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Molecular Genetics and Metabolism
|
February 6, 2022
Early clinical phenotype of late onset Pompe disease: Lessons learned from newborn screening
Erin Huggins, Maggie Holland, Laura E Case, et al.
Journal of the American Heart Association
|
September 21, 2022
Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes
Qixin Yang, Amy M Berkman, Jordan E Ezekian, et al.
Journal of Cardiovascular Translational Research
|
February 11, 2014
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise
Jamie D Kapplinger, Andrew P Landstrom, J Martijn Bos, et al.
The Journal of Biological Chemistry
|
July 21, 2012
A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation
Michelle S Parvatiyar, Andrew P Landstrom, Cicero Figueiredo-Freitas, et al.
Advances in Medical Sciences
|
January 2, 2021
Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies
Isela C Valera, Amanda L Wacker, Hyun Seok Hwang, et al.
Clinical Case Reports
|
January 19, 2019
A 14-year-old in heart failure with multiple cardiomyopathy variants illustrates a role for signal-to-noise analysis in gene test re-interpretation
Patrick S Connell, Aamir Jeewa, Debra L Kearney, et al.
Physiological Genomics
|
March 26, 2009
Molecular evolution of the junctophilin gene family
Alejandro Garbino, Ralph J van Oort, Sayali S Dixit, et al.
Journal of Adolescent and Young Adult Oncology
|
January 23, 2024
Cardiovascular Disease in Childhood, Adolescent, and Young Adult Cancer Survivors: The Impact of Family History of Premature Heart Disease
Amy M Berkman, Clark R Andersen, Andrew P Landstrom, et al.
Scientific Reports
|
May 17, 2022
BRG1 is a biomarker of hypertrophic cardiomyopathy in human heart specimens
Jacob C Scherba, Marc K Halushka, Nicholas D Andersen, et al.
Journal of Cardiac Failure
|
September 2, 2023
LMNA Cardiomyopathy: Important Considerations for the Heart Failure Clinician
Karen Flores Rosario, Ravi Karra, Kaitlyn Amos, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 113) with videos related to
Sort By:
Page
of 12
Molecular Genetics and Metabolism
|
February 6, 2022
Early clinical phenotype of late onset Pompe disease: Lessons learned from newborn screening
Erin Huggins, Maggie Holland, Laura E Case, et al.
Journal of the American Heart Association
|
September 21, 2022
Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes
Qixin Yang, Amy M Berkman, Jordan E Ezekian, et al.
Journal of Cardiovascular Translational Research
|
February 11, 2014
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise
Jamie D Kapplinger, Andrew P Landstrom, J Martijn Bos, et al.
The Journal of Biological Chemistry
|
July 21, 2012
A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation
Michelle S Parvatiyar, Andrew P Landstrom, Cicero Figueiredo-Freitas, et al.
Advances in Medical Sciences
|
January 2, 2021
Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies
Isela C Valera, Amanda L Wacker, Hyun Seok Hwang, et al.
Clinical Case Reports
|
January 19, 2019
A 14-year-old in heart failure with multiple cardiomyopathy variants illustrates a role for signal-to-noise analysis in gene test re-interpretation
Patrick S Connell, Aamir Jeewa, Debra L Kearney, et al.
Physiological Genomics
|
March 26, 2009
Molecular evolution of the junctophilin gene family
Alejandro Garbino, Ralph J van Oort, Sayali S Dixit, et al.
Journal of Adolescent and Young Adult Oncology
|
January 23, 2024
Cardiovascular Disease in Childhood, Adolescent, and Young Adult Cancer Survivors: The Impact of Family History of Premature Heart Disease
Amy M Berkman, Clark R Andersen, Andrew P Landstrom, et al.
Scientific Reports
|
May 17, 2022
BRG1 is a biomarker of hypertrophic cardiomyopathy in human heart specimens
Jacob C Scherba, Marc K Halushka, Nicholas D Andersen, et al.
Journal of Cardiac Failure
|
September 2, 2023
LMNA Cardiomyopathy: Important Considerations for the Heart Failure Clinician
Karen Flores Rosario, Ravi Karra, Kaitlyn Amos, et al.
Page
of 12