Last Updated: 09/26/2026
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Found 6 publications
Medically ready for discharge: A multisite "point-in-time" assessment of hospitalized patients.
Journal: Journal of hospital medicine
Published: March 23, 2023
Phenotypes and Genotypes in Patients with SMC1A-Related Developmental and Epileptic Encephalopathy.
Journal: Genes
Published: February 17, 2023
Two Missense CACNA1A Variants in a Single Family with Variable Neurobehavioral, Cerebellar, Epileptic, and Oculomotor Features.
Journal: Neuropediatrics
Published: January 14, 2021
Awake Mapping of the Auditory Cortex during Tumor Resection in an Aspiring Musical Performer: A Case Report.
Journal: Pediatric neurosurgery
Published: January 23, 2020
Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development.
Journal: American journal of medical genetics. Part A
Published: June 01, 2017
Showing 1-6 of 6
Last Updated: 09/26/2026