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Neurology|April 19, 2013
Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosisAshley Cannon, Shinsuke Fujioka, Nicola J Rutherford, et al.BMC Medical Genetics|March 20, 2012
Polymorphic genes of detoxification and mitochondrial enzymes and risk for progressive supranuclear palsy: a case control studyLisa F Potts, Alex C Cambon, Owen A Ross, et al.Experimental Neurology|January 10, 2016
C9orf72 promoter hypermethylation is reduced while hydroxymethylation is acquired during reprogramming of ALS patient cellsRustam Esanov, Kinsley C Belle, Marka van Blitterswijk, et al.Cell Reports Methods|April 27, 2022
Probe design for simultaneous, targeted capture of diverse metagenomic targetsZachery W Dickson, Dirk Hackenberger, Melanie Kuch, et al.Acta Neuropathologica Communications|September 18, 2020
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measuresRebecca R Valentino, Nikoleta Tamvaka, Michael G Heckman, et al.Neurology|July 30, 2024
Clinicopathologic and Neuroimaging Correlations of Nonverbal Oral Apraxia in Patients With Neurodegenerative DiseaseDanna P Garcia-Guaqueta, Hugo Botha, Rene L Utianski, et al.Nature Medicine|April 15, 1999
Tau gene mutation in familial progressive subcortical gliosisM Goedert, M G Spillantini, R A Crowther, et al.Annals of Neurology|January 7, 2015
Defining neurodegeneration on Guam by targeted genomic sequencingJohn C Steele, Ilaria Guella, Chelsea Szu-Tu, et al.Neurology|November 4, 2009
Two distinct subtypes of right temporal variant frontotemporal dementiaK A Josephs, J L Whitwell, D S Knopman, et al.European Journal of Neurology|August 3, 2021
Clinical, pathological and genetic characteristics of Perry disease-new cases and literature reviewJarosław Dulski, Catalina Cerquera-Cleves, Lukasz Milanowski, et al.Pageof 152