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JCI Insight|February 8, 2019
Distinct pathological signatures in human cellular models of myotonic dystrophy subtypesEllis Y Kim, David Y Barefield, Andy H Vo, et al.Journal of the American College of Cardiology|February 2, 2010
Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathyNeal K Lakdawala, Lisa Dellefave, Charles S Redwood, et al.Journal of the American Heart Association|May 18, 2024
Reduction of Filamin C Results in Altered Proteostasis, Cardiomyopathy, and ArrhythmiasJoyce C Ohiri, Lisa Dellefave-Castillo, Garima Tomar, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 9, 2022
Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of resultsAlborz Sherafati, Omar Elsekaily, Seyedmohammad Saadatagah, et al.JACC. Advances|July 4, 2025
Cardiologists' Perceptions of Cardiogenetic Testing and ManagementW H Wilson Tang, Quan M Bui, Allison L Cirino, et al.The Journal of Clinical Investigation|May 20, 2024
Susceptibility to innate immune activation in genetically mediated myocarditisDaniel F Selgrade, Dominic E Fullenkamp, Ivana A Chychula, et al.Pageof 3