Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome.

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Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome. is …
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scholarly articleQ13442814

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P356DOI10.1371/JOURNAL.PONE.0195594
P932PMC publication ID5898761
P698PubMed publication ID29652902

P50authorChristopher SemsarianQ88316745
Belinda GrayQ96192114
Rajesh PuranikQ113675570
Laura YeatesQ113675603
Richard D BagnallQ60006690
Jodie InglesQ63363978
P2093author name stringRaymond W Sy
Stuart M Grieve
Charlotte Burns
Ganesh Kumar Gnanappa
Giuseppe Femia
P2860cites workBrugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parametersQ86576230
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Magnetic resonance imaging findings in patients with Brugada syndromeQ47911860
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Right ventricular outflow tract dimensions in arrhythmogenic right ventricular cardiomyopathy/dysplasia-a multicentre study comparing echocardiography and cardiovascular magnetic resonance.Q50855137
How to measure the right ventricular outflow tract with cardiovascular magnetic resonance imaging: a head-to-head comparison of methods.Q51098727
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis.Q51204140
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.Q55638651
Insights into the location of type I ECG in patients with Brugada syndrome: correlation of ECG and cardiovascular magnetic resonance imagingQ82690026
Prevention of ventricular fibrillation episodes in Brugada syndrome by catheter ablation over the anterior right ventricular outflow tract epicardiumQ83609756
Echocardiographic tissue deformation imaging quantifies abnormal regional right ventricular function in arrhythmogenic right ventricular dysplasia/cardiomyopathyQ84121874
Brugada Syndrome Phenotype Elimination by Epicardial Substrate AblationQ85936811
Atlas of the clinical genetics of human dilated cardiomyopathyQ28246768
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathQ28294931
Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotypeQ28304358
Mouse model of SCN5A-linked hereditary Lenègre's disease: age-related conduction slowing and myocardial fibrosisQ28585881
Results of ajmaline testing in patients with arrhythmogenic right ventricular dysplasia-cardiomyopathyQ33151484
Cardiac histological substrate in patients with clinical phenotype of Brugada syndromeQ33153396
Fragmented QRS as a marker of conduction abnormality and a predictor of prognosis of Brugada syndromeQ33156672
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndromeQ33158197
Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry.Q33160801
Guidelines for the echocardiographic assessment of the right heart in adults: a report from the American Society of Echocardiography endorsed by the European Association of Echocardiography, a registered branch of the European Society of Cardiology,Q34125322
Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndromeQ34232976
SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractilityQ34372532
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular PathologyQ34465792
Electrocardiographic features of disease progression in arrhythmogenic right ventricular cardiomyopathy/dysplasiaQ35531136
Cardiac electrophysiological substrate underlying the ECG phenotype and electrogram abnormalities in Brugada syndrome patientsQ35674798
Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.Q36245208
Simultaneous Non-Invasive Epicardial and Endocardial Mapping in Patients With Brugada Syndrome: New Insights Into Arrhythmia MechanismsQ37556015
HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.Q38134931
Brugada syndrome: a heterogeneous disease with a common ECG phenotype?Q38176956
Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?Q38407903
Twelve-lead ambulatory electrocardiographic monitoring in Brugada syndrome: Potential diagnostic and prognostic implicationsQ39320655
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.Q40355175
Spontaneous type 1 electrocardiographic pattern is associated with cardiovascular magnetic resonance imaging changes in Brugada syndromeQ42912081
The Australian Genetic Heart Disease RegistryQ44223320
Inferior and lateral electrocardiographic repolarization abnormalities in Brugada syndromeQ44436850
Characterization of the epicardial substrate for catheter ablation of Brugada syndrome.Q46317627
Magnetic resonance investigations in Brugada syndrome reveal unexpectedly high rate of structural abnormalities.Q46634056
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue4
P407language of work or nameEnglishQ1860
P304page(s)e0195594
P577publication date2018-04-13
P1433published inPLOS OneQ564954
P1476titleRelations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome.
P478volume13

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Q92893542Speckle tracking echocardiography data in Brugada syndrome patientscites workP2860

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