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Results 21 - 40 of 131,722  for All Library Resources

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21
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
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Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature genetics, 2021-02, Vol.53 (2), p.128-134 [Peer Reviewed Journal]

COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2021 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-00762-2 ;PMID: 33495596

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22
Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes
Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes
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Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes

Journal of molecular and cellular cardiology, 2010-05, Vol.48 (5), p.899 [Peer Reviewed Journal]

Copyright (c) 2010 Elsevier Ltd. All rights reserved. ;EISSN: 1095-8584 ;DOI: 10.1016/j.yjmcc.2010.03.005 ;PMID: 20298698

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23
Integrated multi-omic characterization of congenital heart disease
Integrated multi-omic characterization of congenital heart disease
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Integrated multi-omic characterization of congenital heart disease

Nature (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: 35732239

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24
Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chains
Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chains
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Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chains

Pflügers Archiv, 2019-05, Vol.471 (5), p.683-699 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2019 ;Pflügers Archiv - European Journal of Physiology is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 0031-6768 ;EISSN: 1432-2013 ;DOI: 10.1007/s00424-019-02257-4 ;PMID: 30706179

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25
Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)
Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)
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Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)

European heart journal, 2019-01, Vol.40 (1), p.19-33 [Peer Reviewed Journal]

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2018. For permissions, please email: journals.permissions@oup.com. 2018 ;ISSN: 0195-668X ;ISSN: 1522-9645 ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehy730 ;PMID: 30561613

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26
ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in cats
ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in cats
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ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in cats

Journal 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: 32243654

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27
Telomere shortening is a hallmark of genetic cardiomyopathies
Telomere shortening is a hallmark of genetic cardiomyopathies
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Telomere shortening is a hallmark of genetic cardiomyopathies

Proceedings of the National Academy of Sciences - PNAS, 2018-09, Vol.115 (37), p.9276-9281 [Peer Reviewed Journal]

Volumes 1–89 and 106–115, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright © 2018 the Author(s). Published by PNAS. ;Copyright National Academy of Sciences Sep 11, 2018 ;Copyright © 2018 the Author(s). Published by PNAS. 2018 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1714538115 ;PMID: 30150400

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28
Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strain
Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strain
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Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strain

PloS 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: 31437176

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29
Cardiovascular highlights from non-cardiology journals
Cardiovascular highlights from non-cardiology journals
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Cardiovascular highlights from non-cardiology journals

Heart (British Cardiac Society), 2016-08, Vol.102 (16), p.1334-1334 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Copyright: 2016 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2016-310217

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30
Speckle tracking imaging in hypertrophic cardiomyopathy
Speckle tracking imaging in hypertrophic cardiomyopathy
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Speckle tracking imaging in hypertrophic cardiomyopathy

Herz, 2019-05, Vol.44 (3), p.265-265 [Peer Reviewed Journal]

Herz is a copyright of Springer, (2017). All Rights Reserved. ;ISSN: 0340-9937 ;EISSN: 1615-6692 ;DOI: 10.1007/s00059-017-4653-3

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31
MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM
MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM
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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 DCM

Journal 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: 29885652

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32
Arrhythmogenic Cardiomyopathy
Arrhythmogenic Cardiomyopathy
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Arrhythmogenic Cardiomyopathy

Circulation research, 2017-09, Vol.121 (7), p.784-802 [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.117.309345 ;PMID: 28912183

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33
Alcohol use disorders and the heart
Alcohol use disorders and the heart
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Alcohol use disorders and the heart

Addiction (Abingdon, England), 2019-09, Vol.114 (9), p.1670-1678 [Peer Reviewed Journal]

2019 The Authors. published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction ;2019 The Authors. Addiction published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction. ;2019 Society for the Study of Addiction ;ISSN: 0965-2140 ;EISSN: 1360-0443 ;DOI: 10.1111/add.14703 ;PMID: 31309639

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34
Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association
Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association
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Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association

Circulation (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: 27832612

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35
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)
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)
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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: 34969177

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36
Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance
Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance
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Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance

Journal of the American College of Cardiology, 2017-02, Vol.69 (6), p.661-676 [Peer Reviewed Journal]

2017 ;Published by Elsevier Inc. ;Copyright Elsevier Limited Feb 14, 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.11.051 ;PMID: 28183509

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37
Genetics of Hypertrophic Cardiomyopathy After 20 Years: Clinical Perspectives
Genetics of Hypertrophic Cardiomyopathy After 20 Years: Clinical Perspectives
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Genetics of Hypertrophic Cardiomyopathy After 20 Years: Clinical Perspectives

Journal of the American College of Cardiology, 2012-08, Vol.60 (8), p.705-715 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.02.068 ;PMID: 22796258 ;CODEN: JACCDI

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38
The genetic basis for cardiac remodeling
The genetic basis for cardiac remodeling
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The genetic basis for cardiac remodeling

Annual review of genomics and human genetics, 2005-01, Vol.6 (1), p.185-216 [Peer Reviewed Journal]

ISSN: 1527-8204 ;EISSN: 1545-293X ;DOI: 10.1146/annurev.genom.6.080604.162132 ;PMID: 16124859

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39
Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy
Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy
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Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy

Journal of the American College of Cardiology, 2016-12, Vol.68 (25), p.2871-2886 [Peer Reviewed Journal]

The Authors ;2016 The Authors ;Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Dec 27, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.08.079 ;PMID: 28007147

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40
Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism
Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism
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Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism

Circulation research, 2017-09, Vol.121 (7), p.838-854 [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.117.310987 ;PMID: 28912186

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