SUBACUTE SPONGIFORM ENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE): THE NATURE AND PROGRESSION OF SPONGIFORM CHANGE

MASTERS, c.L., RICHARDSON, E.P.·1978·Brain

Cited by (309)

Items 101–200 of 309

  1. Expression of Excitatory Amino Acid Transporter-1 (EAAT-1) in Brain Macrophages and Microglia of Patients with Prion Diseases
    Fabrice C Chrétien, Gwenaëlle Le Pavec, Anne‐Valérie Decouvelaere, Marie-Bernadette-Delisle, Emmanuelle Uro‐Coste, James W. Ironside, Pierluigi L. Gambetti, Piero Parchi, Christophe Créminon, Dominique Dormont et al. · 2004 · Journal of Neuropathology & Experimental Neurology
  2. Human prion diseases
    Matti Haltia · 2000 · Annals of Medicine
  3. Panencephalopathic Creutzfeldt–Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patients
    Carmen Jansen, Mark W. Head, Annemieke J.M. Rozemüller, James W. Ironside · 2009 · Neuropathology and Applied Neurobiology
  4. The ubiquitin–proteasome system in spongiform degenerative disorders
    Brandi Whatley, Lian Li, Lih‐Shen Chin · 2008 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  5. Diffusion-weighted imaging and magnetic resonance spectroscopy of sporadic Creutzfeldt–Jakob disease: correlation with clinical course
    Jae Hyoung Kim, Byung Se Choi, Cheolkyu Jung, YoungHee Chang, SangYun Kim · 2011 · Neuroradiology
  6. Impairment of the Peripheral Nervous System in Creutzfeldt-Jakob Disease
    Maria Niewiadomska, Jerzy Kulczycki, Danuta Wochnik-Dyjas, Grazyna Maria Szpak, Maria J. Rakowicz, Wanda Łojkowska, Krystyna Niedzielska, Ewa Inglot, Małgorzata Więcławska, Czesław Głazowski et al. · 2002 · Archives of Neurology
  7. Magnetic resonance imaging in Creutzfeldt-Jakob disease: evidence of focal involvement of the cortex
    Markus Schwaninger, Rebecca Winter, Werner Hacke, Rüdiger von Kummer, Claudia Sommer, Marika Kiessling, Walter Schulz‐Schaeffer, Hans A. Kretzschmar · 1997 · Journal of Neurology Neurosurgery & Psychiatry
  8. Thalamic and Subcortical Gliosis With Dementia
    John Jefferson Moossy, A. J. Martinez, Israel Hanin, GUTTI R. RAO, Howard Yonas, François Boller · 1987 · Archives of Neurology
  9. Gerstmann‐Sträussler‐Scheinker's disease
    Shigeki Kuzuhara, Ichiro KANAZAWA, Hidenao Sasaki, Takao Nakanishi, Kayako Shimamura · 1983 · Annals of Neurology
  10. Cytology and organization of reactive astroglia in human cerebellar cortex with severe loss of granule cells: A study on the ataxic form of creutzfeldt-jakob disease
    Miguel Lafarga, Maria Teresa Berciano, I. Suarez, Carlos Fernández Viadero, M.A. Andrés, José Berciano · 1991 · Neuroscience
  11. Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein
    Alessandro Corsaro, Stefano Thellung, Claudio Russo, Valentina Villa, S. Arena, Maria Cristina D’Adamo, Domenico Paludi, Daniela Rossi Principe, Gianluca Damonte, Umberto Benatti et al. · 2002 · Neurochemistry International
  12. Rabies: Spongiform lesions in the brain
    Kenneth Charlton · 1984 · Acta Neuropathologica
  13. Serial ultrastructural study of experimental Creutzfeldt-Jacob disease in guinea pigs
    J. H. Kim, Elias E. Manuelidis · 1986 · Acta Neuropathologica
  14. Chapter 37: PrPSc causes nerve cell death and stimulates astrocyte proliferation: a paradox
    Stephen J. DeArmond, Krister Kristensson, Russel P. Bowler · 1992 · Progress in brain research
  15. Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype
    Koichi Kawasaki, Koichi Wakabayashi, Akio Kawakami, Masami Higuchi, Tetsuyuki Kitamoto, Shoji Tsuji, Hitoshi Takahashi · 1997 · Acta Neuropathologica
  16. PATHOLOGY OF CREUTZFELDT‐JAKOB DISEASE ASSOCIATED WITH PITUITARY‐DERIVED HUMAN GROWTH HORMONE ADMINISTRATION
    Roy O. Weller, Philip V. Steart, J D Powell-Jackson · 1986 · Neuropathology and Applied Neurobiology
  17. Neil3 induced neurogenesis protects against prion disease during the clinical phase
    Clara M.O. Jalland, Katja Scheffler, Sylvie Lafond Benestad, Torfinn Moldal, Cecilie Ersdal, Gjermund Gunnes, Rajikala Suganthan, Magnar Bjørås, Michael Andreas Tranulis · 2016 · Scientific Reports
  18. Pathways to the discovery of the Aβ amyloid of Alzheimer's disease
    Colin Louis Masters, Konrad T. Beyreuther · 2006 · Journal of Alzheimer s Disease
  19. Combined diffusion-weighted and spectroscopic MR imaging in Creutzfeldt-Jakob disease
    C. C. Tchoyoson Lim, Kevin Tan, Kamal Kumar Verma, Hong J. Yin, Narayanaswamy Venketasubramanian · 2004 · Magnetic Resonance Imaging
  20. Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt–Jakob disease: Proposed staging of cerebral cortical pathology
    Yasushi Iwasaki, Shinsui Tatsumi, Maya Mimuro, Tetsuyuki Kitamoto, Yoshio Hashizume, Mari Yoshida · 2014 · Journal of the Neurological Sciences
  21. Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
    C M Hulette, Nancy L. Earl, Barbara J. Crain · 1992 · Archives of Neurology
  22. A morphometric and immunohistochemical study of the vestibular nuclear complex in bovine spongiform encephalopathy
    M. Jeffrey, W.G. Halliday, Caroline M. Goodsir · 1992 · Acta Neuropathologica
  23. Creutzfeldt-Jakob disease: a case with extensive white matter degeneration and optic atrophy
    Y. Kitagawa, Fumio Gotoh, Akiko Koto, Shinichiro Ebihara, Hiroyuki Okayasu, Toshiharu Ishii, H Matsuyama · 1983 · Journal of Neurology
  24. Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease
    Margarita Diez, Jari Koıstınaho, Stephen J. DeArmond, Darlene Groth, Stanley B. Prusiner, Tomas G. M. Hökfelt · 1997 · Proceedings of the National Academy of Sciences
  25. Gerstmann‐Sträussler‐Scheinker disease with coincidental familial onset
    Arthur J. Hudson, Michael Anthony Farrell, Renate M. Kalnins, John C.E. Kaufmann · 1983 · Annals of Neurology
  26. Experimental transmission of human subacute spongiform encephalopathy to small rodents
    Jun Tateishi, Yuji Sato, Hitoshi Nagara, J. W. Boellaard · 1984 · Acta Neuropathologica
  27. Iatrogenic and zoonotic Creutzfeldt–Jakob disease: the Australian perspective
    Steven John Collins, Colin Louis Masters · 1996 · The Medical Journal of Australia
  28. Human prion diseases (spongiform encephalopathies)
    Hans A. Kretzschmar · 1993 · Archives of virology. Supplementum
  29. Familial Creutzfeldt-Jakob disease with extensive degeneration of white matter
    Jean‐Michel Vallat, Michel Dumas, N. Corvisier, M. J. Leboutet, Anne Loubet, P Dumas, Françoise Cathala · 1983 · Journal of the Neurological Sciences
  30. Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
    Hannah Song Lee, Oren S. Cohen, Hannah Rosenmann, C. Hoffmann, Peter B. Kingsley, Amos D. Korczyn, Joab Chapman, I. Prohovnik · 2012 · American Journal of Neuroradiology
  31. Magnetic resonance imaging follow-up in Creutzfeldt-Jakob disease
    Joachim Röthert, Andreas Schwartz, Michael Härle, Klaus U. Wentz, Peter Berlit, Michael G. Hennerici · 1992 · Journal of Neurology
  32. Different susceptibilities of the geniculate and extrageniculate visual pathways to human Creutzfeldt-Jakob disease (a combined neurophysiological-neuropathological study)
    Umberto Aguglia, Danièle Gambarelli, Guy Farnarier, Aldo Quattrone · 1991 · Electroencephalography and Clinical Neurophysiology
  33. Dialysis encephalopathy: Neuropathologic aspects
    Marc D. Winkelman, Edmond S. Ricanati · 1986 · Human Pathology
  34. PrPSc accumulation in neuronal plasma membranes links Notch-1 activation to dendritic degeneration in prion diseases
    Stephen J. DeArmond, Krystyna Bajsarowicz · 2010 · Molecular Neurodegeneration
  35. Apolipoprotein E Phenotype Frequency and Cerebrospinal Fluid Concentration Are Not Associated With Creutzfeldt-Jakob Disease
    Inga Zerr, Marion Helmhold, S. Poser, Victor W. Armstrong, Thomas Weber · 1996 · Archives of Neurology
  36. Increased Detection of 14-3-3 Protein in Cerebrospinal Fluid in Sporadic Creutzfeldt-Jakob Disease during the Disease Course
    Pierric Giraud, Anne-Gaëlle Biacabé, Guy Chazot, Roger Later, Olivier Joyeux, Yves Moene, Armand Perret‐Liaudet · 2002 · European Neurology
  37. Creutzfeldt-Jakob disease and the eye. I. Background and patient management
    Christian Joseph Lueck, Gawn G. McIlwaine, Martin Zeidler · 2000 · Eye
  38. Case 45-1980
    Richard C. Cabot, Robert E. Scully, James J. Galdabini, Betty U. McNeely, Edward R. Wolpow, George M. Kleinman · 1980 · New England Journal of Medicine
  39. Role of Viruses in Chronic Neurological Diseases
    Jerry S. Wolinsky, Richard T. Johnson · 1980 · Springer eBooks
  40. Otolaryngological Manifestations of Creutzfeldt-Jakob Disease
    Douglas C. Bigelow, Marc D. Eisen, David M. Yen, Sondra C. Saull, David Solomon, David E. Schmidt · 1998 · Archives of Otolaryngology - Head and Neck Surgery
  41. Neuropathologic characteristics of spinal cord lesions in sporadic Creutzfeldt-Jakob disease
    Yasushi Iwasaki, Mari Yoshida, Yoshio Hashizume, Tetsuyuki Kitamoto, Gen Sobue · 2005 · Acta Neuropathologica
  42. Virus Infections of the Nervous System
    Tom Solomon · 2013 · Elsevier eBooks
  43. Comparison of spongiform lesions in experimental scrapie and rabies in skunks
    A. Bundza, Kenneth Charlton · 1988 · Acta Neuropathologica
  44. Role of Formyl Peptide Receptors (FPR) in Abnormal Inflammation Responses Involved in Neurodegenerative Diseases
    Adriano Mollica, Azzurra Stefanucci, Roberto Costante, Francesco Pinnen · 2012 · Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry
  45. Numbers of neurons in vacuolated and non-vacuolated neuroanatomical nuclei in bovine spongiform encephalopathy-affected brains
    M. Jeffrey, W.G. Halliday · 1994 · Journal of Comparative Pathology
  46. Early MRI findings in Creutzfeldt-Jakob disease
    MARCO C. ONOFRJ, T. Fulgente, Domenico Gambi, Giorgio Macchi · 1993 · Journal of Neurology
  47. Spongy Degeneration of the CNS in Infancy
    Y. Luo, K. Huang · 1984 · Archives of Neurology
  48. Multimodal MRI staging for tracking progression and clinical-imaging correlation in sporadic Creutzfeldt-Jakob disease
    Simone Sacco, Matteo Paoletti, Adam M. Staffaroni, Huicong Kang, Julio C. Rojas, Gabe A. Marx, Sheng‐Yang M. Goh, Maria Luisa Mandelli, Isabel Elaine Allen, Joel H. Kramer et al. · 2020 · NeuroImage Clinical
  49. Doença de Creutzfeldt-Jakob forma Heidenhain: relato de caso com achados de ressonância magnética e DWI
    Walter Oleschko Arruda, Kelly Cristina Bordignon, Jerônimo Buzetti Milano, Ricardo Ramina · 2004 · Arquivos de Neuro-Psiquiatria
  50. MRI alterations as an early finding in Creutzfeld-Jakob disease
    Armando Tartaro, T. Fulgente, Camillo Delli Pizzi, Lorenzo Bonomo, Vittorio Bocola, MARCO C. ONOFRJ · 1993 · European Journal of Radiology
  51. The neuropathologic diagnostic criteria of frontal lobe dementia revisited. A study of ten consecutive cases
    Jean‐Jacques Hauw, Charles J. Duyckaerts, Danielle Seilhean, Sophie Camilleri‐Broët, Véronique Sazdovitch, G Rancurel · 1996 · Journal of neural transmission. Supplementum
  52. Creutzfeldt-Jakob disease with severe involvement of cerebral white matter and cerebellum
    José Berciano, Maria Teresa Berciano, J. M. Polo, Javier Figols, J. Ciudad, Miguel Lafarga · 1990 · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin
  53. Discovering the Mechanisms of Neurodegeneration in Prion Diseases
    Stephen J. DeArmond · 2004 · Neurochemical Research
  54. Ultrastructural neuropathology of chronic wasting disease in captive mule deer
    Don C. Guiroy, ELIZABETH S. WILLIAMS, Pawel Piotr Liberski, Ikuro WAKAYAMA, Daniel Carleton Gajdusek · 1993 · Acta Neuropathologica
  55. Case 34-1987
    Richard C. Cabot, Robert E. Scully, Eugene Jerome Mark, William F. McNeely, Betty U. McNeely, Shirley H. Wray, Edward P. Richardson · 1987 · New England Journal of Medicine
  56. Selective neuronal vulnerability during experimental scrapie infection:
    Essia Bouzamondo, Antonia M. Milroy, Henry J. Ralston, Stanley B. Prusiner, Stephen J. DeArmond · 2000 · Brain Research
  57. The spatial pattern of the vacuolation in patients with sporadic Creutzfeldt–Jakob disease
    Richard A. Armstrong, Nigel J. Cairns, Peter L Lantos · 2000 · Neuroscience Letters
  58. Pharmacological modulation of TSPO in microglia/macrophages and neurons in a chronic neurodegenerative model of prion disease
    Vicente-Rodríguez, Marta, Mancuso, Renzo, Peris-Yague, Alba, Simmons, Camilla, NIMA Consortium, Wlazly, Dominika, Dickinson, Amber, Foster, Andy, Knight, Clare, Leckey, Claire et al. · 2023 · Journal of Neuroinflammation
  59. Oligodendroglial deletion of ESCRT‐I component TSG101 causes spongiform encephalopathy
    Will P. Walker, Abby Oehler, Aimee L. Edinger, Kay‐Uwe Wagner, Teresa M. Gunn · 2016 · Biology of the Cell
  60. Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation
    Akio Akagi, Yasushi Iwasaki, Maya Mimuro, Tetsuyuki Kitamoto, Masahito Yamada, Mari Yoshida · 2017 · Prion
  61. Creutzfeldt‐Jakob's disease presenting with ataxia and a movement disorder
    Kapil D. Sethi, David Charles Hess · 1991 · Movement Disorders
  62. Human prion diseases
    James W. Ironside · 1996 · Journal of neural transmission. Supplementum
  63. Spongiform-like changes in Alzheimer's disease
    Gianluigi Mancardi, T. I. Mandybur, Boleslaw H. Liwnicz · 1982 · Acta Neuropathologica
  64. Familial Alzheimer's Disease With Myoclonus and 'Spongy Change'
    Philip E. Duffy, Richard P Mayeux, William J. Kupsky · 1988 · Archives of Neurology
  65. Computed tomography during Creutzfeldt-Jakob disease
    Klaus Peter Westphal, Walter Schachenmayr · 1985 · Neuroradiology
  66. An autopsy case of MM2‐cortical + thalamic‐type sporadic Creutzfeldt‐Jakob disease
    Yufuko Saito, Yasushi Iwasaki, Ikuko Aiba, Tetsuyuki Kitamoto, Mari Yoshida, Yoshio Hashizume · 2010 · Neuropathology
  67. Infections of the Central Nervous System
    John Stevens · 1990 · Clinical medicine and the nervous system
  68. Brain monoamine abnormalities in the two types of Creutzfeldt-Jakob disease
    P. Nyberg, Béla G.L. Almay, Arvid Carlsson, Colin Louis Masters, Bengt G. Winblad · 2009 · Acta Neurologica Scandinavica
  69. Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease
    Richard A. Armstrong, Nigel J. Cairns, Peter L Lantos · 2001 · Neuropathology
  70. Creutzfeldt-Jakob disease: Clinical, EEG and neuropathological findings in a cluster of eleven patients
    Alfredo Lechi, Filomeno Tedeschi, D. Mancia, Vladimiro Pietrini, Fabrizio Tagliavini, M. G. Terzano, Gianriccardo Trabattoni · 1983 · Neurological Sciences
  71. Immunolocalization of the cellular prion protein in normal brain
    Kenneth L. Moya, Nicole Sal�s, Raymonde H�ssig, Christophe Cr�minon, Jacques J. Grassi, Luigi Di Giamberardino · 2000 · Microscopy Research and Technique
  72. APOE gene polymorphisms and susceptibility to Creutzfeldt–Jakob disease
    Yunfei Wei, Yanyan Tang, Wenwu He, Zhanli Qu, Jinming Zeng, Chao Qin · 2013 · Journal of Clinical Neuroscience
  73. Biology and Neuropathology of Prion Diseases
    James W. Ironside, Mark W. Head · 2008 · Handbook of clinical neurology
  74. Spatial correlations between the vacuolation, prion protein deposits, and surviving neurons in the cerebral cortex in sporadic Creutzfeldt–Jakob disease
    Richard A. Armstrong, Peter L Lantos, Nigel J. Cairns · 2001 · Neuropathology
  75. Diffusion-Weighted MR Imaging in Biopsy-Proven Creutzfeldt-Jakob Disease
    Hyo‐Cheol Kim, K H Chang, In Chan Song, Sang Hyun Lee, Bae Ju Kwon, Moon Hee Han, SangYun Kim · 2001 · Korean Journal of Radiology
  76. Prion Diseases and Neurodegeneration
    Stanley B. Prusiner · 1994 · Annual Review of Neuroscience
  77. Jakob-Creutzfeldt Disease Associated with Wernicke Encephalopathy
    S. Gaytan-Garcia, J. J. Gilbert, John H. N. Deck, Jörg Kaufmann · 1988 · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
  78. Neuropathological study of cerebellar degeneration in prion disease
    Qing H. Yang, Yoshio Hashizume, Mari Yoshida, Yin Wang · 1999 · Neuropathology
  79. Spectrum and Pattern of Movement Disorders in Patients with Sporadic Creutzfeldt-Jakob Disease
    Sandeep Gurram, Vikram Venkappayya Holla, Praveen Kumar Sharma, Nitish L. Kamble, Jitender S. Saini, Manjunath Netravathi, Ravi Yadav, Pramod Kumar Pal · 2023 · Tremor and Other Hyperkinetic Movements
  80. Hearing Loss as the Initial Presentation of Creutzfeldt-Jakob Disease
    Priya D. Krishna, Carol A. Bauer · 2004 · Ear Nose & Throat Journal
  81. Quantification of the vacuolation (spongiform change) and prion protein deposition in 11 patients with sporadic Creutzfeldt-Jakob disease
    Richard A. Armstrong, Nigel J. Cairns, Peter L Lantos · 2001 · Acta Neuropathologica
  82. Serial computed tomographic and electroencephalographic studies in Creutzfeldt-Jakob disease
    R. Hayashi, Norinao Hanyu, T. Kuwabara, S. Moriyama · 2009 · Acta Neurologica Scandinavica
  83. The Human Spongiform Encephalopathies
    Paul E. Bendheim · 1984 · Neurologic Clinics
  84. Gerstmann-Str�ussler's disease, atypical multiple sclerosis and carcinomas in a family of sheepbreeders
    J. Peiffer · 1982 · Acta Neuropathologica
  85. Prion Protein Disease and Neuropathology of Prion Disease
    Daniel du Plessis · 2008 · Neuroimaging Clinics of North America
  86. Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family
    Svetlana N. Popova, Ilkka Tarvainen, Sabina Capellari, Piero Parchi, P. Hannikainen, Elina Pirinen, Hannu K. Haapasalo, Irina I. Alafuzoff · 2012 · Acta Neurologica Scandinavica
  87. MM2‐cortical‐type sporadic Creutzfeldt‐Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course
    Yoshiki Niimi, Yasushi Iwasaki, Toshitaka Umemura, Fumiaki Tanaka, Mari Yoshida, Yoshio Hashizume, Tetsuyuki Kitamoto, Mikio Hirayama, Gen Sobue · 2008 · Neuropathology
  88. Neuropathological Diagnosis of Human Prion Disease: Morphological Studies
    James W. lronside · 2003 · Humana Press eBooks
  89. Enhanced expression of 14-3-3 proteins in reactive astrocytes in Creutzfeldt-Jakob disease brains
    Yasuhiro Kawamoto, Ichiro Akiguchi, Christa Jarius, Herbert Budka · 2004 · Acta Neuropathologica
  90. Deciphering the BSE-type specific cell and tissue tropisms of atypical (H and L) and classical BSE
    Anne Balkema‐Buschmann, Grit Priemer, Reiner Ulrich, Romano Strobelt, Bob Hills, Martin H. Groschup · 2019 · Prion
  91. Extensive cortical damage in a case of Creutzfeldt-Jacob disease: clinicoradiological correlations
    Mauro Bergui, Gianni Boris Bradač, Giacomina Rossi, L. Orsi · 2003 · Neuroradiology
  92. Distribution of Cellular Prion Protein in Normal Human Cerebral Cortex – Does It Have Relevance to Creutzfeldt-Jakob Disease?
    Gerard H. Jansen, Christina Francisca Vogelaar, Sabrina Elshof · 2001 · Clinical Chemistry and Laboratory Medicine (CCLM)
  93. Viral Encephalitis and Its Pathology
    J. R. Anderson · 1988 · Current topics in pathology
  94. Neuropathology of Unconventional Virus Infections: Molecular Pathology of Spongiform Change and Amyloid Plaque Deposition
    Colin Louis Masters, Konrad Beyreuther · 2007 · Novartis Foundation symposium
  95. Pathology and Diagnosis of Central Nervous System Infections
    C. Sundaram, S K Shankar, Wong Kum Thong, Carlos Pardo‐Villamizar · 2011 · Pathology Research International
  96. Prion Infections of the Brain
    Ryan Wada, Walter Kucharczyk · 2008 · Neuroimaging Clinics of North America
  97. Elevated Cerebrospinal Fluid Lactic Acid Levels in Creutzfeldt-Jakob Disease
    Gavin I. Awerbuch, Patti L. Peterson, Reuven Sandyk · 1988 · International Journal of Neuroscience
  98. Impairment of the cortical and thalamic electrical activity in scrapie-infected rats
    Marie H. Bassant, L. Court, F Cathala · 1987 · Electroencephalography and Clinical Neurophysiology
  99. Spongiform Encephalopathy of Long Duration: A Family Study
    George P. Rice, Donald W. Paty, Melvin Ball, R. Tatham, ANDREW E. KERTESZ · 1980 · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
  100. Brain stem lesions in sporadic Creutzfeldt–Jakob disease: A histopathological and immunohistochemical study
    Masayuki Shintaku, Chikao Yutani, Katsumi Doh‐ura · 2006 · Neuropathology