Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
Advanced Molecular Detection Clips
Non-Genomics Precision Health Scan
CDC-authored Publications Scan
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
All Databases
COVID-19 GPH (47415)
CDC/NIH Web Information Database (32174)
CDC-Authored Genomics and Precision Health Publications Database (5825)
Precision Health Database (63627)
Tier-Classified Guidelines Database (533)
Pathogen Advanced Molecular Detection Database (26729)
All of Us Reports and Publications Database (656)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226255)
Epigenetic Epidemiology Publications Database (22724)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 19, 2024
. (Total: 63627 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 30 (of 149 Records)
Next
Query Trace:
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns.
Andrey V Marakhonov et al. J Clin Immunol 2024 44(4) 93
Similar articles in PubMed
Parental Engagement in Identifying Information Needs After Newborn Screening for Families of Infants with Suspected Athymia.
Evey Howley et al. J Clin Immunol 2024 44(3) 79
Similar articles in PubMed
Newborn Screening for Severe Combined Immunodeficiency: Lessons Learned from Screening and Follow-Up of the Preterm Newborn Population
A Gaviglio et al, IJNS, December 2023
Efficient screening strategies for severe combined immunodeficiencies in newborns.
Maartje Blom et al. Expert Rev Mol Diagn 2023 1-11
Similar articles in PubMed
Measuring the effect of newborn screening on survival after haematopoietic cell transplantation for severe combined immunodeficiency: a 36-year longitudinal study from the Primary Immune Deficiency Treatment Consortium.
Monica S Thakar et al. Lancet 2023
Similar articles in PubMed
Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20-year single centre experience.
Sevim Busra Korkmaz et al. Int J Immunogenet 2023
Similar articles in PubMed
Newborn Screening Conditions: Early Intervention and Probability of Developmental Delay.
Elizabeth Reynolds et al. J Dev Behav Pediatr
Similar articles in PubMed
Implementation of Newborn Screening for Conditions in the United States First Recommended during 2010-2018.
Sikha Singh et al. Int J Neonatal Screen 9(2)
Similar articles in PubMed
Genomic-Based Newborn Screening for Inborn Errors of Immunity: Practical and Ethical Considerations.
Jovanka R King et al. Int J Neonatal Screen 9(2)
Similar articles in PubMed
Uncertainties experienced by parents of children diagnosed with severe combined immunodeficiency through newborn screening.
Melissa Raspa et al. European journal of human genetics : EJHG 2023 1-7
Similar articles in PubMed
Newborn screening for spinal muscular atrophy in Osaka -challenges in a Japanese pilot study.
Tomokazu Kimizu et al. Brain & development 2023
Similar articles in PubMed
A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry.
Rafael Tesorero et al. PloS one 2023 18(3) e0283024
Similar articles in PubMed
Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan.
Inoue Kento et al. Journal of clinical immunology 2022
Similar articles in PubMed
Newborn screening for severe combined immunodeficiency: The results of the first pilot TREC and KREC study in Ukraine with involving of 10,350 neonates.
Boyarchuk Oksana et al. Frontiers in immunology 2022 13999664
Similar articles in PubMed
The Euroflow PID Orientation Tube in the diagnostic workup of primary immunodeficiency: Daily practice performance in a tertiary university hospital.
Neirinck Jana et al. Frontiers in immunology 2022 13937738
Similar articles in PubMed
TRECs/KRECs: Beyond the Diagnosis of Severe Combined Immunodeficiency.
Ramos Barbara Cristina et al. Journal of clinical immunology 2022
Similar articles in PubMed
Newborn Tandem Mass Spectroscopy Screening for Adenosine Deaminase Deficiency-First Two Years' Experience.
Hartog Nicholas et al. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 2022
Similar articles in PubMed
Economic Evaluation of Newborn Screening for Severe Combined Immunodeficiency.
Shih Sophy T F et al. International journal of neonatal screening 2022 8(3)
Similar articles in PubMed
Modelling the Cost-Effectiveness and Budget Impact of a Newborn Screening Program for Spinal Muscular Atrophy and Severe Combined Immunodeficiency.
Shih Sophy T F et al. International journal of neonatal screening 2022 8(3)
Similar articles in PubMed
Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity.
Chan Koon-Wing et al. Frontiers in immunology 2022 13883446
Similar articles in PubMed
Modelling the Cost-Effectiveness and Budget Impact of a Newborn Screening Program for Spinal Muscular Atrophy and Severe Combined Immunodeficiency
STF Shih et al, IJNS, July 20, 2022
Introducing Newborn Screening for Severe Combined Immunodeficiency-The New Zealand Experience.
Heather Natasha et al. International journal of neonatal screening 2022 8(2)
Similar articles in PubMed
SCID and Other Inborn Errors of Immunity with Low TRECs - the Brazilian Experience.
Barreiros Lucila Akune et al. Journal of clinical immunology 2022
Similar articles in PubMed
Lessons Learned from Five Years of Newborn Screening for Severe Combined Immunodeficiency (SCID) in Israel.
Lev Atar et al. The journal of allergy and clinical immunology. In practice 2022
Similar articles in PubMed
Severe Combined Immunodeficiency: Knowledge and Information Needs Among Healthcare Providers.
Kutsa Oksana et al. Frontiers in pediatrics 2022 10804709
Similar articles in PubMed
Study Design for an Evaluation of Newborn Screening for SCID in the UK.
Elliman David et al. International journal of neonatal screening 2022 8(1)
Similar articles in PubMed
Implementation of Universal Newborn Screening for Severe Combined Immunodeficiency in Singapore While Continuing Routine Bacille-Calmette-Guerin Vaccination Given at Birth.
Chan Su-Wan Bianca et al. Frontiers in immunology 2022 12794221
Similar articles in PubMed
Future Perspectives of Newborn Screening for Inborn Errors of Immunity.
Blom Maartje et al. International journal of neonatal screening 2021 7(4)
Similar articles in PubMed
Establishing Newborn Screening for SCID in the USA; Experience in California.
Puck Jennifer M et al. International journal of neonatal screening 2021 7(4)
Similar articles in PubMed
Genetic screening techniques and diseases for neonatal genetic diseases.
Han Lianshu et al. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2021 50(4) 429-435
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
TOP