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Nature Genetics|April 17, 2012
Common variants at 6q22 and 17q21 are associated with intracranial volumeM Arfan Ikram, Myriam Fornage, Albert V Smith, 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.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 21, 2024
Presenilin-1 mutation position influences amyloidosis, small vessel disease, and dementia with disease stageNelly Joseph-Mathurin, Rebecca L Feldman, Ruijin Lu, et al.The Lancet. Neurology|March 22, 2025
Safety and efficacy of long-term gantenerumab treatment in dominantly inherited Alzheimer's disease: an open-label extension of the phase 2/3 multicentre, randomised, double-blind, placebo-controlled platform DIAN-TU trialRandall J Bateman, Yan Li, Eric M McDade, et al.Neurology|September 11, 2020
Association of common genetic variants with brain microbleeds: A genome-wide association studyMaria J Knol, Dongwei Lu, Matthew Traylor, et al.Nature Medicine|June 22, 2021
A trial of gantenerumab or solanezumab in dominantly inherited Alzheimer's diseaseStephen Salloway, Martin Farlow, Eric McDade, et al.Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Safety and efficacy of long-term gantenerumab treatment in dominantly inherited Alzheimer's disease: an open label extension of the phase 2/3 multicentre, randomised, double-blind, placebo-controlled platform DIAN-TU TrialRandall J Bateman, Yan Li, Eric M McDade, et al.Stroke|June 11, 2020
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter HyperintensitiesNicola J Armstrong, Karen A Mather, Muralidharan Sargurupremraj, et al.Nature Genetics|April 17, 2012
Common variants at 12q14 and 12q24 are associated with hippocampal volumeJoshua C Bis, Charles DeCarli, Albert Vernon Smith, et al.Nature Neuroscience|July 16, 2025
Tau PET positivity in individuals with and without cognitive impairment varies with age, amyloid-β status, APOE genotype and sexRik Ossenkoppele, Emma M Coomans, Liana G Apostolova, et al.Pageof 131