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British Journal of Sports Medicine
|
January 11, 2013
Abnormal electrocardiographic findings in athletes: recognising changes suggestive of cardiomyopathy
Jonathan A Drezner, Euan Ashley, Aaron L Baggish, et al.
Circulation
|
November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function
Stephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.
Communications Medicine
|
May 23, 2022
Implementation of a fully remote randomized clinical trial with cardiac monitoring
Jacob J Mayfield, Neal A Chatterjee, Peter A Noseworthy, et al.
Open Heart
|
June 28, 2019
Heritability in genetic heart disease: the role of genetic background
Joeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Circulation
|
August 28, 2016
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study
Arthur A M Wilde, Arthur J Moss, Elizabeth S Kaufman, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 21, 2013
Autotaxin production of lysophosphatidic acid mediates allergic asthmatic inflammation
Gye Young Park, Yong Gyu Lee, Evgeny Berdyshev, et al.
Heart Rhythm
|
December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndrome
Christian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Human Molecular Genetics
|
January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations
Enkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
Nature Genetics
|
July 3, 2007
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
Bhaswati Pandit, Anna Sarkozy, Len A Pennacchio, et al.
Journal of the American College of Cardiology
|
March 19, 2013
Prevention of sudden cardiac death with implantable cardioverter-defibrillators in children and adolescents with hypertrophic cardiomyopathy
Barry J Maron, Paolo Spirito, Michael J Ackerman, et al.
Page
of 114
Search research articles
Search
Showing results (1071-1080 of 1,140) with videos related to
Sort By:
Page
of 114
British Journal of Sports Medicine
|
January 11, 2013
Abnormal electrocardiographic findings in athletes: recognising changes suggestive of cardiomyopathy
Jonathan A Drezner, Euan Ashley, Aaron L Baggish, et al.
Circulation
|
November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function
Stephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.
Communications Medicine
|
May 23, 2022
Implementation of a fully remote randomized clinical trial with cardiac monitoring
Jacob J Mayfield, Neal A Chatterjee, Peter A Noseworthy, et al.
Open Heart
|
June 28, 2019
Heritability in genetic heart disease: the role of genetic background
Joeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Circulation
|
August 28, 2016
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study
Arthur A M Wilde, Arthur J Moss, Elizabeth S Kaufman, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 21, 2013
Autotaxin production of lysophosphatidic acid mediates allergic asthmatic inflammation
Gye Young Park, Yong Gyu Lee, Evgeny Berdyshev, et al.
Heart Rhythm
|
December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndrome
Christian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Human Molecular Genetics
|
January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations
Enkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
Nature Genetics
|
July 3, 2007
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
Bhaswati Pandit, Anna Sarkozy, Len A Pennacchio, et al.
Journal of the American College of Cardiology
|
March 19, 2013
Prevention of sudden cardiac death with implantable cardioverter-defibrillators in children and adolescents with hypertrophic cardiomyopathy
Barry J Maron, Paolo Spirito, Michael J Ackerman, et al.
Page
of 114