NAB2::STAT6 fusions and genome-wide DNA methylation profiling: Predictors of patient outcomes in meningeal solitary fibrous tumors (2024) Eschbacher KL, Tran QT, Moskalev E, Jenkins S, Fritchie K, Stöhr R, Caron A, et al. Journal article Leigh syndrome is the main clinical characteristic of PTCD3 deficiency (2022) Muñoz-Pujol G, Ortigoza-Escobar JD, Paredes-Fuentes AJ, Jou C, Ugarteburu O, Gort L, Yubero D, et al. Journal article Variable histopathology features of neuronal dyslamination in the cerebral neocortex adjacent to epilepsy-associated vascular malformations suggest complex pathogenesis of focal cortical dysplasia ILAE type IIIc (2022) Miyata H, Kuwashige H, Hori T, Kubota Y, Pieper T, Coras R, Blümcke I, Yoshida Y Journal article Molecular diagnostics in drug-resistant focal epilepsy define new disease entities. (2021) Kobow K, Baulac S, von Deimling A, Lee JH Journal article Focal cortical dysplasia type 1 (2021) Coras R, Holthausen H, Sarnat HB Journal article Toward a refined genotype–phenotype classification scheme for the international consensus classification of Focal Cortical Dysplasia (2021) Blümcke I, Cendes F, Miyata H, Thom M, Aronica E, Najm I Journal article An introduction to the mini-symposium on “The Neuropathology of Focal Human Epilepsy” (2021) Blümcke I Journal article NanoString technology distinguishes anti-TIF-1γ+ from anti-Mi-2+ dermatomyositis patients (2021) Preusse C, Eede P, Heinzerling L, Freitag K, Koll R, Froehlich W, Schneider U, et al. Journal article Integrated genotype–phenotype analysis of long-term epilepsy-associated ganglioglioma (2021) Wang Y, Wang L, Blümcke I, Zhang W, Fu Y, Shan Y, Piao Y, Zhao G Journal article It is time to move on: Commentary to: Genotype-phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery (DOI: 10.1111/bpa.12686) (2019) Blümcke I Journal article, Note