Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Phenotype-driven molecular autopsy for sudden cardiac deathClinical 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: 27000522Digital Resources/Online E-Resources |
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2 |
Material Type: Article
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NGS testing for cardiomyopathy: Utility of adding RASopathy‐associated genesHuman mutation, 2018-07, Vol.39 (7), p.954-958 [Peer Reviewed Journal]2018 Wiley Periodicals, Inc. ;Copyright © 2018 Wiley Periodicals, Inc. ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.23535 ;PMID: 29696744Digital Resources/Online E-Resources |
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3 |
Material Type: Article
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Hypertrophic Cardiomyopathy With Left Ventricular Apical Aneurysm: Implications for Risk Stratification and ManagementJournal of the American College of Cardiology, 2017-02, Vol.69 (7), p.761-773 [Peer Reviewed Journal]Copyright © 2017 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Feb 21, 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.11.063 ;PMID: 28209216Full text available |
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4 |
Material Type: Article
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Clinical Profile and Consequences of Atrial Fibrillation in Hypertrophic CardiomyopathyCirculation (New York, N.Y.), 2017-12, Vol.136 (25), p.2420-2436 [Peer Reviewed Journal]2017 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2017 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.117.029267 ;PMID: 28916640Full text available |
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5 |
Material Type: Article
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An assessment of the role of vinculin loss of function variants in inherited cardiomyopathyHuman mutation, 2020-09, Vol.41 (9), p.1577-1587 [Peer Reviewed Journal]2020 Wiley Periodicals LLC ;2020 Wiley Periodicals LLC. ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.24061 ;PMID: 32516855Digital Resources/Online E-Resources |
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6 |
Material Type: Article
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Low-grade inflammation and the phenotypic expression of myocardial fibrosis in hypertrophic cardiomyopathyHeart (British Cardiac Society), 2012-07, Vol.98 (13), p.1007-1013 [Peer Reviewed Journal]2012, 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. ;2015 INIST-CNRS ;Copyright: 2012 (c) 2012, 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. ;2012, 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. 2012 ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2011-300960 ;PMID: 22447464Full text available |
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7 |
Material Type: Article
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Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic CardiomyopathiesJournal of the American College of Cardiology, 2016-12, Vol.68 (22), p.2440-2451 [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 Dec 6, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.09.927 ;PMID: 27908349Full text available |
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8 |
Material Type: Article
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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) MutationsJournal of the American College of Cardiology, 2018-11, Vol.72 (20), p.2471-2481 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright © 2018 American College of Cardiology Foundation. All rights reserved. ;Copyright Elsevier Limited Nov 13, 2018 ;Distributed under a Creative Commons Attribution 4.0 International License ;2018 Elsevier Inc. All rights reserved. 2018 American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.08.2181 ;PMID: 30442290Full text available |
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9 |
Material Type: Article
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Significance of High-Sensitivity Cardiac Troponin T in Hypertrophic CardiomyopathyJournal of the American College of Cardiology, 2013-10, Vol.62 (14), p.1252-1259 [Peer Reviewed Journal]American College of Cardiology Foundation ;2013 American College of Cardiology Foundation ;2014 INIST-CNRS ;Copyright © 2013 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Oct 1, 2013 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2013.03.055 ;PMID: 23623916 ;CODEN: JACCDIFull text available |
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10 |
Material Type: Article
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Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological studyHeart (British Cardiac Society), 2011-11, Vol.97 (21), p.1744-1752 [Peer Reviewed Journal]2011, 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. ;2015 INIST-CNRS ;Copyright: 2011 (c) 2011, 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/hrt.2011.227967 ;PMID: 21859740Full text available |
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11 |
Material Type: Article
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T1 measurements identify extracellular volume expansion in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophyCirculation. Cardiovascular imaging, 2013-05, Vol.6 (3), p.415-422 [Peer Reviewed Journal]ISSN: 1941-9651 ;EISSN: 1942-0080 ;DOI: 10.1161/CIRCIMAGING.112.000333 ;PMID: 23549607Full text available |
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12 |
Material Type: Article
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Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivityGenetics in medicine, 2015-11, Vol.17 (11), p.880-888 [Peer Reviewed Journal]Copyright Nature Publishing Group Nov 2015 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2014.205 ;PMID: 25611685Full text available |
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13 |
Material Type: Article
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WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signalingNature communications, 2019-08, Vol.10 (1), p.3616-19, Article 3616 [Peer Reviewed Journal]2019. 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. ;Attribution ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-11551-9 ;PMID: 31399586Full text available |
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14 |
Material Type: Article
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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic CardiomyopathyJournal of the American College of Cardiology, 2018-11, Vol.72 (20), p.2457-2467 [Peer Reviewed Journal]2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Nov 13, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.10.001 ;PMID: 30442288Full text available |
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15 |
Material Type: Article
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Outcomes of Contemporary Family Screening in Hypertrophic CardiomyopathyCirculation. Cardiovascular genetics, 2018-04, Vol.11 (4), p.e001896-e001896 [Peer Reviewed Journal]2018 American Heart Association, Inc. ;Copyright American Heart Association, Inc. Apr 2018 ;ISSN: 2574-8300 ;ISSN: 1942-325X ;EISSN: 2574-8300 ;EISSN: 1942-3268 ;DOI: 10.1161/circgen.117.001896 ;PMID: 29661763Full text available |
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16 |
Material Type: Article
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Hypertrophic Cardiomyopathy Phenotype Revisited After 50 Years With Cardiovascular Magnetic ResonanceJournal of the American College of Cardiology, 2009-07, Vol.54 (3), p.220-228 [Peer Reviewed Journal]American College of Cardiology Foundation ;2009 American College of Cardiology Foundation ;Copyright Elsevier Limited Jul 14, 2009 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2009.05.006 ;PMID: 19589434Full text available |
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17 |
Material Type: Article
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Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathyHeart (British Cardiac Society), 2015-02, Vol.101 (4), p.294-301 [Peer Reviewed Journal]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 ;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: 2015 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 ;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 2015 ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2014-306387 ;PMID: 25351510Full text available |
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18 |
Material Type: Article
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Mutations in FLNC are Associated with Familial Restrictive CardiomyopathyHuman mutation, 2016-03, Vol.37 (3), p.269-279 [Peer Reviewed Journal]2015 WILEY PERIODICALS, INC. ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.22942 ;PMID: 26666891Full text available |
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19 |
Material Type: Article
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Direct comparison of the diagnostic capability of cardiac magnetic resonance and endomyocardial biopsy in patients with heart failureEuropean journal of heart failure, 2013-02, Vol.15 (2), p.166-175 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © 2013 the Authors ;ISSN: 1388-9842 ;EISSN: 1879-0844 ;DOI: 10.1093/eurjhf/hfs206 ;PMID: 23329703Full text available |
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20 |
Material Type: Article
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Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM systemInternational journal of molecular medicine, 2016-06, Vol.37 (6), p.1511-1520 [Peer Reviewed Journal]Copyright: © Zhao et al. ;COPYRIGHT 2016 Spandidos Publications ;Copyright: © Zhao et al. 2016 ;ISSN: 1107-3756 ;EISSN: 1791-244X ;DOI: 10.3892/ijmm.2016.2565 ;PMID: 27082122Full text available |