Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Richard B Parad

Showing results (31-40 of 59) with videos related to

Pageof 6
Sort By:
Pediatric Pulmonology|December 26, 2025
Increasing Access to Genetic Counselors With Disease-Specific Expertise: Development of a Centralized Cystic Fibrosis Genetic Counseling Telehealth ModelElinor Langfelder-Schwind, Melissa Basile, Rachel Moyal-Smith, et al.
Journal of the American College of Surgeons|February 22, 2020
Is Abdominal Sonography a Useful Adjunct to Abdominal Radiography in Evaluating Neonates with Suspected Necrotizing Enterocolitis?Sarah A Tracy, Stefanie P Lazow, Ilse M Castro-Aragon, et al.
American Journal of Surgery|May 7, 2021
Abdominal ultrasound findings contribute to a multivariable predictive risk score for surgical necrotizing enterocolitis: A pilot studyStefanie P Lazow, Sarah A Tracy, Steven J Staffa, et al.
Pediatric Surgery International|September 28, 2021
A role for abdominal ultrasound in discriminating suspected necrotizing enterocolitis in congenital heart disease patientsStefanie P Lazow, Sarah A Tracy, Judy A Estroff, et al.
Pediatrics|June 3, 2004
Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detectionsAnne Marie Comeau, Richard B Parad, Henry L Dorkin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2017
A curated gene list for reporting results of newborn genomic sequencingOzge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, et al.
JCO Precision Oncology|June 3, 2026
Germline Whole-Genome Sequencing in Early-Onset Pediatric Solid Tumors Implicates Novel Risk FactorsMatthew Nagy, Andy Bhattacharjee, Abigail Cinelli, et al.
Neonatology|May 29, 2013
Low urine vascular endothelial growth factor levels are associated with mechanical ventilation, bronchopulmonary dysplasia and retinopathy of prematurityBernadette M Levesque, Leslie A Kalish, Abigail B Winston, et al.
Pediatrics|February 3, 2007
Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop reportAnne Marie Comeau, Frank J Accurso, Terry B White, et al.
The Journal of Pediatrics|July 22, 2008
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus reportPhilip M Farrell, Beryl J Rosenstein, Terry B White, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Pediatric Pulmonology|December 26, 2025
Increasing Access to Genetic Counselors With Disease-Specific Expertise: Development of a Centralized Cystic Fibrosis Genetic Counseling Telehealth ModelElinor Langfelder-Schwind, Melissa Basile, Rachel Moyal-Smith, et al.
Journal of the American College of Surgeons|February 22, 2020
Is Abdominal Sonography a Useful Adjunct to Abdominal Radiography in Evaluating Neonates with Suspected Necrotizing Enterocolitis?Sarah A Tracy, Stefanie P Lazow, Ilse M Castro-Aragon, et al.
American Journal of Surgery|May 7, 2021
Abdominal ultrasound findings contribute to a multivariable predictive risk score for surgical necrotizing enterocolitis: A pilot studyStefanie P Lazow, Sarah A Tracy, Steven J Staffa, et al.
Pediatric Surgery International|September 28, 2021
A role for abdominal ultrasound in discriminating suspected necrotizing enterocolitis in congenital heart disease patientsStefanie P Lazow, Sarah A Tracy, Judy A Estroff, et al.
Pediatrics|June 3, 2004
Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detectionsAnne Marie Comeau, Richard B Parad, Henry L Dorkin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2017
A curated gene list for reporting results of newborn genomic sequencingOzge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, et al.
JCO Precision Oncology|June 3, 2026
Germline Whole-Genome Sequencing in Early-Onset Pediatric Solid Tumors Implicates Novel Risk FactorsMatthew Nagy, Andy Bhattacharjee, Abigail Cinelli, et al.
Neonatology|May 29, 2013
Low urine vascular endothelial growth factor levels are associated with mechanical ventilation, bronchopulmonary dysplasia and retinopathy of prematurityBernadette M Levesque, Leslie A Kalish, Abigail B Winston, et al.
Pediatrics|February 3, 2007
Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop reportAnne Marie Comeau, Frank J Accurso, Terry B White, et al.
The Journal of Pediatrics|July 22, 2008
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus reportPhilip M Farrell, Beryl J Rosenstein, Terry B White, et al.
Pageof 6