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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 18, 2024
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Records 1 - 18 (of 18 Records)
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Newborn Screening in the Diagnosis of Primary Immunodeficiency.
Kobrynski Lisa J et al. Clinical reviews in allergy & immunology 2021
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Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India.
Vignesh Pandiarajan et al. Frontiers in immunology 2021 11619146
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Methods and feasibility study for exome sequencing as a universal second-tier test in newborn screening.
Ruiz-Schultz Nicole et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jan
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Molecular Diagnosis of Inherited Immune Disorders.
Farmer Jocelyn R et al. Clinics in laboratory medicine 2019 39(4) 685-697
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Information and Emotional Support Needs of Families Whose Infant Was Diagnosed With SCID Through Newborn Screening.
Raspa Melissa et al. Frontiers in immunology 2020 11885
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Next generation sequencing analysis of consecutive Russian patients with clinical suspicion of inborn errors of immunity.
Suspitsin Evgeny N et al. Clinical genetics 2020 May
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Identification of non-severe combined immune deficiency T-cell lymphopenia at newborn screening for severe combined immune deficiency.
Kobrynski Lisa J et al. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 2019 123(5) 424-427
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What to Do with an Abnormal Newborn Screen for Severe Combined Immune Deficiency.
Chong Hey J et al. Immunology and allergy clinics of North America 2019 Nov 39(4) 535-546
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Societal value of newborn screening for severe combined immune deficiency in Arkansas: An economic analysis.
Hays Laura H et al. Public health nursing (Boston, Mass.) 2019 Apr
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The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience.
Grosse Scott D et al. The Milbank quarterly 2016 94(2) 366-91
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Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency.
Kohn Donald B et al. The Journal of allergy and clinical immunology 2018 Sep
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Genetic testing is coming of age, but for consumers it's buyer beware
E Sheng, CNBC, July 17, 2018
Newborn screening for severe combined immune deficiency (SCID) saves lives and money: a cost-effective public health policy
SD Grosse, CDC Blog Post, 2016
Idiopathic T cell lymphopenia identified in New York State Newborn Screening.
Albin-Leeds Stephanie et al. Clinical immunology (Orlando, Fla.) 2017 Jul
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Overview of 15-year severe combined immunodeficiency in the Netherlands: towards newborn blood spot screening.
de Pagter Anne P J et al. European journal of pediatrics 2015 Sep 174(9) 1183-8
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Cost-Effectiveness/Cost-Benefit Analysis of Newborn Screening for Severe Combined Immune Deficiency in Washington State.
Ding Yao et al. The Journal of pediatrics 2016 Feb
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Newborn screening for severe combined immune deficiency (technical and political aspects).
Kobrynski Lisa et al. Current opinion in allergy and clinical immunology 2015 Oct
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Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans.
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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