Biomarkers in neonatal encephalopathy: new approaches and ongoing questions
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://www.nature.com/articles/s41390-021-01616-1.pdf
Reference6 articles.
1. Piñeiro-Ramos, J. et al. Non-invasive monitoring of evolving urinary metabolic patterns in neonatal encephalopathy. Pediatr. Res. https://doi.org/10.1038/s41390-021-01553-z (2021).
2. Nuñez-Ramiro, A. et al. Topiramate plus cooling for hypoxic-ischemic encephalopathy: a randomized, controlled, multicenter, double-blinded trial. Neonatology 116, 76–84 (2019).
3. O’Boyle, D. S. et al. Improvement in the Prediction of neonatal hypoxic-ischemic encephalopathy with the integration of umbilical cord metabolites and current clinical makers. J. Pediatr. 229, 175–181.e1 (2021).
4. O’Sullivan, M. P. et al. Up-regulation of Nfat5 mRNA and Fzd4 mRNA as a marker of poor outcome in neonatal hypoxic-ischemic encephalopathy. J. Pediatr. 228, 74–81.e2 (2021).
5. Pappas, A. et al. Blood biomarkers and 6- to 7-year childhood outcomes following neonatal encephalopathy. Am. J. Perinatol. https://doi.org/10.1055/s-0040-1717072 (2020).
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