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Metallomics : Integrated Biometal Science|January 22, 2016
Tyrosine hydroxylase regulation in adult rat striatum following short-term neonatal exposure to manganeseTanara V Peres, Lin K Ong, Ana Paula Costa, et al.
Journal of Alzheimer'S Disease : JAD|November 26, 2023
Amyloid and Tau PET Positivity in Progressive Agrammatic Aphasia and Apraxia of SpeechKaterina A Tetzloff, Joseph R Duffy, Heather M Clark, et al.
The Journal of Clinical Investigation|February 12, 2019
APOE4-mediated amyloid-β pathology depends on its neuronal receptor LRP1Masaya Tachibana, Marie-Louise Holm, Chia-Chen Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 31, 2017
Cognitive impairment in progressive supranuclear palsy is associated with tau burdenShunsuke Koga, Adam Parks, Koji Kasanuki, et al.
Brain : a Journal of Neurology|January 30, 2013
Corticospinal tract degeneration associated with TDP-43 type C pathology and semantic dementiaKeith A Josephs, Jennifer L Whitwell, Melissa E Murray, et al.
Neurology. Genetics|January 19, 2017
ABCA7 loss-of-function variants, expression, and neurologic disease riskMariet Allen, Sarah J Lincoln, Morgane Corda, et al.
Brain Pathology (Zurich, Switzerland)|July 11, 2024
Upper motor neuron-predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological studyAya Murakami, Shunsuke Koga, Shinsuke Fujioka, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisZhengrong Zhang, Kaiwen Yu, Hanmei Bao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 21, 2019
In vivo binding of a tau imaging probe, [11 C]PBB3, in patients with progressive supranuclear palsyHironobu Endo, Hitoshi Shimada, Naruhiko Sahara, et al.
Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.
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