Search research articles
Contact Us
Filters
Showing results (121-130 of 147) with videos related to
Page
of 15
Sort By:
Frontiers in Genetics
|
November 4, 2024
Case Report: An association of left ventricular outflow tract obstruction with 5p deletions
Kira Mascho, Svetlana A Yatsenko, Cecilia W Lo, et al.
Circulation. Heart Failure
|
December 5, 2025
Cardiomyopathy-Associated Pathogenic Variants in Pediatric Myocarditis: A Study From the Pediatric Cardiomyopathy Registry
Alicia M Kamsheh, Stephanie M Ware, Surbhi Bhatnagar, et al.
Orphanet Journal of Rare Diseases
|
September 9, 2022
A multi-disciplinary, comprehensive approach to management of children with heterotaxy
Thomas G Saba, Gabrielle C Geddes, Stephanie M Ware, et al.
Circulation. Heart Failure
|
February 15, 2017
Differences in Presentation and Outcomes Between Children With Familial Dilated Cardiomyopathy and Children With Idiopathic Dilated Cardiomyopathy: A Report From the Pediatric Cardiomyopathy Registry Study Group
Paolo Rusconi, James D Wilkinson, Lynn A Sleeper, et al.
Genetics in Medicine Open
|
December 13, 2024
A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices
Matthew D Durbin, Lindsey R Helvaty, Ming Li, et al.
The Journal of Allergy and Clinical Immunology
|
April 24, 2013
High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders
J Pablo Abonia, Ting Wen, Emily M Stucke, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Mark D Levin, Sulagna C Saitta, Karen W Gripp, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2021
Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents
Priyanka Ahimaz, Maya Sabatello, Min Qian, et al.
Plos Genetics
|
February 27, 2016
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
You Li, Hisato Yagi, Ezenwa Obi Onuoha, et al.
Journal of the American Heart Association
|
September 8, 2023
A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease
Benjamin J Landis, Lindsey R Helvaty, Gabrielle C Geddes, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 147) with videos related to
Sort By:
Page
of 15
Frontiers in Genetics
|
November 4, 2024
Case Report: An association of left ventricular outflow tract obstruction with 5p deletions
Kira Mascho, Svetlana A Yatsenko, Cecilia W Lo, et al.
Circulation. Heart Failure
|
December 5, 2025
Cardiomyopathy-Associated Pathogenic Variants in Pediatric Myocarditis: A Study From the Pediatric Cardiomyopathy Registry
Alicia M Kamsheh, Stephanie M Ware, Surbhi Bhatnagar, et al.
Orphanet Journal of Rare Diseases
|
September 9, 2022
A multi-disciplinary, comprehensive approach to management of children with heterotaxy
Thomas G Saba, Gabrielle C Geddes, Stephanie M Ware, et al.
Circulation. Heart Failure
|
February 15, 2017
Differences in Presentation and Outcomes Between Children With Familial Dilated Cardiomyopathy and Children With Idiopathic Dilated Cardiomyopathy: A Report From the Pediatric Cardiomyopathy Registry Study Group
Paolo Rusconi, James D Wilkinson, Lynn A Sleeper, et al.
Genetics in Medicine Open
|
December 13, 2024
A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices
Matthew D Durbin, Lindsey R Helvaty, Ming Li, et al.
The Journal of Allergy and Clinical Immunology
|
April 24, 2013
High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders
J Pablo Abonia, Ting Wen, Emily M Stucke, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Mark D Levin, Sulagna C Saitta, Karen W Gripp, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2021
Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents
Priyanka Ahimaz, Maya Sabatello, Min Qian, et al.
Plos Genetics
|
February 27, 2016
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
You Li, Hisato Yagi, Ezenwa Obi Onuoha, et al.
Journal of the American Heart Association
|
September 8, 2023
A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease
Benjamin J Landis, Lindsey R Helvaty, Gabrielle C Geddes, et al.
Page
of 15