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Public Health Genomics and Precision Health Knowledge Base (v7.8)
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Newborn Screening[original query]>>Reviews/Commentaries[Product Type]
Migration and newborn screening: time to build on the European Asylum, Integration and Migration Fund?
Tsagkaris Christos et al. The European journal of contraception & reproductive health care : the official journal of the European Society of Contraception 2022 1-5
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The cost-effectiveness of newborn screening for spinal muscular atrophy.
Landfeldt Erik et al. Developmental medicine and child neurology 2022
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Inborn error of metabolism precipitated by COVID-19: challenges in the absence of an expanded newborn screening as state health programmes.
Olety Priyanka et al. BMJ case reports 2022 15(6)
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Estimating the Prevalence of Rare Diseases: Long-Chain Fatty Acid Oxidation Disorders as an Illustrative Example.
Kruger Eliza et al. Advances in therapy 2022
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Towards Achieving Equity and Innovation in Newborn Screening across Europe.
Sikonja Jaka et al. International journal of neonatal screening 2022 8(2)
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Accelerating the Pace of Newborn Screening Research to Advance Disease Understanding and Improve Health Outcomes:: Key Efforts of the Newborn Screening Translational Research Network (NBSTRN).
Brower Amy et al. Delaware journal of public health 2022 7(5) 36-37
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A Window of Opportunity for Newborn Screening.
Bailey Donald B et al. Molecular diagnosis & therapy 2022
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COVID-19 Pandemic-Related Impacts on Newborn Screening Public Health Surveillance.
Singh Sikha et al. International journal of neonatal screening 2022 8(2)
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How longitudinal observational studies can guide screening strategy for rare diseases.
Mütze Ulrike et al. Journal of inherited metabolic disease 2022
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Onasemnogene abeparvovec for the treatment of spinal muscular atrophy.
McMillan Hugh J et al. Expert opinion on biological therapy 2022
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Newborn Screening: Review of its Impact for Cystinosis.
Hohenfellner Katharina et al. Cells 2022 11(7)
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Advances in the Management of Sickle Cell Disease: New Concepts and Future Horizons.
Higgins Tara et al. The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG 2022 27(3) 206-213
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50 Years Ago in TheJournalofPediatrics: Newborn Screening for Sickle Cell Disease: A Promise (Un)Fulfilled.
Strumph Kaitlin et al. The Journal of pediatrics 2022 24368
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Ethical Considerations for Equitable Access to Genomic Sequencing for Critically Ill Neonates in the United States.
P Fishler Kristen et al. International journal of neonatal screening 2022 8(1)
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Perspective on newborn screening (NBS): Evidence sharing on conditions to be included in NBS in Pakistan.
Majid Hafsa et al. JPMA. The Journal of the Pakistan Medical Association 2022 72(3) 526-531
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Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening.
Mütze Ulrike et al. European journal of pediatrics 2022
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From Guthrie to Genomes: Expanding Bioinformatic Capabilities in Newborn Screening Programs
A Gaviglio et al, CDC Blog Post, March 21, 2022
[Genomic newborn screening. Perspective from the Ethics Commission of the Spanish Society for Human Genetics. Part II: Ethical, legal and social issues (ELSIs) of the introduction of next generation sequencing technologies in a public health newborn screening program.]
Pàmpols Ros Teresa et al. Revista espanola de salud publica 2022 96
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Acute complications in children with sickle cell disease: Prevention and management.
Beck Carolyn E et al. Paediatrics & child health 2022 27(1) 50-62
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Making Decisions About Krabbe Disease Newborn Screening.
Schrier Vergano Samantha A et al. Pediatrics 2022
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Newborn Screening for X-Linked Adrenoleukodystrophy: Past, Present, and Future.
Moser Ann B et al. International journal of neonatal screening 2022 8(1)
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Global impact of COVID-19 on newborn screening programmes.
Koracin Vanesa et al. BMJ global health 2022 7(3)
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Insights into National Laboratory Newborn Screening and Future Prospects.
Mujamammi Ahmed H et al. Medicina (Kaunas, Lithuania) 2022 58(2)
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Nursing engagement in genetics and genomics: A developing country's perspective.
Abad Peter James B et al. International nursing review 2022
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Sudden Death in Diabetic Ketoacidosis Complicated by Sickle Cell Trait.
Dau Georgia E et al. The American journal of forensic medicine and pathology 2022
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Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassaemia and fetal haemoglobin in HbSS.
Serjeant Graham R et al. Expert review of hematology 2022
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Clinical Phenotypes of Cystic Fibrosis Carriers.
Polgreen Philip M et al. Annual review of medicine 2022 73563-574
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Revisiting a diagnosis of cystic fibrosis - Uncertainties and considerations.
Balfour-Lynn I M et al. Paediatric respiratory reviews 2022
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Early Development of Newborn Screening for HCU and Current Challenges.
Levy Harvey L et al. International journal of neonatal screening 2021 7(4)
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Select Ethical Aspects of Next-Generation Sequencing Tests for Newborn Screening and Diagnostic Evaluation of Critically Ill Newborns.
Sen Kuntal et al. International journal of neonatal screening 2021 7(4)
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Page last reviewed:
Oct 1, 2021
Page last updated:
Jun 24, 2022
Content source:
Office of Genomics and Precision Public Health
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