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1
Inflammatory Cardiomyopathic Syndromes
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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2
Recent Findings Related to Cardiomyopathy and Genetics
Recent Findings Related to Cardiomyopathy and Genetics
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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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3
Dystrophin-Deficient Cardiomyopathy
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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4
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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5
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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6
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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7
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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8
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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9
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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10
Myocarditis and inflammatory cardiomyopathy: current evidence and future directions
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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11
Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy
Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy
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Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy

Nature (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: 35732739

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12
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
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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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13
Arrhythmias as Presentation of Genetic Cardiomyopathy
Arrhythmias as Presentation of Genetic Cardiomyopathy
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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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14
Current state of knowledge on Takotsubo syndrome: a Position Statement from the Taskforce on Takotsubo Syndrome of the Heart Failure Association of the European Society of Cardiology
Current state of knowledge on Takotsubo syndrome: a Position Statement from the Taskforce on Takotsubo Syndrome of the Heart Failure Association of the European Society of Cardiology
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Current state of knowledge on Takotsubo syndrome: a Position Statement from the Taskforce on Takotsubo Syndrome of the Heart Failure Association of the European Society of Cardiology

European journal of heart failure, 2016-01, Vol.18 (1), p.8-27 [Peer Reviewed Journal]

2015 The Authors © 2015 European Society of Cardiology ;2015 The Authors European Journal of Heart Failure © 2015 European Society of Cardiology. ;ISSN: 1388-9842 ;ISSN: 1879-0844 ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.424 ;PMID: 26548803

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15
Efficacy of CD34+ Stem Cell Therapy in Nonischemic Dilated Cardiomyopathy Is Absent in Patients With Diabetes but Preserved in Patients With Insulin Resistance
Efficacy of CD34+ Stem Cell Therapy in Nonischemic Dilated Cardiomyopathy Is Absent in Patients With Diabetes but Preserved in Patients With Insulin Resistance
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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 Resistance

Stem 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: 27025690

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16
Dilated Cardiomyopathy: Genetic Determinants and Mechanisms
Dilated Cardiomyopathy: Genetic Determinants and Mechanisms
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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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17
Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry
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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18
Peripartum Cardiomyopathy: JACC State-of-the-Art Review
Peripartum Cardiomyopathy: JACC State-of-the-Art Review
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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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19
Familial Hypertrophic Cardiomyopathy: Diagnosis and Management
Familial Hypertrophic Cardiomyopathy: Diagnosis and Management
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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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20
T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure
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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