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E Seidman

Showing results (331-340 of 533) with videos related to

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Circulation. Cardiovascular Genetics|September 6, 2012
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathyNeal K Lakdawala, Jens J Thune, Steven D Colan, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 29, 2024
Predictive modeling of endocardial fibroelastosis recurrence in patients with congenital heart diseaseDaniel Diaz-Gil, Natalia Silva-Gomez, Sarah U Morton, et al.
The New England Journal of Medicine|January 28, 2005
Glycogen storage diseases presenting as hypertrophic cardiomyopathyMichael Arad, Barry J Maron, Joshua M Gorham, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in <i>LMNA</i> and <i>MYBPC3</i> that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
Circulation Research|June 28, 2017
Fundamental Cardiovascular Research: Returns on Societal Investment: A Scientific Statement From the American Heart AssociationJoseph A Hill, Reza Ardehali, Kimberli Taylor Clarke, et al.
International Journal of Molecular Sciences|March 11, 2023
Multi-Omics Profiling of Hypertrophic Cardiomyopathy Reveals Altered Mechanisms in Mitochondrial Dynamics and Excitation-Contraction CouplingJarrod Moore, Jourdan Ewoldt, Gabriela Venturini, et al.
Cell|July 3, 2007
A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system developmentIvan P G Moskowitz, Jae B Kim, Meredith L Moore, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 20, 2019
Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart DiseaseSarah U Morton, Lara Maleyeff, David Wypij, et al.
JAMA|March 26, 2009
Clinical outcome and phenotypic expression in LAMP2 cardiomyopathyBarry J Maron, William C Roberts, Michael Arad, et al.
Human Mutation|June 19, 2013
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing lossKerry K Brown, Lucas M Viana, Cecilia C Helwig, et al.
Pageof 54

Showing results (331-340 of 533) with videos related to

Sort By:
Pageof 54
Circulation. Cardiovascular Genetics|September 6, 2012
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathyNeal K Lakdawala, Jens J Thune, Steven D Colan, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 29, 2024
Predictive modeling of endocardial fibroelastosis recurrence in patients with congenital heart diseaseDaniel Diaz-Gil, Natalia Silva-Gomez, Sarah U Morton, et al.
The New England Journal of Medicine|January 28, 2005
Glycogen storage diseases presenting as hypertrophic cardiomyopathyMichael Arad, Barry J Maron, Joshua M Gorham, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in <i>LMNA</i> and <i>MYBPC3</i> that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
Circulation Research|June 28, 2017
Fundamental Cardiovascular Research: Returns on Societal Investment: A Scientific Statement From the American Heart AssociationJoseph A Hill, Reza Ardehali, Kimberli Taylor Clarke, et al.
International Journal of Molecular Sciences|March 11, 2023
Multi-Omics Profiling of Hypertrophic Cardiomyopathy Reveals Altered Mechanisms in Mitochondrial Dynamics and Excitation-Contraction CouplingJarrod Moore, Jourdan Ewoldt, Gabriela Venturini, et al.
Cell|July 3, 2007
A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system developmentIvan P G Moskowitz, Jae B Kim, Meredith L Moore, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 20, 2019
Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart DiseaseSarah U Morton, Lara Maleyeff, David Wypij, et al.
JAMA|March 26, 2009
Clinical outcome and phenotypic expression in LAMP2 cardiomyopathyBarry J Maron, William C Roberts, Michael Arad, et al.
Human Mutation|June 19, 2013
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing lossKerry K Brown, Lucas M Viana, Cecilia C Helwig, et al.
Pageof 54