Schweizerisches Epilepsie-Zentrum

Combining magnetic resonance fingerprinting with voxel-based morphometric analysis to reduce false positives for focal cortical dysplasia detection (2024) Ding Z, Hu S, Su TY, Choi JY, Morris S, Wang X, Sakaie K, et al. Journal article Neurofilaments and progranulin are related to atrophy in frontotemporal lobar degeneration – A transdiagnostic study cross-validating atrophy and fluid biomarkers (2024) Hüper L, Steinacker P, Polyakova M, Mueller K, Godulla J, Herzig S, Danek A, et al. Journal article Multiclass prediction of different dementia syndromes based on multi-centric volumetric MRI imaging (2023) Lampe L, Huppertz HJ, Anderl-Straub S, Albrecht F, Ballarini T, Bisenius S, Mueller K, et al. Journal article Relationship of serum beta-synuclein with blood biomarkers and brain atrophy (2022) Oeckl P, Anderl-Straub S, Danek A, Diehl-Schmid J, Fassbender K, Fliessbach K, Halbgebauer S, et al. Journal article Correction to: Routine diagnostics for neural antibodies, clinical correlates, treatment and functional outcome (Journal of Neurology, (2020), 267, 7, (2101-2114), 10.1007/s00415-020-09814-3) (2021) Bien CG, Bien CI, Onugoren MD, De Simoni D, Eigler V, Haensch CA, Holtkamp M, et al. Journal article, Erratum Quantifying progression in primary progressive aphasia with structural neuroimaging (2021) Lombardi J, Mayer B, Semler E, Anderl-Straub S, Uttner I, Kassubek J, Diehl-Schmid J, et al. Journal article Routine diagnostics for neural antibodies, clinical correlates, treatment and functional outcome (2020) Bien CG, Bien CI, Onugoren M, De Simoni D, Eigler V, Haensch CA, Holtkamp M, et al. Journal article Correction to: Routine diagnostics for neural antibodies, clinical correlates, treatment and functional outcome (Journal of Neurology, (2020), 10.1007/s00415-020-09814-3) (2020) Bien CG, Bien CI, Dogan Onugoren M, De Simoni D, Eigler V, Haensch CA, Holtkamp M, et al. Journal article, Erratum The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study (2019) Papuc SM, Abela L, Steindl K, Begemann A, Simmons TL, Schmitt B, Zweier M, et al. Journal article Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes (2019) Begemann A, Acuna MA, Zweier M, Vincent M, Steindl K, Bachmann-Gagescu R, Hackenberg A, et al. Journal article