scholarly article | Q13442814 |
P50 | author | Christopher Semsarian | Q88316745 |
Belinda Gray | Q96192114 | ||
Rajesh Puranik | Q113675570 | ||
Laura Yeates | Q113675603 | ||
Richard D Bagnall | Q60006690 | ||
Jodie Ingles | Q63363978 | ||
P2093 | author name string | Raymond W Sy | |
Stuart M Grieve | |||
Charlotte Burns | |||
Ganesh Kumar Gnanappa | |||
Giuseppe Femia | |||
P2860 | cites work | Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters | Q86576230 |
Evaluation of Brugada syndrome by cardiac magnetic resonance | Q46768818 | ||
Magnetic resonance imaging findings in patients with Brugada syndrome | Q47911860 | ||
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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 imaging | Q82690026 | ||
Prevention of ventricular fibrillation episodes in Brugada syndrome by catheter ablation over the anterior right ventricular outflow tract epicardium | Q83609756 | ||
Echocardiographic tissue deformation imaging quantifies abnormal regional right ventricular function in arrhythmogenic right ventricular dysplasia/cardiomyopathy | Q84121874 | ||
Brugada Syndrome Phenotype Elimination by Epicardial Substrate Ablation | Q85936811 | ||
Atlas of the clinical genetics of human dilated cardiomyopathy | Q28246768 | ||
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death | Q28294931 | ||
Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype | Q28304358 | ||
Mouse model of SCN5A-linked hereditary Lenègre's disease: age-related conduction slowing and myocardial fibrosis | Q28585881 | ||
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Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome | Q33153396 | ||
Fragmented QRS as a marker of conduction abnormality and a predictor of prognosis of Brugada syndrome | Q33156672 | ||
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SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility | Q34372532 | ||
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Electrocardiographic features of disease progression in arrhythmogenic right ventricular cardiomyopathy/dysplasia | Q35531136 | ||
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Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome. | Q36245208 | ||
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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 implications | Q39320655 | ||
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 syndrome | Q42912081 | ||
The Australian Genetic Heart Disease Registry | Q44223320 | ||
Inferior and lateral electrocardiographic repolarization abnormalities in Brugada syndrome | Q44436850 | ||
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 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e0195594 | |
P577 | publication date | 2018-04-13 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome. | |
P478 | volume | 13 |
Q92893542 | Speckle tracking echocardiography data in Brugada syndrome patients | cites work | P2860 |
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