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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Heart, Lung, Blood and Sleep Disorders
Last data update: Mar 28, 2024
. (Total: 63390 Documents since 2012)
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Records 1 - 14 (of 14 Records)
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Lymphopenia[original query]>>Reviews/Commentaries[Product Type]
Genomic-Based Newborn Screening for Inborn Errors of Immunity: Practical and Ethical Considerations.
Jovanka R King et al. Int J Neonatal Screen 9(2)
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GATA2 Related Conditions and Predisposition to Pediatric Myelodysplastic Syndromes.
Bruzzese Antonella et al. Cancers 2020 Oct 12(10)
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Review: Why screen for severe combined immunodeficiency disease?
Thomas C et al. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie 2020 Sep
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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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The case for severe combined immunodeficiency (SCID) and T cell lymphopenia newborn screening: saving lives…one at a time.
Quinn Jessica et al. Immunologic research 2020 Mar
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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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Nonsevere combined immunodeficiency T-cell lymphopenia identified through newborn screening.
Patrawala Meera et al. Current opinion in allergy and clinical immunology 2019 Sep
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Newborn screening for severe combined immunodeficiency and T-cell lymphopenia.
Puck Jennifer M et al. Immunological reviews 2019 Jan 287(1) 241-252
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Newborn Screening for Severe Combined Immunodeficiency.
Routes John et al. Current allergy and asthma reports 2018 May 18(6) 34
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A Practical Approach to Newborn Screening for Severe Combined Immunodeficiency Using the T Cell Receptor Excision Circle Assay.
Thakar Monica S et al. Frontiers in immunology 2017 81470
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Newborn Screening for Primary Immunodeficiency Diseases: History, Current and Future Practice.
King Jovanka R et al. Journal of clinical immunology 2017 Nov
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Newborn Screening for SCID: Lessons Learned.
Buelow Becky J et al. Expert review of hematology 2016 May
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Guidelines for Screening, Early Diagnosis and Management of Severe Combined Immunodeficiency (SCID) in India.
Madkaikar Manisha et al. Indian 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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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 28, 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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