-
1
-
-
0002554696
-
Transmissible human spongiform encephalopathy (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker syndrome, and kuru
-
Calne DB, ed. Philadelphia: WB Saunders
-
Brown P. Transmissible human spongiform encephalopathy (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker syndrome, and kuru. In: Calne DB, ed. Neurodegenerative diseases. Philadelphia: WB Saunders, 1994:839-876.
-
(1994)
Neurodegenerative Diseases
, pp. 839-876
-
-
Brown, P.1
-
2
-
-
0000620908
-
Prions
-
Fields BN, Knipe DM, Howley PM, eds. Philadelphia: Lippincott-Raven
-
Prusiner SB. Prions. In: Fields BN, Knipe DM, Howley PM, eds. Fields virology. 3rd ed, vol 2. Philadelphia: Lippincott-Raven, 1996:2901-2950.
-
(1996)
Fields Virology. 3rd Ed
, vol.2
, pp. 2901-2950
-
-
Prusiner, S.B.1
-
3
-
-
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
-
4
-
-
0001289828
-
Pathologie animale - La maladie dite tremblante du mouton est-elle inoculable
-
Paris
-
Cuille J, Chelle PL. Pathologie animale - la maladie dite tremblante du mouton est-elle inoculable. CR Acad Sci (Paris) 1936;203:1552-1554.
-
(1936)
CR Acad Sci
, vol.203
, pp. 1552-1554
-
-
Cuille, J.1
Chelle, P.L.2
-
5
-
-
49749220574
-
Scrapie and kuru
-
Hadlow WJ. Scrapie and kuru. Lancet 1959;2:289-290.
-
(1959)
Lancet
, vol.2
, pp. 289-290
-
-
Hadlow, W.J.1
-
6
-
-
0014430962
-
Creutzfeldt-Jakob disease (subacute spongiform encephalopathy): Transmission to the chimpanzee
-
Gibbs CJ, Gajdusek DC, Asher DM, et al. Creutzfeldt-Jakob disease (subacute spongiform encephalopathy): transmission to the chimpanzee. Science 1968;161:388-389.
-
(1968)
Science
, vol.161
, pp. 388-389
-
-
Gibbs, C.J.1
Gajdusek, D.C.2
Asher, D.M.3
-
7
-
-
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
-
8
-
-
0023669586
-
A novel progressive spongiform encephalopathy in cattle
-
Wells GAH, Scott AC, Johnson CT, et al. A novel progressive spongiform encephalopathy in cattle. 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
-
9
-
-
0028809091
-
The neuropathology and epidemiology of bovine spongiform encephalopathy
-
Wells GA, Wilesmith JW. The neuropathology and epidemiology of bovine spongiform encephalopathy [review]. Brain Pathol 1995;5:91-103.
-
(1995)
Brain Pathol
, vol.5
, pp. 91-103
-
-
Wells, G.A.1
Wilesmith, J.W.2
-
10
-
-
0342951746
-
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
-
11
-
-
0022973492
-
Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases
-
Brown P, Cathala F, Castaigne P, Gajdusek DC. Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 1986;20:597-602.
-
(1986)
Ann Neurol
, vol.20
, pp. 597-602
-
-
Brown, P.1
Cathala, F.2
Castaigne, P.3
Gajdusek, D.C.4
-
12
-
-
0344342110
-
New variant of Creutzfeldt-Jakob disease in a 26-year-old French man
-
Chazot G, Broussolle E, Lapras CI, Blättler T, Aguzzi A, Kopp N. New variant of Creutzfeldt-Jakob disease in a 26-year-old French man. Lancet 1996;347:1181.
-
(1996)
Lancet
, vol.347
, pp. 1181
-
-
Chazot, G.1
Broussolle, E.2
Lapras, C.I.3
Blättler, T.4
Aguzzi, A.5
Kopp, N.6
-
13
-
-
0002313311
-
Infectious amyloids: Subacute spongiform encephalopathies as transmissible cerebral amyloidosis
-
Fields BN, Knipe DM, Howley PM, eds. Philadelphia: Lippincott-Raven
-
Gajdusek DC. Infectious amyloids: subacute spongiform encephalopathies as transmissible cerebral amyloidosis. In: Fields BN, Knipe DM, Howley PM, eds. Fields virology. 3rd ed, vol 2. Philadelphia: Lippincott-Raven, 1996:2851-2900.
-
(1996)
Fields Virology. 3rd Ed
, vol.2
, pp. 2851-2900
-
-
Gajdusek, D.C.1
-
14
-
-
0025244011
-
Transgenetic studies implicate interaction between homologous PrP isoforms in scrapie prion replication
-
Prusiner SB, Scott M, Foster D, et al. Transgenetic studies implicate interaction between homologous PrP isoforms in scrapie prion replication. Cell 1990;63:673-686.
-
(1990)
Cell
, vol.63
, pp. 673-686
-
-
Prusiner, S.B.1
Scott, M.2
Foster, D.3
-
15
-
-
0028782015
-
Transmission of bovine spongiform encephalopathy and scrapie to mice: Strain variation and the species barrier
-
Bruce M, Chree A, McConnell I, Foster J, Pearson G, Fraser H. Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier. Philos Trans R Soc Lond [Biol] 1994;343:405-411.
-
(1994)
Philos Trans R Soc Lond [Biol]
, vol.343
, pp. 405-411
-
-
Bruce, M.1
Chree, A.2
McConnell, I.3
Foster, J.4
Pearson, G.5
Fraser, H.6
-
16
-
-
13344293718
-
Unaltered susceptibility to BSE in transgenic mice expressing human prion protein
-
Collinge J, Palmer MS, Sidle KC, et al. Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. Nature 1995;378:779-783.
-
(1995)
Nature
, vol.378
, pp. 779-783
-
-
Collinge, J.1
Palmer, M.S.2
Sidle, K.C.3
-
17
-
-
0029810684
-
New diagnostic tests for prion diseases
-
Collinge J. New diagnostic tests for prion diseases. N Engl J Med 1996;335:963-965.
-
(1996)
N Engl J Med
, vol.335
, pp. 963-965
-
-
Collinge, J.1
-
18
-
-
0025820942
-
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
-
Erratum, Nature 1991;352:547
-
Palmer MS, Dryden AJ, Hughes JT, Collinge J. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 1991;352:340-342. [Erratum, Nature 1991;352:547.]
-
(1991)
Nature
, vol.352
, pp. 340-342
-
-
Palmer, M.S.1
Dryden, A.J.2
Hughes, J.T.3
Collinge, J.4
-
19
-
-
0025859996
-
Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease
-
Collinge J, Palmer MS, Dryden AJ. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 1991;337:1441-1442.
-
(1991)
Lancet
, vol.337
, pp. 1441-1442
-
-
Collinge, J.1
Palmer, M.S.2
Dryden, A.J.3
-
20
-
-
0028235176
-
Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
-
Brown P, Gibbs CJ, Rodgers-Jackson 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-Jackson, P.3
-
21
-
-
0027925797
-
Failure to transmit bovine spongiform encephalopathy to mice by feeding them with extraneural tissues of affected cattle
-
Meddleton DJ, Barlow RM. Failure to transmit bovine spongiform encephalopathy to mice by feeding them with extraneural tissues of affected cattle. Vet Rec 1993;132:545-547.
-
(1993)
Vet Rec
, vol.132
, pp. 545-547
-
-
Meddleton, D.J.1
Barlow, R.M.2
-
22
-
-
0029840653
-
The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
-
Hsich G, Kenney K, Gibbs CJ Jr, Lee KH, Harrington MG. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 1996;335:924-930.
-
(1996)
N Engl J Med
, vol.335
, pp. 924-930
-
-
Hsich, G.1
Kenney, K.2
Gibbs C.J., Jr.3
Lee, K.H.4
Harrington, M.G.5
-
23
-
-
0029110015
-
The prion diseases
-
Prusiner SB. The prion diseases. Sci Am 1995;272:30-37.
-
(1995)
Sci Am
, vol.272
, pp. 30-37
-
-
Prusiner, S.B.1
|