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

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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
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
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
Neutrophil degranulation biomarkers characterize restrictive echocardiographic pattern with diastolic dysfunction in patients with diabetes
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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8
Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)
Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)
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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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9
54 Characterisation of systolic myocardial strain in patients with fabry disease
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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10
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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11
16 MRI imaging in obstructive hypertrophic cardiomyopathy, our experience in a district general hospital
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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12
Arrhythmogenic Cardiomyopathy
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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13
Classification, Epidemiology, and Global Burden of Cardiomyopathies
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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14
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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15
The Relevance of Takotsubo Cardiomyopathy as a Stress-Induced Disease
The Relevance of Takotsubo Cardiomyopathy as a Stress-Induced Disease
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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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16
Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?
Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?
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Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

Journal of molecular and cellular cardiology, 2010-05, Vol.48 (5), p.882 [Peer Reviewed Journal]

Copyright (c) 2009 Elsevier Ltd. All rights reserved. ;EISSN: 1095-8584 ;DOI: 10.1016/j.yjmcc.2009.10.031 ;PMID: 19914256

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17
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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18
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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19
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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20
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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