The magnitude and challenge of false-positive newborn screening test results.
about
Another look at Emergency Department HIV screening in practice: no need to revise expectations.Genetic screening: A primer for primary care.Validation and development of an immunonephelometric assay for the determination of alpha-1 antitrypsin levels in dried blood spots from patients with COPD.Indicators of newborn screening for congenital hypothyroidism in Sri Lanka: program challenges and way forwardBetter off not knowing: improving clinical care by limiting physician access to unsolicited diagnostic information.Neonatal screening of inborn errors of metabolism using tandem mass spectrometry: an evidence-based analysisDried blood spot testing for seven steroids using liquid chromatography-tandem mass spectrometry with reference interval determination in the Korean population.Neonatal screening for congenital adrenal hyperplasia in Southern Brazil: a population based study with 108,409 infants.Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen statesClinical and environmental influences on metabolic biomarkers collected for newborn screening.A review of the psychosocial effects of false-positive results on parents and current communication practices in newborn screening.Universal newborn screening and adverse medical outcomes: a historical note.How many deaths can be prevented by newborn screening for congenital adrenal hyperplasia?Policy issues related to expanded newborn screening: a review of three genetic/metabolic disorders.Congenital hypothyroidism: recommendations of the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism.Questioning the Need for Informed Consent: A Case Study of California's Experience with a Pilot Newborn Screening Research Project.Comparing the clinical and economic effects of clinical examination, pulse oximetry, and echocardiography in newborn screening for congenital heart defects: a probabilistic cost-effectiveness model and value of information analysis.Mutation database for the galactose-1-phosphate uridyltransferase (GALT) gene.Unusual Case of Phenylketonuria With Atypical Brain Magnetic Resonance Imaging Findings.Mutations at the galactose-1-p-uridyltransferase gene in infants with a positive galactosemia newborn screening test.Galactosaemia in a Brazilian population: high incidence and cost-benefit analysis.Two-year pilot study of newborn screening for congenital adrenal hyperplasia in New South Wales compared with nationwide case surveillance in Australia.The inclusion of succinylacetone as marker for tyrosinemia type I in expanded newborn screening programs.Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.Effects of birth weight on profiles of dried blood amino-acids and acylcarnitines.Worldwide Recall Rate in Newborn Screening Programs for Congenital Hypothyroidism.Metabolic etiologies in West syndrome.More than half of abnormal results from laboratory tests ordered by family physicians could be false-positive.Psychosocial Aspects of Newborn Screening Programs for Cystic Fibrosis
P2860
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P2860
The magnitude and challenge of false-positive newborn screening test results.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
The magnitude and challenge of false-positive newborn screening test results.
@en
type
label
The magnitude and challenge of false-positive newborn screening test results.
@en
prefLabel
The magnitude and challenge of false-positive newborn screening test results.
@en
P1433
P1476
The magnitude and challenge of false-positive newborn screening test results.
@en
P2093
P304
P356
10.1001/ARCHPEDI.154.7.714
P407
P577
2000-07-01T00:00:00Z