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1
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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2
Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strain
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Speckle tracking echocardiographic deformation indices in Chagas and idiopathic dilated cardiomyopathy: Incremental prognostic value of longitudinal strain

PloS one, 2019-08, Vol.14 (8), p.e0221028-e0221028 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Santos Junior 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. ;2019 Santos Junior et al 2019 Santos Junior et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0221028 ;PMID: 31437176

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3
MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM
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MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM

Journal of translational medicine, 2018-06, Vol.16 (1), p.161-161, Article 161 [Peer Reviewed Journal]

COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. This work is licensed 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) 2018 ;ISSN: 1479-5876 ;EISSN: 1479-5876 ;DOI: 10.1186/s12967-018-1534-3 ;PMID: 29885652

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4
Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance
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Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance

Journal of the American College of Cardiology, 2017-02, Vol.69 (6), p.661-676 [Peer Reviewed Journal]

2017 ;Published by Elsevier Inc. ;Copyright Elsevier Limited Feb 14, 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.11.051 ;PMID: 28183509

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5
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin
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Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin

PloS one, 2013-12, Vol.8 (12), p.e83403-e83403 [Peer Reviewed Journal]

2013 Sommese 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. ;2013 Sommese et al 2013 Sommese et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0083403 ;PMID: 24367593

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6
Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy
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Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy

Circulation (New York, N.Y.), 2021-11, Vol.144 (21), p.1714-1731 [Peer Reviewed Journal]

ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/circulationaha.121.053575 ;PMID: 34672721

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7
Efficacy of CD34+ Stem Cell Therapy in Nonischemic Dilated Cardiomyopathy Is Absent in Patients With Diabetes but Preserved in Patients With Insulin Resistance
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Efficacy of CD34+ Stem Cell Therapy in Nonischemic Dilated Cardiomyopathy Is Absent in Patients With Diabetes but Preserved in Patients With Insulin Resistance

Stem cells translational medicine, 2016-05, Vol.5 (5), p.632-638 [Peer Reviewed Journal]

2016 AlphaMed Press ;AlphaMed Press. ;Copyright John Wiley & Sons, Inc. May 2016 ;AlphaMed Press 2016 ;ISSN: 2157-6564 ;EISSN: 2157-6580 ;DOI: 10.5966/sctm.2015-0172 ;PMID: 27025690

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8
Phenotype-driven molecular autopsy for sudden cardiac death
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Phenotype-driven molecular autopsy for sudden cardiac death

Clinical 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: 27000522

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9
T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure
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T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure

JACC. Cardiovascular imaging, 2016-01, Vol.9 (1), p.40 [Peer Reviewed Journal]

Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;EISSN: 1876-7591 ;DOI: 10.1016/j.jcmg.2015.12.001 ;PMID: 26762873

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10
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)
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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: 30297972

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11
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy
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Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy

JAMA : the journal of the American Medical Association, 2022-02, Vol.327 (5), p.454 [Peer Reviewed Journal]

EISSN: 1538-3598 ;DOI: 10.1001/jama.2021.24674 ;PMID: 35103767

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12
Vector Flow Mapping in Obstructive Hypertrophic Cardiomyopathy to Assess the Relationship of Early Systolic Left Ventricular Flow and the Mitral Valve
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Vector Flow Mapping in Obstructive Hypertrophic Cardiomyopathy to Assess the Relationship of Early Systolic Left Ventricular Flow and the Mitral Valve

Journal of the American College of Cardiology, 2014-11, Vol.64 (19), p.1984-1995 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2014 American College of Cardiology Foundation ;2015 INIST-CNRS ;Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Nov 11, 2014 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2014.04.090 ;PMID: 25440093 ;CODEN: JACCDI

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13
Natural History and Expansive Clinical Profile of Stress (Tako-Tsubo) Cardiomyopathy
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Natural History and Expansive Clinical Profile of Stress (Tako-Tsubo) Cardiomyopathy

Journal of the American College of Cardiology, 2010-01, Vol.55 (4), p.333-341 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2010 American College of Cardiology Foundation ;Copyright (c) 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Jan 26, 2010 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2009.08.057 ;PMID: 20117439

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14
Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction: Insights From the SHaRe Registry
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Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction: Insights From the SHaRe Registry

Circulation (New York, N.Y.), 2020-04, Vol.141 (17), p.1371-1383 [Peer Reviewed Journal]

2020 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2020 The Authors. 2020 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.119.044366 ;PMID: 32228044

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15
Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI HCM Registry
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Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI HCM Registry

Journal of the American College of Cardiology, 2019-11, Vol.74 (19), p.2333-2345 [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.2019.08.1057 ;PMID: 31699273

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16
Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants
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Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants

The 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: 32480058

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17
Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders
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Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders

Circulation (New York, N.Y.), 2018-06, Vol.137 (25), p.2716-2726 [Peer Reviewed Journal]

2018 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2018 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.117.032175 ;PMID: 29915098

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18
Recommendations for cardiomyopathy surveillance for survivors of childhood cancer: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group
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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 Group

The 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: LANCAO

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19
Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling
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Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling

Scientific reports, 2018-01, Vol.8 (1), p.1998-11, Article 1998 [Peer Reviewed Journal]

2018. 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) 2018 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-20114-9 ;PMID: 29386531

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20
Towards a Paradigm Shift in the Treatment of Chronic Chagas Disease
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Towards a Paradigm Shift in the Treatment of Chronic Chagas Disease

Antimicrobial 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: AACHAX

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