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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Metabolomic insights in advanced cardiomyopathy of chronic chagasic and idiopathic patients that underwent heart transplantScientific reports, 2024-04, Vol.14 (1), p.9810-9810 [Peer Reviewed Journal]2024. The Author(s). ;The Author(s) 2024. 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. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-53875-7 ;PMID: 38684702Full text available |
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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. ;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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Human umbilical cord-derived mesenchymal stromal cells improve myocardial fibrosis and restore miRNA-133a expression in diabetic cardiomyopathyStem cell research & therapy, 2024-04, Vol.15 (1), p.120-120 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1757-6512 ;EISSN: 1757-6512 ;DOI: 10.1186/s13287-024-03715-2 ;PMID: 38659015Full text available |
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Incidence and risk factors for development of left ventricular hypertrophy in Fabry diseaseHeart (British Cardiac Society), 2024-04, p.heartjnl-2023-323783 [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-2023-323783 ;PMID: 38688703Full text available |
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Association of uncertain significance genetic variants with myocardial mechanics and morphometrics in patients with nonischemic dilated cardiomyopathyBMC cardiovascular disorders, 2024-04, Vol.24 (1), p.224-224 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1471-2261 ;EISSN: 1471-2261 ;DOI: 10.1186/s12872-024-03888-x ;PMID: 38664609Full text available |
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Restrictive annuloplasty or replacement on reverse remodeling for nonischemic dilated cardiomyopathyJournal of cardiothoracic surgery, 2024-04, Vol.19 (1), p.201-201 [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. ;ISSN: 1749-8090 ;EISSN: 1749-8090 ;DOI: 10.1186/s13019-024-02719-6 ;PMID: 38609986Full text available |
| 7 |
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Evaluating the efficacy and safety of mavacamten in hypertrophic cardiomyopathy: A systematic review and meta-analysis focusing on qualitative assessment, biomarkers, and cardiac imagingPloS one, 2024-04, Vol.19 (4), p.e0301704-e0301704 [Peer Reviewed Journal]Copyright: © 2024 Vyas et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. ;COPYRIGHT 2024 Public Library of Science ;2024 Vyas et al 2024 Vyas et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0301704 ;PMID: 38635724Full text available |
| 8 |
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Genotype-Phenotype Insights of Inherited Cardiomyopathies-A ReviewMedicina (Kaunas, Lithuania), 2024-03, Vol.60 (4), p.543 [Peer Reviewed Journal]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. ;ISSN: 1010-660X ;EISSN: 1648-9144 ;DOI: 10.3390/medicina60040543 ;PMID: 38674189Full text available |
| 9 |
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A therapeutic leap: how myosin inhibitors moved from cardiac interventions to skeletal muscle myopathy solutionsThe Journal of clinical investigation, 2024-05, Vol.134 (9) [Peer Reviewed Journal]2024 Bogomolovas et al. 2024 Bogomolovas et al. ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI179958 ;PMID: 38690729Full text available |
| 10 |
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Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and FibrosisThe New England journal of medicine, 2024-04, Vol.390 (16), p.1537-1540 [Peer Reviewed Journal]Copyright © 2024 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMc2313870 ;PMID: 38657259Full text available |
| 11 |
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Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated CardiomyopathyInternational journal of molecular sciences, 2024-04, Vol.25 (7), p.3807 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25073807 ;PMID: 38612618Full text available |
| 12 |
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Identifying predictors and determining mortality rates of septic cardiomyopathy and sepsis-related cardiogenic shock: A retrospective, observational studyPloS one, 2024-04, Vol.19 (4), p.e0299876-e0299876 [Peer Reviewed Journal]Copyright: © 2024 Hendrickson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. ;COPYRIGHT 2024 Public Library of Science ;2024 Hendrickson et al 2024 Hendrickson et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0299876 ;PMID: 38662672Full text available |
| 13 |
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Metoprolol Lack of efficacy1Reactions weekly, 2024-04 (2005), p.536-536Copyright Springer Nature B.V. Apr 27, 2024 ;ISSN: 0114-9954 ;EISSN: 1179-2051Digital Resources/Online E-Resources |
| 14 |
Material Type: Article
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Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic CardiomyopathyBMC cardiovascular disorders, 2024-04, Vol.24 (1), p.220-220 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1471-2261 ;EISSN: 1471-2261 ;DOI: 10.1186/s12872-024-03878-z ;PMID: 38654147Full text available |
| 15 |
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OP-04. Biventricular Noncompaction with Ascending Aortic Dilatation Presenting with Congestive Heart Failure: A Rare Case of Nonischemic CardiomyopathyThe European research journal, 2024-03, Vol.10, p.S10-S11 [Peer Reviewed Journal]Copyright The Association of Health Research & Strategy Mar 2024 ;EISSN: 2149-3189Full text available |
| 16 |
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Prognosis value of galectin-3 in patients with dilated cardiomyopathy: a meta-analysisPeerJ (San Francisco, CA), 2024, Vol.12, p.e17201-e17201 [Peer Reviewed Journal]2024 Xiong and Zhang. ;EISSN: 2167-8359 ;DOI: 10.7717/peerj.17201 ;PMID: 38680895Full text available |
| 17 |
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The feasibility of left ventricular strain and strain rate for evaluating patients with risk factors of sudden cardiac death in hypertrophic cardiomyopathy by Feature-tracking Cardiac Magnetic ResonanceThe American journal of cardiology, 2024-04 [Peer Reviewed Journal]2024 ;Copyright © 2024 Elsevier Inc. All rights reserved. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2024.04.025 ;PMID: 38642869Digital Resources/Online E-Resources |
| 18 |
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Association between dietary selenium and zinc intake and risk of dilated cardiomyopathy in children: a case-control studyBMC pediatrics, 2024-04, Vol.24 (1), p.251-251 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-024-04706-1 ;PMID: 38605385Full text available |
| 19 |
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Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathyinfo:eu-repo/semantics/OpenAccess ;ISSN: 1568-5888 ;EISSN: 1876-6250Full text available |
| 20 |
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KBTBD13 is a novel cardiomyopathy geneinfo:eu-repo/semantics/OpenAccess ;ISSN: 1059-7794 ;EISSN: 1098-1004Digital Resources/Online E-Resources |
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