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1 |
Material Type: Article
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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 CardiologyJournal 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: 26542657Full text available |
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2 |
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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3 |
Material Type: Article
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Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variantsThe American heart journal, 2020-07, Vol.225, p.108-119 [Peer Reviewed Journal]2020 The Author(s) ;Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved. ;2020. The Author(s) ;ISSN: 0002-8703 ;EISSN: 1097-6744 ;DOI: 10.1016/j.ahj.2020.03.023 ;PMID: 32480058Full text available |
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4 |
Material Type: Article
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Presence and utility of electrocardiographic abnormalities in long-term childhood cancer survivorsHeart (British Cardiac Society), 2024-05, Vol.110 (10), p.726-734 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2024 ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2023-323474 ;PMID: 38503487Digital Resources/Online E-Resources |
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5 |
Material Type: Article
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Towards a Paradigm Shift in the Treatment of Chronic Chagas DiseaseAntimicrobial Agents and Chemotherapy, 2014-02, Vol.58 (2), p.635-639 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright © 2014, American Society for Microbiology. All Rights Reserved. ;Copyright © 2014, American Society for Microbiology. All Rights Reserved. 2014 American Society for Microbiology ;ISSN: 0066-4804 ;EISSN: 1098-6596 ;DOI: 10.1128/AAC.01662-13 ;PMID: 24247135 ;CODEN: AACHAXFull text available |
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6 |
Material Type: Article
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Recommendations for cardiomyopathy surveillance for survivors of childhood cancer: a report from the International Late Effects of Childhood Cancer Guideline Harmonization GroupThe lancet oncology, 2015-03, Vol.16 (3), p.e123-e136 [Peer Reviewed Journal]Elsevier Ltd ;2015 Elsevier Ltd ;Copyright © 2015 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited Mar 2015 ;2015 Elsevier Ltd. All rights reserved. Elsevier Ltd. All rights reserved. 2015 ;ISSN: 1470-2045 ;EISSN: 1474-5488 ;DOI: 10.1016/S1470-2045(14)70409-7 ;PMID: 25752563 ;CODEN: LANCAOFull text available |
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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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8 |
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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9 |
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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10 |
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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11 |
Material Type: Article
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Gap junction protein beta 4 plays an important role in cardiac function in humans, rodents, and zebrafishPloS one, 2020-10, Vol.15 (10), p.e0240129 [Peer Reviewed Journal]COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Okamoto 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 Okamoto et al 2020 Okamoto et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0240129 ;PMID: 33048975Full text available |
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12 |
Material Type: Article
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Contemporary Outcomes of Pediatric Restrictive Cardiomyopathy: A Single-Center ExperiencePediatric cardiology, 2019-04, Vol.40 (4), p.694 [Peer Reviewed Journal]EISSN: 1432-1971 ;DOI: 10.1007/s00246-018-2043-0 ;PMID: 30542921Digital Resources/Online E-Resources |
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13 |
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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14 |
Material Type: Article
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Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe RegistryCirculation (New York, N.Y.), 2023-08, Vol.148 (5), p.394-404 [Peer Reviewed Journal]2023 The Authors. 2023 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.122.062517 ;PMID: 37226762Digital Resources/Online E-Resources |
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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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Acute catecholamine cardiomyopathy in patients with phaeochromocytoma or functional paragangliomaHeart (British Cardiac Society), 2013-10, Vol.99 (19), p.1438-1444 [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 ;Copyright: 2013 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-2013-304073 ;PMID: 23837998Full text available |
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18 |
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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19 |
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 |
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20 |
Material Type: Article
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Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation CarriersJournal of the American College of Cardiology, 2020-08, Vol.76 (5), p.550-559 [Peer Reviewed Journal]2020 The Authors ;Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved. ;COPYRIGHT 2020 Elsevier B.V. ;2020 The Authors 2020 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2020.06.011 ;PMID: 32731933Full text available |