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1
Call for Consensus in the Evaluation of Circulating Matrix Metalloproteinases in Chagas Disease
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Call for Consensus in the Evaluation of Circulating Matrix Metalloproteinases in Chagas Disease

The American journal of tropical medicine and hygiene, 2022-07, Vol.107 (3), p.495-499 [Peer Reviewed Journal]

Copyright Institute of Tropical Medicine Sep 2022 ;The author(s) 2022 ;ISSN: 0002-9637 ;EISSN: 1476-1645 ;DOI: 10.4269/ajtmh.21-0860 ;PMID: 35895410

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2
Inflammatory Cardiomyopathic Syndromes
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Inflammatory Cardiomyopathic Syndromes

Circulation 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: 28912184

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3
Human-induced pluripotent stem cells for modelling metabolic perturbations and impaired bioenergetics underlying cardiomyopathies
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Human-induced pluripotent stem cells for modelling metabolic perturbations and impaired bioenergetics underlying cardiomyopathies

Cardiovascular research, 2021-02, Vol.117 (3), p.694-711 [Peer Reviewed Journal]

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com. 2020 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0008-6363 ;EISSN: 1755-3245 ;DOI: 10.1093/cvr/cvaa125 ;PMID: 32365198

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4
Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies
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Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies

Annual review of genomics and human genetics, 2019-08, Vol.20 (1), p.129-153 [Peer Reviewed Journal]

Copyright Annual Reviews, Inc. 2019 ;ISSN: 1527-8204 ;EISSN: 1545-293X ;DOI: 10.1146/annurev-genom-083118-015306 ;PMID: 30978303

Digital Resources/Online E-Resources

5
Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 3: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy and Other Cardiomyopathies, and Myocarditis: A Scientific Statement From the American Heart Association and American College of Cardiology
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Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 3: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy and Other Cardiomyopathies, and Myocarditis: A Scientific Statement From the American Heart Association and American College of Cardiology

Journal of the American College of Cardiology, 2015-12, Vol.66 (21), p.2362-2371 [Peer Reviewed Journal]

EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2015.09.035 ;PMID: 26542657

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6
Inherited Cardiomyopathies
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Inherited Cardiomyopathies

The New England journal of medicine, 2011-04, Vol.364 (17), p.1643-1656 [Peer Reviewed Journal]

Copyright © 2011 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMra0902923 ;PMID: 21524215

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7
Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)
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Article
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Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)

Genetics in medicine, 2019-10, Vol.21 (10), p.2406-2409 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0521-2

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8
54 Characterisation of systolic myocardial strain in patients with fabry disease
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54 Characterisation of systolic myocardial strain in patients with fabry disease

Heart (British Cardiac Society), 2018-06, Vol.104 (Suppl 6), p.A50-A50 [Peer Reviewed Journal]

2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;2018 2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2018-BCS.54

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9
Recent Findings Related to Cardiomyopathy and Genetics
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Article
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Recent Findings Related to Cardiomyopathy and Genetics

International 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: 34830403

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10
16 MRI imaging in obstructive hypertrophic cardiomyopathy, our experience in a district general hospital
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16 MRI imaging in obstructive hypertrophic cardiomyopathy, our experience in a district general hospital

Heart (British Cardiac Society), 2018-05, Vol.104 (Suppl 5), p.A11 [Peer Reviewed Journal]

2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2018 © 2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2018-BCVI.31

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11
Arrhythmogenic Cardiomyopathy
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Arrhythmogenic Cardiomyopathy

Circulation research, 2017-12, Vol.121 (12), p.1296-1298 [Peer Reviewed Journal]

Copyright Lippincott Williams & Wilkins Ovid Technologies Dec 8, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.312211

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12
Classification, Epidemiology, and Global Burden of Cardiomyopathies
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Classification, Epidemiology, and Global Burden of Cardiomyopathies

Circulation research, 2017-09, Vol.121 (7), p.722-730 [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.117.309711 ;PMID: 28912179

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13
Dystrophin-Deficient Cardiomyopathy
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Article
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Dystrophin-Deficient Cardiomyopathy

Journal 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: 27230049

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14
The Relevance of Takotsubo Cardiomyopathy as a Stress-Induced Disease
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Article
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The Relevance of Takotsubo Cardiomyopathy as a Stress-Induced Disease

Cardiometry, 2023-03 (26), p.105-113 [Peer Reviewed Journal]

2023. This work is published under http://www.cardiometry.net/issues (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2304-7232 ;DOI: 10.18137/cardiometry.2023.26.105113

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15
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
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Article
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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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16
Integrated multi-omic characterization of congenital heart disease
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Article
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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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17
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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18
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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Article
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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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19
ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in cats
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Article
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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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20
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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