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Author Details

Stephen J DeArmond
1971
267
97
PMIDPaper TitleJournal TitlePublished Year
35662331Default Mode Network quantitative diffusion and resting-state functional magnetic resonance imaging correlates in sporadic Creutzfeldt-Jakob disease.Hum Brain Mapp2022
29453245Early vs late age at onset frontotemporal dementia and frontotemporal lobar degeneration.Neurology2018
28264087Precipitous Deterioration of Motor Function, Cognition, and Behavior.JAMA Neurol2017
28863454Autobiography Series: From Sleep-Wake Mechanisms to Prion Diseases.Journal of Neuropathology and Experimental Neurology2017
26851378Brain Aggregates: An Effective In Vitro Cell Culture System Modeling Neurodegenerative Diseases.J Neuropathol Exp Neurol2016
26796215Selective Frontoinsular von Economo Neuron and Fork Cell Loss in Early Behavioral Variant Frontotemporal Dementia.Cereb Cortex2016
26116725Use of a 2-aminothiazole to Treat Chronic Wasting Disease in Transgenic Mice.J Infect Dis2015
26137419Metabolic disorders with clinical and radiologic features of sporadic Creutzfeldt-Jakob disease.Neurol Clin Pract2015
26094969Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation.Ann Neurol2015
26226132Prion Disease Induces Alzheimer Disease-Like Neuropathologic Changes.J Neuropathol Exp Neurol2015
26224882Different 2-Aminothiazole Therapeutics Produce Distinct Patterns of Scrapie Prion Neuropathology in Mouse Brains.J Pharmacol Exp Ther2015
24699458Evidence that bank vole PrP is a universal acceptor for prions.PLoS Pathog2014
25367029White matter involvement in sporadic Creutzfeldt-Jakob disease.Brain2014
24419081AAV9-mediated expression of a non-self protein in nonhuman primate central nervous system triggers widespread neuroinflammation driven by antigen-presenting cell transduction.Molecular Therapy2014
24866748Convection-enhanced delivery of AAV2-PrPshRNA in prion-infected mice.PLoS One2014
24982139Serial propagation of distinct strains of Aβ prions from Alzheimer's disease patients.Proc Natl Acad Sci U S A2014
24982137Distinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice.Proc Natl Acad Sci U S A2014
24624328Application of quantitative DTI metrics in sporadic CJD.Neuroimage Clin2014
23383230Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease.PLoS One2013
22367382Patterns of striatal degeneration in frontotemporal dementia.Alzheimer Dis Assoc Disord2013
24218576Transmission of multiple system atrophy prions to transgenic mice.Proc Natl Acad Sci U S A2013
24122181Quinacrine treatment trial for sporadic Creutzfeldt-Jakob disease.Neurology2013
24330864Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases.Acta Neuropathol Commun2013
23965382Biaryl amides and hydrazones as therapeutics for prion disease in transgenic mice.J Pharmacol Exp Ther2013
24128760Drug resistance confounding prion therapeutics.Proc Natl Acad Sci U S A2013
23400721Sporadic Jakob-Creutzfeldt disease presenting as primary progressive aphasia.JAMA Neurol2013
23438476Convergent replication of mouse synthetic prion strains.Am J Pathol2013
23100369Chimeric elk/mouse prion proteins in transgenic mice.J Gen Virol2013
22017504Safety and tolerability of magnetic resonance imaging-guided convection-enhanced delivery of AAV2-hAADC with a novel delivery platform in nonhuman primate striatum.Hum Gene Ther2012
22438549Identification of I137M and other mutations that modulate incubation periods for two human prion strains.J Virol2012
22547509Clinical overlap between Jakob-Creutzfeldt disease and Lewy body disease.Can J Neurol Sci2012
22507918A brain aggregate model gives new insights into the pathobiology and treatment of prion diseases.Journal of Neuropathology and Experimental Neurology2012
22331873Spontaneous generation of rapidly transmissible prions in transgenic mice expressing wild-type bank vole prion protein.Proc Natl Acad Sci U S A2012
22491196Saccade abnormalities in autopsy-confirmed frontotemporal lobar degeneration and Alzheimer disease.Arch Neurol2012
22768295Pharmacokinetics of quinacrine efflux from mouse brain via the P-glycoprotein efflux transporter.PLoS One2012
22453179Salivary prions in sheep and deer.Prion2012
22711819Purified and synthetic Alzheimer's amyloid beta (Aβ) prions.Proc Natl Acad Sci U S A2012
23229042Differential diagnosis of Jakob-Creutzfeldt disease.Arch Neurol2012
23344724Intracerebral Infusion of Antisense Oligonucleotides Into Prion-infected Mice.Mol Ther Nucleic Acids2012
21653702Selective frontoinsular von Economo neuron and fork cell loss in early behavioral variant frontotemporal dementia.Cereb Cortex2012
22163178Protease-resistant prions selectively decrease Shadoo protein.PLoS Pathog2011
21262831Bioluminescence imaging of Abeta deposition in bigenic mouse models of Alzheimer's disease.Proc Natl Acad Sci U S A2011
20562461Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family.J Neurol Neurosurg Psychiatry2011
21727894Conserved properties of human and bovine prion strains on transmission to guinea pigs.Lab Invest2011
21881831Behavioral variant frontotemporal dementia with corticobasal degeneration pathology: phenotypic comparison to bvFTD with Pick's disease.J Mol Neurosci2011
21839745Conformational transformation and selection of synthetic prion strains.J Mol Biol2011
22160704Spontaneous generation of anchorless prions in transgenic mice.Proc Natl Acad Sci U S A2011
22131541Amyloid vs FDG-PET in the differential diagnosis of AD and FTLD.Neurology2011
22114562Down-regulation of Shadoo in prion infections traces a pre-clinical event inversely related to PrP(Sc) accumulation.PLoS Pathog2011
21823158Clinicopathological correlations in corticobasal degeneration.Ann Neurol2011
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