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1 |
Material Type: Article
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Call for Consensus in the Evaluation of Circulating Matrix Metalloproteinases in Chagas DiseaseThe American journal of tropical medicine and hygiene, 2022-07, Vol.107 (3), p.495-499 [Peer Reviewed Journal]Copyright Institute of Tropical Medicine Sep 2022 ;The author(s) 2022 ;ISSN: 0002-9637 ;EISSN: 1476-1645 ;DOI: 10.4269/ajtmh.21-0860 ;PMID: 35895410Full text available |
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Material Type: Article
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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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3 |
Material Type: Article
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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 |
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4 |
Material Type: Article
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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 |
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5 |
Material Type: Article
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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 |
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6 |
Material Type: Article
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GW29-e0130 Variants in Sarcomere Genes Played a Potential Role in Arrhythmogenic CardiomyopathyJournal of the American College of Cardiology, 2018-10, Vol.72 (16), p.C69-C69 [Peer Reviewed Journal]2018 ;Copyright Elsevier Limited Oct 16, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.08.403Full text available |
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7 |
Material Type: Article
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Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)Genetics in medicine, 2019-10, Vol.21 (10), p.2406-2409 [Peer Reviewed Journal]American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0521-2Full text available |
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8 |
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 |
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9 |
Material Type: Article
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LEFT BUNDLE BRANCH CARDIOMYOPATHY: AN OLD FOE TREATED BY A NEW TOOLJournal of the American College of Cardiology, 2018-03, Vol.71 (11), p.A937-A937 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright Elsevier Limited Mar 10, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/S0735-1097(18)31478-5Full text available |
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10 |
Material Type: Article
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PREDICTORS OF EXERCISE CAPACITY AFTER SEPTAL MYECTOMY IN PATIENTS WITH HYPERTROPHIC CARDIOMYOPATHYJournal of the American College of Cardiology, 2018-03, Vol.71 (11), p.A733-A733 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright Elsevier Limited Mar 10, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/S0735-1097(18)31274-9Full text available |
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11 |
Material Type: Article
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OUTCOMES OF HYPERTROPHIC CARDIOMYOPATHY IN A MULTI ETHNIC SOCIETYJournal of the American College of Cardiology, 2018-03, Vol.71 (11), p.A905-A905 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright Elsevier Limited Mar 10, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/S0735-1097(18)31446-3Full text available |
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12 |
Material Type: Article
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54 Characterisation of systolic myocardial strain in patients with fabry diseaseHeart (British Cardiac Society), 2018-06, Vol.104 (Suppl 6), p.A50-A50 [Peer Reviewed Journal]2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;2018 2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2018-BCS.54Full text available |
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13 |
Material Type: Article
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16 MRI imaging in obstructive hypertrophic cardiomyopathy, our experience in a district general hospitalHeart (British Cardiac Society), 2018-05, Vol.104 (Suppl 5), p.A11 [Peer Reviewed Journal]2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2018 © 2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2018-BCVI.31Full text available |
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14 |
Material Type: Article
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Arrhythmogenic CardiomyopathyCirculation research, 2017-12, Vol.121 (12), p.1296-1298 [Peer Reviewed Journal]Copyright Lippincott Williams & Wilkins Ovid Technologies Dec 8, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.312211Full text available |
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15 |
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 |
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16 |
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 |
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17 |
Material Type: Article
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The Relevance of Takotsubo Cardiomyopathy as a Stress-Induced DiseaseCardiometry, 2023-03 (26), p.105-113 [Peer Reviewed Journal]2023. This work is published under http://www.cardiometry.net/issues (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2304-7232 ;DOI: 10.18137/cardiometry.2023.26.105113Full text available |
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18 |
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 |
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19 |
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 |
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20 |
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 |