 Neonatal Screening
"Neonatal Screening" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The identification of selected parameters in newborn infants by various tests, examinations, or other procedures. Screening may be performed by clinical or laboratory measures. A screening test is designed to sort out healthy neonates (INFANT, NEWBORN) from those not well, but the screening test is not intended as a diagnostic device, rather instead as epidemiologic.
| Descriptor ID |
D015997
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| MeSH Number(s) |
E01.370.225.910 E01.370.500.580 E05.200.910 E05.318.308.980.438.580.580 L01.280.960.500.580.580 N02.421.726.233.443.816 N05.715.360.300.800.438.500.575 N06.850.520.308.980.438.580.580 N06.850.780.500.580
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| Concept/Terms |
Neonatal Screening- Neonatal Screening
- Neonatal Screenings
- Screening, Neonatal
- Screenings, Neonatal
- Infant, Newborn, Screening
- Newborn Infant Screening
- Newborn Infant Screenings
- Screening, Newborn Infant
- Screenings, Newborn Infant
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Below are MeSH descriptors whose meaning is more general than "Neonatal Screening".
Below are MeSH descriptors whose meaning is more specific than "Neonatal Screening".
This graph shows the total number of publications written about "Neonatal Screening" by people in this website by year, and whether "Neonatal Screening" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2017 | 1 | 0 | 1 | | 2019 | 0 | 1 | 1 | | 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Neonatal Screening" by people in Profiles.
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Dunn JJ, Selvarangan R, Maggert K, Young S, Leber AL. Multicenter Evaluation of the DiaSorin Molecular Simplexa Congenital CMV Direct PCR Test on Neonatal Saliva and Urine Specimens. J Clin Microbiol. 2023 06 20; 61(6):e0028323.
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Repnikova E, Roberts J, Mc Dermott S, Farooqi MS, Iqbal NT, Silvey M, Nolen J, Taboada E, Li W. Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two cases. Pathol Res Pract. 2019 Oct; 215(10):152578.
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Ehmann P, Lantos JD. Ethical issues with testing and treatment for Krabbe disease. Dev Med Child Neurol. 2019 12; 61(12):1358-1361.
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Knapp B, Decker C, Lantos JD. Neonatologists' Attitudes About Diagnostic Whole-Genome Sequencing in the NICU. Pediatrics. 2019 01; 143(Suppl 1):S54-S57.
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Lantos JD. Ethical and Psychosocial Issues in Whole Genome Sequencing (WGS) for Newborns. Pediatrics. 2019 01; 143(Suppl 1):S1-S5.
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Johnston J, Lantos JD, Goldenberg A, Chen F, Parens E, Koenig BA. Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies. Hastings Cent Rep. 2018 Jul; 48 Suppl 2:S2-S6.
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Berg JS, Agrawal PB, Bailey DB, Beggs AH, Brenner SE, Brower AM, Cakici JA, Ceyhan-Birsoy O, Chan K, Chen F, Currier RJ, Dukhovny D, Green RC, Harris-Wai J, Holm IA, Iglesias B, Joseph G, Kingsmore SF, Koenig BA, Kwok PY, Lantos J, Leeder SJ, Lewis MA, McGuire AL, Milko LV, Mooney SD, Parad RB, Pereira S, Petrikin J, Powell BC, Powell CM, Puck JM, Rehm HL, Risch N, Roche M, Shieh JT, Veeraraghavan N, Watson MS, Willig L, Yu TW, Urv T, Wise AL. Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017 Feb; 139(2).
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Smith LD, Willig LK, Kingsmore SF. Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders. Cold Spring Harb Perspect Med. 2015 Dec 18; 6(2):a023168.
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Poretti A, Blaser SI, Lequin MH, Fatemi A, Meoded A, Northington FJ, Boltshauser E, Huisman TA. Neonatal neuroimaging findings in inborn errors of metabolism. J Magn Reson Imaging. 2013 Feb; 37(2):294-312.
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Lantos JD. Dangerous and expensive screening and treatment for rare childhood diseases: the case of Krabbe disease. Dev Disabil Res Rev. 2011; 17(1):15-8.
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