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Neuropathology and Applied Neurobiology|March 1, 1986
Spongiform encephalopathy: a neurocytologist's viewpoint with a note on Alzheimer's diseaseE G Gray
Neuropathology and Applied Neurobiology|July 27, 2022
DNA methylation profiling improves routine diagnosis of paediatric central nervous system tumours: A prospective population-based studyElizabeth Schepke, Maja Löfgren, Torsten Pietsch, et al.
Neuropathology and Applied Neurobiology|July 28, 2022
A novel SREBF1::NACC1 gene fusion in an unclassifiable intracranial tumourYasuhide Takeuchi, Yohei Mineharu, Yoshiki Arakawa, et al.
Neuropathology and Applied Neurobiology|February 13, 2022
The S1PR2-CCL2-BDNF-TrkB pathway mediates neuroinflammation and motor incoordination in hyperammonaemiaYaiza M Arenas, Tiziano Balzano, Gergana Ivaylova, et al.
Neuropathology and Applied Neurobiology|October 14, 2021
TRAPPC11-related muscular dystrophy with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brainPinki Munot, Nadine McCrea, Silvia Torelli, et al.
Neuropathology and Applied Neurobiology|March 11, 2022
Extracellular tau oligomers affect extracellular glutamate handling by astrocytes through downregulation of GLT-1 expression and impairment of NKA1A2 functionDomenica Donatella Li Puma, Cristian Ripoli, Giulia Puliatti, et al.
Neuropathology and Applied Neurobiology|July 31, 2023
First report of medulloblastoma in a patient with MUTYH-associated polyposisMarie-Charlotte Villy, Mathilde Warcoin, Mathilde Filser, et al.
Neuropathology and Applied Neurobiology|October 9, 2023
A high-throughput single-cell RNA expression profiling method identifies human pericyte markersAndras Sziraki, Yu Zhong, Allison M Neltner, et al.
Neuropathology and Applied Neurobiology|June 30, 2023
Psychotic symptoms in frontotemporal dementia with TDP-43 tend to be associated with type B pathologyVeronica Hirsch-Reinshagen, Christa Hercher, Fidel Vila-Rodriguez, et al.
Neuropathology and Applied Neurobiology|March 29, 2003
Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein geneA King, L Doey, M Rossor, et al.
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