Barba-Reyes, J.M.* et al. Oligodendroglia vulnerability in the human dorsal striatum in Parkinson's disease. Acta Neuropathol. 149:46 (2025)
Corrêa-da-Silva, F.* et al. Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion. Acta Neuropathol. 147:64 (2024)
Mori, K.* et al. Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins. Acta Neuropathol. 148:48 (2024)
Ryan, F.* et al. Ferroptosis inhibitor improves outcome after early and delayed treatment in mild spinal cord injury. Acta Neuropathol. 147:106 (2024)
Matosin, N.* et al. Associations of psychiatric disease and ageing with FKBP5 expression converge on superficial layer neurons of the neocortex. Acta Neuropathol. 145, 439-459 (2023)
LaClair, K.D.* et al. Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALS. Acta Neuropathol. 140, 121–142 (2020)
Gomes, L.A.* et al. A beta-induced acceleration of Alzheimer-related tau-pathology spreading and its association with prion protein. Acta Neuropathol. 138, 913-941 (2019)
Hellwig, M.* et al. TCF4 (E2-2) harbors tumor suppressive functions in SHH medulloblastoma. Acta Neuropathol. 137, 657-673 (2019)
Doppler, K.* et al. Dermal phospho-alpha-synuclein deposits confirm REM sleep behaviour disorder as prodromal Parkinson's disease. Acta Neuropathol. 133, 535-545 (2017)
Schludi, M.H.* et al. Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss. Acta Neuropathol. 134, 241–254 (2017)
Suárez-Calvet, M.* et al. Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS. Acta Neuropathol. 131, 587-604 (2016)
Mackenzie, I.R.* et al. Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers. Acta Neuropathol. 130, 845-861 (2015)
Schludi, M.H.* et al. Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing. Acta Neuropathol. 130, 537-555 (2015)
Schludi, M.H.* et al. Erratum to: Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing. Acta Neuropathol. 130, 557-558 (2015)
Götzl, J.K.* et al. Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis. Acta Neuropathol. 127, 845-860 (2014)
May, S.* et al. C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration. Acta Neuropathol. 128, 485-503 (2014)
van der Zee, J.* et al. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathol. 128, 397-410 (2014)
Kreth, S.* et al. In human glioblastomas transcript elongation by alternative polyadenylation and miRNA targeting is a potent mechanism of MGMT silencing. Acta Neuropathol. 125, 671-681 (2013)
Lee, M.S. et al. Transcriptome analysis of MENX-associated rat pituitary adenomas identifies novel molecular mechanisms involved in the pathogenesis of human pituitary gonadotroph adenomas. Acta Neuropathol. 126, 137-150 (2013)
Mackenzie, I.R.* et al. Dipeptide repeat protein pathology in C9ORF72 mutation cases: Clinico-pathological correlations. Acta Neuropathol. 126, 859-879 (2013)
Mori, K.* et al. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins. Acta Neuropathol. 126, 881-893 (2013)
Irmler, M. et al. Long-term proteasomal inhibition in transgenic mice by UBB+1 expression results in dysfunction of central respiration control reminiscent of brainstem neuropathology in Alzheimer patients. Acta Neuropathol. 124, 187-197 (2012)
Elstner, M. et al. Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death. Acta Neuropathol. 122, 75-86 (2011)
Neumann, M.* et al. Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies. Acta Neuropathol. 117, 137-149 (2009)
Alldinger, S.* ; Fonfara, S.* ; Kremmer, E. & Baumgärtner, W.* Up-regulation of the hyaluronate receptor CD44 in canine distemper demyelinated plaques. Acta Neuropathol. 99, 138-146 (2000)
Neumann, M.* et al. alpha-Synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies. Acta Neuropathol. 100, 568-574 (2000)
Schmahl, W. ; Knödlseder, M. ; Favor, J. & Davidson, D. Defects of Neuronal Migration and the Phatogenesis of Cortical Malformations are associated with Small eye (Sey) in the Mouse, a Point Mutation at the Pax-6-locus. Acta Neuropathol. 86, 126-135 (1993)
Schmahl, W.G. ; Knoedlseder, M. ; Favor, J. & Davidson, D.R.* Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus. Acta Neuropathol. 86, 126-135 (1993)
Stavrou, D.K.* et al. Localization of experimental glioma grafts by means of iodinated monoclonal antibodies and radionuclide imaging. Acta Neuropathol. 66, 340-342 (1985)