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The Journal of Thoracic and Cardiovascular Surgery
|
June 1, 2022
Validation of donor fraction cell-free DNA with biopsy-proven cardiac allograft rejection in children and adults
Marc E Richmond, Shriprasad R Deshpande, Steven D Zangwill, et al.
Clinical Transplantation
|
October 14, 2021
Increase in nuclear cell-free DNA is associated with major adverse events in adult and pediatric heart transplant recipients
Steven D Zangwill, Shriprasad R Deshpande, Pippa M Simpson, et al.
Pediatric Transplantation
|
March 8, 2022
Relationship between donor fraction cell-free DNA and clinical rejection in heart transplantation
Shriprasad R Deshpande, Steven D Zangwill, Steven J Kindel, et al.
Journal of the American College of Cardiology
|
September 27, 2023
Outcomes After Hybrid Palliation for Infants With Critical Left Heart Obstruction
Madison B Argo, David J Barron, Pirooz Eghtesady, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
February 21, 2023
Norwood operation versus comprehensive stage II after bilateral pulmonary artery banding palliation for infants with critical left heart obstruction
Madison B Argo, David J Barron, Pirooz Eghtesady, et al.
Plos Genetics
|
September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Plos Genetics
|
July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Circulation. Cardiovascular Genetics
|
October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3
Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome
Jhih-Rong Lin, Daniella Miller, Dana Luong, et al.
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of 16
Search research articles
Search
Showing results (151-160 of 159) with videos related to
Sort By:
Page
of 16
You have reached the last page of results.
This site can display upto 159 results.
The Journal of Thoracic and Cardiovascular Surgery
|
June 1, 2022
Validation of donor fraction cell-free DNA with biopsy-proven cardiac allograft rejection in children and adults
Marc E Richmond, Shriprasad R Deshpande, Steven D Zangwill, et al.
Clinical Transplantation
|
October 14, 2021
Increase in nuclear cell-free DNA is associated with major adverse events in adult and pediatric heart transplant recipients
Steven D Zangwill, Shriprasad R Deshpande, Pippa M Simpson, et al.
Pediatric Transplantation
|
March 8, 2022
Relationship between donor fraction cell-free DNA and clinical rejection in heart transplantation
Shriprasad R Deshpande, Steven D Zangwill, Steven J Kindel, et al.
Journal of the American College of Cardiology
|
September 27, 2023
Outcomes After Hybrid Palliation for Infants With Critical Left Heart Obstruction
Madison B Argo, David J Barron, Pirooz Eghtesady, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
February 21, 2023
Norwood operation versus comprehensive stage II after bilateral pulmonary artery banding palliation for infants with critical left heart obstruction
Madison B Argo, David J Barron, Pirooz Eghtesady, et al.
Plos Genetics
|
September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Plos Genetics
|
July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Circulation. Cardiovascular Genetics
|
October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3
Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome
Jhih-Rong Lin, Daniella Miller, Dana Luong, et al.
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of 16