Last Updated: 09/26/2026
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Found 34 publications
Deep Brain Stimulation for Dystonia and Epilepsy in Alternating Hemiplegia of Childhood.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 02, 2026
A Systematic Review of Race or Ethnicity and Risk of Death in Spina Bifida in the United States.
Journal: Journal of child neurology
Published: July 04, 2025
Natural History of Alternating Hemiplegia of Childhood: Vulnerabilities in Early Childhood and Predictive Factors for Long-Term Outcomes.
Journal: Annals of the Child Neurology Society
Published: June 14, 2025
Sequencing Analysis Demonstrates That a Complex Genetic Architecture Contributes to Risk for Spina Bifida.
Journal: Birth defects research
Published: June 04, 2025
Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.
Journal: Annals of the Child Neurology Society
Published: March 03, 2025
Motor function and safety after allogeneic cord blood and cord tissue-derived mesenchymal stromal cells in cerebral palsy: An open-label, randomized trial.
Journal: Developmental medicine and child neurology
Published: March 14, 2022
Characterization of sedation and anesthesia complications in patients with alternating hemiplegia of childhood.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: October 09, 2021
The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder.
Journal: Human molecular genetics
Published: August 23, 2021
Opportunities, barriers, and recommendations in down syndrome research.
Journal: Translational science of rare diseases
Published: July 16, 2021
A Systematic Review of Cognitive Function in Adults with Spina Bifida.
Journal: Developmental neurorehabilitation
Published: April 19, 2021
Alternating hemiplegia of childhood: evolution over time and mouse model corroboration.
Journal: Brain communications
Published: March 05, 2021
Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features.
Journal: Human molecular genetics
Published: January 05, 2021
Last Updated: 09/26/2026