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Pediatrics|March 12, 2025
Evidence and Recommendation for Infantile Krabbe Disease Newborn ScreeningMargie A Ream, Wendy K K Lam, Scott D Grosse, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2024
Can Incorporating Molecular Testing Improve the Accuracy of Newborn Screening for Congenital Adrenal Hyperplasia?Kyriakie Sarafoglou, Amy Gaviglio, Carrie Wolf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 29, 2022
Evidence and recommendation for mucopolysaccharidosis type II newborn screening in the United StatesMargie A Ream, Wendy K K Lam, Scott D Grosse, et al.
MMWR. Morbidity and Mortality Weekly Report|September 11, 2020
Infants with Congenital Disorders Identified Through Newborn Screening - United States, 2015-2017Marci K Sontag, Careema Yusuf, Scott D Grosse, et al.
MMWR. Recommendations and Reports : Morbidity and Mortality Weekly Report. Recommendations and Reports|January 16, 2004
Applying public health strategies to primary immunodeficiency diseases: a potential approach to genetic disordersMary Lou Lindegren, Lisa Kobrynski, Sonja A Rasmussen, et al.
European Journal of Human Genetics : EJHG|June 3, 2026
Health economic evaluations of genomic newborn screening: Approaches by studies within the international consortium on newborn sequencingHadley Stevens Smith, Martin Vu, Tamara Dangouloff, et al.
Vaccine|October 8, 2023
Vaccine value profile for cytomegalovirusSuresh B Boppana, Michiel van Boven, William J Britt, et al.
Emerging Infectious Diseases|November 3, 2016
Cost-effectiveness of Increasing Access to Contraception during the Zika Virus Outbreak, Puerto Rico, 2016Rui Li, Katharine B Simmons, Jeanne Bertolli, et al.
BMC Pediatrics|April 18, 2015
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric diseaseSara D Khangura, Maria D Karaceper, Yannis Trakadis, et al.
Orphanet Journal of Rare Diseases|February 5, 2016
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort studyMaria D Karaceper, Pranesh Chakraborty, Doug Coyle, et al.
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