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Debra L Kearney

Showing results (31-40 of 37) with videos related to

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Journal of the American College of Cardiology|October 19, 2010
Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosisEnkhsaikhan Purevjav, Jaquelin Varela, Micaela Morgado, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysisSirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, et al.
Journal of the American College of Cardiology|August 7, 2010
Viral endomyocardial infection is an independent predictor and potentially treatable risk factor for graft loss and coronary vasculopathy in pediatric cardiac transplant recipientsMousumi Moulik, John P Breinholt, William J Dreyer, et al.
Circulation Research|August 19, 2006
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathyZhao Yang, Neil E Bowles, Steven E Scherer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2006
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathyPrince J Kannankeril, Brett M Mitchell, Sanjeewa A Goonasekera, et al.
Circulation|September 8, 2005
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in childrenZhao Yang, Colin J McMahon, Liana R Smith, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Journal of the American College of Cardiology|October 19, 2010
Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosisEnkhsaikhan Purevjav, Jaquelin Varela, Micaela Morgado, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysisSirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, et al.
Journal of the American College of Cardiology|August 7, 2010
Viral endomyocardial infection is an independent predictor and potentially treatable risk factor for graft loss and coronary vasculopathy in pediatric cardiac transplant recipientsMousumi Moulik, John P Breinholt, William J Dreyer, et al.
Circulation Research|August 19, 2006
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathyZhao Yang, Neil E Bowles, Steven E Scherer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2006
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathyPrince J Kannankeril, Brett M Mitchell, Sanjeewa A Goonasekera, et al.
Circulation|September 8, 2005
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in childrenZhao Yang, Colin J McMahon, Liana R Smith, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
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