Showing results (211-220 of 231) with videos related to
Sort By:
Pageof 24
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2012
Sickle cell disease incidence among newborns in New York State by maternal race/ethnicity and nativityYing Wang, Joseph Kennedy, Michele Caggana, et al.Pediatrics|August 14, 2013
Factors associated with late detection of critical congenital heart disease in newbornsApril L Dawson, Cynthia H Cassell, Tiffany Riehle-Colarusso, et al.MMWR. Morbidity and Mortality Weekly Report|March 30, 2023
Trends in Stimulant Prescription Fills Among Commercially Insured Children and Adults - United States, 2016-2021Melissa L Danielson, Michele K Bohm, Kimberly Newsome, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 4, 2013
Hospitalizations, costs, and mortality among infants with critical congenital heart disease: how important is timely detection?Cora Peterson, April Dawson, Scott D Grosse, et al.Annals of the New York Academy of Sciences|July 4, 2019
Data needed to respond appropriately to anemia when it is a public health problemAnne M Williams, O Yaw Addo, Scott D Grosse, et al.Genetics in Medicine Open|March 4, 2025
Association of HFE genotypes with hemochromatosis-related phenotypes in the All of Us research programNandana D Rao, Ramal Moonesinghe, Lu Shi, et al.Public Health Reports (Washington, D.C. : 1974)|January 2, 2014
A public health economic assessment of hospitals' cost to screen newborns for critical congenital heart diseaseCora Peterson, Scott D Grosse, Jill Glidewell, et al.Pediatrics|October 12, 2011
Strategies for implementing screening for critical congenital heart diseaseAlex R Kemper, William T Mahle, Gerard R Martin, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 24, 2016
Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendationAlex R Kemper, Jeffrey Brosco, Anne Marie Comeau, et al.Pediatrics|July 19, 2023
Evidence and Recommendation for Guanidinoacetate Methyltransferase Deficiency Newborn ScreeningMargie A Ream, Wendy K K Lam, Scott D Grosse, et al.Pageof 24