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Shannon N Nees

Showing results (11-20 of 20) with videos related to

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The Journal of Urology|March 12, 2013
Incidence, significance and natural history of persistent retrograde venous flow after varicocelectomy in children and adolescents: correlation with catch-up growthJason P Van Batavia, Angela M Fast, Shannon N Nees, et al.
Journal of Pediatric Hematology/Oncology|April 25, 2013
Use of complementary and alternative medicine among children, adolescent, and young adult cancer survivors: a survey studyDeborah H Ndao, Elena J Ladas, Yuanyuan Bao, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 13, 2018
Patients with anomalous aortic origin of the coronary artery remain at risk after surgical repairShannon N Nees, Jonathan N Flyer, Anjali Chelliah, et al.
The Annals of Thoracic Surgery|May 27, 2020
Assessment of Anomalous Coronary Arteries by Imagers and Surgeons: Comparison of Imaging ModalitiesKanwal M Farooqi, Shannon N Nees, Jennifer Smerling, et al.
Journal of Patient Experience|February 28, 2024
User-Centered Development of HEARTPrep, a Digital Health Psychosocial Intervention for Prenatally Diagnosed Congenital Heart DiseaseErica Sood, Kimberly S Canter, Steven Battisti, et al.
Pediatric Cardiology|June 24, 2023
Virtually Delivered Psychosocial Intervention for Prenatally Diagnosed Congenital Heart Disease: Feasibility and Acceptability of HEARTPrepErica Sood, Shannon N Nees, Shubhika Srivastava, et al.
Kidney International|June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndromeSimone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.
Circulation. Genomic and Precision Medicine|February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.
The New England Journal of Medicine|July 19, 2013
Mutations in DSTYK and dominant urinary tract malformationsSimone Sanna-Cherchi, Rosemary V Sampogna, Natalia Papeta, et al.
American Journal of Human Genetics|November 20, 2012
Copy-number disorders are a common cause of congenital kidney malformationsSimone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
The Journal of Urology|March 12, 2013
Incidence, significance and natural history of persistent retrograde venous flow after varicocelectomy in children and adolescents: correlation with catch-up growthJason P Van Batavia, Angela M Fast, Shannon N Nees, et al.
Journal of Pediatric Hematology/Oncology|April 25, 2013
Use of complementary and alternative medicine among children, adolescent, and young adult cancer survivors: a survey studyDeborah H Ndao, Elena J Ladas, Yuanyuan Bao, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 13, 2018
Patients with anomalous aortic origin of the coronary artery remain at risk after surgical repairShannon N Nees, Jonathan N Flyer, Anjali Chelliah, et al.
The Annals of Thoracic Surgery|May 27, 2020
Assessment of Anomalous Coronary Arteries by Imagers and Surgeons: Comparison of Imaging ModalitiesKanwal M Farooqi, Shannon N Nees, Jennifer Smerling, et al.
Journal of Patient Experience|February 28, 2024
User-Centered Development of HEARTPrep, a Digital Health Psychosocial Intervention for Prenatally Diagnosed Congenital Heart DiseaseErica Sood, Kimberly S Canter, Steven Battisti, et al.
Pediatric Cardiology|June 24, 2023
Virtually Delivered Psychosocial Intervention for Prenatally Diagnosed Congenital Heart Disease: Feasibility and Acceptability of HEARTPrepErica Sood, Shannon N Nees, Shubhika Srivastava, et al.
Kidney International|June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndromeSimone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.
Circulation. Genomic and Precision Medicine|February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.
The New England Journal of Medicine|July 19, 2013
Mutations in DSTYK and dominant urinary tract malformationsSimone Sanna-Cherchi, Rosemary V Sampogna, Natalia Papeta, et al.
American Journal of Human Genetics|November 20, 2012
Copy-number disorders are a common cause of congenital kidney malformationsSimone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, et al.
Pageof 2