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Jill D Siegfried

Showing results (1-10 of 15) with videos related to

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Journal of the American College of Cardiology|April 16, 2011
Update 2011: clinical and genetic issues in familial dilated cardiomyopathyRay E Hershberger, Jill D Siegfried
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2010
Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsRay E Hershberger, Ana Morales, Jill D Siegfried
Clinical and Translational Science|October 28, 2011
Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathyNadine Norton, Jill D Siegfried, Duanxiang Li, et al.
Circulation. Heart Failure|October 8, 2009
Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathyRay E Hershberger, Jason Cowan, Ana Morales, et al.
Progress in Pediatric Cardiology|April 13, 2011
Rare variant mutations identified in pediatric patients with dilated cardiomyopathyEvadnie Rampersaud, Jill D Siegfried, Nadine Norton, et al.
Circulation. Cardiovascular Genetics|March 11, 2010
Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathyRay E Hershberger, Nadine Norton, Ana Morales, et al.
Circulation|May 12, 2010
Rare variant mutations in pregnancy-associated or peripartum cardiomyopathyAna Morales, Thomas Painter, Ran Li, et al.
Clinical and Translational Science|July 2, 2010
Identification of novel mutations in RBM20 in patients with dilated cardiomyopathyDuanxiang Li, Ana Morales, Jorge Gonzalez-Quintana, et al.
Journal of Cardiac Failure|April 16, 2013
Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathyChad Brodt, Jill D Siegfried, Mark Hofmeyer, et al.
Clinical and Translational Science|December 21, 2010
SCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and common splice variant Q1077delJianding Cheng, Ana Morales, Jill D Siegfried, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of the American College of Cardiology|April 16, 2011
Update 2011: clinical and genetic issues in familial dilated cardiomyopathyRay E Hershberger, Jill D Siegfried
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2010
Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsRay E Hershberger, Ana Morales, Jill D Siegfried
Clinical and Translational Science|October 28, 2011
Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathyNadine Norton, Jill D Siegfried, Duanxiang Li, et al.
Circulation. Heart Failure|October 8, 2009
Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathyRay E Hershberger, Jason Cowan, Ana Morales, et al.
Progress in Pediatric Cardiology|April 13, 2011
Rare variant mutations identified in pediatric patients with dilated cardiomyopathyEvadnie Rampersaud, Jill D Siegfried, Nadine Norton, et al.
Circulation. Cardiovascular Genetics|March 11, 2010
Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathyRay E Hershberger, Nadine Norton, Ana Morales, et al.
Circulation|May 12, 2010
Rare variant mutations in pregnancy-associated or peripartum cardiomyopathyAna Morales, Thomas Painter, Ran Li, et al.
Clinical and Translational Science|July 2, 2010
Identification of novel mutations in RBM20 in patients with dilated cardiomyopathyDuanxiang Li, Ana Morales, Jorge Gonzalez-Quintana, et al.
Journal of Cardiac Failure|April 16, 2013
Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathyChad Brodt, Jill D Siegfried, Mark Hofmeyer, et al.
Clinical and Translational Science|December 21, 2010
SCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and common splice variant Q1077delJianding Cheng, Ana Morales, Jill D Siegfried, et al.
Pageof 2