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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosisEuropean heart journal, 2020-04, Vol.41 (14), p.1414-1429 [Peer Reviewed Journal]The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology. 2019 ;info:eu-repo/semantics/openAccess ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz669 ;PMID: 31637441Full text available |
| 2 |
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Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseasesEuropean heart journal, 2016-06, Vol.37 (23), p.1850-1858 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2016. For permissions please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehv727 ;PMID: 26792875Full text available |
| 3 |
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Peripartum cardiomyopathy: current management and future perspectivesEuropean heart journal, 2015-05, Vol.36 (18), p.1090-1097 [Peer Reviewed Journal]The Author 2015. Published by Oxford University Press on behalf of the European Society of Cardiology. ;The Author 2015. Published by Oxford University Press on behalf of the European Society of Cardiology 2015 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehv009 ;PMID: 25636745Full text available |
| 4 |
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Atlas of the clinical genetics of human dilated cardiomyopathyEuropean heart journal, 2015-05, Vol.36 (18), p.1123-1135 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2014. For permissions please email: journals.permissions@oup.com. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0195-668X ;ISSN: 1522-9645 ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehu301 ;PMID: 25163546Full text available |
| 5 |
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Peripartum cardiomyopathy: from genetics to managementEuropean heart journal, 2021-08, Vol.42 (32), p.3094-3102 [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/ehab458Full text available |
| 6 |
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Clinical genetics and outcome of left ventricular non-compaction cardiomyopathyEuropean heart journal, 2017-12, Vol.38 (46), p.3449-3460 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2017. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx545 ;PMID: 29029073Full text available |
| 7 |
Material Type: Article
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Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differencesEuropean heart journal, 2021-01, Vol.42 (2), p.162-174 [Peer Reviewed Journal]The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. 2020 ;The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehaa841 ;PMID: 33156912Full text available |
| 8 |
Material Type: Article
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Apical ballooning syndrome or takotsubo cardiomyopathy : a systematic reviewEuropean heart journal, 2006-07, Vol.27 (13), p.1523-1529 [Peer Reviewed Journal]2006 INIST-CNRS ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehl032 ;PMID: 16720686Full text available |
| 9 |
Material Type: Article
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Human atrial fibrillation substrate: towards a specific fibrotic atrial cardiomyopathyEuropean heart journal, 2013-09, Vol.34 (35), p.2731-2738 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/eht194 ;PMID: 23761394Full text available |
| 10 |
Material Type: Article
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The role of genetics in cardiovascular disease: arrhythmogenic cardiomyopathyEuropean heart journal, 2020-04, Vol.41 (14), p.1393-1400 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com. 2020 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehaa141 ;PMID: 32191298Full text available |
| 11 |
Material Type: Article
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Bromocriptine for the treatment of peripartum cardiomyopathy: a multicentre randomized studyEuropean heart journal, 2017-09, Vol.38 (35), p.2671-2679 [Peer Reviewed Journal]The Author 2017. Published by Oxford University Press on behalf of the European Society of Cardiology ;The Author 2017. Published by Oxford University Press on behalf of the European Society of Cardiology 2017 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx355 ;PMID: 28934837Full text available |
| 12 |
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Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantationEuropean heart journal, 2018-03, Vol.39 (10), p.853-860 [Peer Reviewed Journal]The Author 2017. Published by Oxford University Press on behalf of the European Society of Cardiology. 2017 ;info:eu-repo/semantics/openAccess ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx596 ;PMID: 29095976Full text available |
| 13 |
Material Type: Article
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Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriersEuropean heart journal, 2015-04, Vol.36 (14), p.847-855 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehu509 ;PMID: 25616645Full text available |
| 14 |
Material Type: Article
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Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genesEuropean heart journal, 2017-12, Vol.38 (46), p.3461-3468 [Peer Reviewed Journal]The Author 2017. Published by Oxford University Press on behalf of the European Society of Cardiology. ;The Author 2017. Published by Oxford University Press on behalf of the European Society of Cardiology. 2016 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehw603 ;PMID: 28082330Full text available |
| 15 |
Material Type: Article
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Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-term life-threatening arrhythmiasEuropean heart journal, 2018-03, Vol.39 (10), p.864-873 [Peer Reviewed Journal]2018 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx808 ;PMID: 29377983Full text available |
| 16 |
Material Type: Article
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Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United KingdomEuropean heart journal, 2019-03, Vol.40 (12), p.986-993 [Peer Reviewed Journal]The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Cardiology. 2018 ;The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Cardiology. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehy798 ;PMID: 30535072Full text available |
| 17 |
Material Type: Article
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Tako-Tsubo cardiomyopathy: intraindividual structural analysis in the acute phase and after functional recoveryEuropean heart journal, 2007-10, Vol.28 (20), p.2456-2464 [Peer Reviewed Journal]The European Society of Cardiology 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org 2007 ;2007 INIST-CNRS ;The European Society of Cardiology 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehl570 ;PMID: 17395683Full text available |
| 18 |
Material Type: Article
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A signature of circulating microRNAs differentiates takotsubo cardiomyopathy from acute myocardial infarctionEuropean heart journal, 2014-04, Vol.35 (15), p.999-1006 [Peer Reviewed Journal]The Author 2013. Published by Oxford University Press on behalf of the European Society of Cardiology. 2013 ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/eht392 ;PMID: 24046434Full text available |
| 19 |
Material Type: Article
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Extracellular vesicles from immortalized cardiosphere-derived cells attenuate arrhythmogenic cardiomyopathy in desmoglein-2 mutant miceEuropean heart journal, 2021-09, Vol.42 (35), p.3558-3571 [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 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehab419 ;PMID: 34345905Full text available |
| 20 |
Material Type: Article
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Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathyEuropean heart journal, 2016-03, Vol.37 (9), p.755-763 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehv387 ;PMID: 26314686Full text available |
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