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Humans
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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The innate immune system in chronic cardiomyopathy: a European Society of Cardiology (ESC) scientific statement from the Working Group on Myocardial Function of the ESCEuropean journal of heart failure, 2018-03, Vol.20 (3), p.445 [Peer Reviewed Journal]2018 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.1138 ;PMID: 29333691Digital Resources/Online E-Resources |
| 2 |
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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 |
| 3 |
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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 |
| 4 |
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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 |
| 5 |
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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 |
| 6 |
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Inherited CardiomyopathiesThe New England journal of medicine, 2011-04, Vol.364 (17), p.1643-1656 [Peer Reviewed Journal]Copyright © 2011 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMra0902923 ;PMID: 21524215Full text available |
| 7 |
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Neutrophil degranulation biomarkers characterize restrictive echocardiographic pattern with diastolic dysfunction in patients with diabetesEuropean journal of clinical investigation, 2021-12, Vol.51 (12), p.e13640 [Peer Reviewed Journal]2021 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation. ;EISSN: 1365-2362 ;DOI: 10.1111/eci.13640 ;PMID: 34129696Digital Resources/Online E-Resources |
| 8 |
Material Type: Article
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Diabetes, oxidative stress, molecular mechanism, and cardiovascular disease--an overviewToxicology mechanisms and methods, 2012-06, Vol.22 (5), p.330 [Peer Reviewed Journal]EISSN: 1537-6524 ;DOI: 10.3109/15376516.2012.666648 ;PMID: 22394340Digital Resources/Online E-Resources |
| 9 |
Material Type: Article
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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 |
| 10 |
Material Type: Article
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Incidence, risk assessment and prevention of sudden cardiac death in cardiomyopathiesEuropean journal of heart failure, 2023-12, Vol.25 (12), p.2144 [Peer Reviewed Journal]2023 European Society of Cardiology. ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.3076 ;PMID: 37905371Digital Resources/Online E-Resources |
| 11 |
Material Type: Article
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HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)Heart rhythm, 2011-08, Vol.8 (8), p.1308 [Peer Reviewed Journal]EISSN: 1556-3871 ;DOI: 10.1016/j.hrthm.2011.05.020 ;PMID: 21787999Digital Resources/Online E-Resources |
| 12 |
Material Type: Article
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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 |
| 13 |
Material Type: Article
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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 |
| 14 |
Material Type: Article
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Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?Journal of molecular and cellular cardiology, 2010-05, Vol.48 (5), p.882 [Peer Reviewed Journal]Copyright (c) 2009 Elsevier Ltd. All rights reserved. ;EISSN: 1095-8584 ;DOI: 10.1016/j.yjmcc.2009.10.031 ;PMID: 19914256Digital Resources/Online E-Resources |
| 15 |
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 |
| 16 |
Material Type: Article
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Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypesJournal of molecular and cellular cardiology, 2010-05, Vol.48 (5), p.899 [Peer Reviewed Journal]Copyright (c) 2010 Elsevier Ltd. All rights reserved. ;EISSN: 1095-8584 ;DOI: 10.1016/j.yjmcc.2010.03.005 ;PMID: 20298698Digital Resources/Online E-Resources |
| 17 |
Material Type: Article
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Integrated multi-omic characterization of congenital heart diseaseNature (London), 2022-08, Vol.608 (7921), p.181-191 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature Limited. ;Copyright Nature Publishing Group Aug 4, 2022 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-022-04989-3 ;PMID: 35732239Full text available |
| 18 |
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 |
| 19 |
Material Type: Article
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Telomere shortening is a hallmark of genetic cardiomyopathiesProceedings of the National Academy of Sciences - PNAS, 2018-09, Vol.115 (37), p.9276-9281 [Peer Reviewed Journal]Volumes 1–89 and 106–115, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright © 2018 the Author(s). Published by PNAS. ;Copyright National Academy of Sciences Sep 11, 2018 ;Copyright © 2018 the Author(s). Published by PNAS. 2018 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1714538115 ;PMID: 30150400Full text available |
| 20 |
Material Type: Article
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Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strainPloS one, 2019-08, Vol.14 (8), p.e0221028-e0221028 [Peer Reviewed Journal]COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Santos Junior et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Santos Junior et al 2019 Santos Junior et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0221028 ;PMID: 31437176Full text available |
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