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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trialThe Lancet (British edition), 2020-09, Vol.396 (10253), p.759-769 [Peer Reviewed Journal]2020 Elsevier Ltd ;Copyright © 2020 Elsevier Ltd. All rights reserved. ;2020. Elsevier Ltd ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(20)31792-X ;PMID: 32871100Full text available |
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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 |
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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) MutationsJournal of the American College of Cardiology, 2018-11, Vol.72 (20), p.2471-2481 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright © 2018 American College of Cardiology Foundation. All rights reserved. ;Copyright Elsevier Limited Nov 13, 2018 ;Distributed under a Creative Commons Attribution 4.0 International License ;2018 Elsevier Inc. All rights reserved. 2018 American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.08.2181 ;PMID: 30442290Full text available |
| 4 |
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A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanismCardiovascular research, 2016-10, Vol.112 (1), p.452-463 [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: 0008-6363 ;EISSN: 1755-3245 ;DOI: 10.1093/cvr/cvw192 ;PMID: 27496873Full text available |
| 5 |
Material Type: Article
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European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of CardiologyEuropean heart journal, 2016-01, Vol.37 (2), p.164-173 [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/ehv497 ;PMID: 26409010Full text available |
| 6 |
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Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriersEuropean journal of heart failure, 2013-04, Vol.15 (4), p.376-384 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © 2013 the Authors ;ISSN: 1388-9842 ;EISSN: 1879-0844 ;DOI: 10.1093/eurjhf/hfs191 ;PMID: 23183350Full text available |
| 7 |
Material Type: Article
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Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathyCirculation (New York, N.Y.), 2005-08, Vol.112 (5), p.636-642 [Peer Reviewed Journal]2005 INIST-CNRS ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/circulationaha.104.532234 ;PMID: 16061754 ;CODEN: CIRCAZFull text available |
| 8 |
Material Type: Article
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Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive PhenotypeJournal of the American College of Cardiology, 2007-06, Vol.49 (25), p.2419-2426 [Peer Reviewed Journal]American College of Cardiology Foundation ;2007 American College of Cardiology Foundation ;Copyright Elsevier Limited Jun 26, 2007 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2007.02.061 ;PMID: 17599605Full text available |
| 9 |
Material Type: Article
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Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutationsThe Journal of clinical investigation, 2003-01, Vol.111 (2), p.209-216 [Peer Reviewed Journal]Copyright American Society for Clinical Investigation Jan 2003 ;Copyright © 2003, American Society for Clinical Investigation 2003 ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/jci200316336 ;PMID: 12531876Full text available |
| 10 |
Material Type: Article
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Dilated Cardiomyopathy Mutations in Three Thin Filament Regulatory Proteins Result in a Common Functional PhenotypeThe Journal of biological chemistry, 2005-08, Vol.280 (31), p.28498-28506 [Peer Reviewed Journal]ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.M412281200 ;PMID: 15923195Full text available |
| 11 |
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Quantitative Expression of the Mutated Lamin A/C Gene in Patients With CardiolaminopathyJournal of the American College of Cardiology, 2012-11, Vol.60 (19), p.1916-1920 [Peer Reviewed Journal]American College of Cardiology Foundation ;2012 American College of Cardiology Foundation ;2015 INIST-CNRS ;Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Nov 6, 2012 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.05.059 ;PMID: 23062543 ;CODEN: JACCDIFull text available |
| 12 |
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Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathyThe Lancet (British edition), 2004-01, Vol.363 (9406), p.371-372 [Peer Reviewed Journal]2004 Elsevier Ltd ;2004 INIST-CNRS ;Copyright Lancet Ltd. Jan 31, 2004 ;Copyright Elsevier Limited Jan 31, 2004 ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(04)15468-8 ;PMID: 15070570 ;CODEN: LANCAOFull text available |
| 13 |
Material Type: Article
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Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formationThe FEBS journal, 2005-04, Vol.272 (8), p.2037-2049 [Peer Reviewed Journal]2005 FEBS ;ISSN: 1742-464X ;EISSN: 1742-4658 ;DOI: 10.1111/j.1742-4658.2005.04630.x ;PMID: 15819894Full text available |
| 14 |
Material Type: Article
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Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation CarriersJournal of the American College of Cardiology, , Vol.59 (5), p.493-500 [Peer Reviewed Journal]American College of Cardiology Foundation ;2012 American College of Cardiology Foundation ;Copyright Elsevier Limited Jan 31, 2012 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2011.08.078Full text available |
| 15 |
Material Type: Book
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Dictionary Visions, Research and Practice: Selected papers from the 12th International Symposium on Lexicography, Copenhagen 2004ISBN: 9027223343 ;ISBN: 9789027223340 ;EISBN: 9789027291196 ;EISBN: 9027291195 ;OCLC: 237387041Full text available |
| 16 |
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| 17 |
Material Type: Article
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Reply to Finsterer and Mehri—Leber’s Hereditary Optic Neuropathy: Mind the HeartCJC open (Online), 2023-01, Vol.5 (1), p.36-36 [Peer Reviewed Journal]2022 The Authors ;2022 The Authors 2022 ;ISSN: 2589-790X ;EISSN: 2589-790X ;DOI: 10.1016/j.cjco.2022.11.005 ;PMID: 36700185Full text available |
| 18 |
Material Type: Article
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Jørgen Bang & Karl Hårbøl: Omvendt fremmedordbog. København: Munksgaard, 1991Hermes (Århus, Denmark), 2015-07, Vol.6 (10), p.143 [Peer Reviewed Journal]ISSN: 0904-1699 ;EISSN: 1903-1785 ;DOI: 10.7146/hjlcb.v6i10.21528Full text available |
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| 20 |
Material Type: Article
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Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial DiseasesEuropean heart journal, 2013-09, Vol.34 (33), p.2636-2648 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/eht210 ;PMID: 23824828Full text available |
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