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Annals of Neurology|July 11, 2023
Network Connectivity Alterations across the MAPT Mutation Clinical SpectrumLiwen Zhang, Taru M Flagan, Suvi Häkkinen, et al.Annals of Clinical and Translational Neurology|September 17, 2025
Functional Connectivity Associations With Markers of Disease Progression in GRN Pathogenic Variant CarriersTaru M Flagan, Stephanie A Chu, Suvi Häkkinen, et al.Journal of Neurology|April 30, 2026
Factors influencing accelerated progression in behavioral variant frontotemporal dementiaMolly Split, Zachary J Kunicki, Daliah Ross, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 23, 2019
The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodologyBradley Boeve, Jessica Bove, Patrick Brannelly, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 13, 2021
Harmonizing neuropsychological assessment for mild neurocognitive disorders in EuropeMarina Boccardi, Andreas U Monsch, Clarissa Ferrari, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 14, 2020
Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohortMelanie T Gentry, Maria I Lapid, Jeremy Syrjanen, et al.Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia casesEliana Marisa Ramos, Deepika Reddy Dokuru, Victoria Van Berlo, et al.Neurobiology of Aging|October 5, 2019
Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriersQin Chen, Bradley F Boeve, Christopher G Schwarz, et al.Annals of Clinical and Translational Neurology|November 28, 2020
Brain volumetric deficits in MAPT mutation carriers: a multisite studyStephanie A Chu, Taru M Flagan, Adam M Staffaroni, et al.Pageof 42