Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identifying Genetic Susceptibility in Neonates With Hypoxic-Ischemic Encephalopathy: A Retrospective Case Series.

Journal of child neurology - 1 Feb 2023

Woodward Kristine E, Murthy Prashanth, Mineyko Aleksandra, Mohammad Khorshid, Esser Michael J

Abstract excerpt

Neonatal hypoxic-ischemic encephalopathy is a clinical phenomenon that often results from perinatal asphyxia. To mitigate secondary neurologic injury, prompt initial assessment and diagnosis is needed to identify patients eligible for therapeutic hypothermia. However, occasionally neonates present with a clinical picture of hypoxic-ischemic encephalopathy without significant risk factors for perinatal asphyxia....

Topics

Join the communities discussing this publication.

Genetic Predisposition to Disease
Hypoxia-Ischemia, Brain
Infant, Newborn
Kinesins
NAV1.7 Voltage-Gated Sodium Channel

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Neonatal and fetal brain pathology

Steroid 21-Hydroxylase

Source

Identifiers

PMID: 36628482
DOI: 10.1177/08830738221147805

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identifying Genetic Susceptibility in Neonates With Hypoxic-Ischemic Encephalopathy: A Retrospective Case Series.PMID 36628482Read ↗

Genetic Diagnosis in Neonatal Encephalopathy With Hypoxic Brain Damage Using Targeted Gene Panel SequencingSemantic proximity Read ↗

Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis.Semantic proximity Read ↗

Genetic and epigenetic contributors and mimickers of phenotypic hypoxic-ischemic encephalopathy (HIE).Semantic proximity Read ↗

Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study.Semantic proximity Read ↗

Exploring the genetic landscape of neurotransmitter alterations in hypoxic-ischemic encephalopathy: A personalized medicine perspectiveSemantic proximity Read ↗

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A ReviewSemantic proximity Read ↗

Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing.Semantic proximity Read ↗

[Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event].Semantic proximity Read ↗

The NESHIE and CP Genetics Resource (NCGR): A database of genes and variants reported in neonatal encephalopathy with suspected hypoxic ischemic encephalopathy (NESHIE) and consequential cerebral palsy (CP)Semantic proximity Read ↗

Congenital anomalies and genetic disorders in neonates and infants: a single-center observational cohort studySemantic proximity Read ↗

Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infantSemantic proximity Read ↗

Genomic testing in the neonatal intensive care unit: a 5-year retrospective single-centre study from a tertiary care hospital in Bengaluru, India.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.