Results 1 - 20 of 53,160 for All Library Resources
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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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Inflammatory Cardiomyopathic SyndromesCirculation research, 2017-09, Vol.121 (7), p.803-818 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Sep 15, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.310221 ;PMID: 28912184Full text available |
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Human-induced pluripotent stem cells for modelling metabolic perturbations and impaired bioenergetics underlying cardiomyopathiesCardiovascular research, 2021-02, Vol.117 (3), p.694-711 [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: 0008-6363 ;EISSN: 1755-3245 ;DOI: 10.1093/cvr/cvaa125 ;PMID: 32365198Full text available |
| 3 |
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Advances in the Genetic Basis and Pathogenesis of Sarcomere CardiomyopathiesAnnual review of genomics and human genetics, 2019-08, Vol.20 (1), p.129-153 [Peer Reviewed Journal]Copyright Annual Reviews, Inc. 2019 ;ISSN: 1527-8204 ;EISSN: 1545-293X ;DOI: 10.1146/annurev-genom-083118-015306 ;PMID: 30978303Digital Resources/Online E-Resources |
| 4 |
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Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 3: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy and Other Cardiomyopathies, and Myocarditis: A Scientific Statement From the American Heart Association and American College of CardiologyJournal of the American College of Cardiology, 2015-12, Vol.66 (21), p.2362-2371 [Peer Reviewed Journal]EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2015.09.035 ;PMID: 26542657Full text available |
| 5 |
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Recent Findings Related to Cardiomyopathy and GeneticsInternational journal of molecular sciences, 2021-11, Vol.22 (22), p.12522 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms222212522 ;PMID: 34830403Full text available |
| 6 |
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Classification, Epidemiology, and Global Burden of CardiomyopathiesCirculation research, 2017-09, Vol.121 (7), p.722-730 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Sep 15, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.309711 ;PMID: 28912179Full text available |
| 7 |
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Dystrophin-Deficient CardiomyopathyJournal of the American College of Cardiology, 2016-05, Vol.67 (21), p.2533-2546 [Peer Reviewed Journal]American College of Cardiology Foundation ;2016 American College of Cardiology Foundation ;Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited May 31, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.02.081 ;PMID: 27230049Full text available |
| 8 |
Material Type: Article
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Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectNature genetics, 2021-02, Vol.53 (2), p.128-134 [Peer Reviewed Journal]COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2021 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-00762-2 ;PMID: 33495596Full text available |
| 9 |
Material Type: Article
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Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chainsPflügers Archiv, 2019-05, Vol.471 (5), p.683-699 [Peer Reviewed Journal]Springer-Verlag GmbH Germany, part of Springer Nature 2019 ;Pflügers Archiv - European Journal of Physiology is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 0031-6768 ;EISSN: 1432-2013 ;DOI: 10.1007/s00424-019-02257-4 ;PMID: 30706179Full text available |
| 10 |
Material Type: Article
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Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)European heart journal, 2019-01, Vol.40 (1), p.19-33 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2018. For permissions, please email: journals.permissions@oup.com. 2018 ;ISSN: 0195-668X ;ISSN: 1522-9645 ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehy730 ;PMID: 30561613Full text available |
| 11 |
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ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in catsJournal of veterinary internal medicine, 2020-05, Vol.34 (3), p.1062-1077 [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. ;2020 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. ;2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0891-6640 ;ISSN: 1939-1676 ;EISSN: 1939-1676 ;DOI: 10.1111/jvim.15745 ;PMID: 32243654Full text available |
| 12 |
Material Type: Article
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Arrhythmogenic CardiomyopathyCirculation research, 2017-09, Vol.121 (7), p.784-802 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Sep 15, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.309345 ;PMID: 28912183Full text available |
| 13 |
Material Type: Article
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MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCMJournal of translational medicine, 2018-06, Vol.16 (1), p.161-161, Article 161 [Peer Reviewed Journal]COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 1479-5876 ;EISSN: 1479-5876 ;DOI: 10.1186/s12967-018-1534-3 ;PMID: 29885652Full text available |
| 14 |
Material Type: Article
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Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart AssociationCirculation (New York, N.Y.), 2016-12, Vol.134 (23), p.e579-e646 [Peer Reviewed Journal]2016 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIR.0000000000000455 ;PMID: 27832612Full text available |
| 15 |
Material Type: Article
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Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC)European journal of heart failure, 2022-03, Vol.24 (3), p.406 [Peer Reviewed Journal]ISSN: 1879-0844 ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.2414Digital Resources/Online E-Resources |
| 16 |
Material Type: Article
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Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic ResonanceJournal of the American College of Cardiology, 2017-02, Vol.69 (6), p.661-676 [Peer Reviewed Journal]2017 ;Published by Elsevier Inc. ;Copyright Elsevier Limited Feb 14, 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.11.051 ;PMID: 28183509Full text available |
| 17 |
Material Type: Article
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Disease features and management of cardiomyopathies in womenHeart failure reviews, 2024-05, Vol.29 (3), p.663-674 [Peer Reviewed Journal]The Author(s) 2024 ;EISSN: 1573-7322 ;DOI: 10.1007/s10741-024-10386-xDigital Resources/Online E-Resources |
| 18 |
Material Type: Article
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Genetics of Hypertrophic Cardiomyopathy After 20 Years: Clinical PerspectivesJournal of the American College of Cardiology, 2012-08, Vol.60 (8), p.705-715 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.02.068 ;PMID: 22796258 ;CODEN: JACCDIFull text available |
| 19 |
Material Type: Article
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The genetic basis for cardiac remodelingAnnual review of genomics and human genetics, 2005-01, Vol.6 (1), p.185-216 [Peer Reviewed Journal]ISSN: 1527-8204 ;EISSN: 1545-293X ;DOI: 10.1146/annurev.genom.6.080604.162132 ;PMID: 16124859Full text available |
| 20 |
Material Type: Article
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Clinical and Mechanistic Insights Into the Genetics of CardiomyopathyJournal of the American College of Cardiology, 2016-12, Vol.68 (25), p.2871-2886 [Peer Reviewed Journal]The Authors ;2016 The Authors ;Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Dec 27, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.08.079 ;PMID: 28007147Full text available |
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