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41 |
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Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosinPloS one, 2013-12, Vol.8 (12), p.e83403-e83403 [Peer Reviewed Journal]2013 Sommese 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. ;2013 Sommese et al 2013 Sommese et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0083403 ;PMID: 24367593Full text available |
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42 |
Material Type: Article
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Lamin A/C CardiomyopathyCirculation. Cardiovascular genetics, 2017-12, Vol.10 (6), p.e002004-e002004 [Peer Reviewed Journal]Copyright American Heart Association, Inc. Dec 2017 ;ISSN: 1942-325X ;EISSN: 1942-3268 ;DOI: 10.1161/CIRCGENETICS.117.002004Full text available |
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43 |
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Correction: Clinical profile and prognostic factors of alcoholic cardiomyopathy in tribal and non-tribal populationOpen heart, 2020-12, Vol.7 (2), p.e001335corr1 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2020 Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2020 ;ISSN: 2053-3624 ;ISSN: 2398-595X ;EISSN: 2053-3624 ;DOI: 10.1136/openhrt-2020-001335corr1 ;PMID: 33303621Full text available |
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44 |
Material Type: Article
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Myocarditis and inflammatory cardiomyopathy: current evidence and future directionsNature reviews cardiology, 2021-03, Vol.18 (3), p.169-193 [Peer Reviewed Journal]COPYRIGHT 2021 Nature Publishing Group ;Springer Nature Limited 2020. ;Springer Nature Limited 2020 ;ISSN: 1759-5002 ;EISSN: 1759-5010 ;DOI: 10.1038/s41569-020-00435-x ;PMID: 33046850Full text available |
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45 |
Material Type: Article
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Hypertrophic Cardiomyopathy Gene TestingCirculation. Cardiovascular genetics, 2017-10, Vol.10 (5), p.e001951-e001951 [Peer Reviewed Journal]Copyright American Heart Association, Inc. Oct 2017 ;ISSN: 1942-325X ;EISSN: 1942-3268 ;DOI: 10.1161/CIRCGENETICS.117.001951Full text available |
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46 |
Material Type: Article
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Towards etiological treatments in cardiomyopathiesLa Presse médicale (1983), 2024-03, Vol.53 (1), p.104223 [Peer Reviewed Journal]Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved. ;EISSN: 2213-0276 ;DOI: 10.1016/j.lpm.2024.104223 ;PMID: 38309622Digital Resources/Online E-Resources |
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47 |
Material Type: Article
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Molecular mechanisms in cardiomyopathyClinical science (1979), 2017-07, Vol.131 (13), p.1375-1392 [Peer Reviewed Journal]2017 The Author(s). published by Portland Press Limited on behalf of the Biochemical Society. ;ISSN: 0143-5221 ;EISSN: 1470-8736 ;DOI: 10.1042/cs20160170 ;PMID: 28645928Digital Resources/Online E-Resources |
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48 |
Material Type: Article
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Single-nucleus profiling of human dilated and hypertrophic cardiomyopathyNature (London), 2022-08, Vol.608 (7921), p.174-180 [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/s41586-022-04817-8 ;PMID: 35732739Full text available |
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49 |
Material Type: Article
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Predicting the Development of Dilated Cardiomyopathy in Kindred With Genetic Risk: Family MattersJournal of the American College of Cardiology, 2024-04, Vol.83 (17), p.1652-1655 [Peer Reviewed Journal]2024 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2024.03.381Full text available |
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50 |
Material Type: Article
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Genetic Restrictive Cardiomyopathy: Causes and Consequences-An Integrative ApproachInternational journal of molecular sciences, 2021-01, Vol.22 (2), p.558 [Peer Reviewed Journal]2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). 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/ijms22020558 ;PMID: 33429969Full text available |
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51 |
Material Type: Article
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Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and TherapyCirculation research, 2017-09, Vol.121 (7), p.749-770 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.311059 ;PMID: 28912181Full text available |
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52 |
Material Type: Article
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The role of mutations in the SCN5A gene in cardiomyopathiesBiochimica et biophysica acta, 2016-07, Vol.1863 (7 Pt B), p.1799 [Peer Reviewed Journal]Copyright © 2016 Elsevier B.V. All rights reserved. ;ISSN: 0006-3002 ;EISSN: 1878-2434 ;DOI: 10.1016/j.bbamcr.2016.02.014 ;PMID: 26916278Digital Resources/Online E-Resources |
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53 |
Material Type: Article
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Cardiomyopathy phenotypes in human-induced pluripotent stem cell-derived cardiomyocytes—a systematic reviewPflügers Archiv, 2019-05, Vol.471 (5), p.755-768 [Peer Reviewed Journal]The Author(s) 2018 ;Pflügers Archiv - European Journal of Physiology is a copyright of Springer, (2018). All Rights Reserved. © 2018. 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: 0031-6768 ;EISSN: 1432-2013 ;DOI: 10.1007/s00424-018-2214-0 ;PMID: 30324321Full text available |
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54 |
Material Type: Article
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Investigation of de novo variation in pediatric cardiomyopathyAmerican journal of medical genetics. Part C, Seminars in medical genetics, 2020-03, Vol.184 (1), p.1162020 Wiley Periodicals, Inc. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31764 ;PMID: 31912959Digital Resources/Online E-Resources |
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55 |
Material Type: Article
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Dilated cardiomyopathy: the complexity of a diverse genetic architectureNature reviews cardiology, 2013-09, Vol.10 (9), p.531-547 [Peer Reviewed Journal]COPYRIGHT 2013 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2013 ;ISSN: 1759-5002 ;EISSN: 1759-5010 ;DOI: 10.1038/nrcardio.2013.105 ;PMID: 23900355Full text available |
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56 |
Material Type: Article
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Inherited cardiomyopathies in veterinary medicinePflügers Archiv, 2019-05, Vol.471 (5), p.745-753 [Peer Reviewed Journal]Springer-Verlag GmbH Germany, part of Springer Nature 2018 ;Pflügers Archiv - European Journal of Physiology is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 0031-6768 ;EISSN: 1432-2013 ;DOI: 10.1007/s00424-018-2209-x ;PMID: 30284024Full text available |
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57 |
Material Type: Article
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Significance of abnormal and late ventricular signals in ventricular tachycardia ablation of ischemic and nonischemic cardiomyopathiesHeart rhythm, 2022-12, Vol.19 (12), p.2075 [Peer Reviewed Journal]Copyright © 2022 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved. ;EISSN: 1556-3871 ;DOI: 10.1016/j.hrthm.2022.08.008 ;PMID: 35964871Digital Resources/Online E-Resources |
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58 |
Material Type: Article
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Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic CardiomyopathyCirculation (New York, N.Y.), 2021-11, Vol.144 (21), p.1714-1731 [Peer Reviewed Journal]ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/circulationaha.121.053575 ;PMID: 34672721Full text available |
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59 |
Material Type: Article
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Development of plasma and whole blood taurine reference ranges and identification of dietary features associated with taurine deficiency and dilated cardiomyopathy in golden retrievers: A prospective, observational studyPloS one, 2020-05, Vol.15 (5), p.e0233206 [Peer Reviewed Journal]COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Ontiveros 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. ;2020 Ontiveros et al 2020 Ontiveros et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0233206 ;PMID: 32413894Full text available |
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60 |
Material Type: Article
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2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathyHeart rhythm, 2019-11, Vol.16 (11), p.e301 [Peer Reviewed Journal]Copyright © 2019 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved. ;EISSN: 1556-3871 ;DOI: 10.1016/j.hrthm.2019.05.007 ;PMID: 31078652Digital Resources/Online E-Resources |