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Alzheimer'S & Dementia (New York, N. Y.)|August 8, 2019
Rates of lobar atrophy in asymptomatic MAPT mutation carriersQin Chen, Bradley F Boeve, Matthew Senjem, et al.Brain : a Journal of Neurology|November 3, 2020
18F-flortaucipir PET to autopsy comparisons in Alzheimer's disease and other neurodegenerative diseasesDavid N Soleimani-Meigooni, Leonardo Iaccarino, Renaud La Joie, et al.Alzheimer'S Research & Therapy|February 2, 2019
18F-flortaucipir (AV-1451) tau PET in frontotemporal dementia syndromesRichard M Tsai, Alexandre Bejanin, Orit Lesman-Segev, et al.Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Longitudinal functional network connectivity changes across the clinical stages of C9orf72 hexanucleotide repeat expansion carriersLiwen Zhang, Suvi Häkkinen, Youjin Jung, et al.Brain : a Journal of Neurology|November 21, 2023
Clinical dimensions along the non-fluent variant primary progressive aphasia spectrumIgnacio Illán-Gala, Diego L Lorca-Puls, Boon Lead Tee, et al.Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
The BEYONDD Pilot Study: A Decentralized Community-Engaged Research Framework for Multimodal Characterization of Neurodegenerative Risk in a Multi-Ethnic, Midlife Cohort with Subjective Cognitive or Behavioral ComplaintsMonica Rivera-Mindt, Micah J Savin, Vanessa Guzman, et al.Parkinsonism & Related Disorders|May 6, 2025
Peripheral Immune pattern in a genetic cohort of p.A53T alpha-synuclein carriersChristos Koros, Athina-Maria Simitsi, Nikolaos Papagiannakis, et al.Medrxiv : the Preprint Server for Health Sciences|July 17, 2026
In-clinic validation of a smartphone-based finger tapping test for use in neurodegenerative and neurological populationsMorgan O'Connor, Mark E Sanderson-Cimino, Zi Li, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 9, 2012
Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansionBaber K Khan, Jennifer S Yokoyama, Leonel T Takada, et al.Alzheimer'S & Dementia (New York, N. Y.)|November 11, 2017
An 8-week, open-label, dose-finding study of nimodipine for the treatment of progranulin insufficiency from GRN gene mutationsSharon J Sha, Zachary A Miller, Sang-Won Min, et al.Pageof 43