Acta Neuropathologica

ISSN: 0001-6322
eISSN: 1432-0533
Publisher: Springer

Publications (23)

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Journal article
Unpublished / Preprint

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Abstract

Temporal change of DNA methylation subclasses between matched newly diagnosed and recurrent glioblastoma (2024) Drexler R, Khatri R, Schüller U, Eckhardt A, Ryba A, Sauvigny T, Dührsen L, et al. Journal article Correction to: Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genes (Acta Neuropathologica, (2023), 10.1007/s00401-023-02561-5) (2023) Hoffmann L, Coras R, Kobow K, López-Rivera JA, Lal D, Leu C, Najm I, et al. Journal article, Erratum Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genes (2023) Hoffmann L, Coras R, Kobow K, López-Rivera JA, Lal D, Leu C, Najm I, et al. Journal article Aberrant NOVA1 function disrupts alternative splicing in early stages of amyotrophic lateral sclerosis (2022) Krach F, Wheeler EC, Regensburger M, Börstler T, Wend H, Vu AQ, Wang R, et al. Journal article, Original article DNA methylation-based classification of malformations of cortical development in the human brain (2022) Jabari S, Kobow K, Pieper T, Hartlieb T, Kudernatsch M, Polster T, Bien CG, et al. Journal article Making sense of missense variants in TTN-related congenital myopathies (2021) Rees M, Nikoopour R, Fukuzawa A, Kho AL, Fernandez-Garcia MA, Wraige E, Bodi I, et al. Journal article Genetic and epigenetic characterization of posterior pituitary tumors (2021) Schmid S, Solomon DA, Perez E, Thieme A, Kleinschmidt-Demasters BK, Giannini C, Reinhardt A, et al. Journal article A glutaminyl cyclase-catalyzed α-synuclein modification identified in human synucleinopathies (2021) Hartlage-Rübsamen M, Bluhm A, Moceri S, Machner L, Köppen J, Schenk M, Hilbrich I, et al. Journal article PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment (2020) Kleineidam L, Chouraki V, Próchnicki T, van der Lee SJ, Madrid-Márquez L, Wagner-Thelen H, Karaca I, et al. Journal article Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay (2020) Kobow K, Jabari S, Pieper T, Kudernatsch M, Polster T, Woermann FG, Kalbhenn T, et al. Journal article
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