StephenJ.DeArmondMD

PubMed

• 2 citations
  Default Mode Network quantitative diffusion and resting-state functional magnetic resonance imaging correlates in sporadic Creutzfeldt-Jakob disease.
  Matteo Paoletti, Eduardo Caverzasi, Maria Luisa Mandelli, Jesse A Brown, Roland G Henry
  Human Brain Mapping. 2022-09-01
• 31 citations
  Early vs late age at onset frontotemporal dementia and frontotemporal lobar degeneration
  Sang Won Seo, Marie-Pierre Thibodeau, David C. Perry, Alice Y. Hua, Manu Sidhu
  Neurology. 2018-03-20
• Autobiography Series: From Sleep-Wake Mechanisms to Prion Diseases.
  Stephen J. DeArmond
  Journal of Neuropathology and Experimental Neurology. 2017-07-01

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
• Cerebellar plaques in presenile dementia: Gerstmann-Straussler syndrome or Alzheimer's disease?  
  Koo EH, DeArmond SJ, Hart J, Gordon B, Selkoe DJ, Price DL, J Neuropathol Exp Neurol
• Scrapie prions caused decreased membrane fluidity in cultured cells.  
  Wong K, Qui Y, VanCleff J, Prusiner SB, DeArmond SJ, J Neuropathol Exp Neurol
• 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
• 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
• Prion diseases and neurodegeneration.  
  Prusiner SB, DeArmond SJ, Annu Rev Neurosci
• The molecular pathology of prion diseases.  
  DeArmond SJ, West J Med
• 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
• 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
• 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
• Proliferative potential of human neuroepithelial tumors in situ.  
  Hoshino T, Nagashima T, Cho KG, Davis RL, DeArmond SJ, J Neuropathol Exp Neurol
• Distinct MRI athropy patterns in autopsy-proven Alzheimer's disease and frontotemporal lobar degenration.  
  Rabinovici GD, Seeley WW, Kim EJ, Gorno-Tempini ML, Rascovsky K, Pagliaro TA, Allison SC, Halabi C, Kramer JH, Johnson HK, Weiner MW, Forman MS, Trojanowski JQ, DeArmo..., Am J Alzheimers Disease and Other Dementias
• Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein.  
  Tamguney G, Miller MW, Giles K, Lemus A, Glidden DV, DeArmond SJ, Prusiner SB, J Gen Virol
• T cells infiltrate the brain in murine and human transmissible spongiform encephalopathies.  
  Lewicki H, Tishon A, Homann D, Mazarguil H, Laval F, Asensio VC, Campbell IL, DeArmond SJ, Coon B, Teng C, Gairin JE, Oldstone MB, J Virol
• Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein.  
  Schmitt-Ulms G, Legname G, Baldwin MA, Ball HL, Bradon N, Bosque PJ, Crossin KL, Edelman GM, DeArmond SJ, Cohen FE, Prusiner SB, J Mol Biol
• Clinical, neuroimaging and neuropathologyical features of a new chromosome 9p-linked FTD-ALS family.  
  Boxer AL, Mackenzie IR, Boeve BF, Baker M, Seeley WW, Crook R, Feldman H, Hsiung GY, Tutherford N, Laluz V, Whitwell J, Foti D., McDade E, Molano J, Karydas A, Wojtas ..., J Neurol Neurosurg Psychiatry
• Behavioral variant frontotemporal dementia with corticobasal degeneration pathology: phenotypic comparison to bvFTD with Pick's Disease.  
  Rankin KP, Mayo MC, Seeley WW, Lee S, Rabinovici G, Gorno-Tempini ML, Boxer AL, Weiner MW, Trojanowski0020JQ, DeArmond SJ, Miller BL, J Mol Neurosci
• Sporadic Jakob-Creutzfeldt Disease Presenting as Primary Progressive Aphasia.  
  Johnson DY, Dunkelberger DL, Henry M, Haman A, Greicius MD, Wong K, DeArmond SJ, Miller BL, Gorno-Tempini ML, Geschwind MD, JAMA Neurol
• Propagation of prion strains through specific conformers of the prion protein.  
  Scott MR, Groth D, Tatzelt J, Torchia M, Tremblay P, DeArmond SJ, Prusiner SB, J Virol
• A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis.  
  Schätzl HM, Laszlo L, Holtzman DM, Tatzelt J, DeArmond SJ, Weiner RI, Mobley WC, Prusiner SB, J Virol
• An immunocytochemical study of P2 protein in the human.  
  DeArmond SJ, Deibler GE, Bacon M, Kies MW, Eng LF, J Neuropathol Exp Neurol
• Chemical and biological properties of the prion protein and its cellular isoform.  
  DeArmond SJ, Kretzschmar H, McKinley M, Barry R, Meyer R, Westaway D, Prusiner S, J Neuropathol Exp Neurol
• Proliferative potential of malignant and non-malignant meningiomas.  
  Hoshino T, Nagashima T, Cho KG, Murovic JA, Zhang R, Davis RL, DeArmond SJ, J Neuropathol Exp Neurol
• Immunohistochemical demonstration of S phase cells in human brain tumor tissues exposed to bromodeoxyuridine (BrdU) in situ.  
  Hoshino T, Nagashima T, Murovic JA, DeArmond SJ, Davis RL, J Neuropathol Exp Neurol
• Identification of prion filaments in scrapie infected brain.  
  DeArmond SJ, Kretzschmar HA, McKinley MP, Barry MB, Braunfeld MB, Prusiner SB, J Neuropathol Exp Neurol
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Books/Book Chapters

• 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
• 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
• 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
• Prion Diseases. 
  Chapter: Greenfield's Neuropathology 
  Page 273 - 323DeArmond SJ, Kretzschmar HA, Prusiner SBEditors: Graham, DI and Lantos, PL.Arnold, LondonEdition 1-> ,
• 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,
• 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
• 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
• 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
• 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
• 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
• Structure of the Human Brain, a Photographic Atlas. 
  DeArmond SJ, Fusco MM, Dewey MOxford Press, New YorkEdition 1st,,
• 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
• 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
• 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
• 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
• Immunochemistry of the glial fibrillary acidic (GFA) protein. 
  Chapter: Progress in Neuropathology 
  Page 19 - 39Eng LF, DeArmond SJEditors: Zimmerman HM.Raven Press, New York
• 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
• Ice Skating: Steps to Success. 
  Künzle-Watson K, DeArmond SJHuman Kinetics Press, Champaign, IL
• 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
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Abstracts/Posters

• The application of glial fibrillary acidic (GFA) protein immunohistochemistry in neurooncology. A progress report.
  DeArmond SJ, Eng LF, Rubinstein LJ, Pathol Res Pract
• Glial fibrillary acidic (GFA) protein immunocytochemistry in development and neuropathology.
  Eng LF, DeArmond SJ, Prog Clin Biol Res
• Neural differentiation in the OTT-6050 mouse teratoma. Production of a tumor fraction restricted to stem cells and neural cells after centrifugal elutriation.
  VandenBerg SR, Chatel M, Griffiths OM, DeArmond SJ, Pappas C, Herman MM, Virchows Arch A Pathol Anat Histol
• Neural differentiation in the OTT-6050 mouse teratoma. Production of a tumor fraction showing melanogenesis in neuroepithelial cells after centrifugal elutriation.
  VandenBerg SR, Hess JR, Herman MM, DeArmond SJ, Halks-Miller M, Rubinstein LJ, Virchows Arch A Pathol Anat Histol
• Neural differentiation in the OTT-6050 mouse teratoma: effects of intracerebral environment on the neural differentiation of embryoid bodies.
  DeArmond SJ, VandenBerg SR, Herman MM, Virchows Arch A Pathol Anat Histol
• Prolonged brain retention of contrast agent in neonatal herpes simplex encephalitis.
  Junck L, Enzmann DR, DeArmond SJ, Okerlund M, Radiology
• Degradation of glial fibrillary acidic protein by a calcium dependent proteinase: an electroblot study.
  DeArmond SJ, Fajardo M, Naughton SA, Eng LF, Brain Res
• Antibodies to a scrapie prion protein.
  Bendheim PE, Barry RA, DeArmond SJ, Stites DP, Prusiner SB, Nature
• Immunohistochemistry: techniques and application to neurooncology.
  DeArmond SJ, Eng LF, Prog Exp Tumor Res
• Immunocytochemical demonstration of S-phase cells by anti-bromodeoxyuridine monoclonal antibody in human brain tumor tissues.
  Nagashima T, DeArmond SJ, Murovic J, Hoshino T, Acta Neuropathol (Berl)
• Scrapie and Creutzfeldt-Jakob disease prions.
  Prusiner SB, Barry RA, McKinley MP, Bellinger CG, Meyer RK, DeArmond SJ, Kingsbury DT, Microbiol Sci
• Identification of prion amyloid filaments in scrapie-infected brain.
  DeArmond SJ, McKinley MP, Barry RA, Braunfeld MB, McColloch JR, Prusiner SB, Cell
• Propagation of infectious miniprions in transgenic mice expressing truncated and partially deleted PrP molecules.
  Supattapone S, Muramoto Tagaard C, Peretz D, Willie H, Ngyuen O, Cohen FE, DeArmond SJ, Prusiner SB, Scott M, Am Soc of Cell Biology Meeting, San Francisco, CA
• Impairment of the GABAergic system during scrapie infection in hamsters: Insights from functional and structural studies.
  Bouzamondo E, Milroy AM, Lisse T, Ralston HJ, Prusiner SB, DeArmond SJ, 29th Annual Meeting of the Society of Neuroscience, Miami, FL
• New functional, structural and ultrastructural insights on the GABAergic system during scrapie: Relevance for neurodegenerative mechanisms.
  Bouzamondo-Bernstein E, Hopkins SD, Ralston HJ III, Prusiner SB, DeArmond SJ, 6th International Symposium on NeuroVirology
• Changes in the localization of brain prion proteins during scrapie infection.
  DeArmond SJ, Mobley WC, DeMott DL, Barry RA, Beckstead JH, Prusiner SB, Neurology
• PrPSc accumulation in neuronal plasma membranes links Notch-1 activation to dendritic degeneration in prion diseases.
  DeArmond SJ, Bajsarowicz K, Mol Neurodegener
• Characterization of normal human brain cultures. Evidence for the outgrowth of leptomeningeal cells.
  Rutka JT, Kleppe-Hoifodt H, Emma DA, Giblin JR, Dougherty DV, McCulloch JR, DeArmond SJ, Rosenblum ML, Lab Invest
• Molecular cloning of a human prion protein cDNA.
  Kretzschmar HA, Stowring LE, Westaway D, Stubblebine WH, Prusiner SB, Dearmond SJ, DNA
• Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies.
  Kitamoto T, Tateishi J, Tashima T, Takeshita I, Barry RA, DeArmond SJ, Prusiner SB, Ann Neurol
• Linkage of prion protein and scrapie incubation time genes.
  Carlson GA, Kingsbury DT, Goodman PA, Coleman S, Marshall ST, DeArmond S, Westaway D, Prusiner SB, Cell
• Sensory reinnervation in microsurgical reconstruction of the heel.
  Chang KN, DeArmond SJ, Buncke HJ, Plast Reconstr Surg
• Whipple's disease confined to the central nervous system.
  Adams M, Rhyner PA, Day J, DeArmond S, Smuckler EA, Ann Neurol
• Pyruvate dehydrogenase complex deficiency as a cause of subacute necrotizing encephalopathy (Leigh disease).
  Kretzschmar HA, DeArmond SJ, Koch TK, Patel MS, Newth CJ, Schmidt KA, Packman S, Pediatrics
• Inhibition of growth and induction of differentiation in a malignant human glioma cell line by normal leptomeningeal extracellular matrix proteins.
  Rutka JT, Giblin JR, Apodaca G, DeArmond SJ, Stern R, Rosenblum ML, Cancer Res
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