Literature DB >> 25979780

Current status of newborn screening worldwide: 2015.

Bradford L Therrell1, Carmencita David Padilla2, J Gerard Loeber3, Issam Kneisser4, Amal Saadallah5, Gustavo J C Borrajo6, John Adams7.   

Abstract

Newborn screening describes various tests that can occur during the first few hours or days of a newborn's life and have the potential for preventing severe health problems, including death. Newborn screening has evolved from a simple blood or urine screening test to a more comprehensive and complex screening system capable of detecting over 50 different conditions. While a number of papers have described various newborn screening activities around the world, including a series of papers in 2007, a comprehensive review of ongoing activities since that time has not been published. In this report, we divide the world into 5 regions (North America, Europe, Middle East and North Africa, Latin America, and Asia Pacific), assessing the current NBS situation in each region and reviewing activities that have taken place in recent years. We have also provided an extensive reference listing and summary of NBS and health data in tabular form.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Inborn errors of metabolism; International screening; Newborn screening; Rare disease screening

Mesh:

Year:  2015        PMID: 25979780     DOI: 10.1053/j.semperi.2015.03.002

Source DB:  PubMed          Journal:  Semin Perinatol        ISSN: 0146-0005            Impact factor:   3.300


  134 in total

1.  Insights in Public Health: Newborn Screening Saves Babies Using Public/Private Partnerships.

Authors:  Sylvia Mann
Journal:  Hawaii J Med Public Health       Date:  2015-12

2.  Metabolic analysis reveals evidence for branched chain amino acid catabolism crosstalk and the potential for improved treatment of organic acidurias.

Authors:  Stephen McCalley; David Pirman; Michelle Clasquin; Kendall Johnson; Shengfang Jin; Jerry Vockley
Journal:  Mol Genet Metab       Date:  2019-05-21       Impact factor: 4.797

3.  Reply to A Mackie.

Authors:  Marleen Jansen
Journal:  Eur J Hum Genet       Date:  2017-04-26       Impact factor: 4.246

Review 4.  International differences in the evaluation of conditions for newborn bloodspot screening: a review of scientific literature and policy documents.

Authors:  Marleen E Jansen; Selina C Metternick-Jones; Karla J Lister
Journal:  Eur J Hum Genet       Date:  2016-11-16       Impact factor: 4.246

5.  Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.

Authors:  Josephine Johnston; John D Lantos; Aaron Goldenberg; Flavia Chen; Erik Parens; Barbara A Koenig
Journal:  Hastings Cent Rep       Date:  2018-07       Impact factor: 2.683

6.  High incidence of maternal vitamin B12 deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel.

Authors:  Gwendolyn Gramer; Junmin Fang-Hoffmann; Patrik Feyh; Glynis Klinke; Peter Monostori; Jürgen G Okun; Georg F Hoffmann
Journal:  World J Pediatr       Date:  2018-06-15       Impact factor: 2.764

7.  The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience.

Authors:  Scott D Grosse; John D Thompson; Yao Ding; Michael Glass
Journal:  Milbank Q       Date:  2016-06       Impact factor: 4.911

8.  Brief Report: Delayed Diagnosis of Treatable Inborn Errors of Metabolism in Children with Autism and Other Neurodevelopmental Disorders.

Authors:  María Elena Márquez-Caraveo; Isabel Ibarra-González; Rocío Rodríguez-Valentín; Miguel Ángel Ramírez-García; Verónica Pérez-Barrón; Eduardo Lazcano-Ponce; Marcela Vela-Amieva
Journal:  J Autism Dev Disord       Date:  2021-06

9.  Development and application of a novel method to characterize methylmercury exposure in newborns using dried blood spots.

Authors:  Niladri Basu; Jenny W L Eng; Marie Perkins; Andrea Santa-Rios; Gordana Martincevic; Krystin Carlson; Richard L Neitzel
Journal:  Environ Res       Date:  2017-08-18       Impact factor: 6.498

10.  The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia.

Authors:  Emma K Baker; Sheena Arora; David J Amor; Perrin Date; Meagan Cross; James O'Brien; Chloe Simons; Carolyn Rogers; Stephen Goodall; Jennie Slee; Chris Cahir; David E Godler
Journal:  J Autism Dev Disord       Date:  2021-07-22
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