Last Updated: 09/26/2026
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Found 12 publications
Disney to Pixar Transition Causing Epilepsy: A Case Report of Reflex Epilepsy.
Journal: Journal of child neurology
Published: October 29, 2024
Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A-related epilepsy and/or neurodevelopmental disorders.
Journal: Epilepsia
Published: November 13, 2023
GPI-anchoring disorders and the heart: Is cardiomyopathy an overlooked feature?
Journal: Clinical genetics
Published: June 26, 2023
N-methyl-d-aspartate (NMDA) receptor genetics: The power of paralog homology and protein dynamics in defining dominant genetic variants.
Journal: American journal of medical genetics. Part A
Published: May 11, 2021
SLC6A1 G443D associated with developmental delay and epilepsy.
Journal: Cold Spring Harbor molecular case studies
Published: March 09, 2020
The effect of increased intracranial EEG sampling rates in clinical practice.
Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Published: August 21, 2017
Two patients with a GRIN2A mutation and childhood-onset epilepsy.
Journal: Pediatric neurology
Published: May 30, 2013
Metastatic epidural bacterial abscess in a 4-year-old boy.
Journal: JAMA neurology
Published: April 05, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026