메뉴 건너뛰기




Volumn 53, Issue 9, 1996, Pages 913-920

Diagnostic criteria for sporadic Creutzfeldt-Jakob disease

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATAXIA; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIAGNOSTIC PROCEDURE; ELECTROENCEPHALOGRAM; HUMAN; HUMAN CELL; HUMAN TISSUE; LABORATORY DIAGNOSIS; MICROSCOPY; MYOCLONUS; NEUROPATHOLOGY; PRION; PRIORITY JOURNAL; RELIABILITY;

EID: 0029741936     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.1996.00550090125018     Document Type: Article
Times cited : (267)

References (51)
  • 2
    • 0023669586 scopus 로고
    • A novel progressive spongiform encephalopathy
    • Wells GAH, Scott AC, Johnson CT, et al. A novel progressive spongiform encephalopathy. Vet Rec. 1987;121:419-420.
    • (1987) Vet Rec , vol.121 , pp. 419-420
    • Wells, G.A.H.1    Scott, A.C.2    Johnson, C.T.3
  • 3
    • 0009831646 scopus 로고
    • Minutes of the second meeting in Rome, July 3, and the third meeting in Paris, April 29-30
    • Concerted Action of the EU. Surveillance of Creutzfeldt-Jakob disease in the European community. Minutes of the second meeting in Rome, July 3, 1993 and the third meeting in Paris, April 29-30, 1994.
    • (1993) Surveillance of Creutzfeldt-Jakob Disease in the European Community
  • 4
    • 0028235176 scopus 로고
    • Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
    • Brown P, Gibbs CJ, Rodgers-Johnson P, et al. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol. 1994;35:513-529.
    • (1994) Ann Neurol , vol.35 , pp. 513-529
    • Brown, P.1    Gibbs, C.J.2    Rodgers-Johnson, P.3
  • 5
    • 0027922756 scopus 로고
    • EEG findings in Creutzteldt-Jakob disease
    • Brown P. EEG findings in Creutzteldt-Jakob disease. JAMA. 1993;269:3168.
    • (1993) JAMA , vol.269 , pp. 3168
    • Brown, P.1
  • 7
    • 0029128592 scopus 로고
    • Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)
    • Budka H, Aguzzi A, Brown P, et al. Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol. 1995;5:319-322.
    • (1995) Brain Pathol , vol.5 , pp. 319-322
    • Budka, H.1    Aguzzi, A.2    Brown, P.3
  • 8
    • 0018360851 scopus 로고
    • Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
    • Masters CL, Harris JO, Gajdusek DC, Gibbs CJ Jr, Bernoulli C, Asher DM. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol. 1979;5:177-188.
    • (1979) Ann Neurol , vol.5 , pp. 177-188
    • Masters, C.L.1    Harris, J.O.2    Gajdusek, D.C.3    Gibbs Jr., C.J.4    Bernoulli, C.5    Asher, D.M.6
  • 9
    • 0000781428 scopus 로고
    • Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomischem Befunde (spastische Pseudosklerose-Encephalomyelopathie mit disseminierten Degenerationsherden)
    • Jakob A. Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomischem Befunde (spastische Pseudosklerose-Encephalomyelopathie mit disseminierten Degenerationsherden). Dtsch Z Nervenheilkunde. 1921;70:132-146.
    • (1921) Dtsch Z Nervenheilkunde , vol.70 , pp. 132-146
    • Jakob, A.1
  • 10
    • 0025330687 scopus 로고
    • Prion dementia without characteristic pathology
    • Collinge J, Owen F, Poulter M, et al. Prion dementia without characteristic pathology. Lancet. 1990;336:7-9.
    • (1990) Lancet , vol.336 , pp. 7-9
    • Collinge, J.1    Owen, F.2    Poulter, M.3
  • 11
    • 0024406472 scopus 로고
    • A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change
    • Hansen LA, Masliah E, Terry RO, Mirra SS. A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change. Acta Neuropathol (Berl). 1989;78:194-201.
    • (1989) Acta Neuropathol (Berl) , vol.78 , pp. 194-201
    • Hansen, L.A.1    Masliah, E.2    Terry, R.O.3    Mirra, S.S.4
  • 12
    • 0019514305 scopus 로고
    • Panencephalopathic type of Creutzfeldt-Jakob disease: Primary involvement of the cerebral white matter
    • Mizutani T, Okumura A, Oda M, Shiraki H. Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter. J Neurol. 1981;44:103-115.
    • (1981) J Neurol , vol.44 , pp. 103-115
    • Mizutani, T.1    Okumura, A.2    Oda, M.3    Shiraki, H.4
  • 13
    • 0026751775 scopus 로고
    • Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
    • Kitamoto T, Shin R-W, Doh-ura K, et al. Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol. 1992;140:1285-1294.
    • (1992) Am J Pathol , vol.140 , pp. 1285-1294
    • Kitamoto, T.1    Shin, R.-W.2    Doh-ura, K.3
  • 14
    • 0028040838 scopus 로고
    • Prion protein immunocytochemistry: Reliable protocols for the investigation of Creutzfeldt-Jakob disease
    • Hayward PAR, Bell JE, Ironside JW. Prion protein immunocytochemistry: Reliable protocols for the investigation of Creutzfeldt-Jakob disease. Neuropathol Appl Neurobiol. 1994;20:375-383.
    • (1994) Neuropathol Appl Neurobiol , vol.20 , pp. 375-383
    • Hayward, P.A.R.1    Bell, J.E.2    Ironside, J.W.3
  • 15
    • 0027342789 scopus 로고
    • Human prion diseases (spongiform encephalopathies)
    • Kretzschmar MA. Human prion diseases (spongiform encephalopathies). Arch Virol Suppl. 1993;7:261-293.
    • (1993) Arch Virol Suppl , vol.7 , pp. 261-293
    • Kretzschmar, M.A.1
  • 17
    • 0024827258 scopus 로고
    • Levels of infectivity in the blood throughout the incubation period of hamsters peripherally injected with scrapie
    • Casaccia P, Ladogana A, Xi YG, Pocchiari M. Levels of infectivity in the blood throughout the incubation period of hamsters peripherally injected with scrapie. Arch Virol. 1989;108:145-150.
    • (1989) Arch Virol , vol.108 , pp. 145-150
    • Casaccia, P.1    Ladogana, A.2    Xi, Y.G.3    Pocchiari, M.4
  • 18
    • 0023928966 scopus 로고
    • Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies
    • Kitamoto T, Tateishi J. Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies. Am J Pathol. 1988;131:435-443.
    • (1988) Am J Pathol , vol.131 , pp. 435-443
    • Kitamoto, T.1    Tateishi, J.2
  • 19
    • 0025372832 scopus 로고
    • A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease
    • Brown P, Wolff A, Gajdusek DC. A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease. Neurology. 1990;40:887-890.
    • (1990) Neurology , vol.40 , pp. 887-890
    • Brown, P.1    Wolff, A.2    Gajdusek, D.C.3
  • 20
    • 0025826175 scopus 로고
    • Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments
    • Doi-Yi R, Kitamoto T, Tateishi J. Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments. Acta Neumpathol (Berl). 1991; 82:260-265.
    • (1991) Acta Neumpathol (Berl) , vol.82 , pp. 260-265
    • Doi-Yi, R.1    Kitamoto, T.2    Tateishi, J.3
  • 21
    • 0028069275 scopus 로고
    • Hydrated autoclave pretreatment enhancement of prion protein immunoreactivity in formalin-fixed bovine spongiform encephalopathy-affected brain
    • Haritani M, Spencer Yl, Wells GAH. Hydrated autoclave pretreatment enhancement of prion protein immunoreactivity in formalin-fixed bovine spongiform encephalopathy-affected brain. Acta Neuropathol (Berl). 1994;87:86-90;
    • (1994) Acta Neuropathol (Berl) , vol.87 , pp. 86-90
    • Haritani, M.1    Spencer, Yl.2    Wells, G.A.H.3
  • 22
    • 0026730281 scopus 로고
    • The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system
    • Kitamoto T, Doh-ura K, Muramoto T, Miyazono M, Tateishi J. The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system. Am J Pathol. 1992;141:271-277.
    • (1992) Am J Pathol , vol.141 , pp. 271-277
    • Kitamoto, T.1    Doh-ura, K.2    Muramoto, T.3    Miyazono, M.4    Tateishi, J.5
  • 23
    • 0028922696 scopus 로고
    • Etiology and pathogenesis of prion diseases
    • DeArmond SJ, Prusiner MB. Etiology and pathogenesis of prion diseases. Am J Pathol. 1995;146:785-811.
    • (1995) Am J Pathol , vol.146 , pp. 785-811
    • DeArmond, S.J.1    Prusiner, M.B.2
  • 24
    • 0028814065 scopus 로고
    • Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldl-Jakob disease
    • Goodbrand IA, Ironside JW, Nicolson D, Bell JE. Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldl-Jakob disease. Neurosci Lett. 1995;183:127-130.
    • (1995) Neurosci Lett , vol.183 , pp. 127-130
    • Goodbrand, I.A.1    Ironside, J.W.2    Nicolson, D.3    Bell, J.E.4
  • 25
    • 0026729945 scopus 로고
    • Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters
    • Hecker R, Taraboulos A, Scott M, et al. Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters. Genes Dev. 1992;6:1213-1228.
    • (1992) Genes Dev , vol.6 , pp. 1213-1228
    • Hecker, R.1    Taraboulos, A.2    Scott, M.3
  • 28
    • 0028139422 scopus 로고
    • Tubulovesicular structures in Gerstmann-Sträussler-Scheinker disease
    • Liberski PP, Budka H. Tubulovesicular structures in Gerstmann-Sträussler-Scheinker disease. Acta Neuropathol (Berl). 1994;88:491-492.
    • (1994) Acta Neuropathol (Berl) , vol.88 , pp. 491-492
    • Liberski, P.P.1    Budka, H.2
  • 29
    • 0025159389 scopus 로고
    • Appearance of tubulovesicular structures in experimental Creutzfeldt-Jakob disease and scrapie precedes the onset of clinical disease
    • Liberski PP, Yanagihara R, Gibbs CJ Jr, Gajdusek DC. Appearance of tubulovesicular structures in experimental Creutzfeldt-Jakob disease and scrapie precedes the onset of clinical disease. Acta Neuropathol (Berl). 1990;79:349-354.
    • (1990) Acta Neuropathol (Berl) , vol.79 , pp. 349-354
    • Liberski, P.P.1    Yanagihara, R.2    Gibbs Jr., C.J.3    Gajdusek, D.C.4
  • 32
    • 0022639482 scopus 로고
    • Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue
    • Brown P, Coker-Vann M, Pomeroy K, et al. Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue. N Engl J Med. 1986;314:547-551.
    • (1986) N Engl J Med , vol.314 , pp. 547-551
    • Brown, P.1    Coker-Vann, M.2    Pomeroy, K.3
  • 33
    • 0028223595 scopus 로고
    • Detection of proteinase-resistant protein (PrP) in small brain tissue samples from Creutzfeldt-Jakob disease patients
    • Xi YG, Cardone F, Pocchiari M. Detection of proteinase-resistant protein (PrP) in small brain tissue samples from Creutzfeldt-Jakob disease patients. J Neurol Sci. 1994;124:171-173.
    • (1994) J Neurol Sci , vol.124 , pp. 171-173
    • Xi, Y.G.1    Cardone, F.2    Pocchiari, M.3
  • 34
    • 0026725538 scopus 로고
    • The phenotypic expression of different mutations in transmissible human spongiform encephalopathy
    • Brown P. The phenotypic expression of different mutations in transmissible human spongiform encephalopathy. Rev Neurol (Paris). 1992;148:317-327.
    • (1992) Rev Neurol (Paris) , vol.148 , pp. 317-327
    • Brown, P.1
  • 35
    • 0025230662 scopus 로고
    • Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant protein common to Gerstmann-StrZussier syndrome
    • Doh-ura K, Tateishi J, Kitamoto T. Sasaki H, Sakaki Y, Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant protein common to Gerstmann-StrZussier syndrome. Ann Neurol. 1990;27:121-126.
    • (1990) Ann Neurol , vol.27 , pp. 121-126
    • Doh-ura, K.1    Tateishi, J.2    Kitamoto, T.3    Sasaki, H.4    Sakaki, Y.5
  • 36
    • 0014430962 scopus 로고
    • Creutzfeldt-Jakob disease (spongiform encephalopathy): Transmission to the chimpanzee
    • Gibbs CJ Jr, Gajdusek DG, Asher DM, et al. Creutzfeldt-Jakob disease (spongiform encephalopathy): transmission to the chimpanzee. Science. 1968;161: 388-389.
    • (1968) Science , vol.161 , pp. 388-389
    • Gibbs Jr., C.J.1    Gajdusek, D.G.2    Asher, D.M.3
  • 38
    • 0024375840 scopus 로고
    • Positive transmission of Creutzfeldt-Jakob disease verified by murine kuru plaques
    • KitamotoT, Tateishi J, Sawa H, Doh-ura K. Positive transmission of Creutzfeldt-Jakob disease verified by murine kuru plaques. Lab Invest. 1989;60:507-512.
    • (1989) Lab Invest , vol.60 , pp. 507-512
    • Kitamoto, T.1    Tateishi, J.2    Sawa, H.3    Doh-ura, K.4
  • 39
    • 0141467070 scopus 로고
    • Prion protein gene analysis and transmission studies of Creutzfeldt-Jakob disease
    • Prusiner SB, Collinge J, Powell J, Anderton B, eds. London, England: Ellis Horwood
    • Tateishi J, Doh-ura K, Kitamoto T, et al. Prion protein gene analysis and transmission studies of Creutzfeldt-Jakob disease. In: Prusiner SB, Collinge J, Powell J, Anderton B, eds. Prion Diseases of Humans and Animals. London, England: Ellis Horwood; 1992:129-138.
    • (1992) Prion Diseases of Humans and Animals , pp. 129-138
    • Tateishi, J.1    Doh-ura, K.2    Kitamoto, T.3
  • 40
    • 0027076372 scopus 로고
    • Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains
    • Muramoto T, Kitamoto T, Tateishi J, Goto I. Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains. Brain Res. 1992;559:309-316.
    • (1992) Brain Res , vol.559 , pp. 309-316
    • Muramoto, T.1    Kitamoto, T.2    Tateishi, J.3    Goto, I.4
  • 41
    • 0028102794 scopus 로고
    • Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein
    • Telling GC, Scott M, Hsiao KK, et al. Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Proc Natl Acad Sci U S A. 1994;91:9936-9940.
    • (1994) Proc Natl Acad Sci U S A , vol.91 , pp. 9936-9940
    • Telling, G.C.1    Scott, M.2    Hsiao, K.K.3
  • 43
    • 0021019026 scopus 로고
    • Scrapie prions aggregate to form amyloid-like birefringent rods
    • Prusiner SB, McKinley MP, Bowman KA, et al. Scrapie prions aggregate to form amyloid-like birefringent rods. Cell. 1983;35:349-358.
    • (1983) Cell , vol.35 , pp. 349-358
    • Prusiner, S.B.1    McKinley, M.P.2    Bowman, K.A.3
  • 46
    • 0026482458 scopus 로고
    • High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease
    • Jimi T, Wakayama Y, Shibuya S, et al. High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease. Clin Chim Acta. 1992;211:37-46.
    • (1992) Clin Chim Acta , vol.211 , pp. 37-46
    • Jimi, T.1    Wakayama, Y.2    Shibuya, S.3
  • 47
    • 0023243715 scopus 로고
    • High neuron-specific enolase level of cerebrospinal fluid in the early stage of Creutzfeldt-jakob disease
    • Wakayama Y, Shibuya S, Kawase J, Sagawa F, Hashizume Y. High neuron-specific enolase level of cerebrospinal fluid in the early stage of Creutzfeldt-jakob disease. Klin Wochenschr. 1987;65:798-801.
    • (1987) Klin Wochenschr , vol.65 , pp. 798-801
    • Wakayama, Y.1    Shibuya, S.2    Kawase, J.3    Sagawa, F.4    Hashizume, Y.5
  • 48
    • 0029078348 scopus 로고
    • Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease
    • Zerr I, Bodemer M, Räcker S, et al. Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease. Lancet. 1995;345: 1609-1610.
    • (1995) Lancet , vol.345 , pp. 1609-1610
    • Zerr, I.1    Bodemer, M.2    Räcker, S.3
  • 49
    • 0022606619 scopus 로고
    • Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
    • Harrington MG, Merril CR, Asher DM, Gajdusek DC. Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. N Engl J Med. 1986;315:279-283.
    • (1986) N Engl J Med , vol.315 , pp. 279-283
    • Harrington, M.G.1    Merril, C.R.2    Asher, D.M.3    Gajdusek, D.C.4
  • 50
    • 0342951746 scopus 로고    scopus 로고
    • A new variant of Creutzfeldt-Jakob disease in the UK
    • Will RG, Ironside JW, Zeidler M, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet. 1996;347:921-925.
    • (1996) Lancet , vol.347 , pp. 921-925
    • Will, R.G.1    Ironside, J.W.2    Zeidler, M.3
  • 51
    • 0023499868 scopus 로고
    • Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
    • Kascsak RJ, Rubenstein R, Merz PA, et al. Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins. J Virol. 1987;61:3688-3693.
    • (1987) J Virol , vol.61 , pp. 3688-3693
    • Kascsak, R.J.1    Rubenstein, R.2    Merz, P.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.