Kristine E. Woodward
Calgary, AB, Canada
Last Updated: 09/26/2026
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Found 14 publications
EEG criticality as a prognostic tool for functional outcomes in sedated pediatric intensive care patients.
Journal: Frontiers in computational neuroscience
Published: March 16, 2026
Successful Treatment of Pediatric Neurosarcoidosis With Corticosteroids, Infliximab, and Methotrexate.
Journal: Pediatric neurology
Published: March 31, 2025
The future is in the background: background EEG patterns, not acute seizures, predict epilepsy and neurodevelopmental outcomes in neonatal HIE.
Journal: Frontiers in pediatrics
Published: January 14, 2025
Motor and default mode network states of rest in frontal lobe epilepsy.
Journal: Neuroimage. Reports
Published: September 30, 2024
Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 13, 2023
Identifying Genetic Susceptibility in Neonates With Hypoxic-Ischemic Encephalopathy: A Retrospective Case Series.
Journal: Journal of child neurology
Published: January 11, 2023
Pearls & Oy-sters: Cerebral Abscess Secondary to Pulmonary Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia.
Journal: Neurology
Published: December 09, 2021
Neuroinflammation and Precision Medicine in Pediatric Neurocritical Care: Multi-Modal Monitoring of Immunometabolic Dysfunction.
Journal: International journal of molecular sciences
Published: October 22, 2020
Antenatal diagnosis of fetal intraventricular hemorrhage: systematic review and meta-analysis.
Journal: Developmental medicine and child neurology
Published: September 18, 2020
Isolated convergence-retraction nystagmus secondary to intralesional haemorrhage of a pineal cyst: an easily missed neurological finding with potentially life-threatening consequences.
Journal: BMJ case reports
Published: September 15, 2020
Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism.
Journal: Pediatric blood & cancer
Published: January 02, 2020
Last Updated: 09/26/2026