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Journal of the American Heart Association|December 11, 2025
Polygenic Risk Scores for Preeclampsia Prediction Beyond Gold-Standard Clinical Models in Multiethnic PopulationsMaddalena Ardissino, Kypros Nicolaides, Frances Conti-Ramsden, et al.
Journal of Medical Genetics|August 6, 2026
The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testingSian Ellard, Helen Hanson, Emma-Jane Cassidy, et al.
JACC. Clinical Electrophysiology|February 19, 2021
Late-Gadolinium Enhancement Interface Area and Electrophysiological Simulations Predict Arrhythmic Events in Patients With Nonischemic Dilated CardiomyopathyGabriel Balaban, Brian P Halliday, Bradley Porter, et al.
European Journal of Heart Failure|September 30, 2024
Long-term follow-up of the TRED-HF trial: Implications for therapy in patients with dilated cardiomyopathy and heart failure remissionLeanne Cheng, Daniel Hammersley, Aaraby Ragavan, et al.
PLOS Digital Health|February 25, 2026
AI-ECG classification for Brugada syndrome: A study of machine learning techniques to optimise for limited datasetsKeenan Saleh, Raaif Hadadi, Yixiu Liang, et al.
Circulation|October 2, 2024
Long-Term Outcomes After Septal Reduction Therapies in Obstructive Hypertrophic Cardiomyopathy: Insights From the SHARE RegistryNiccolò Maurizi, Panagiotis Antiochos, Anjali Owens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHDAlice Garrett, Chey Loveday, Laura King, et al.
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