DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 56 · October 2025 DOI: 10.1055/s-015-62321


NEP 50th Annual Meeting of the Society for Neuropediatrics, 2025
Bern, Switzerland, 02.–04.10.2025

Abstracts (HTML) Abstracts (PDF) List of Authors
  • A-230
    Japaridze, N.; Vogt, N.; Niklaus, M.:

    A Case Report of an Infant with De Barsy Syndrome with Intractable Seizures and Severe Gastro-Esophageal Reflux

  • A-250
    Dafsari, H. S.; Deneubourg, C.; EPG5 epilepsy working group; Jungbluth, H.; Fanto, M.:

    Epg5 Links Proteotoxic Stress Due to Defective Autophagic Clearance and Epileptogenesis in Drosophila and Vici Syndrome Patients

  • A-190
    Schönberger, J.; Jaiser, M.; Klotz, K. A.; Reinacher, P. C.; Wagner, K.; Schulze-Bonhage, A.; Antonio-Arce, V. San; Jacobs, J.:

    Intracranial Sleep Spindles and High-Frequency Oscillations in Children with Focal Epilepsy and Developmental Delay

  • A-249
    Alber, M.; Kern, J.; Gröschel, S.; Floess, S.; Rosewich, H.:

    Milde Arthrogryposis und Neonatal Beginnende Tonische Anfälle, Klinischer Verlauf, und Therapieansprechen bei SCN1A-c.2345C>T-Mutation als Hinweis auf eine GOF-Variante im Rahmen Eines NDEEMA-Spektrums

  • A-115
    Knupp, K. G.; Schoonjans, A.-S.; Sullivan, J.; Lagae, L.; Guerrini, R.; Zuberi, S. M.; Nabbout, R.; Riney, K.; Nickels, K. C.; Davis, R.; Lock, M. D.; Dai, D.; Minh, T.; Roper, R. Zhang; Lothe, A.; Langlois, M.; Haas, S.; Gil-Nagel, A.:

    Safety and Effectiveness of Fenfluramine for the Treatment of Seizures in Lennox-Gastaut Syndrome: Results from the Final Analysis of an Open-Label Extension Study

  • A-176
    Becker, L.-L.; Jolitz, L.; Helbig, I.; Ruggiero, S. McKeown; Cohen, S.; Angelini, C.; Vallespin, E.; Michaud, V.; Gerasimenko, A.; Cogne, B.; Isidor, B.; Keren, B.; Dyment, D.; Heron, D.; Karstensen, H. Gásdal; Cuppen, I.; Christodoulou, J.; Wilson, M.; Lake, N. J.; Biskup, S.; Syrbe, S.; Mori, T.; Kaindl, A. M.:

    TRPM3-Associated Disorders: Clinical Spectrum and Treatment Options

  • A-287
    Bader, I.; Feichtinger, R.; Carvalhal, S.; Beichler, C.; Wolthuis, R.; van Hagen, J.; van Haelst, M.; Oliveira, R.; Mayr, J.; de Lange, J.:

    Genotypes and Phenotypes of a Novel Neurodevelopmental Disorder Caused by Biallelic Mutations in BUB1