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1 |
Material Type: Article
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10-year survival in patients undergoing cardiac resynchronization therapyEuropean heart journal, 2021-10, Vol.42 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com. 2021 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehab724.0936Full text available |
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2 |
Material Type: Article
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105 The effect of biventricular pacing on myocardial function and oxidative metabolism in severe dilated cardiomyopathyEuropean heart journal, 2003-03, Vol.24 (5), p.3 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1016/S0195-668X(03)93656-6Full text available |
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3 |
Material Type: Article
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1169Interim analysis of data from a long-term, extension trial of tafamidis meglumine in patients with transthyretin amyloid cardiomyopathyEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0011Full text available |
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4 |
Material Type: Article
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1174Characterization of disease hot-phases using 18f-fluorodeoxyglucose positron emission tomography in arrhythmogenic cardiomyopathy caused by desmosomal gene mutationsEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0016Full text available |
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5 |
Material Type: Article
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1175Structural progression increases the risk of ventricular arrhythmias in patients with arrhythmogenic cardiomyopathyEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0017Full text available |
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6 |
Material Type: Article
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1177Insights on mitochondrial energetics in obstructive hypertrophic cardiomyopathyEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0019Full text available |
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7 |
Material Type: Article
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1180Cardiomyocyte-specific deletion of Brd4 induces hypertrophic cardiomyopathy and suggests a novel function for the chromatin reader as co-repressor in the healthy heartEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0022Full text available |
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8 |
Material Type: Article
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1183Beta-Adrenoceptor activation increases cardiac galectin-3 levels via the hippo signaling pathwayEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0025Full text available |
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9 |
Material Type: Article
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1183Clinical screening for hypertrophic cardiomyopathy in paediatric first-degree relatives: evidence for a change in paradigmEuropean heart journal, 2018-08, Vol.39 (suppl_1) [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehy565.1183Full text available |
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10 |
Material Type: Article
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1214Desmoglein 2 gene mutation (DSG2-F531C) caused arrhythmogenic right ventricular cardiomyopathy in human and mice is gene dose-dependentEuropean heart journal, 2017-08, Vol.38 (suppl_1) [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx502.1214Full text available |
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11 |
Material Type: Article
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122Left atrial diameter predicted from left atrial volume in the risk assessment of sudden cardiac death in hypertrophic cardiomyopathy - potential clinical consequence for the individual patientEuropean heart journal, 2017-08, Vol.38 (suppl_1) [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx501.122Full text available |
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12 |
Material Type: Article
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124Predictive value of classic sudden death risk factors in pediatric-onset hypertrophic cardiomyopathyEuropean heart journal, 2017-08, Vol.38 (suppl_1) [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx501.124Full text available |
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13 |
Material Type: Article
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1290 Gene dose-dependent atrial arrhythmias, heart block and atrial cardiomyopathy in mice overexpressing the A3 adenosine receptorEuropean heart journal, 2003-03, Vol.24 (5), p.244 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1016/S0195-668X(03)94552-0Full text available |
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14 |
Material Type: Article
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1292 Genotype-phenotype correlation in arrhythmogenic right-ventricular cardiomyopathy linked to desmoplakin mutation (ARVD8)European heart journal, 2003-03, Vol.24 (5), p.244 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1016/S0195-668X(03)94554-4Full text available |
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15 |
Material Type: Article
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1309 Drosophila melanogaster: a powerful genetic model to identify members of a particular human genetic pathway related to cardiomyopathiesEuropean heart journal, 2003-03, Vol.24 (5), p.248 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1016/S0195-668X(03)94567-2Full text available |
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16 |
Material Type: Article
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1310 Expression profiling of human hypertrophic cardiomyopathy progressed to dilated cardiomyopathy by DNA microarray analysis: Insight into the pathogenesis of phenotypesEuropean heart journal, 2003-03, Vol.24 (5), p.248 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1016/S0195-668X(03)94568-4Full text available |
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17 |
Material Type: Article
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1348Impact of genetically determined differences in ECG parameters on risk of AF in c. 300,000 UK Biobank participantsEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0048Full text available |
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18 |
Material Type: Article
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1350Outcome after diagnosis with hypertrophic cardiomyopathy: a nationwide studyEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0050Full text available |
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19 |
Material Type: Article
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1386Reduction of mitral regurgitation in patients with heart failure and secondary mitral regurgitation: relationship between changes in brain natriuretic peptide and outcomes from the COAPT trialEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0053Full text available |
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20 |
Material Type: Article
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1411The effect of eplerenone on fibrosis in hypertrophic cardiomyopathy. A randomised controlled trial assessed using cardiopulmonary exercise testing and cardiovascular magnetic resonanceEuropean heart journal, 2019-10, Vol.40 (Supplement_1) [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz748.0059Full text available |