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1
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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2
Neutrophil degranulation biomarkers characterize restrictive echocardiographic pattern with diastolic dysfunction in patients with diabetes
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Neutrophil degranulation biomarkers characterize restrictive echocardiographic pattern with diastolic dysfunction in patients with diabetes

European journal of clinical investigation, 2021-12, Vol.51 (12), p.e13640 [Peer Reviewed Journal]

2021 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation. ;EISSN: 1365-2362 ;DOI: 10.1111/eci.13640 ;PMID: 34129696

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3
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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4
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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5
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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6
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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7
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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8
Investigation of de novo variation in pediatric cardiomyopathy
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Investigation of de novo variation in pediatric cardiomyopathy

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-03, Vol.184 (1), p.116

2020 Wiley Periodicals, Inc. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31764 ;PMID: 31912959

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9
Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy
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Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy

Circulation (New York, N.Y.), 2021-11, Vol.144 (21), p.1714-1731 [Peer Reviewed Journal]

ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/circulationaha.121.053575 ;PMID: 34672721

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10
Development of plasma and whole blood taurine reference ranges and identification of dietary features associated with taurine deficiency and dilated cardiomyopathy in golden retrievers: A prospective, observational study
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Development of plasma and whole blood taurine reference ranges and identification of dietary features associated with taurine deficiency and dilated cardiomyopathy in golden retrievers: A prospective, observational study

PloS one, 2020-05, Vol.15 (5), p.e0233206 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Ontiveros 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. ;2020 Ontiveros et al 2020 Ontiveros et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0233206 ;PMID: 32413894

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11
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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12
Outcomes of Restrictive Cardiomyopathy in Childhood and the Influence of Phenotype: A Report From the Pediatric Cardiomyopathy Registry
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Outcomes of Restrictive Cardiomyopathy in Childhood and the Influence of Phenotype: A Report From the Pediatric Cardiomyopathy Registry

Circulation (New York, N.Y.), 2012-09, Vol.126 (10), p.1237-1244 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.112.104638 ;PMID: 22843787 ;CODEN: CIRCAZ

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13
Phenotype-driven molecular autopsy for sudden cardiac death
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Phenotype-driven molecular autopsy for sudden cardiac death

Clinical genetics, 2017-01, Vol.91 (1), p.22 [Peer Reviewed Journal]

2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. ;EISSN: 1399-0004 ;DOI: 10.1111/cge.12778 ;PMID: 27000522

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14
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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15
Clinical profile and outcome of cardiomyopathies in infants and children seen at a tertiary centre
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Clinical profile and outcome of cardiomyopathies in infants and children seen at a tertiary centre

International journal of cardiology, 2023-01, Vol.371, p.516 [Peer Reviewed Journal]

Copyright © 2022 Elsevier B.V. All rights reserved. ;EISSN: 1874-1754 ;DOI: 10.1016/j.ijcard.2022.09.034 ;PMID: 36130621

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16
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)
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Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)

Circulation (New York, N.Y.), 2018-10, Vol.138 (14), p.1387-1398 [Peer Reviewed Journal]

2018 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2018 The Authors. 2018 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.117.033200 ;PMID: 30297972

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17
Taurine deficiency and dilated cardiomyopathy in golden retrievers fed commercial diets
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Taurine deficiency and dilated cardiomyopathy in golden retrievers fed commercial diets

PloS one, 2018-12, Vol.13 (12), p.e0209112-e0209112 [Peer Reviewed Journal]

COPYRIGHT 2018 Public Library of Science ;COPYRIGHT 2018 Public Library of Science ;2018 Kaplan 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. ;2018 Kaplan et al 2018 Kaplan et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0209112 ;PMID: 30543707

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18
Clinical Features and Outcomes of Takotsubo (Stress) Cardiomyopathy
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Clinical Features and Outcomes of Takotsubo (Stress) Cardiomyopathy

The New England journal of medicine, 2015-09, Vol.373 (10), p.929-938 [Peer Reviewed Journal]

Copyright © 2015 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1406761 ;PMID: 26332547

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19
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy
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Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy

JAMA : the journal of the American Medical Association, 2022-02, Vol.327 (5), p.454 [Peer Reviewed Journal]

EISSN: 1538-3598 ;DOI: 10.1001/jama.2021.24674 ;PMID: 35103767

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20
Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial
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Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial

The Lancet (British edition), 2019-01, Vol.393 (10166), p.61-73 [Peer Reviewed Journal]

2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved. ;Copyright Elsevier Limited Jan 5, 2019 ;2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license 2019 ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(18)32484-X ;PMID: 30429050

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