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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|June 6, 2023
D-galactose Supplementation for the Treatment of Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE): A Pilot Trial of Precision Medicine After Epilepsy SurgeryÁngel Aledo-Serrano, Adrián Valls-Carbó, Christina D Fenger, et al.
Brain : a Journal of Neurology|October 13, 2022
The genomic landscape across 474 surgically accessible epileptogenic human brain lesionsJavier A López-Rivera, Costin Leu, Marie Macnee, et al.
Orphanet Journal of Rare Diseases|May 23, 2026
Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephalyChristiane R Proepper, Lisa-Maria Schwarz, Sofia M Schuetz, et al.
Epilepsia|March 1, 2025
Seizure outcomes following epilepsy surgery in pediatric and young adult patients with high-grade brain tumors: Results from a European surveyRobert Lersch, Till Hartlieb, Tom Pieper, et al.
Neuropediatrics|August 30, 2024
Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly PatientsChristiane R Proepper, Sofia M Schuetz, Lisa-Maria Schwarz, et al.
Neurology|October 28, 2022
Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the <i>SLC35A2</i> GeneCarmen Barba, Ingmar Blumcke, Melodie R Winawer, et al.
Neurology|November 11, 2018
Neurologic phenotypes associated with <i>COL4A1</i>/<i>2</i> mutations: Expanding the spectrum of diseaseSara Zagaglia, Christina Selch, Jelena Radic Nisevic, et al.
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