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Circulation|May 7, 2020
Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular CardiomyopathyEric D Smith, Neal K Lakdawala, Nikolaos Papoutsidakis, et al.JAMA Cardiology|August 11, 2021
Genomic Autopsy of Sudden Deaths in Young IndividualsGregory Webster, Megan J Puckelwartz, Lorenzo L Pesce, et al.Journal of the American Heart Association|March 25, 2021
Genomic Context Differs Between Human Dilated Cardiomyopathy and Hypertrophic CardiomyopathyMegan J Puckelwartz, Lorenzo L Pesce, Lisa M Dellefave-Castillo, et al.Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.Genome Medicine|January 16, 2024
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.European Heart Journal|August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onsetRenee Johnson, Robert A Fletcher, Stacey Peters, et al.Pageof 2