A T-cell antigen atlas for meningioma: novel options for immunotherapy Gioele MediciLena K. FreudenmannMarian C. Neidert Original Paper Open access 27 June 2023 Pages: 173 - 190
Tau seeding and spreading in vivo is supported by both AD-derived fibrillar and oligomeric tau Anastasie Mate De GerandoLindsay A. WelikovitchBradley T. Hyman Original Paper Open access 21 June 2023 Pages: 191 - 210
Mutation ∆K281 in MAPT causes Pick’s disease Manuel SchweighauserHolly J. GarringerKathy L. Newell Original Paper Open access 23 June 2023 Pages: 211 - 226
Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes Chiara CappellettiSandra Pilar HenriksenMathias Toft Original Paper Open access 22 June 2023 Pages: 227 - 244
Mutant LRRK2 exacerbates immune response and neurodegeneration in a chronic model of experimental colitis Diego CabezudoGeorge TsafarasVeerle Baekelandt Original Paper Open access 08 June 2023 Pages: 245 - 261
Central and peripheral myeloid-derived suppressor cell-like cells are closely related to the clinical severity of multiple sclerosis María Cristina OrtegaRafael Lebrón-GalánDiego Clemente Original Paper Open access 27 May 2023 Pages: 263 - 282
From methylation to myelination: epigenomic and transcriptomic profiling of chronic inactive demyelinated multiple sclerosis lesions Assia TianeMelissa SchepersTim Vanmierlo Original Paper Open access 07 June 2023 Pages: 283 - 299
Defective cerebellar ryanodine receptor type 1 and endoplasmic reticulum calcium ‘leak’ in tremor pathophysiology Regina T. MartuscelloMeng-Ling ChenPhyllis L. Faust Original Paper 19 June 2023 Pages: 301 - 318
Individual myasthenia gravis autoantibody clones can efficiently mediate multiple mechanisms of pathology Minh C. PhamGianvito MasiKevin C. O’Connor Original Paper 21 June 2023 Pages: 319 - 336
SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders Benjamin EllezamMatsanga L. KasekaJean Michaud Original Paper 15 May 2023 Pages: 337 - 352
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model Ruizhi DengEva Medico-SalsenchTahsin Stefan Barakat Original Paper Open access 29 April 2023 Pages: 353 - 368