Last Updated: 09/26/2026
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Found 14 publications
Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.
Journal: Epilepsia
Published: December 02, 2025
Medication Barriers in Pediatric Patients With Epilepsy.
Journal: Pediatric neurology
Published: October 02, 2025
A Simple Intervention Improves Access to Telemedicine for Spanish-Speaking Families in an Outpatient Pediatric Epilepsy Clinic.
Journal: Journal of child neurology
Published: May 14, 2025
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Journal: American journal of human genetics
Published: May 09, 2024
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Journal: American journal of human genetics
Published: March 20, 2024
Endoscopic transventricular "inside-out" corpus callosotomy: illustrative case.
Journal: Journal of neurosurgery. Case lessons
Published: March 04, 2024
Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus.
Journal: medRxiv : the preprint server for health sciences
Published: January 18, 2024
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.
Journal: American journal of human genetics
Published: December 07, 2023
Corrigendum: Intrafamilial variability in SLC6A1-related neurodevelopmental disorders.
Journal: Frontiers in neuroscience
Published: July 31, 2023
Intrafamilial variability in SLC6A1-related neurodevelopmental disorders.
Journal: Frontiers in neuroscience
Published: May 08, 2023
Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy.
Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2023
Last Updated: 09/26/2026