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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular CardiomyopathyCirculation (New York, N.Y.), 2020-06, Vol.141 (23), p.1872-1884 [Peer Reviewed Journal]2020 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.119.044934 ;PMID: 32372669Full text available |
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Genotype-Dependent and -Independent Calcium Signaling Dysregulation in Human Hypertrophic CardiomyopathyCirculation (New York, N.Y.), 2016-11, Vol.134 (22), p.1738-1748 [Peer Reviewed Journal]2016 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2016 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.115.020086 ;PMID: 27688314Full text available |
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Physiologic biomechanics enhance reproducible contractile development in a stem cell derived cardiac muscle platformNature communications, 2021-10, Vol.12 (1), p.6167-6167, Article 6167 [Peer Reviewed Journal]2021. The Author(s). ;The Author(s) 2021. 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. ;The Author(s) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-26496-1 ;PMID: 34697315Full text available |
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Genetic testing impacts the utility of prospective familial screening in hypertrophic cardiomyopathy through identification of a nonfamilial subgroupGenetics in medicine, 2018-01, Vol.20 (1), p.69-75 [Peer Reviewed Journal]2018 The Author(s) ;Copyright Nature Publishing Group Jan 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.79 ;PMID: 28640247Full text available |
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Integrating mechanical cues with engineered platforms to explore cardiopulmonary development and diseaseiScience, 2023-12, Vol.26 (12), p.108472-108472, Article 108472 [Peer Reviewed Journal]2023 The Author(s) ;2023 The Author(s). ;ISSN: 2589-0042 ;EISSN: 2589-0042 ;DOI: 10.1016/j.isci.2023.108472 ;PMID: 38077130Full text available |
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HSC70 is a chaperone for wild-type and mutant cardiac myosin binding protein CJCI insight, 2018-06, Vol.3 (11) [Peer Reviewed Journal]Copyright © 2018, American Society for Clinical Investigation 2018 American Society for Clinical Investigation ;ISSN: 2379-3708 ;EISSN: 2379-3708 ;DOI: 10.1172/jci.insight.99319 ;PMID: 29875314Full text available |
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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: 30297972Full text available |
| 8 |
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Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathyEuropean heart journal, 2021-05, Vol.42 (20), p.1988-1996 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehab148 ;PMID: 33769460Full text available |
| 9 |
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Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathyEuropean heart journal, 2021-10, Vol.42 (38), p.3932-3944 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com. 2021 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehab598 ;PMID: 34491319Full text available |
| 10 |
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Other side of the coin: the missing heritability in hypertrophic cardiomyopathyEuropean heart journal, 2017-12, Vol.38 (46), p.3469-3471 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehx024 ;PMID: 28201496Full text available |
| 11 |
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Translation of New and Emerging Therapies for Genetic CardiomyopathiesJACC. Basic to translational science, 2022-01, Vol.7 (1), p.70-83 [Peer Reviewed Journal]2022 The Authors ;2022 The Authors. ;2022 The Authors 2022 ;ISSN: 2452-302X ;EISSN: 2452-302X ;DOI: 10.1016/j.jacbts.2021.07.012 ;PMID: 35128211Full text available |
| 12 |
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Hypertrophic cardiomyopathy: single gene disease or complex trait?European heart journal, 2016-06, Vol.37 (23), p.1823-1825 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehv562 ;PMID: 26508162Full text available |
| 13 |
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A Case of Reverse McConnell's Sign Associated With Acute Respiratory Distress Syndrome and Septic ShockCurēus (Palo Alto, CA), 2024-01, Vol.16 (1), p.e52166 [Peer Reviewed Journal]Copyright © 2024, Curtis et al. ;Copyright © 2024, Curtis et al. This work is published under https://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. ;Copyright © 2024, Curtis et al. 2024 Curtis et al. ;ISSN: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.52166 ;PMID: 38357087Full text available |
| 14 |
Material Type: Article
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Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathyEuropean heart journal, 2021-10, Vol.42 (38), p.3932 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com. ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehab598 ;PMID: 36282238Full text available |
| 15 |
Material Type: Article
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Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretationGenetics in medicine, 2021-07, Vol.23 (7), p.1281-1287 [Peer Reviewed Journal]2021 The Author(s) ;The Author(s) 2021. 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. ;The Author(s) 2021 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01134-9 ;PMID: 33782553Full text available |
| 16 |
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Whole-Exome Sequencing Reveals GATA4 and PTEN Mutations as a Potential Digenic Cause of Left Ventricular NoncompactionCirculation. Cardiovascular genetics, 2018-01, Vol.11 (1), p.e001966-e001966 [Peer Reviewed Journal]Copyright American Heart Association, Inc. Jan 2018 ;ISSN: 2574-8300 ;ISSN: 1942-325X ;EISSN: 2574-8300 ;EISSN: 1942-3268 ;DOI: 10.1161/CIRCGEN.117.001966 ;PMID: 29874181Full text available |
| 17 |
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Sarcomere mutation-specific expression patterns in human hypertrophic cardiomyopathyCirculation. Cardiovascular genetics, 2014-08, Vol.7 (4), p.434-443 [Peer Reviewed Journal]2014 American Heart Association, Inc. ;ISSN: 1942-325X ;EISSN: 1942-3268 ;DOI: 10.1161/CIRCGENETICS.113.000448 ;PMID: 25031304Full text available |
| 18 |
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Response by Ho et al to Letter Regarding Article, “Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)”Circulation (New York, N.Y.), 2019-03, Vol.139 (12), p.1559-1560 [Peer Reviewed Journal]2019 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.118.039069 ;PMID: 30883221Full text available |
| 19 |
Material Type: Article
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Effects of MYBPC3 loss-of-function mutations preceding hypertrophic cardiomyopathyJCI insight, 2020-01, Vol.5 (2) [Peer Reviewed Journal]2020 American Society for Clinical Investigation 2020 American Society for Clinical Investigation ;ISSN: 2379-3708 ;EISSN: 2379-3708 ;DOI: 10.1172/jci.insight.133782 ;PMID: 31877118Full text available |
| 20 |
Material Type: Article
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Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic CardiomyopathyCirculation. Genomic and precision medicine, 2020-10, Vol.13 (5), p.396-405 [Peer Reviewed Journal]2020 The Authors. 2020 ;ISSN: 2574-8300 ;EISSN: 2574-8300 ;DOI: 10.1161/CIRCGEN.120.002929 ;PMID: 32841044Full text available |
Results 1 - 20 of 49 for All Library Resources
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