ScreenPlus: A comprehensive, multi-disorder newborn screening program-Reference-Cited by-同舟云学术

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ScreenPlus: A comprehensive, multi-disorder newborn screening program

Published:2024-03 Issue: Volume:38 Page:101037
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Kelly Nicole R.,Orsini Joseph J.,Goldenberg Aaron J.,Mulrooney Niamh S.,Boychuk Natalie A.,Clarke Megan J.,Paleologos Katrina,Martin Monica M.,McNeight Hannah,Caggana Michele,Bailey Sean M.,Eiland Lisa R.,Ganesh Jaya,Kupchik Gabriel,Lumba Rishi,Nafday Suhas,Stroustrup Annemarie,Gelb Michael H.,Wasserstein Melissa P.

Funder

Takeda Pharmaceuticals USA Inc

BioMarin Pharmaceutical Inc

National Institute of Child Health and Human Development

Abeona Therapeutics Inc

Alexion Pharmaceuticals Inc

Ultragenyx Pharmaceutical Inc

Genzyme Corporation

Ara Parseghian Medical Research Fund

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference25 articles.

1. Influence of phenylalanine intake on phenylketonuria;Bickel;Lancet Lond. Engl.,1953

2. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963

3. Phenylpyruvic Oligophrenia: introductory study of fifty cases of mental deficiency associated with excretion of Phenylpyruvic acid;Jervis;Arch. Neurol. Psychiatr.,1937

4. After 50 years, newborn screening continues to yield public health gains;Kuehn;JAMA,2013

5. Committee report: method for evaluating conditions nominated for population-based screening of newborns and children;Calonge;Genet. Med.,2010

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1. Current Status of Newborn Bloodspot Screening Worldwide 2024: A Comprehensive Review of Recent Activities (2020–2023);International Journal of Neonatal Screening;2024-05-23

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