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1 |
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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2 |
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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3 |
Material Type: Article
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Clinical Trajectories and Long-Term Outcomes of Alcoholic Versus Other Forms of Dilated CardiomyopathyHeart, lung & circulation, 2024-03, Vol.33 (3), p.368 [Peer Reviewed Journal]Copyright © 2023 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved. ;EISSN: 1444-2892 ;DOI: 10.1016/j.hlc.2023.11.025 ;PMID: 38336540Digital Resources/Online E-Resources |
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4 |
Material Type: Article
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Histological and functional assessment of a Takotsubo cardiomyopathy model established by immobilization stressPacing and clinical electrophysiology, 2024-03, Vol.47 (3), p.373 [Peer Reviewed Journal]2024 Wiley Periodicals LLC. ;EISSN: 1540-8159 ;DOI: 10.1111/pace.14930 ;PMID: 38341623Digital Resources/Online E-Resources |
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5 |
Material Type: Article
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Role of the Alpha-B-Crystallin Protein in Cardiomyopathic DiseaseInternational journal of molecular sciences, 2024-03, Vol.25 (5), p.2826 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;2024 by the authors. 2024 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25052826 ;PMID: 38474073Full text available |
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6 |
Material Type: Article
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Truncated titin protein in dilated cardiomyopathy incorporates into the sarcomere and transmits forceThe Journal of clinical investigation, 2024-01, Vol.134 (2), p.1-3 [Peer Reviewed Journal]Copyright American Society for Clinical Investigation Jan 2024 ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI17019GFull text available |
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7 |
Material Type: Article
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Myocardial bridging in obstructive hypertrophic cardiomyopathy: a risk factor for myocardial fibrosisBMC medicine, 2024-02, Vol.22 (1), p.86-86 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1741-7015 ;EISSN: 1741-7015 ;DOI: 10.1186/s12916-024-03301-6 ;PMID: 38413945Full text available |
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Material Type: Article
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Assessing the impact of atrial fibrillation on symptoms and quality of life in hypertrophic cardiomyopathyJournal of cardiovascular electrophysiology, 2024-04, Vol.35 (4), p.654 [Peer Reviewed Journal]2024 Wiley Periodicals LLC. ;EISSN: 1540-8167 ;DOI: 10.1111/jce.16192 ;PMID: 38288888Digital Resources/Online E-Resources |
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9 |
Material Type: Article
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Aggressive treatment of atrial fibrillation in hypertrophic cardiomyopathy patients improve quality of lifeJournal of cardiovascular electrophysiology, 2024-04, Vol.35 (4), p.664 [Peer Reviewed Journal]EISSN: 1540-8167 ;DOI: 10.1111/jce.16210 ;PMID: 38332487Digital Resources/Online E-Resources |
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10 |
Material Type: Article
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Dilated cardiomyopathy due to hypocalcaemia: a case reportJournal of medical case reports, 2024-04, Vol.18 (1), p.204-204 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/s13256-024-04505-3 ;PMID: 38600559Full text available |
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11 |
Material Type: Article
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Advances in the Management of Hypertrophic Cardiomyopathy Leading to Low Disease-Related Mortality in 2023The American journal of cardiology, 2024-02, Vol.212, p.S77-S82 [Peer Reviewed Journal]2023 The Author(s) ;Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved. ;2023. The Author(s) ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2023.10.073 ;PMID: 38368039Full text available |
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12 |
Material Type: Article
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More Than Meets the Eye: Defining the Prevalence, Pathophysiology, and Approach to Myocardial Iron OverloadThe American journal of cardiology, 2024-05, Vol.219, p.38-43 [Peer Reviewed Journal]2024 Elsevier Inc. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2024.01.033 ;PMID: 38461925Full text available |
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13 |
Material Type: Article
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14 Myocardial sheetlet abnormality as a marker of sarcomere dysfunction in carriers of rare HCM-causing sarcomere gene variants before phenotypic conversionHeart (British Cardiac Society), 2024-03, Vol.110 (Suppl 1), p.A7-A9 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2024-BSCMR.12Digital Resources/Online E-Resources |
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14 |
Material Type: Article
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26 Phenotype, outcomes and natural history of early-stage non-ischaemic cardiomyopathyHeart (British Cardiac Society), 2024-03, Vol.110 (Suppl 1), p.A19-A20 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2024-BSCMR.23Digital Resources/Online E-Resources |
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15 |
Material Type: Article
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25 Residual structural, functional and myocardial tissue abnormalities in patients with dilated cardiomyopathy in clinical remissionHeart (British Cardiac Society), 2024-03, Vol.110 (Suppl 1), p.A18-A19 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2024-BSCMR.22Digital Resources/Online E-Resources |
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16 |
Material Type: Article
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Role of experience in myectomy for hypertrophic cardiomyopathy: With very high procedural volume, myectomy remains low-risk even with concomitant procedure needInternational journal of cardiology, 2024-06, Vol.404, p.131961 [Peer Reviewed Journal]EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2024.131961 ;PMID: 38499250Digital Resources/Online E-Resources |
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17 |
Material Type: Article
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Genetic Testing in Hypertrophic CardiomyopathyThe American journal of cardiology, 2024-02, Vol.212, p.S4-S13 [Peer Reviewed Journal]2023 The Authors ;Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved. ;2023. The Authors ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2023.10.032 ;PMID: 38368035Full text available |
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18 |
Material Type: Article
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Hypertrophic Cardiomyopathy: The Patient Perspective–Turning Tragedy into ActionThe American journal of cardiology, 2024-02, Vol.212, p.S83-S86 [Peer Reviewed Journal]2023 The Author(s) ;2023. The Author(s) ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2023.10.063 ;PMID: 38368040Full text available |
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19 |
Material Type: Article
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Retracted: Multiomics Analysis of Transcriptome, Epigenome, and Genome Uncovers Putative Mechanisms for Dilated CardiomyopathyBioMed research international, 2024, Vol.2024, p.9898717-9898717 [Peer Reviewed Journal]Copyright © 2024 BioMed Research International. ;Copyright © 2024 BioMed Research International. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2024 BioMed Research International. 2024 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2024/9898717 ;PMID: 38550143Full text available |
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20 |
Material Type: Article
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Cardiotoxicity Risk of Cancer Treatment in Patients With Underlying Cardiomyopathies: Is Hypertrophic Cardiomyopathy Any Different?Mayo Clinic proceedings, 2024-02, Vol.99 (2), p.191-193 [Peer Reviewed Journal]COPYRIGHT 2024 Elsevier, Inc. ;ISSN: 0025-6196 ;EISSN: 1942-5546 ;DOI: 10.1016/j.mayocp.2023.12.013 ;PMID: 38309931Digital Resources/Online E-Resources |