PROTECT Studie EASEE4YOU Studie ESCO Natural History Study Longitudinaler Verlauf und Einflussfaktoren von genetischen Entwicklungsstörungen und Epilepsien

Patientenregister aRgus - Multilevel visualization of non-synonymous single nucleotide variants & advanced pathogenicity score modeling for genetic vulnerability assessment Dup15q Forschungsprojekt

Diagnostic Yield of Genome-Wide Sequencing and Genotype-Phenotype Correlations in Children with Epilepsy and Neurodevelopmental Disorders Dup15q Syndrome: Registry-Based Analyses of Genetic Landscape, Quantitative Natural History of Clinical Phenotypes, and EEG Biomarkers L-Serine Supplementation in Individuals with Monogenic Neurodevelopmental Disorders Analysis of Molecular Genetic Alterations in People with Therapy-Refractory Structural Epilepsies and Epilepsy Syndromes Defining Age-Dependent Metagenomic Reference Profiles in Cerebrospinal Fluid of Paediatric Patients without Inflammatory CNS Disease