StephenJ.DeArmondMD

PubMed

• Autobiography Series: From Sleep-Wake Mechanisms to Prion Diseases.
  DeArmond, S. J.> ;Journal of neuropathology and experimental neurology. 2017 Sep 3
• 55 citations
  Selective Frontoinsular von Economo Neuron and Fork Cell Loss in Early Behavioral Variant Frontotemporal Dementia.
  Kim, E., Sidhu, M., Gaus, S. E., Huang, E. J., Hof, P. R., Miller, B. L., DeArmond, S. J., Seeley, W. W.> ;Cerebral cortex (New York, N.Y. : 1991). 2016 Jan 23
• Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation
  Joel C. Watts, Kurt Giles, Ana Serban, Smita S. Patel, Abby Oehler, Sumita Bhardwaj, Shenheng Guan, Mph Michael D. Greicius Md, Bruce L. Miller, Stephen J. DeArmond, M...> ;Annals of Neurology. 2015 Oct 1
• White matter involvement in sporadic Creutzfeldt-Jakob disease
  Eduardo Caverzasi, Maria Luisa Mandelli, Stephen J. DeArmond, Christopher P. Hess, Paolo Vitali, Nico Papinutto, Abby Oehler, Bruce L. Miller, Irina V. Lobach, Stefano...> ;Brain. 2014 Dec 1
• Distinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice
  Jan Stöhr, Carlo Condello, Joel C. Watts, Lillian Bloch, Abby Oehler, Mimi Nick, Stephen J. DeArmond, Kurt Giles, William F. DeGrado, Stanley B. Prusiner> ;Proceedings of the National Academy of Sciences of the United States of America. 2014 Jul 15
• Serial propagation of distinct strains of Aβ prions from Alzheimer’s disease patients
  Joel C. Watts, Carlo Condello, Jan Stöhr, Abby Oehler, Joanne Lee, Stephen J. DeArmond, Lars Lannfelt, Martin Ingelsson, Kurt Giles, Stanley B. Prusiner> ;Proceedings of the National Academy of Sciences of the United States of America. 2014 Jul 15
• Evidence that bank vole PrP is a universal acceptor for prions.
  Joel C. Watts, Kurt Giles, Smita S. Patel, Abby Oehler, Stephen J. DeArmond, Stanley B. Prusiner> ;PLOS Pathogens. 2014 Apr 3
• 5 citations
  Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases
  Mee Ohk Kim, Ignazio Cali, Abby Oehler, Jamie Fong, Katherine Wong, Tricia See, Jonathan S. Katz, Pierluigi Gambetti, Brianne M. Bettcher, Stephen J. DeArmond, Michael...> ;Acta neuropathologica communications. 2013 Dec 12
• 23 citations
  Quinacrine treatment trial for sporadic Creutzfeldt-Jakob disease
  Michael D. Geschwind, Amy Kuo, Katherine Wong, Aissa Haman, Gillian Devereux, Benjamin J. Raudabaugh, David Y. Johnson, Charles C. Torres-Chae, Ron Finley, Paul A. Gar...> ;Neurology. 2013 Dec 3
• 103 citations
  Transmission of multiple system atrophy prions to transgenic mice
  Joel C. Watts, Kurt Giles, Abby Oehler, Lefkos T. Middleton, David T. Dexter, S. M. Gentleman, Stephen J. DeArmond, Stanley B. Prusiner> ;Proceedings of the National Academy of Sciences of the United States of America. 2013 Nov 26
• Drug resistance confounding prion therapeutics
  David B. Berry, Duo Lu, Michal Geva, Joel C. Watts, Sumita Bhardwaj, Abby Oehler, Adam R. Renslo, Stephen J. DeArmond, Stanley B. Prusiner, Kurt Giles> ;Proceedings of the National Academy of Sciences of the United States of America. 2013 Oct 29
• 1 citations
  Biaryl amides and hydrazones as therapeutics for prion disease in transgenic mice.
  Lu, D., Giles, K., Li, Z., Rao, S., Dolghih, E., Gever, J. R., Geva, M., Elepano, M. L., Oehler, A., Bryant, C., Renslo, A. R., Jacobson, M. P., Dearmond, S. J., Silbe...> ;The Journal of pharmacology and experimental therapeutics. 2013 Aug 24
• 1 citations
  Convergent Replication of Mouse Synthetic Prion Strains
  Sina Ghaemmaghami, David W. Colby, Hoang-Oanh B. Nguyen, Shigenari Hayashi, Abby Oehler, Stephen J. DeArmond, Stanley B. Prusiner> ;American Journal of Pathology. 2013 Mar 1
• 6 citations
  Sporadic Jakob-Creutzfeldt disease presenting as primary progressive aphasia.
  Johnson, D. Y., Dunkelberger, D. L., Henry, M. L., Haman, A., Greicius, M. D., Wong, K., DeArmond, S. J., Miller, B. L., Gorno-Tempini, M. L., Geschwind, M. D.> ;JAMA neurology. 2013 Feb 13
• Chimeric elk/mouse prion proteins in transgenic mice
  Gültekin Tamgüney, Kurt Giles, Abby Oehler, Natrina L. Johnson, Stephen J. DeArmond, Stanley B. Prusiner> ;Journal of General Virology. 2013 Feb 1
• Levels of the Mahogunin Ring Finger 1 E3 Ubiquitin Ligase Do Not Influence Prion Disease
  Derek Silvius, Rose Pitstick, Misol Ahn, Delisha Meishery, Abby Oehler, Gregory S. Barsh, Stephen J. DeArmond, George A. Carlson, Teresa M. Gunn> ;PLOS ONE. 2013 Jan 30
• Patterns of striatal degeneration in frontotemporal dementia.
  Cathra Halabi, Anasheh Halabi, David Dean, Pei-Ning Wang, Adam L. Boxer, John Q. Trojanowski, Stephen J. DeArmond, Bruce L. Miller, Joel H. Kramer, William W. Seeley> ;Alzheimer Disease & Associated Disorders. 2013 Jan 1
• 18 citations
  Differential diagnosis of Jakob-Creutzfeldt disease.
  Ross W. Paterson, Charles C. Torres-Chae, Amy Kuo, Tim Ando, Elizabeth A. Nguyen, Katherine Wong, Stephen J. DeArmond, Aissa Haman, Paul A. Garcia, David Y. Johnson, B...> ;JAMA Neurology. 2012 Dec 1
• Differential Diagnosis of Jakob-Creutzfeldt Disease.
  Paterson RW Torres-Chae CC Kuo AL Ando T Nguyen EA Wong K Dearmond SJ Haman A Garcia P Johnson DY Miller BL Geschwind MD> ;Arch Neurol. 2012 Sep 24
• 3 citations
  Pharmacokinetics of quinacrine efflux from mouse brain via the P-glycoprotein efflux transporter.
  Ahn, M., Ghaemmaghami, S., Huang, Y., Phuan, P., May, B. C., Giles, K., DeArmond, S. J., Prusiner, S. B.> ;PloS one. 2012 Jul 7
• Purified and synthetic Alzheimer’s amyloid beta (Aβ) prions
  Jan Stöhr, Joel C. Watts, Zachary L. Mensinger, Abby Oehler, Sunny K. Grillo, Stephen J. DeArmond, Stanley B. Prusiner, Kurt Giles> ;Proceedings of the National Academy of Sciences of the United States of America. 2012 Jul 3
• 5 citations
  Identification of I137M and Other Mutations That Modulate Incubation Periods for Two Human Prion Strains
  Kurt Giles, Gian Felice De Nicola, Smita S. Patel, David V. Glidden, Carsten Korth, Abby Oehler, Stephen J. DeArmond, Stanley B. Prusiner> ;Journal of Virology. 2012 Jun 1
• 4 citations
  A brain aggregate model gives new insights into the pathobiology and treatment of prion diseases.
  Krystyna Bajsarowicz, Misol Ahn, Larry Ackerman, Bernadette N. DeArmond, George A. Carlson, Stephen J. DeArmond> ;Journal of Neuropathology and Experimental Neurology. 2012 May 1
• Clinical overlap between Jakob-Creutzfeldt disease and Lewy body disease.
  Maria Carmela Tartaglia, David Y. Johnson, Julie Ngoc Thai, Tatiana Cattaruzza, Katherine Wong, Paul A. Garcia, Stephen J. DeArmond, Bruce L. Miller, Michael D. Geschwind> ;Canadian Journal of Neurological Sciences. 2012 May 1
• 18 citations
  Salivary prions in sheep and deer.
  Tamgüney, G., Richt, J. A., Hamir, A. N., Greenlee, J. J., Miller, M. W., Wolfe, L. L., Sirochman, T. M., Young, A. J., Glidden, D. V., Johnson, N. L., Giles, K., DeAr...> ;Prion. 2012 Mar 29
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Journal Articles

• Cytosolic prion protein in neurons.  
  Mironov A, Latawiec D, Wille H, Bouzamondo-Bernstein E, Legname G, Williamson RA, Burton D, DeArmond SJ, Prusiner SB, Peters PJ, J Neurosci
• The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system.  
  Bouzamondo-Bernstein E, Hopkins SD, Spilman P, Uyehara-Lock J, Deering C, Safar J, Prusiner SB, Ralston HJ, DeArmond SJ, J Neuropathol Exp Neurol
• Prion clearance in bigenic mice.  
  Safar JG, DeArmond SJ, Kociuba K, Deering C, Didorenko S, Bouzamondo-Bernstein E, Prusiner SB, Tremblay P, J Gen Virol
• Etiology and pathogenesis of prion diseases.  
  DeArmond SJ, Prusiner SB, Am J Pathol
• Patterns of MRI atrophy in tau-positive and ubiquitin-positive frontotemporal lobar degeneration.  
  Kim EJ, Rabinovici GD, Seeley WW, Halabi C, Shu H, Weiner MW, DeArmond SJ, Trojanowski JQ, Gorno-Tempini ML, Miller BL, Rosen HJ, J Neurol Neurosurg Psychiatry
• The molecular pathology of prion diseases.  
  DeArmond SJ, West J Med
• Prion diseases and neurodegeneration.  
  Prusiner SB, DeArmond SJ, Annu Rev Neurosci
• The effect of preoptic warming on the arousal system of the mesencephalic reticular formation.  
  DeArmond SJ, Fusco MM, Exp Neurol
• Radiation-induced large intracranial vessel occlusive vasculopathy.  
  Brant-Zawadzki M, Anderson M, DeArmond SJ, Conley FK, Jahnke RW, AJR Am J Roentgenol
• A neurochemical and immunocytochemical study of P2 protein in human and bovine nervous systems.  
  DeArmond SJ, Deibler GE, Bacon M, Kies MW, Eng LF, J Histochem Cytochem
• The application of glial fibrillary acidic (GFA) protein immunohistochemistry in neurooncology. A progress report.  
  DeArmond SJ, Eng LF, Rubinstein LJ, Pathol Res Pract
• The neurochemistry of prion diseases.  
  DeArmond SJ, Prusiner SB, J Neurochem
• Glial fibrillary acidic (GFA) protein immunocytochemistry in development and neuropathology.  
  DeArmond SJ, Deibler GE, Bacon M, Kies MW, Eng LF, J Histochem Cytochem
• Development of a non-selecting, non-perturbing method to study human brain tumor cell invasion in murine brain.  
  DeArmond SJ, Stowring L, Amar A, Coopersmith P, Dougherty D, Spencer D, Mikkelsen T, Rosenblum M, J Neurooncol
• Development of an in vitro extracellular matrix assay for studies of brain tumor cell invasion.  
  Amar AP, DeArmond SJ, Spencer DR, Coopersmith PF, Ramos DM, Rosenblum ML, J Neurooncol
• Post-embedding immunoperoxidase staining of glial fibrillary acidic protein for light and electron microscopy.  
  DeArmond SJ, Siegel MW, Dixon RG, Eng LF, J Neuroimmunol
• Glial fibrillary acidic protein in hepatic encephalopathy. An immunohistochemical study.  
  Sobel RA, DeArmond SJ, Forno LS, Eng LF, J Neuropathol Exp Neurol
• Type I fiber predominance can be caused by isolated mitochondrial respiratory chain complex I deficiency.  
  Enns GM, Hopper CL, DeArmond SJ, Bass NE, Zanko A, Weisiger K, Ohnstad C, Bolabi M, Packman S, Am. J. Hum. Genet
• Brain region differences in prion protein structure and selective vulnerability of neurons in scrapie.  
  Qui Y, Ninchak-Casey A, Yehiely F, Prusiner SB, DeArmond SJ, J Neuropathol Exp Neurol
• Antibodies to the scrapie protein decorate prion rods.  
  Barry RA, McKinley MP, Bendheim PE, Lewis GK, DeArmond SJ, Prusiner SB, J Immunol
• A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice.  
  Kaneko K, Ball HL, Wille H, Zhang H, Groth D, Torchia M, Tremblay P, Safar J, Prusiner SB, DeArmond SJ, Baldwin MA, Cohen FE, J Mol Biol
• A microangiopathic syndrome of encephalopathy, hearing loss, and retinal arteriolar occlusions.  
  Monteiro ML, Swanson RA, Coppeto JR, Cuneo RA, DeArmond SJ, Prusiner SB, Neurology
• Cerebral amyloidosis in prion diseases.  
  DeArmond SJ, Amyloid: Int. J. Exp. Clin. Invest
• An unusual spinal meningioma in a child: case report.  
  Liu HC, DeArmond SJ, Edwards MS, Neurosurgery
• Measurement of GFAP in hepatic encephalopathy by ELISA and transblots.  
  Kretzschmar HA, DeArmond SJ, Forno LS, J Neuropathol Exp Neurol
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Books/Book Chapters

• Immunocytochemical studies of astrocytes in normal development and disease. 
  Chapter: Advances in Cellular Neurobiology 
  Page 145 - 171Eng LF, DeArmond SJEditors: Federoff S, Hertz L.Academic Press, New York
• Immunochemistry of the glial fibrillary acidic (GFA) protein. 
  Chapter: Progress in Neuropathology 
  Page 19 - 39Eng LF, DeArmond SJEditors: Zimmerman HM.Raven Press, New York
• Structure of the Human Brain, a Photographic Atlas. 
  DeArmond SJ, Fusco MM, Dewey MOxford Press, New YorkEdition 1st,,
• Pathogenesis of Prion Diseases. 
  Chapter: Protein misfolding, aggregataion, and conformational diseases 
  Page 125 - 146Legname G, DeArmond SJ, Cohen FE, Prusiner SBEditors: Uversky VN and Fink A.Springer Science+Business Media, LLC, NY
• Glial fibrillary acidic (GFA) protein immunocytochemistry in development and neuropathology. 
  Chapter: Proceedings of the XI International Congress of Anatomy, Part A: Alan R. Liss 
  Page 65 - 79Eng LF, DeArmond SJEditors: Fedoroff S, Hertz L.New York
• Ice Skating: Steps to Success. 
  Künzle-Watson K, DeArmond SJHuman Kinetics Press, Champaign, IL
• Immunohistochemistry: Techniques and application to neurooncology. 
  Chapter: Progress in Experimental Brain Tumor Research: Brain Tumor Biology 
  Page 92 - 117DeArmond SJ, Eng LFEditors: Rosenblum ML, Wilson CB.Karger Medical and Scientific Publishers, Basel, Switzerland
• Ultrastructural and immunological investigations of scrapie prions. 
  Chapter: The Biological Substrates of Alzheimer's Disease 
  Page 145 - 160McKinley MP, Barry RA, Braunfeld MB, Prusiner SB, DeArmond SJEditors: Scheibel AB, Wechsler AF, Brazier MAB.UCLA Forum Medical Sciences: Academic Press, New York
• The molecular pathology of prion diseases. 
  Chapter: Prions: Novel Infectious Pathogens Causing Scrapie and Creutzfeldt-Jakob Disease 
  Page 387 - 414DeArmond SJ, Kretzschmar HA, McKinley MP, Prusiner SBEditors: Prusiner SB, McKinley MP.Academic Press, New York
• Correlation of in situ cell kinetics and degree of anaplasia in human brain tumors: Identification of S-phase cells with anti-BUdR antibodies. 
  Page 67 - 74DeArmond SJ, Nagashima T, Cho KG, Murovic JA, Davis RL, Hoshino TLEditors: Chatel M, Darcel F, Pecker J.Brain Oncology: Martinus Nijhoff Publishers, Dordrecht, The Netherlands
• Novel mechanisms of CNS degeneration - prion structure and biology. 
  Chapter: Novel Infectious Agents and the Central Nervous System 
  Page 239 - 256Prusiner SB, Stahl N, DeArmond SJEditors: John Wiley and Sons.London
• Prion diseases. 
  Chapter: Handbook of Clinical Neurology 
  Page 543 - 580Prusiner SB, Hsiao KK, Bredesen DE, DeArmond SJEditors: Vinken PJ, Bruyn GW, Klawans HL, McKendall RR.Elsevier, Amsterdam, Netherlands
• The Molecular and Genetic Basis of Neurodegenerative Diseases. 
  Chapter: Modern Surgical Pathology 
  Page 2039 - 2068Tousseyn TA, Simko JP, Gaskin DA, DeArmond SJEditors: Weidner, N, Cote, RJ, Suster, S, Weiss, LM.WB Saunders Co, Philadelphia, PA
• Biosafety issues in prion diseases. 
  Chapter: Prion Biology and Diseases 
  Page 921 - 960Harris DA, Peters PJ, Taraboulos A, Lingappa V, DeArmond SJ, Prusiner SBEditors: Prusiner, SB.Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
• Some strategies and methods for the study of prions. 
  Chapter: Prion Biology and Diseases 
  Page 857 - 920Harris DA, Peters PJ, Taraboulos A, Lingappa V, DeArmond SJ, Prusiner SBEditors: Prusiner, SB.Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
• Cell biology of prions. 
  Chapter: Prion Biology and Diseases 
  Page 483 - 544Harris DA, Peters PJ, Taraboulos A, Lingappa V, DeArmond SJ, Prusiner SBEditors: Prusiner, SB.Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NYEdition 2nd,
• Prion Diseases. 
  Chapter: Greenfield's Neuropathology 
  Page 273 - 323DeArmond SJ, Kretzschmar HA, Prusiner SBEditors: Graham, DI and Lantos, PL.Arnold, LondonEdition 1-> ,
• Perspectives on prion biology, prion disease pathogenesis, and pharmacological approaches to treatment. 
  Chapter: Clinics in Laboratory Medicine 
  Page 1 - 41DeArmond SJ and Prusiner SBEditors: Ghetti, B and Piccardo, P. Prion Diseases.WB Saunders Company, Philadelphia
• The molecular and genetic basis of neurodegenerative diseases. 
  Chapter: Modern Surgical Pathology 
  Page 2121 - 2153DeArmond SJ, Simko JP, Gaskin DAEditors: Weidner, N, Cote, RJ, Suster, S, Weiss, LM.WB Saunders Co, Philadelphia, PA
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Abstracts/Posters

• Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters.
  Hecker R, Taraboulos A, Scott M, Pan KM, Yang SL, Torchia M, Jendroska K, DeArmond SJ, Prusiner SB, Genes Dev
• Sporadic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease.
  Martindale J, Geschwind MD, DeArmond SJ, Young G, Dillon WP, Henry R, Uyehara-Lock JH, Gaskin DA, Miller BL, Arch Neurol
• Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.
  Carlson GA, Ebeling C, Yang SL, Telling G, Torchia M, Groth D, Westaway D, DeArmond SJ, Prusiner SB, Proc Natl Acad Sci U S A
• Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease.
  Geschwind MD, Martindale J, Miller D, DeArmond SJ, Uyehara-Lock J, Gaskin D, Kramer JH, Barbaro NM, Miller BL, Arch Neurol
• Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein.
  Hsiao KK, Groth D, Scott M, Yang SL, Serban H, Rapp D, Foster D, Torchia M, DeArmond SJ, Prusiner SB, Proc Natl Acad Sci U S A
• Notch-1 activation and dendritic atrophy in prion disease.
  Ishikura N, Clever JL, Bouzamondo-Bernstein E, Samayoa E, Prusiner SB, Huang EJ, DeArmond SJ, Proc Natl Acad Sci U S A
• Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
  Telling GC, Scott M, Hsiao KK, Foster D, Yang SL, Torchia M, Sidle KC, Collinge J, DeArmond SJ, Prusiner SB, Proc Natl Acad Sci U S A
• Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle.
  Enns GM, Hoppel CL, DeArmond SJ, Schelley S, Bass N, Weisiger K, Horoupian D, Packman S, Clin Genet
• Ischemic stress induces deposition of amyloid beta immunoreactivity in human brain.
  Jendroska K, Poewe W, Daniel SE, Pluess J, Iwerssen-Schmidt H, Paulsen J, Barthel S, Schelosky L, Cervós-Navarro J, DeArmond SJ, Acta Neuropathol (Berl)
• First symptom in sporadic Creutzfeldt-Jakob disease.
  Rabinovici GD, Wang PN, Levin J, Cook L, Pravdin M, Davis J, DeArmond SJ, Barbaro NM, Martindale J, Miller BL, Geschwind MD, Neurology
• Developmental expression of PrP in the post-implantation embryo.
  Tremblay P, Bouzamondo-Bernstein E, Heinrich C, Prusiner SB, DeArmond, SJ, Brain Research
• Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein.
  Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ, Prusiner SB, Cell
• Prion disease (PrP-A117V) presenting with ataxia instead of dementia.
  Mastrianni JA, Curtis MT, Oberholtzer JC, Da Costa MM, DeArmond SJ, Prusiner SB, Garbern JY, Neurology
• Changes in neuropeptide expression in mice infected with prions.
  Diez M, Groth D, DeArmond SJ, Prusiner SB, Hökfelt, Neurobiology of Aging
• Creutzfeldt-Jakob disease in a pregnant woman with an implanted dura mater graft.
  Lane KL, Brown P, Howell DN, Crain BJ, Hulette CM, Burger PC, DeArmond SJ, Neurosurgery
• . Genetics of prion diseases and prion diversity in mice.
  Carlson GA, DeArmond SJ, Torchia M, Westaway D, Prusiner SB, Philos Trans R Soc Lond B Biol Sci
• Regional mapping of prion proteins in brain.
  Taraboulos A, Jendroska K, Serban D, Yang SL, DeArmond SJ, Prusiner SB, Proc Natl Acad Sci U S A
• Central nervous system systemic lupus erythematosus mimicking progressive multifocal leucoencephalopathy.
  Kaye BR, Neuwelt CM, London SS, DeArmond SJ, Ann Rheum Dis
• Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.
  Scott M, Groth D, Foster D, Torchia M, Yang SL, DeArmond SJ, Prusiner SB, Cell
• Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform.
  DeArmond SJ, Yang SL, Lee A, Bowler R, Taraboulos A, Groth D, Prusiner SB, Proc Natl Acad Sci U S A
• Overview of the transmissible spongiform encephalopathies: prion protein disorders.
  DeArmond SJ, Br Med Bull
• The neuropathological phenotype in transgenic mice expressing different prion protein constructs.
  DeArmond SJ, Yang SL, Cayetano-Canlas J, Groth D, Prusiner SB, Philos Trans R Soc Lond B Biol Sci
• Scrapie prions alter receptor-mediated calcium responses in cultured cells.
  Kristensson K, Feuerstein B, Taraboulos A, Hyun WC, Prusiner SB, DeArmond SJ, Neurology
• Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.
  Prusiner SB, Groth D, Serban A, Koehler R, Foster D, Torchia M, Burton D, Yang SL, DeArmond SJ, Proc Natl Acad Sci U S A
• The application of glial fibrillary acidic (GFA) protein immunohistochemistry in neurooncology. A progress report.
  DeArmond SJ, Eng LF, Rubinstein LJ, Pathol Res Pract
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