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Acta Neuropathologica Communications|June 1, 2023
Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degenerationShunsuke Koga, Michael A Metrick, Lawrence I Golbe, et al.Arthritis Care & Research|December 2, 2025
Clinical Practice Guideline for Evaluation and Management of Peripheral Nervous System Manifestations in Sjögren's DiseaseAnahita Deboo, Robert Fox, Katherine M Hammitt, et al.Human Molecular Genetics|June 23, 2017
Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patientsMercedes Prudencio, Patrick K Gonzales, Casey N Cook, et al.Parkinsonism & Related Disorders|August 30, 2008
Pallidonigral TDP-43 pathology in Perry syndromeChristian Wider, Dennis W Dickson, A Jon Stoessl, et al.Neurology|February 11, 2021
Association of Mitochondrial DNA Genomic Variation With Risk of Pick DiseaseRebecca R Valentino, Michael G Heckman, Patrick W Johnson, et al.Brain Pathology (Zurich, Switzerland)|August 17, 2016
FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372GPawel Tacik, Michael A DeTure, Yari Carlomagno, et al.Acta Neuropathologica|April 23, 2015
A novel tau mutation, p.K317N, causes globular glial tauopathyPawel Tacik, Michael DeTure, Wen-Lang Lin, et al.Brain : a Journal of Neurology|December 17, 2021
Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutationsCyril Pottier, Ligia Mateiu, Matthew C Baker, et al.Acta Neuropathologica|April 19, 2024
Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansionEvan Udine, Mariely DeJesus-Hernandez, Shulan Tian, et al.Acta Neuropathologica|February 26, 2021
Latent trait modeling of tau neuropathology in progressive supranuclear palsyNaomi Kouri, Melissa E Murray, Joseph S Reddy, et al.Pageof 15