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21
Valsartan in early-stage hypertrophic cardiomyopathy: a randomized phase 2 trial
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Article
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Valsartan in early-stage hypertrophic cardiomyopathy: a randomized phase 2 trial

Nature medicine, 2021-10, Vol.27 (10), p.1818-1824 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to Springer Nature America, Inc. ;COPYRIGHT 2021 Nature Publishing Group ;The Author(s), under exclusive licence to Springer Nature America, Inc. 2021. ;ISSN: 1078-8956 ;EISSN: 1546-170X ;DOI: 10.1038/s41591-021-01505-4 ;PMID: 34556856

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22
Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype
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Article
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Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

British journal of dermatology (1951), 2019-05, Vol.180 (5), p.1114 [Peer Reviewed Journal]

2018 British Association of Dermatologists. ;EISSN: 1365-2133 ;DOI: 10.1111/bjd.17388 ;PMID: 30382575

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23
Discordant clinical features of identical hypertrophic cardiomyopathy twins
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Article
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Discordant clinical features of identical hypertrophic cardiomyopathy twins

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (10), p.1 [Peer Reviewed Journal]

Copyright National Academy of Sciences Mar 9, 2021 ;2021 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2021717118 ;PMID: 33658374

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24
Hypertrophic Cardiomyopathy–Related Sudden Cardiac Death in Young People in Ontario
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Article
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Hypertrophic Cardiomyopathy–Related Sudden Cardiac Death in Young People in Ontario

Circulation (New York, N.Y.), 2019-11, Vol.140 (21), p.1706-1716 [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.119.040271 ;PMID: 31630535

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25
Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy
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Article
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Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy

Journal of cardiovascular magnetic resonance, 2017-12, Vol.19 (1), p.107-107, Article 107 [Peer Reviewed Journal]

COPYRIGHT 2017 BioMed Central Ltd. ;COPYRIGHT 2017 BioMed Central Ltd. ;The Author(s). 2017 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-017-0420-0 ;PMID: 29284499

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26
Clinical Profiles of Hypertrophic Cardiomyopathy With Apical Phenotype: Comparison of Pure-Apical Form and Distal-Dominant Form
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Article
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Clinical Profiles of Hypertrophic Cardiomyopathy With Apical Phenotype: Comparison of Pure-Apical Form and Distal-Dominant Form

Circulation Journal, 2009, Vol.73(12), pp.2330-2336 [Peer Reviewed Journal]

2009 THE JAPANESE CIRCULATION SOCIETY ;ISSN: 1346-9843 ;EISSN: 1347-4820 ;DOI: 10.1253/circj.CJ-09-0438 ;PMID: 19838003

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27
Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene
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Article
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Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene

PloS one, 2016-07, Vol.11 (7), p.e0158730-e0158730 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Toro 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. ;Attribution 4.0 Spain info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/es/ ;2016 Toro et al 2016 Toro et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0158730 ;PMID: 27391596

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28
Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2–Mediated COVID-19
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Article
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Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2–Mediated COVID-19

Mayo Clinic proceedings, 2020-07, Vol.95 (7), p.1354-1368 [Peer Reviewed Journal]

2020 Mayo Foundation for Medical Education and Research ;Copyright © 2020 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved. ;COPYRIGHT 2020 Elsevier, Inc. ;2020 Mayo Foundation for Medical Education and Research. 2020 Mayo Foundation for Medical Education and Research ;ISSN: 0025-6196 ;EISSN: 1942-5546 ;DOI: 10.1016/j.mayocp.2020.04.028 ;PMID: 32448590

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29
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy
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Article
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The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy

Nature communications, 2019-05, Vol.10 (1), p.2267-2267, Article 2267 [Peer Reviewed Journal]

The Author(s) 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. ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-09929-w ;PMID: 31118417

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30
Myocardial Fibrosis as an Early Manifestation of Hypertrophic Cardiomyopathy
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Article
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Myocardial Fibrosis as an Early Manifestation of Hypertrophic Cardiomyopathy

The New England journal of medicine, 2010-08, Vol.363 (6), p.552-563 [Peer Reviewed Journal]

Copyright © 2010 Massachusetts Medical Society. All rights reserved. ;2015 INIST-CNRS ;Copyright © 2010 Massachusetts Medical Society. 2010 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1002659 ;PMID: 20818890 ;CODEN: NEJMAG

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31
Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment
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Article
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Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

Genetics in medicine, 2014-04, Vol.16 (4), p.286-293 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2014. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2013.138 ;PMID: 24113344

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32
Hemodynamic effects of myocardial bridging in patients with hypertrophic cardiomyopathy
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Article
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Hemodynamic effects of myocardial bridging in patients with hypertrophic cardiomyopathy

American journal of physiology. Heart and circulatory physiology, 2019-12, Vol.317 (6), p.H1282-H1291 [Peer Reviewed Journal]

Copyright American Physiological Society Dec 2019 ;ISSN: 0363-6135 ;EISSN: 1522-1539 ;DOI: 10.1152/ajpheart.00466.2019 ;PMID: 31674812

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33
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
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Article
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Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Nature genetics, 2021-02, Vol.53 (2), p.135-142 [Peer Reviewed Journal]

COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2021 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-00764-0 ;PMID: 33495597

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34
Cardiac magnetic resonance detection of myocardial scarring in hypertrophic cardiomyopathy: correlation with histopathology and prevalence of ventricular tachycardia
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Article
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Cardiac magnetic resonance detection of myocardial scarring in hypertrophic cardiomyopathy: correlation with histopathology and prevalence of ventricular tachycardia

Journal of the American College of Cardiology, 2009-07, Vol.54 (3), p.242-249 [Peer Reviewed Journal]

Copyright Elsevier Limited Jul 14, 2009 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2009.04.026 ;PMID: 19589437

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35
MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy
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Article
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MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy

PloS one, 2017-06, Vol.12 (6), p.e0180064-e0180064 [Peer Reviewed Journal]

COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 McNamara 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. ;2017 McNamara et al 2017 McNamara et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0180064 ;PMID: 28658286

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36
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy
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Article
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Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy

PloS one, 2015-04, Vol.10 (4), p.e0121723-e0121723 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Forleo 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. ;2015 Forleo et al 2015 Forleo et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0121723 ;PMID: 25837155

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37
Family screening in black patients with isolated left ventricular non-compaction: the Chris Hani Baragwanath experience
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Article
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Family screening in black patients with isolated left ventricular non-compaction: the Chris Hani Baragwanath experience

Cardiovascular Journal of Africa, 2020-07, Vol.31 (4), p.180-184 [Peer Reviewed Journal]

Copyright © 2020 Clinics Cardive Publishing 2020 ;ISSN: 1995-1892 ;EISSN: 1680-0745 ;DOI: 10.5830/CVJA-2020-003 ;PMID: 32159583

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38
Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy
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Article
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Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy

Journal of the American College of Cardiology, 2019-04, Vol.73 (13), p.1601-1611 [Peer Reviewed Journal]

2019 American College of Cardiology Foundation ;Copyright © 2019 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;2019. American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.12.085 ;PMID: 30947911

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39
Septal Myectomy in Hypertrophic Cardiomyopathy: National Outcomes of Concomitant Mitral Surgery
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Article
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Septal Myectomy in Hypertrophic Cardiomyopathy: National Outcomes of Concomitant Mitral Surgery

Mayo Clinic proceedings, 2019-01, Vol.94 (1), p.66-73 [Peer Reviewed Journal]

2018 Mayo Foundation for Medical Education and Research ;Copyright © 2018 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved. ;COPYRIGHT 2019 Frontline Medical Communications Inc. ;Copyright Mayo Foundation for Medical Education and Research Jan 2019 ;ISSN: 0025-6196 ;EISSN: 1942-5546 ;DOI: 10.1016/j.mayocp.2018.07.022 ;PMID: 30611455

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40
Phenotype and Clinical Outcomes of Titin Cardiomyopathy
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Article
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Phenotype and Clinical Outcomes of Titin Cardiomyopathy

Journal of the American College of Cardiology, 2017-10, Vol.70 (18), p.2264-2274 [Peer Reviewed Journal]

2017 The Authors ;Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Oct 31, 2017 ;2017 The Authors 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2017.08.063 ;PMID: 29073955

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