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JAMA Cardiology
|
November 8, 2025
Efficacy of Acoramidis in Wild-Type and Variant Transthyretin Amyloid Cardiomyopathy: Results From ATTRibute-CM and Its Open-Label Extension
Kevin M Alexander, Margot K Davis, Olakunle Akinboboye, et al.
Genome Medicine
|
October 23, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
Katherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Heart Rhythm
|
May 13, 2019
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy
Jeffrey A Towbin, William J McKenna, Dominic J Abrams, et al.
Circulation. Cardiovascular Genetics
|
March 31, 2015
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members
Judith A Groeneweg, Aditya Bhonsale, Cynthia A James, et al.
Heart Rhythm
|
November 3, 2019
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary
Jeffrey A Towbin, William J McKenna, Dominic J Abrams, et al.
Circulation
|
March 20, 2023
Effectiveness of the <i>Family Heart Talk</i> Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial
Daniel D Kinnamon, Elizabeth Jordan, Garrie J Haas, et al.
JAMA
|
February 1, 2022
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy
Gordon S Huggins, Daniel D Kinnamon, Garrie J Haas, et al.
Circulation
|
September 30, 2021
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants
Marta Gigli, Davide Stolfo, Sharon L Graw, et al.
Cardiovascular Research
|
January 11, 2017
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis
Anneline S J M Te Riele, Esperanza Agullo-Pascual, Cynthia A James, et al.
JAMA
|
August 1, 2023
Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry
Elizabeth Jordan, Daniel D Kinnamon, Garrie J Haas, et al.
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of 26
Search research articles
Search
Showing results (241-250 of 260) with videos related to
Sort By:
Page
of 26
JAMA Cardiology
|
November 8, 2025
Efficacy of Acoramidis in Wild-Type and Variant Transthyretin Amyloid Cardiomyopathy: Results From ATTRibute-CM and Its Open-Label Extension
Kevin M Alexander, Margot K Davis, Olakunle Akinboboye, et al.
Genome Medicine
|
October 23, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
Katherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Heart Rhythm
|
May 13, 2019
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy
Jeffrey A Towbin, William J McKenna, Dominic J Abrams, et al.
Circulation. Cardiovascular Genetics
|
March 31, 2015
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members
Judith A Groeneweg, Aditya Bhonsale, Cynthia A James, et al.
Heart Rhythm
|
November 3, 2019
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary
Jeffrey A Towbin, William J McKenna, Dominic J Abrams, et al.
Circulation
|
March 20, 2023
Effectiveness of the <i>Family Heart Talk</i> Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial
Daniel D Kinnamon, Elizabeth Jordan, Garrie J Haas, et al.
JAMA
|
February 1, 2022
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy
Gordon S Huggins, Daniel D Kinnamon, Garrie J Haas, et al.
Circulation
|
September 30, 2021
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants
Marta Gigli, Davide Stolfo, Sharon L Graw, et al.
Cardiovascular Research
|
January 11, 2017
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis
Anneline S J M Te Riele, Esperanza Agullo-Pascual, Cynthia A James, et al.
JAMA
|
August 1, 2023
Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry
Elizabeth Jordan, Daniel D Kinnamon, Garrie J Haas, et al.
Page
of 26