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Results 1 - 20 of 7,735  for All Library Resources

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1
Inflammatory Cardiomyopathic Syndromes
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Article
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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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2
Dystrophin-Deficient Cardiomyopathy
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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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3
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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4
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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5
Myocarditis and inflammatory cardiomyopathy: current evidence and future directions
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Myocarditis and inflammatory cardiomyopathy: current evidence and future directions

Nature 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: 33046850

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6
Arrhythmias as Presentation of Genetic Cardiomyopathy
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Article
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Arrhythmias as Presentation of Genetic Cardiomyopathy

Circulation 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: 35617362

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7
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
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Article
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Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy

Circulation 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: 28912181

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8
Dilated Cardiomyopathy: Genetic Determinants and Mechanisms
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Article
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Dilated Cardiomyopathy: Genetic Determinants and Mechanisms

Circulation 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: 28912180

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9
Peripartum Cardiomyopathy: JACC State-of-the-Art Review
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Article
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Peripartum Cardiomyopathy: JACC State-of-the-Art Review

Journal 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: 31948651

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10
T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure
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T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure

JACC. 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: 26762873

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11
Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry
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Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry

International 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: 36918127

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12
Familial Hypertrophic Cardiomyopathy: Diagnosis and Management
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Article
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Familial Hypertrophic Cardiomyopathy: Diagnosis and Management

Vascular health and risk management, 2023-01, Vol.19, p.211-221 [Peer Reviewed Journal]

2023 Litt et al. ;COPYRIGHT 2023 Dove Medical Press Limited ;2023. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 Litt et al. 2023 Litt et al. ;ISSN: 1178-2048 ;ISSN: 1176-6344 ;EISSN: 1178-2048 ;DOI: 10.2147/VHRM.S365001 ;PMID: 37050929

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13
Clinical utility of cardiovascular magnetic resonance in hypertrophic cardiomyopathy
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Article
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Clinical utility of cardiovascular magnetic resonance in hypertrophic cardiomyopathy

Journal of cardiovascular magnetic resonance, 2012-02, Vol.14 (1), p.13-13, Article 13 [Peer Reviewed Journal]

COPYRIGHT 2012 BioMed Central Ltd. ;COPYRIGHT 2012 BioMed Central Ltd. ;2012 Maron; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2012 Maron; licensee BioMed Central Ltd. 2012 Maron; licensee BioMed Central Ltd. ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/1532-429x-14-13 ;PMID: 22296938

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14
The Remarkable 50 Years of Imaging in HCM and How it Has Changed Diagnosis and Management: From M-Mode Echocardiography to CMR
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The Remarkable 50 Years of Imaging in HCM and How it Has Changed Diagnosis and Management: From M-Mode Echocardiography to CMR

JACC. Cardiovascular imaging, 2016-07, Vol.9 (7), p.858 [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.2016.05.003 ;PMID: 27388665

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15
Phase 2 Study of Aficamten in Patients With Obstructive Hypertrophic Cardiomyopathy
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Article
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Phase 2 Study of Aficamten in Patients With Obstructive Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2023-01, Vol.81 (1), p.34-45 [Peer Reviewed Journal]

2023 The Authors ;Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2022.10.020 ;PMID: 36599608

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16
Phenotype, outcomes and natural history of early-stage non-ischaemic cardiomyopathy
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Article
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Phenotype, outcomes and natural history of early-stage non-ischaemic cardiomyopathy

European journal of heart failure, 2023-11, Vol.25 (11), p.2050 [Peer Reviewed Journal]

2023 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.3037 ;PMID: 37728026

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17
Hypertrophic Cardiomyopathy: Present and Future, With Translation Into Contemporary Cardiovascular Medicine
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Article
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Hypertrophic Cardiomyopathy: Present and Future, With Translation Into Contemporary Cardiovascular Medicine

Journal of the American College of Cardiology, 2014-07, Vol.64 (1), p.83-99 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2014.05.003 ;PMID: 24998133 ;CODEN: JACCDI

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18
Genetics of dilated cardiomyopathy: practical implications for heart failure management
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Article
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Genetics of dilated cardiomyopathy: practical implications for heart failure management

Nature reviews cardiology, 2020-05, Vol.17 (5), p.286-297 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Springer Nature Limited 2019. ;ISSN: 1759-5002 ;EISSN: 1759-5010 ;DOI: 10.1038/s41569-019-0284-0 ;PMID: 31605094

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19
Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis
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Article
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Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis

Journal of the American College of Cardiology, 2015-12, Vol.66 (21), p.2451-2466 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2015 American College of Cardiology Foundation ;Copyright © 2015 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Dec 1, 2015 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2015.09.075 ;PMID: 26610878

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20
Iron Overload Cardiomyopathy: Better Understanding of an Increasing Disorder
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Article
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Iron Overload Cardiomyopathy: Better Understanding of an Increasing Disorder

Journal of the American College of Cardiology, 2010-09, Vol.56 (13), p.1001-1012 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright © 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Sep 21, 2010 ;2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. 2010 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2010.03.083 ;PMID: 20846597 ;CODEN: JACCDI

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