-
1
-
-
0000612171
-
Subacute spongiform encephalopathy - A subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy)
-
Nevin S, McMenemey WH, Behrman S, Jones DP. Subacute spongiform encephalopathy - a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy). Brain 1960;83:519-564.
-
(1960)
Brain
, vol.83
, pp. 519-564
-
-
Nevin, S.1
McMenemey, W.H.2
Behrman, S.3
Jones, D.P.4
-
2
-
-
0001168221
-
Observations on three slow infection of sheep
-
Sigurdsson B. Observations on three slow infection of sheep. Br Vet J 1954;110:225-270, 307-322.
-
(1954)
Br Vet J
, vol.110
, Issue.225-270
, pp. 307-322
-
-
Sigurdsson, B.1
-
3
-
-
0017643758
-
Unconventional viruses and the origin and disappearance of kuru
-
Gajdusek DC. Unconventional viruses and the origin and disappearance of kuru. Science 1977; 197:943-960.
-
(1977)
Science
, vol.197
, pp. 943-960
-
-
Gajdusek, D.C.1
-
4
-
-
0025910229
-
Molecular biology of prion diseases
-
Prusiner SB. Molecular biology of prion diseases. Science 1991;252:1515-1522.
-
(1991)
Science
, vol.252
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
5
-
-
0028235176
-
Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
-
Brown P, Gibbs CJ Jr, 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 Jr., C.J.2
Rodgers-Johnson, P.3
-
6
-
-
0027741446
-
Developments in diagnosis for prion diseases
-
Tateishi J, Kitamoto T. Developments in diagnosis for prion diseases. Br Med Bull 1993;49:971-979.
-
(1993)
Br Med Bull
, vol.49
, pp. 971-979
-
-
Tateishi, J.1
Kitamoto, T.2
-
7
-
-
0018384549
-
Transmission of chronic spongiform encephalopathy with kuru plaques from human to small rodents
-
Tateishi J, Ohta M, Koga M, Sato Y, Kuroiwa Y. Transmission of chronic spongiform encephalopathy with kuru plaques from human to small rodents. Ann Neurol 1979;5:581-584.
-
(1979)
Ann Neurol
, vol.5
, pp. 581-584
-
-
Tateishi, J.1
Ohta, M.2
Koga, M.3
Sato, Y.4
Kuroiwa, Y.5
-
8
-
-
0026751775
-
Abnormal isoform of prion protein 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 protein 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
-
9
-
-
0027076372
-
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;599:309-316.
-
(1992)
Brain Res
, vol.599
, pp. 309-316
-
-
Muramoto, T.1
Kitamoto, T.2
Tateishi, J.3
Goto, I.4
-
10
-
-
0026651376
-
The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease
-
Muramoto T, Kitamoto T, Tateishi J, Goto I. The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease. Am J Pathol 1992;140:1411-1420.
-
(1992)
Am J Pathol
, vol.140
, pp. 1411-1420
-
-
Muramoto, T.1
Kitamoto, T.2
Tateishi, J.3
Goto, I.4
-
11
-
-
0026440020
-
The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration
-
Muramoto T, Kitamoto T, Koga H, Tateishi J. The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration. Acta Neuropathol 1992; 84:686-689.
-
(1992)
Acta Neuropathol
, vol.84
, pp. 686-689
-
-
Muramoto, T.1
Kitamoto, T.2
Koga, H.3
Tateishi, J.4
-
12
-
-
0023919161
-
Degeneration of the thalamus and inferior olives associated with spongiform encephalopathy of the cerebral cortex
-
Mizusawa H, Ohkoshi N, Sasaki H, Kanazawa I, Nakanishi T. Degeneration of the thalamus and inferior olives associated with spongiform encephalopathy of the cerebral cortex. Clin Neuropathol 1988;7:81-86.
-
(1988)
Clin Neuropathol
, vol.7
, pp. 81-86
-
-
Mizusawa, H.1
Ohkoshi, N.2
Sasaki, H.3
Kanazawa, I.4
Nakanishi, T.5
-
13
-
-
0026552043
-
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
-
Medori R, Tritschler H-J, LeBlanc A, et al. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med 1992;326:444-449.
-
(1992)
N Engl J Med
, vol.326
, pp. 444-449
-
-
Medori, R.1
Tritschler, H.-J.2
LeBlanc, A.3
-
14
-
-
0026675218
-
Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): A comparative study of patients with codon 102 point mutation or without mutations
-
Miyazono M, Kitamoto T, Doh-ura K, Iwaki T, Tateishi J. Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations. Acta Neuropathol 1992;84: 349-354.
-
(1992)
Acta Neuropathol
, vol.84
, pp. 349-354
-
-
Miyazono, M.1
Kitamoto, T.2
Doh-ura, K.3
Iwaki, T.4
Tateishi, J.5
-
15
-
-
0028204867
-
Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graft
-
Yamada S, Aiba T, Endo Y, Hara M, Kitamoto T, Tateishi J. Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graft. Neurosurgery 1994;34:740-744.
-
(1994)
Neurosurgery
, vol.34
, pp. 740-744
-
-
Yamada, S.1
Aiba, T.2
Endo, Y.3
Hara, M.4
Kitamoto, T.5
Tateishi, J.6
-
16
-
-
0001294301
-
An autopsy case of Creutzfeldt-Jakob disease associated with cor3 neal transplantation
-
in Japanese
-
Uchiyama K, Ishida C, Yago S, Kurumaya H, Kitamoto T. An autopsy case of Creutzfeldt-Jakob disease associated with cor3 neal transplantation. Dementia 1994;8:466-473 (in Japanese).
-
(1994)
Dementia
, vol.8
, pp. 466-473
-
-
Uchiyama, K.1
Ishida, C.2
Yago, S.3
Kurumaya, H.4
Kitamoto, T.5
-
17
-
-
0025906297
-
Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker
-
Kretzschmar HA, Honold G, Seitelberger F, et al. Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker. Lancet 1991;337:1160.
-
(1991)
Lancet
, vol.337
, pp. 1160
-
-
Kretzschmar, H.A.1
Honold, G.2
Seitelberger, F.3
-
18
-
-
0023821179
-
Gerstmann-Sträussler-Scheinker disease: Immunohistological and experimental studies
-
Tateishi J, Kitamoto T, Hashiguchi H, Shii H. Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies. Ann Neurol 1988;24:35-40.
-
(1988)
Ann Neurol
, vol.24
, pp. 35-40
-
-
Tateishi, J.1
Kitamoto, T.2
Hashiguchi, H.3
Shii, H.4
-
19
-
-
0027497304
-
A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis
-
Kitamoto T, Amano N, Terao Y, et al. A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis. Ann Neurol 1993;34:808-813.
-
(1993)
Ann Neurol
, vol.34
, pp. 808-813
-
-
Kitamoto, T.1
Amano, N.2
Terao, Y.3
-
20
-
-
0026609502
-
Gerstmann-Sträussler Scheinker disease in an Alsatian family: Clinical and genetic studies
-
Tranchant C, Doh-ura K, Warter JM, et al. Gerstmann-Sträussler Scheinker disease in an Alsatian family: clinical and genetic studies. J Neurol Neurosurg Psychiatry 1992;55: 185-187.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 185-187
-
-
Tranchant, C.1
Doh-ura, K.2
Warter, J.M.3
-
21
-
-
84990464525
-
A case with codon 145 mutation of the prion protein gene
-
in Japanese
-
Ichimiya Y, Iizuka R, Iwamoto N, Arai H, Kitamoto T, Tateishi J. A case with codon 145 mutation of the prion protein gene. Dementia 1994;8:391-396 (in Japanese).
-
(1994)
Dementia
, vol.8
, pp. 391-396
-
-
Ichimiya, Y.1
Iizuka, R.2
Iwamoto, N.3
Arai, H.4
Kitamoto, T.5
Tateishi, J.6
-
22
-
-
0028782020
-
Human prion diseases with variant prion protein
-
Biol
-
Kitamoto T, Tateishi J. Human prion diseases with variant prion protein. Philos Trans R Soc Lond [Biol] 1994;343:971-979.
-
(1994)
Philos Trans R Soc Lond
, vol.343
, pp. 971-979
-
-
Kitamoto, T.1
Tateishi, J.2
-
23
-
-
0028206519
-
Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene
-
Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J. Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene. Neurology 1994; 44:299-301.
-
(1994)
Neurology
, vol.44
, pp. 299-301
-
-
Inoue, I.1
Kitamoto, T.2
Doh-ura, K.3
Shii, H.4
Goto, I.5
Tateishi, J.6
-
24
-
-
0000715711
-
Creutzfeldt-Jakob disease presenting as frontal lobe dementia associated with a 96 base pair insertion in the prion protein gene
-
in Japanese
-
Isozaki E, Miyamoto K, Kagamihara Y, et al. Creutzfeldt-Jakob disease presenting as frontal lobe dementia associated with a 96 base pair insertion in the prion protein gene. Dementia 1994;8:363-371 (in Japanese).
-
(1994)
Dementia
, vol.8
, pp. 363-371
-
-
Isozaki, E.1
Miyamoto, K.2
Kagamihara, Y.3
-
25
-
-
0342495573
-
A case of presenile dementia with a 168 base pair insertion in prion protein gene
-
in Japanese
-
Mizushima S, Ishiki K, Nishimaru T. A case of presenile dementia with a 168 base pair insertion in prion protein gene. Dementia 1994;8:380-390 (in Japanese).
-
(1994)
Dementia
, vol.8
, pp. 380-390
-
-
Mizushima, S.1
Ishiki, K.2
Nishimaru, T.3
-
26
-
-
0026496257
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism
-
Goldfarb LG, Petersen RB, Tabaton M, et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science 1992; 258:806-808.
-
(1992)
Science
, vol.258
, pp. 806-808
-
-
Goldfarb, L.G.1
Petersen, R.B.2
Tabaton, M.3
-
27
-
-
0028004290
-
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele
-
Tagliavini F, Prelli F, Porro M, et al. Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele. Cell 1994;79:695-703.
-
(1994)
Cell
, vol.79
, pp. 695-703
-
-
Tagliavini, F.1
Prelli, F.2
Porro, M.3
-
28
-
-
0027332116
-
Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins
-
Pan K-M, Baldwin M, Nguyen J, et al. Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins. Proc Natl Acad Sci USA 1993;90:10962-10966.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10962-10966
-
-
Pan, K.-M.1
Baldwin, M.2
Nguyen, J.3
-
29
-
-
0006071109
-
Experimental Creutzfeldt-Jakob disease: Induction of amyloid plaques in rodents
-
Prusiner SB, McKinley MP, eds. San Diego: Academic Press
-
Tateishi J, Hikita K, Kitamoto T, Nagara H. Experimental Creutzfeldt-Jakob disease: induction of amyloid plaques in rodents. In: Prusiner SB, McKinley MP, eds. Prions novel infectious pathogens causing scrapie and Creutzfeldt-Jakob disease. San Diego: Academic Press, 1987:415-426.
-
(1987)
Prions Novel Infectious Pathogens Causing Scrapie and Creutzfeldt-Jakob Disease
, pp. 415-426
-
-
Tateishi, J.1
Hikita, K.2
Kitamoto, T.3
Nagara, H.4
-
30
-
-
0024828497
-
Organ distribution of proteinase-resistant prion protein in humans and mice with Creutzfeldt-Jakob disease
-
Kitamoto T, Mohri S, Tateishi J. Organ distribution of proteinase-resistant prion protein in humans and mice with Creutzfeldt-Jakob disease. J Gen Virol 1989;70:3371-3379.
-
(1989)
J Gen Virol
, vol.70
, pp. 3371-3379
-
-
Kitamoto, T.1
Mohri, S.2
Tateishi, J.3
|