about
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.Short QT syndrome in pediatrics.Short QT and atrial fibrillation: A KCNQ1 mutation-specific disease. Late follow-up in three unrelated children.Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy.Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.Genetic analysis, in silico prediction, and family segregation in long QT syndrome.Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.Large Genomic Imbalances in Brugada Syndrome.Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic InvestigationAdvances in paediatric interventional cardiology since 2000.Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic AdvancesGenetics of sudden cardiac death in children and young athletes.Genetics of arrhythmogenic right ventricular cardiomyopathy.Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy.Electrical Substrate Elimination in 135 Consecutive Patients With Brugada Syndrome.Brugada syndrome: clinical and genetic findings.Genetics of inherited arrhythmias in pediatrics.Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?Genetic basis of dilated cardiomyopathy.Congenital heart block related to maternal autoantibodies: descriptive analysis of a series of 18 cases from a single center.A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death.Post-mortem genetic analysis in juvenile cases of sudden cardiac death.Correction: Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation.Impact of right ventricular outflow tract size and substrate on outcomes of percutaneous pulmonary valve implantation.Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement.Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients.Prevention of sudden death in adolescent athletes: Incremental diagnostic value and cost-effectiveness of diagnostic tests.Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up.Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis.Effect of dual-chamber pacemaker implantation on aortic dilatation in patients with congenital heart block.Characterizing the spectrum of right ventricular remodelling in response to chronic training.The Utilization of an Insertable Cardiac Monitor in a Child With Pallid Breath-Holding Spells.Fever-Related Arrhythmic Events in the Multicenter Survey on Arrhythmic Events in Brugada Syndrome (SABRUS).A Genetically Vulnerable Myocardium May Predispose to Myocarditis.[Experience with junctional atrioventricular reciprocating tachycardia].Hemodynamic changes alert to spontaneous ductus arteriosus spasm.The role of clinical, genetic and segregation evaluation in sudden infant death.Ventricular dyssynchrony and function improve following catheter ablation of nonseptal accessory pathways in children.Double venous drainage in scimitar syndrome. Ideal anatomy for percutaneous complete cureIdentity crisis of a Mullins Balloon. Is it a balloon-in-balloon catheter?
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
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name
Georgia Sarquella-Brugada
@ast
Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
@es
Georgia Sarquella-Brugada
@nl
Georgia Sarquella-Brugada
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type
label
Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
@sl
prefLabel
Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
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Georgia Sarquella-Brugada
@nl
Georgia Sarquella-Brugada
@sl
P106
P1153
26432928900
P21
P31
P496
0000-0002-6857-8904