Results 1 - 20 of 30 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Viral myocarditis in combination with genetic cardiomyopathy as a cause of sudden death. An autopsy seriesBMC cardiovascular disorders, 2024-05, Vol.24 (1), p.282-282 [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/s12872-024-03913-z ;PMID: 38811883Full text available |
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MiR-31-5p alleviates septic cardiomyopathy by targeting BAP1 to inhibit SLC7A11 deubiquitination and ferroptosisBMC cardiovascular disorders, 2024-05, Vol.24 (1), p.286-286 [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/s12872-024-03954-4 ;PMID: 38816686Full text available |
| 3 |
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Takotsubo syndrome as an acute cardiac complication following combined chemotherapyInternational journal of cardiology. Cardiovascular risk and prevention, 2024-09, Vol.22, p.200292 [Peer Reviewed Journal]EISSN: 2772-4875Full text available |
| 4 |
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Generation of an induced pluripotent stem cell line from a patient with arrhythmogenic right ventricular cardiomyopathy harboring a TMEM43 splice-site variantStem cell research, 2024-05, Vol.78, p.103453-103453, Article 103453 [Peer Reviewed Journal]2024 ;Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved. ;ISSN: 1873-5061 ;EISSN: 1876-7753 ;DOI: 10.1016/j.scr.2024.103453 ;PMID: 38824800Full text available |
| 5 |
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Multilevel modelling for decision support in hypertrophic cardiomyopathy in the SMASH-HCM projectFinnish Journal of eHealth and eWelfare, 2024-05, Vol.16 (2) [Peer Reviewed Journal]EISSN: 1798-0798Full text available |
| 6 |
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USP7 promotes cardiometabolic disorders and mitochondrial homeostasis dysfunction in diabetic mice via stabilizing PGC1βPharmacological research, 2024-05, Vol.205, p.107235 [Peer Reviewed Journal]EISSN: 1096-1186 ;DOI: 10.1016/j.phrs.2024.107235Digital Resources/Online E-Resources |
| 7 |
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This Week in the JournalThe New England journal of medicine, 2024-05, Vol.390 (20), p.1848 [Peer Reviewed Journal]Copyright © 2024 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMtwj240530Full text available |
| 8 |
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Evidence of cardiomyopathy associated with Marfan syndrome in childrenHeart (British Cardiac Society), 2024-05, p.heartjnl-2024-323922 [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-2024-323922 ;PMID: 38816063Full text available |
| 9 |
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An overview of the treatments for hypertrophic cardiomyopathyFrontiers in cardiovascular medicine, 2024-06, Vol.11 [Peer Reviewed Journal]EISSN: 2297-055X ;DOI: 10.3389/fcvm.2024.1387596Full text available |
| 10 |
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Growth hormone releasing peptide-6 (GHRP-6) prevents doxorubicin-induced myocardial and extra-myocardial damages by activating prosurvival mechanismsFrontiers in pharmacology, 2024-05, Vol.15 [Peer Reviewed Journal]EISSN: 1663-9812 ;DOI: 10.3389/fphar.2024.1402138Full text available |
| 11 |
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Arrhythmogenic right ventricular cardiomyopathy with sustained ventricular tachycardia: a case reportBMC cardiovascular disorders, 2024-05, Vol.24 (1), p.284-284 [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/s12872-024-03959-z ;PMID: 38816798Full text available |
| 12 |
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Real-time Three-dimensional Echocardiography for Assessing Left Atrial Structural and Functional Changes in Mutation Carriers of Hypertrophic CardiomyopathyZhongguo quanke yixue, 2024-08, Vol.27 (24), p.2987-2993 [Peer Reviewed Journal]ISSN: 1007-9572 ;DOI: 10.12114/j.issn.1007-9572.2023.0692Digital Resources/Online E-Resources |
| 13 |
Material Type: Article
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Cardiomyopathy in children: a single-centre, retrospective study of genetic and clinical characteristicsBMJ paediatrics open, 2024-05, Vol.8 (1), p.e002024 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ 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)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2024 ;EISSN: 2399-9772 ;DOI: 10.1136/bmjpo-2023-002024 ;PMID: 38823802Full text available |
| 14 |
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Hypertrophic cardiomyopathy-related left ventricular pseudoaneurysm: A case reportHeliyon, 2024-06, Vol.10 (11), p.e32197 [Peer Reviewed Journal]EISSN: 2405-8440Full text available |
| 15 |
Material Type: Article
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Left Ventricular Non-compaction and Associated Cardiomyopathy Presenting With Cardiac Failure: A Case ReportCurēus (Palo Alto, CA), 2024-04, Vol.16 (4), p.e59265 [Peer Reviewed Journal]Copyright © 2024, Azhar et al. ;Copyright © 2024, Azhar et al. This work is published under https://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. ;Copyright © 2024, Azhar et al. 2024 Azhar et al. ;ISSN: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.59265 ;PMID: 38813285Full text available |
| 16 |
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A New Cardiac Myosin Inhibitor for Obstructive Hypertrophic Cardiomyopathy?NEJM journal watch. Cardiology, 2024-05Copyright © 2024 Massachusetts Medical Society. All rights reserved. ;ISSN: 2330-0477Full text available |
| 17 |
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Biomaterial-enhanced cell and drug delivery: lessons learned in the cardiac field and future perspectivesAdvanced Materials, 2016-02 [Peer Reviewed Journal]Attribution-NonCommercial-NoDerivs 3.0 Ireland https://creativecommons.org/licenses/by-nc-nd/3.0/ie ;ISSN: 0935-9648 ;EISSN: 1521-4095 ;DOI: 10.1002/adma.201505349Full text available |
| 18 |
Material Type: Article
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Bone marrow-derived mesenchymal stem cells have innate procoagulant activity and cause microvascular obstruction following intracoronary delivery: amelioration by antithrombin therapySTEM CELLS, 2015-06 [Peer Reviewed Journal]Attribution-NonCommercial-NoDerivs 3.0 Ireland https://creativecommons.org/licenses/by-nc-nd/3.0/ie ;ISSN: 1066-5099 ;EISSN: 1549-4918 ;DOI: 10.1002/stem.2050Digital Resources/Online E-Resources |
| 19 |
Material Type: Article
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The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variantNetherlands Heart Journal, 2023-07, Vol.31 (7-8), p.315-323open access ;DOI: 10.1007/s12471-023-01791-2Digital Resources/Online E-Resources |
| 20 |
Material Type: Article
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Clinical Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives: Who, When, and How?Digital Resources/Online E-Resources |
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