prognosis of women with Brugada syndrome and electrophysiological study
22. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
23. Brugada Syndrome
24. aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes: results from the TETRIS study.
25. Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy.
26. Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis.
27. Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
28. Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
29. Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins
30. Phacomatosis pigmentokeratotica: Exploring extracutaneous comorbidities and topical therapy
31. Chapter 11 - The electrocardiographic spectrum of the long QT syndrome in pediatric patients
32. The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope
33. Can Sudden Cardiac Death Risk in the Young be Identified in the Emergency Department?
34. aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes:results from the TETRIS study
35. Spanish Catheter Ablation Registry. 18th Official Report of the Spanish Society of Cardiology Working Group on Electrophysiology and Arrhythmias (2018)
36. Registro Español de Ablación con Catéter. XVIII Informe Oficial de la Sección de Electrofisiología y Arritmias de la Sociedad Española de Cardiología (2018)
37. Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome
38. Long-term outcome of neonates and infants with permanent junctional reciprocating tachycardia. When cardiac ablation changes natural history
39. Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic Cardiomyopathy
40. Digenic Heterozigosity in SCN5A and CACNA1C Explains the Variable Expressivity of the Long QT Phenotype in a Spanish Family
41. La expresividad variable del síndrome de QT largo de una familia española se explica por la heterocigosis digénica en SCN5A y CACNA1C
42. Genetic analysis, in silico prediction, and family segregation in long QT syndrome
43. Sudden unexplained death in young people: A family matter
44. Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy: A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology – ERRATUM
45. Role of miRNA–mRNA Interactome in Pathophysiology of Arrhythmogenic Cardiomyopathy.
46. A narrative review of inherited arrhythmogenic syndromes in young population: role of genetic diagnosis in exercise recommendations.
47. Update on Genes Associated with Arrhythmogenic Cardiomyopathy
48. Spanish Catheter Ablation Registry. 17th Official Report of the Spanish Society of Cardiology Working Group on Electrophysiology and Arrhythmias (2017)
49. Molecular autopsy in a cohort of infants died suddenly at rest
50. Registro Español de Ablación con Catéter. XVII Informe Oficial de la Sección de Electrofisiología y Arritmias de la Sociedad Española de Cardiología (2017)
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