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Journal of the American Heart Association
|
November 4, 2024
Clinical Features and Outcomes of Pediatric <i>MYH7</i>-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Gregory Webster, et al.
Open Heart
|
November 24, 2024
Hypertrophic cardiomyopathy due to truncating variants in myosin binding protein C: a Spanish cohort
Maria Melendo-Viu, Rafael Salguero-Bodes, María Valverde-Gómez, et al.
Circulation. Heart Failure
|
September 23, 2020
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the <i>TTN</i> Gene
Mohammed Majid Akhtar, Massimiliano Lorenzini, Marcos Cicerchia, et al.
Journal of the American College of Cardiology
|
September 15, 2022
Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy
Luis Escobar-Lopez, Juan Pablo Ochoa, Ana Royuela, et al.
Journal of the American College of Cardiology
|
August 25, 2022
Natural History of MYH7-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Marina Navarro-Peñalver, et al.
JAMA Cardiology
|
May 12, 2021
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure
Mohammed Majid Akhtar, Massimiliano Lorenzini, Menelaos Pavlou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Nature Genetics
|
February 25, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Julien Barc, Rafik Tadros, Charlotte Glinge, et al.
Nature Genetics
|
April 27, 2022
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Julien Barc, Rafik Tadros, Charlotte Glinge, et al.
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Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 19 results.
Journal of the American Heart Association
|
November 4, 2024
Clinical Features and Outcomes of Pediatric <i>MYH7</i>-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Gregory Webster, et al.
Open Heart
|
November 24, 2024
Hypertrophic cardiomyopathy due to truncating variants in myosin binding protein C: a Spanish cohort
Maria Melendo-Viu, Rafael Salguero-Bodes, María Valverde-Gómez, et al.
Circulation. Heart Failure
|
September 23, 2020
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the <i>TTN</i> Gene
Mohammed Majid Akhtar, Massimiliano Lorenzini, Marcos Cicerchia, et al.
Journal of the American College of Cardiology
|
September 15, 2022
Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy
Luis Escobar-Lopez, Juan Pablo Ochoa, Ana Royuela, et al.
Journal of the American College of Cardiology
|
August 25, 2022
Natural History of MYH7-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Marina Navarro-Peñalver, et al.
JAMA Cardiology
|
May 12, 2021
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure
Mohammed Majid Akhtar, Massimiliano Lorenzini, Menelaos Pavlou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Nature Genetics
|
February 25, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Julien Barc, Rafik Tadros, Charlotte Glinge, et al.
Nature Genetics
|
April 27, 2022
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Julien Barc, Rafik Tadros, Charlotte Glinge, et al.
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of 2