-
1
-
-
33746127253
-
Uber eine eigenartige herdformige erkrankung des zentralnervensystems
-
Creutzfeldt HG. Uber eine eigenartige herdformige erkrankung des zentralnervensystems. Z Neurol U Psychiatr 1920 ; 57 : 1-18.
-
(1920)
Z Neurol U Psychiatr
, vol.57
, pp. 1-18
-
-
Creutzfeldt, H.G.1
-
2
-
-
0000781428
-
Uber eine eigenartige Erkrankung des Zentral-nervensystems mit bemerkenswertem anatomischem Befunde (spastische pseudosklerotische Encephalomyelopathie mit disseminierten Degenerationsherden)
-
Jakob A. Uber eine eigenartige Erkrankung des Zentral-nervensystems mit bemerkenswertem anatomischem Befunde (spastische pseudosklerotische Encephalomyelopathie mit disseminierten Degenerationsherden). Dtsch Z Nervenheilk 1921 ; 70 : 132-46.
-
(1921)
Dtsch Z Nervenheilk
, vol.70
, pp. 132-146
-
-
Jakob, A.1
-
3
-
-
0026552043
-
Fatal familial insomnia, a prion disease with a mutation at codon-178 of the prion protein gene
-
Medori R, Tritschler HJ, Leblanc A, Villare F, Manetto V, Chen HY, 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 : 444-9.
-
(1992)
N Engl J Med
, vol.326
, pp. 444-449
-
-
Medori, R.1
Tritschler, H.J.2
Leblanc, A.3
Villare, F.4
Manetto, V.5
Chen, H.Y.6
-
4
-
-
78651041685
-
Degenerative disease of the central nervous system in New Guinea: The endemic occurrence of "kuru" in the native population
-
Gajdusek DC, Zigas V. Degenerative disease of the central nervous system in New Guinea: The endemic occurrence of "kuru" in the native population. N Engl J Med 1957; 257 : 974-8.
-
(1957)
N Engl J Med
, vol.257
, pp. 974-978
-
-
Gajdusek, D.C.1
Zigas, V.2
-
5
-
-
51849178459
-
Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems
-
Gerstmann J, Sträussler E, Scheinker I. Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems. Z Neurol 1936 ; 154 : 736-62.
-
(1936)
Z Neurol
, vol.154
, pp. 736-762
-
-
Gerstmann, J.1
Sträussler, E.2
Scheinker, I.3
-
6
-
-
0001907961
-
La tremblante du mouton est bien inoculable
-
Cuill J, Chelle PL. La tremblante du mouton est bien inoculable. CR Acad Sci Paris 1938 ; 206 : 78-9.
-
(1938)
CR Acad Sci Paris
, vol.206
, pp. 78-79
-
-
Cuill, J.1
Chelle, P.L.2
-
7
-
-
0023669586
-
A novel progressive spongiform encephalopathy in cattle
-
Wells GAH, Scott AC, Johnson CT, Gunning RF, Hancock RD, et al. A novel progressive spongiform encephalopathy in cattle. Vet Rec 1987 ; 121 : 419-20.
-
(1987)
Vet Rec
, vol.121
, pp. 419-420
-
-
Wells, G.A.H.1
Scott, A.C.2
Johnson, C.T.3
Gunning, R.F.4
Hancock, R.D.5
-
8
-
-
0014572261
-
Transmissible mink encephalopathy: Behavior of the disease agent in mink
-
Marsh RF, Burger D, Hanson RP. Transmissible mink encephalopathy: Behavior of the disease agent in mink. Amer J Vet Res 1969 ; 30 : 1637-42.
-
(1969)
Amer J Vet Res
, vol.30
, pp. 1637-1642
-
-
Marsh, R.F.1
Burger, D.2
Hanson, R.P.3
-
9
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science 1982 ; 216 : 136-44.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
11
-
-
0018220615
-
Resistance of scrapie to decontamination
-
Dickinson AG, Taylor DM. Resistance of scrapie to decontamination. New Eng J Med 1978 ; 299 : 1413-4.
-
(1978)
New Eng J Med
, vol.299
, pp. 1413-1414
-
-
Dickinson, A.G.1
Taylor, D.M.2
-
12
-
-
0002388560
-
-
L Court. Paris: Masson
-
Brown P, Rowher RG, Green EM, Gajdusek DC. The Effects of Chemicals, Heat, and Histopathologic Processing on High-infectivity Hamster Adapted Scrapie Virus. Virus non Conventionnels et Affections du Système Nerveux Central. L Court. Paris: Masson; 1983. p. 156-63.
-
(1983)
The Effects of Chemicals, Heat, and Histopathologic Processing on High-infectivity Hamster Adapted Scrapie Virus. Virus non Conventionnels et Affections du Système Nerveux Central
, pp. 156-163
-
-
Brown, P.1
Rowher, R.G.2
Green, E.M.3
Gajdusek, D.C.4
-
13
-
-
0014963710
-
Inactivation of the scrapie agent by near monochromatic ultraviolet light
-
Latarget R, Muel B, Haig DA, Clarke MC, Alper T. Inactivation of the scrapie agent by near monochromatic ultraviolet light. Nature 1970 ; 227 : 1341-3.
-
(1970)
Nature
, vol.227
, pp. 1341-1343
-
-
Latarget, R.1
Muel, B.2
Haig, D.A.3
Clarke, M.C.4
Alper, T.5
-
14
-
-
0001533763
-
Inactivation of the agents of scrapie, Creutzfeldt-Jakob disease, and kuru by radiations
-
SB Prusiner & WJ Hadlow, eds. New York: Academic Press
-
Latarjet R. Inactivation of the agents of scrapie, Creutzfeldt-Jakob disease, and kuru by radiations. In: SB Prusiner & WJ Hadlow, eds. Slow Transmissible Diseases of the Nervous System. New York: Academic Press 1979; 2 : 387-408.
-
(1979)
Slow Transmissible Diseases of the Nervous System
, vol.2
, pp. 387-408
-
-
Latarjet, R.1
-
15
-
-
0023880845
-
Autoclaving does not decontaminate formol-fixed scrapie tissues
-
Taylor DM, McConnell I. Autoclaving does not decontaminate formol-fixed scrapie tissues. Lancet 1988 ; 1 : 1463-4.
-
(1988)
Lancet
, vol.1
, pp. 1463-1464
-
-
Taylor, D.M.1
McConnell, I.2
-
16
-
-
0014331517
-
The effect of β-propiolactone on the scrapie agent
-
Haig DA, Clark MC. The effect of β-propiolactone on the scrapie agent. J Gen Virol 1968 ; 3 : 281-3.
-
(1968)
J Gen Virol
, vol.3
, pp. 281-283
-
-
Haig, D.A.1
Clark, M.C.2
-
17
-
-
0002388560
-
The effect of chemicals, heat, and histopathologic processing on high infectivity hamster-adapted scrapie virus. Virus non conventionnels et affections du système nerveux central
-
Paris: Masson
-
Brown P, Rohwer RG, Green EM, Gajdusek DC. The effect of chemicals, heat, and histopathologic processing on high infectivity hamster-adapted scrapie virus. Virus non conventionnels et affections du système nerveux central. L Court. Paris: Masson; 1983. p. 156-63.
-
(1983)
L Court
, pp. 156-163
-
-
Brown, P.1
Rohwer, R.G.2
Green, E.M.3
Gajdusek, D.C.4
-
18
-
-
0027405681
-
Comparative analysis of scrapie agent inactivation methods
-
Ernst DR, Race RE. Comparative analysis of scrapie agent inactivation methods. J Virol Methods 1993 ; 41 : 193-201.
-
(1993)
J Virol Methods
, vol.41
, pp. 193-201
-
-
Ernst, D.R.1
Race, R.E.2
-
19
-
-
0021019026
-
-
Prusiner SB, McKinley MP, Bowman KA, Bolton DC, Bendheim PE, Groth DF, et al. Cell 1983 ; 35 : 349-58.
-
(1983)
Cell
, vol.35
, pp. 349-358
-
-
Prusiner, S.B.1
McKinley, M.P.2
Bowman, K.A.3
Bolton, D.C.4
Bendheim, P.E.5
Groth, D.F.6
-
20
-
-
0000930692
-
Scrapie strain differences: The implications of stability and mutation. Proceedings of workshop on slow transmissible diseases
-
Dickinson AG, Bruce ME, Outram GW, Kimberlin RH. Scrapie strain differences: The implications of stability and mutation. Proceedings of workshop on slow transmissible diseases (Japanese). Tateishi J 1984 : 105-18.
-
(1984)
Tateishi J
, pp. 105-118
-
-
Dickinson, A.G.1
Bruce, M.E.2
Outram, G.W.3
Kimberlin, R.H.4
-
21
-
-
0017873041
-
Pathogenesis of mouse scrapie: Effect of route of inoculation on infectivity titres and dose-response curves
-
Kimberlin RH, Walker CA. Pathogenesis of mouse scrapie: Effect of route of inoculation on infectivity titres and dose-response curves. J Comp Pathol 1978 ; 88 : 39-47.
-
(1978)
J Comp Pathol
, vol.88
, pp. 39-47
-
-
Kimberlin, R.H.1
Walker, C.A.2
-
22
-
-
2442490085
-
-
Prusiner SB, McKinley MP, Groth DF, Bowman KA, Mock NI, Cochran SP, et al. Proc Natl Acad Sci USA 1981 ; 78 : 6675-9.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 6675-6679
-
-
Prusiner, S.B.1
McKinley, M.P.2
Groth, D.F.3
Bowman, K.A.4
Mock, N.I.5
Cochran, S.P.6
-
23
-
-
0019324430
-
Molecular properties, partial purifications, and assay by incubation period measurements of the hamster scrapie agent
-
Prusiner SB, Groth DF, Cochran SP, Masiarz FR, McKinley MP, Martinez HM. Molecular properties, partial purifications, and assay by incubation period measurements of the hamster scrapie agent. Biochemistry 1980 ; 19 : 4883-91.
-
(1980)
Biochemistry
, vol.19
, pp. 4883-4891
-
-
Prusiner, S.B.1
Groth, D.F.2
Cochran, S.P.3
Masiarz, F.R.4
McKinley, M.P.5
Martinez, H.M.6
-
24
-
-
0022505119
-
Newer data on the inactivation of scrapie virus or Creutzfeldt-Jakob disease virus in brain tissue
-
Brown P, Rohwer RG, Gajdusek DC. Newer data on the inactivation of scrapie virus or Creutzfeldt-Jakob disease virus in brain tissue. J Inf Dis 1986 ; 153 : 1145-8.
-
(1986)
J Inf Dis
, vol.153
, pp. 1145-1148
-
-
Brown, P.1
Rohwer, R.G.2
Gajdusek, D.C.3
-
25
-
-
0020756095
-
Resistance of the scrapie agent to inactivation by psoralens
-
McKinley MP, Masiarz FR, Isaacs ST, Hearst JE, Prusiner SB. Resistance of the scrapie agent to inactivation by psoralens. Photochem Photobiol 1983 ; 37 : 539-45.
-
(1983)
Photochem Photobiol
, vol.37
, pp. 539-545
-
-
McKinley, M.P.1
Masiarz, F.R.2
Isaacs, S.T.3
Hearst, J.E.4
Prusiner, S.B.5
-
26
-
-
0019588431
-
Thiocyanate and hydroxyl ions inactivate the scrapie agent
-
Prusiner SB, Groth DF, McKinley MP, Cochran SP, Bowman KA, Kasper KC. Thiocyanate and hydroxyl ions inactivate the scrapie agent. Proc Natl Acad Sci USA 1981 ; 78 : 4606-10.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 4606-4610
-
-
Prusiner, S.B.1
Groth, D.F.2
McKinley, M.P.3
Cochran, S.P.4
Bowman, K.A.5
Kasper, K.C.6
-
27
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
Oesch B, Westaway D, Walchli M, McKinley MP, Kent SB, Aebersold R, et al. A cellular gene encodes scrapie PrP 27-30 protein. Cell 1985 ; 40 : 735-46.
-
(1985)
Cell
, vol.40
, pp. 735-746
-
-
Oesch, B.1
Westaway, D.2
Walchli, M.3
McKinley, M.P.4
Kent, S.B.5
Aebersold, R.6
-
29
-
-
0000492906
-
The key role of the nerve membrane protein PrP in scrapie-like diseases
-
Hope J, Baybutt H. The key role of the nerve membrane protein PrP in scrapie-like diseases. Neurosciences 1991 ; 3 : 165-71.
-
(1991)
Neurosciences
, vol.3
, pp. 165-171
-
-
Hope, J.1
Baybutt, H.2
-
30
-
-
0025836627
-
Prion protein genes: Evolutionary and functional aspects
-
BW Chesebro, ed. Berlin: Springer-Verlag
-
Oesch B, Westaway D, Prusiner SB. Prion protein genes: Evolutionary and functional aspects. In: BW Chesebro, ed. Current Topics in Microbiology and Immunology. Transmissible Spongiform Encephalopathies: Scrapie, BSE and Related Disorders. Berlin: Springer-Verlag; 991. p. 109-24.
-
Current Topics in Microbiology and Immunology. Transmissible Spongiform Encephalopathies: Scrapie, BSE and Related Disorders
, pp. 109-124
-
-
Oesch, B.1
Westaway, D.2
Prusiner, S.B.3
-
31
-
-
0027466091
-
-
Prusiner SB, Fäzi M, Scott M, Serban D, Serban H, Taraboulos A, et al. J Infect Dis 1993 ; 167 : 602-13.
-
(1993)
J Infect Dis
, vol.167
, pp. 602-613
-
-
Prusiner, S.B.1
Fäzi, M.2
Scott, M.3
Serban, D.4
Serban, H.5
Taraboulos, A.6
-
33
-
-
0029937271
-
NMR structure of the mouse prion protein domain PrP (121-231)
-
Riek R, Hornemann S, Wider G, Billeter M, Glockshuber R, Wäthrich K. NMR structure of the mouse prion protein domain PrP (121-231). Nature 1996 ; 382 : 180-2.
-
(1996)
Nature
, vol.382
, pp. 180-182
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Billeter, M.4
Glockshuber, R.5
Wäthrich, K.6
-
34
-
-
0030836511
-
NMR characterisation of the full-length recombinant murine prion protein mPrP(23-231)
-
Riek R, Hornemann S, Wider G, Glockshuber R, Wäthrich K. NMR characterisation of the full-length recombinant murine prion protein mPrP(23-231). FEBS Letters 1997 ; 413 : 282-8.
-
(1997)
FEBS Letters
, vol.413
, pp. 282-288
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Glockshuber, R.4
Wäthrich, K.5
-
36
-
-
0028866917
-
A mutant prion protein displays an aberrant membrane association when expressed in cultures cells
-
Lehmann S, Harris DA. A mutant prion protein displays an aberrant membrane association when expressed in cultures cells. J Biol Chem 1995 ; 270 : 24589-97.
-
(1995)
J Biol Chem
, vol.270
, pp. 24589-24597
-
-
Lehmann, S.1
Harris, D.A.2
-
37
-
-
0030050733
-
Mutant and infectious prion proteins display common biochemical properties in cultured cells
-
Lehmann S, Harris DA. Mutant and infectious prion proteins display common biochemical properties in cultured cells. J Biol Chem 1996 ; 271 : 1633-7.
-
(1996)
J Biol Chem
, vol.271
, pp. 1633-1637
-
-
Lehmann, S.1
Harris, D.A.2
-
38
-
-
0026600865
-
Normal development and behaviour of mice lacking the neuronal cell surface PrP protein
-
Bäeler H, Fischer M, Lang Y, Bluethmann H, Lipp H-P, De Armond SJ, et al. Normal development and behaviour of mice lacking the neuronal cell surface PrP protein. Nature 1992 ; 356 : 577-82.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Bäeler, H.1
Fischer, M.2
Lang, Y.3
Bluethmann, H.4
Lipp, H.-P.5
De Armond, S.J.6
-
39
-
-
0027997387
-
-
Collinge J, Whittington MA, Sidle KCL, Smith CJ, Palmer MS, Clarke AR, et al. Nature 1994 ; 370 : 295-7.
-
(1994)
Nature
, vol.370
, pp. 295-297
-
-
Collinge, J.1
Whittington, M.A.2
Sidle, K.C.L.3
Smith, C.J.4
Palmer, M.S.5
Clarke, A.R.6
-
40
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homozygous for a disupted PrP gene
-
Sakagushi S, Katamine S, Nishida N, Morluchi R, Shigematsu K, Sugimoto T, et al. Loss of cerebellar Purkinje cells in aged mice homozygous for a disupted PrP gene. Nature 1996 ; 380 : 526-31.
-
(1996)
Nature
, vol.380
, pp. 526-531
-
-
Sakagushi, S.1
Katamine, S.2
Nishida, N.3
Morluchi, R.4
Shigematsu, K.5
Sugimoto, T.6
-
41
-
-
0025244011
-
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
-
Prusiner SB, Scott M, Foster D, Pan KM, Groth D, Mirenda C, et al. Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 1990 ; 63 : 673-86.
-
(1990)
Cell
, vol.63
, pp. 673-686
-
-
Prusiner, S.B.1
Scott, M.2
Foster, D.3
Pan, K.M.4
Groth, D.5
Mirenda, C.6
-
42
-
-
0027924773
-
Transgenetic investigations of prion diseases of humans and animals
-
Prusiner SB. Transgenetic investigations of prion diseases of humans and animals. Philos Trans R Soc Lond [Biol] 1993 ; 339 : 239-54.
-
(1993)
Philos Trans R Soc Lond [Biol]
, vol.339
, pp. 239-254
-
-
Prusiner, S.B.1
-
43
-
-
0000368918
-
Protéine prion: Structure, fonctions, et polymorphismes associés aux encéphalopathies spongiformes humaines
-
Laplanche JL, Beaudry P, Ripoll L, Launay JM. Protéine prion: Structure, fonctions, et polymorphismes associés aux encéphalopathies spongiformes humaines. Path Biol 1995 ; 43 : 104-13.
-
(1995)
Path Biol
, vol.43
, pp. 104-113
-
-
Laplanche, J.L.1
Beaudry, P.2
Ripoll, L.3
Launay, J.M.4
-
44
-
-
0027516141
-
Inherited prion diseases
-
Laplanche JL, Chatelain J, Dussaucy M, Bounneau C, Launay JM, Brandel JP, et al. Inherited prion disease. Br Med J 1993 ; 306 : 794-5.
-
(1993)
Br Med J
, vol.306
, pp. 794-795
-
-
Laplanche, J.L.1
Chatelain, J.2
Dussaucy, M.3
Bounneau, C.4
Launay, J.M.5
Brandel, J.P.6
-
46
-
-
0025820942
-
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
-
Palmer MS, Dryden AJ, Hughes JT, Collinge J. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 1991 ; 352 : 340-2.
-
(1991)
Nature
, vol.352
, pp. 340-342
-
-
Palmer, M.S.1
Dryden, A.J.2
Hughes, J.T.3
Collinge, J.4
-
47
-
-
0027972696
-
Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob disease
-
Deslys JP, Marc D, Dormont D. Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob disease. J Gen Virol 1994 ; 75 : 23-7.
-
(1994)
J Gen Virol
, vol.75
, pp. 23-27
-
-
Deslys, J.P.1
Marc, D.2
Dormont, D.3
-
48
-
-
0027479202
-
Valine homozygous 129 PrP genotype in a French growth-hormone related Creutzfeldt-Jakob disease patient
-
Labauge P, Pages M, Blard JM, Chatelain J, Laplanche JL. Valine homozygous 129 PrP genotype in a French growth-hormone related Creutzfeldt-Jakob disease patient. Neurology 1993 ; 43 : 447.
-
(1993)
Neurology
, vol.43
, pp. 447
-
-
Labauge, P.1
Pages, M.2
Blard, J.M.3
Chatelain, J.4
Laplanche, J.L.5
-
49
-
-
0027319326
-
Mice devoid of PrP are resistant to scrapie
-
Bäeler H, Aguzzi A, Sailer A, Greiner RA, Autenried P, Aguet M, et al. Mice devoid of PrP are resistant to scrapie. Cell 1993 ; 73 : 1339-47.
-
(1993)
Cell
, vol.73
, pp. 1339-1347
-
-
Bäeler, H.1
Aguzzi, A.2
Sailer, A.3
Greiner, R.A.4
Autenried, P.5
Aguet, M.6
-
50
-
-
0030054010
-
Normal host prion protein necessary for scrapie-induced neurotoxicity
-
Brandner S, Isemann S, Raeber A, Fischer M, Sailer A, Kobayashi Y, et al. Normal host prion protein necessary for scrapie-induced neurotoxicity. Nature 1996 ; 379 : 339-43.
-
(1996)
Nature
, vol.379
, pp. 339-343
-
-
Brandner, S.1
Isemann, S.2
Raeber, A.3
Fischer, M.4
Sailer, A.5
Kobayashi, Y.6
-
51
-
-
0018687383
-
Pathogenesis of mouse scrapie: Dynamics of agent replication in spleen, spinal cord and brain after infection by different routes
-
Kimberlin RH, Walker CA. Pathogenesis of mouse scrapie: Dynamics of agent replication in spleen, spinal cord and brain after infection by different routes. J Comp Pathol 1979 ; 89 : 551-62.
-
(1979)
J Comp Pathol
, vol.89
, pp. 551-562
-
-
Kimberlin, R.H.1
Walker, C.A.2
-
52
-
-
0031444295
-
A crucial role for B cells in neuroinvasive scrapie
-
Klein MA, Frigg R, Fleschig E, Raeber AJ, Kalinke U, Bluethmann H, et al. A crucial role for B cells in neuroinvasive scrapie. Nature 1997 ; 390 : 687-90.
-
(1997)
Nature
, vol.390
, pp. 687-690
-
-
Klein, M.A.1
Frigg, R.2
Fleschig, E.3
Raeber, A.J.4
Kalinke, U.5
Bluethmann, H.6
-
53
-
-
0028338441
-
Structural clues to prion replication
-
Cohen FE, Pan KM, Huang Z, Baldwin M, Fletterick RJ, Prusiner SB. Structural clues to prion replication. Science 1994 ; 264 : 530-1.
-
(1994)
Science
, vol.264
, pp. 530-531
-
-
Cohen, F.E.1
Pan, K.M.2
Huang, Z.3
Baldwin, M.4
Fletterick, R.J.5
Prusiner, S.B.6
-
54
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling GC, Scott M, Mastriani J, Gabizon R, Torchia M, Cohen FE, et al. Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell 1995 ; 83 : 79-90.
-
(1995)
Cell
, vol.83
, pp. 79-90
-
-
Telling, G.C.1
Scott, M.2
Mastriani, J.3
Gabizon, R.4
Torchia, M.5
Cohen, F.E.6
-
55
-
-
0027956109
-
Cell-free formation of protease-resistant prion protein
-
Kocisko DA, Come JH, Priola SA, Chesebro B, Raymond GJ, Lansbury PT, et al. Cell-free formation of protease-resistant prion protein. Nature 1994 ; 370 : 471-4.
-
(1994)
Nature
, vol.370
, pp. 471-474
-
-
Kocisko, D.A.1
Come, J.H.2
Priola, S.A.3
Chesebro, B.4
Raymond, G.J.5
Lansbury, P.T.6
-
56
-
-
0026064667
-
Are prions misfolded molecular chaperones?
-
Liautard JP. Are prions misfolded molecular chaperones? FEBS Lett 1991 ; 294 : 155-7.
-
(1991)
FEBS Lett
, vol.294
, pp. 155-157
-
-
Liautard, J.P.1
-
57
-
-
0031015906
-
Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy
-
Hill AF, Zeldler M, Ironside J, Collinge J. Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy. Lancet 1997 ; 349 : 99-100.
-
(1997)
Lancet
, vol.349
, pp. 99-100
-
-
Hill, A.F.1
Zeldler, M.2
Ironside, J.3
Collinge, J.4
-
58
-
-
0033573778
-
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples
-
Hill AF, Butterworth RJ, Jioner S, Jackson G, Rossor MN, Thomas DJ, et al. Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. Lancet 1999 ; 353 : 183-9.
-
(1999)
Lancet
, vol.353
, pp. 183-189
-
-
Hill, A.F.1
Butterworth, R.J.2
Jioner, S.3
Jackson, G.4
Rossor, M.N.5
Thomas, D.J.6
|