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Circulation
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July 1, 2018
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome
S Mohsen Hosseini, Raymond Kim, Sharmila Udupa, et al.
European Heart Journal
|
September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
Roddy Walsh, Arnon Adler, Ahmad S Amin, et al.
European Journal of Heart Failure
|
February 15, 2020
Predictors of left ventricular remodelling in patients with dilated cardiomyopathy - a cardiovascular magnetic resonance study
Upasana Tayal, Ricardo Wage, Simon Newsome, et al.
Cold Spring Harbor Molecular Case Studies
|
January 5, 2017
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>
Gillian Rea, Tessa Homfray, Jan Till, et al.
BMC Cardiovascular Disorders
|
July 25, 2019
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
Hariharan Raju, James S Ware, Jonathan R Skinner, et al.
Journal of the American College of Cardiology
|
September 1, 2024
Arrhythmic Risk Stratification by Cardiovascular Magnetic Resonance Imaging in Patients With Nonischemic Cardiomyopathy
Daniel J Hammersley, Abbasin Zegard, Emmanuel Androulakis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2021
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation
Andrea D Thompson, Adam S Helms, Anamika Kannan, et al.
Nature Communications
|
August 21, 2023
Environmental and genetic predictors of human cardiovascular ageing
Mit Shah, Marco H de A Inácio, Chang Lu, et al.
Circulation
|
February 1, 2019
Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Chris Miles, Gherardo Finocchiaro, Michael Papadakis, et al.
Nature Communications
|
September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart disease
David M McKean, Jason Homsy, Hiroko Wakimoto, et al.
Page
of 73
Search research articles
Search
Showing results (591-600 of 721) with videos related to
Sort By:
Page
of 73
Circulation
|
July 1, 2018
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome
S Mohsen Hosseini, Raymond Kim, Sharmila Udupa, et al.
European Heart Journal
|
September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
Roddy Walsh, Arnon Adler, Ahmad S Amin, et al.
European Journal of Heart Failure
|
February 15, 2020
Predictors of left ventricular remodelling in patients with dilated cardiomyopathy - a cardiovascular magnetic resonance study
Upasana Tayal, Ricardo Wage, Simon Newsome, et al.
Cold Spring Harbor Molecular Case Studies
|
January 5, 2017
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>
Gillian Rea, Tessa Homfray, Jan Till, et al.
BMC Cardiovascular Disorders
|
July 25, 2019
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
Hariharan Raju, James S Ware, Jonathan R Skinner, et al.
Journal of the American College of Cardiology
|
September 1, 2024
Arrhythmic Risk Stratification by Cardiovascular Magnetic Resonance Imaging in Patients With Nonischemic Cardiomyopathy
Daniel J Hammersley, Abbasin Zegard, Emmanuel Androulakis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2021
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation
Andrea D Thompson, Adam S Helms, Anamika Kannan, et al.
Nature Communications
|
August 21, 2023
Environmental and genetic predictors of human cardiovascular ageing
Mit Shah, Marco H de A Inácio, Chang Lu, et al.
Circulation
|
February 1, 2019
Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Chris Miles, Gherardo Finocchiaro, Michael Papadakis, et al.
Nature Communications
|
September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart disease
David M McKean, Jason Homsy, Hiroko Wakimoto, et al.
Page
of 73