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1 |
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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2 |
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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3 |
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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4 |
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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5 |
Material Type: Article
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ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in catsJournal of veterinary internal medicine, 2020-05, Vol.34 (3), p.1062-1077 [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. ;2020 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. ;2020. 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: 0891-6640 ;ISSN: 1939-1676 ;EISSN: 1939-1676 ;DOI: 10.1111/jvim.15745 ;PMID: 32243654Full text available |
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6 |
Material Type: Article
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Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strainPloS one, 2019-08, Vol.14 (8), p.e0221028-e0221028 [Peer Reviewed Journal]COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Santos Junior 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. ;2019 Santos Junior et al 2019 Santos Junior et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0221028 ;PMID: 31437176Full text available |
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Material Type: Article
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MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCMJournal of translational medicine, 2018-06, Vol.16 (1), p.161-161, Article 161 [Peer Reviewed Journal]COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. 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) 2018 ;ISSN: 1479-5876 ;EISSN: 1479-5876 ;DOI: 10.1186/s12967-018-1534-3 ;PMID: 29885652Full text available |
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8 |
Material Type: Article
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Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart AssociationCirculation (New York, N.Y.), 2016-12, Vol.134 (23), p.e579-e646 [Peer Reviewed Journal]2016 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIR.0000000000000455 ;PMID: 27832612Full text available |
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9 |
Material Type: Article
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Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC)European journal of heart failure, 2022-03, Vol.24 (3), p.406 [Peer Reviewed Journal]2021 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. ;ISSN: 1879-0844 ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.2414 ;PMID: 34969177Digital Resources/Online E-Resources |
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10 |
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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11 |
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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12 |
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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13 |
Material Type: Article
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Arrhythmias as Presentation of Genetic CardiomyopathyCirculation research, 2022-05, Vol.130 (11), p.1698-1722 [Peer Reviewed Journal]ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.122.319835 ;PMID: 35617362Full text available |
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14 |
Material Type: Article
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Efficacy of CD34+ Stem Cell Therapy in Nonischemic Dilated Cardiomyopathy Is Absent in Patients With Diabetes but Preserved in Patients With Insulin ResistanceStem cells translational medicine, 2016-05, Vol.5 (5), p.632-638 [Peer Reviewed Journal]2016 AlphaMed Press ;AlphaMed Press. ;Copyright John Wiley & Sons, Inc. May 2016 ;AlphaMed Press 2016 ;ISSN: 2157-6564 ;EISSN: 2157-6580 ;DOI: 10.5966/sctm.2015-0172 ;PMID: 27025690Full text available |
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15 |
Material Type: Article
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Dilated Cardiomyopathy: Genetic Determinants and MechanismsCirculation research, 2017-09, Vol.121 (7), p.731-748 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.116.309396 ;PMID: 28912180Full text available |
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16 |
Material Type: Article
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Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registryInternational journal of cardiology, 2023-05, Vol.379, p.96 [Peer Reviewed Journal]Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2023.03.028 ;PMID: 36918127Digital Resources/Online E-Resources |
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17 |
Material Type: Article
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Peripartum Cardiomyopathy: JACC State-of-the-Art ReviewJournal of the American College of Cardiology, 2020-01, Vol.75 (2), p.207-221 [Peer Reviewed Journal]Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;2020. American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2019.11.014 ;PMID: 31948651Full text available |
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18 |
Material Type: Article
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Dilated cardiomyopathyThe Lancet (British edition), 2010-02, Vol.375 (9716), p.752-762 [Peer Reviewed Journal]Elsevier Ltd ;2010 Elsevier Ltd ;2015 INIST-CNRS ;Copyright 2010 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited Feb 27-Mar 5, 2010 ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(09)62023-7 ;PMID: 20189027 ;CODEN: LANCAOFull text available |
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19 |
Material Type: Article
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T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart FailureJACC. Cardiovascular imaging, 2016-01, Vol.9 (1), p.40 [Peer Reviewed Journal]Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;EISSN: 1876-7591 ;DOI: 10.1016/j.jcmg.2015.12.001 ;PMID: 26762873Digital Resources/Online E-Resources |
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20 |
Material Type: Article
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Dilated cardiomyopathy: from epidemiologic to genetic phenotypes: A translational review of current literatureJournal of internal medicine, 2019-10, Vol.286 (4), p.362-372 [Peer Reviewed Journal]2019 The Association for the Publication of the Journal of Internal Medicine. ;Copyright © 2019 The Association for the Publication of the Journal of Internal Medicine ;ISSN: 0954-6820 ;EISSN: 1365-2796 ;DOI: 10.1111/joim.12944 ;PMID: 31132311Digital Resources/Online E-Resources |