-
1
-
-
0025372832
-
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: 887-90.
-
(1990)
Neurology
, vol.40
, pp. 887-890
-
-
Brown, P.1
Wolff, A.2
Gajdusek, D.C.3
-
2
-
-
0025219885
-
Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue
-
Picardo P, Safar J, Ceroni M, Gajdusek DC, Gibbs CJ. Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue. Neurology 1990; 40: 518-22.
-
(1990)
Neurology
, vol.40
, pp. 518-522
-
-
Picardo, P.1
Safar, J.2
Ceroni, M.3
Gajdusek, D.C.4
Gibbs, C.J.5
-
3
-
-
0025797632
-
Localization of amyloidogenic proteins and sulfated glycosaminoglycans in nontransmissible and transmissible cerebral amyloidoses
-
Guiroy DC, Yanaghihara R, Gajdusek DC. Localization of amyloidogenic proteins and sulfated glycosaminoglycans in nontransmissible and transmissible cerebral amyloidoses. Acta Neuropathol 1991; 82: 87-92.
-
(1991)
Acta Neuropathol
, vol.82
, pp. 87-92
-
-
Guiroy, D.C.1
Yanaghihara, R.2
Gajdusek, D.C.3
-
4
-
-
0021203930
-
Antibodies to protein of scrapie-associated fibrils
-
Diringer H, Rahn HC, Bode L. Antibodies to protein of scrapie-associated fibrils. Lancet 1984; ii: 345.
-
(1984)
Lancet
, vol.2
, pp. 345
-
-
Diringer, H.1
Rahn, H.C.2
Bode, L.3
-
5
-
-
0023499868
-
Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
-
Kascsack RJ, Rubenstein R, Merz PA. Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins. J Virol 1987; 61: 3688-93.
-
(1987)
J Virol
, vol.61
, pp. 3688-3693
-
-
Kascsack, R.J.1
Rubenstein, R.2
Merz, P.A.3
-
6
-
-
0023235753
-
Changes in the localization of brain prion proteins during scrapie infection
-
DeArmond SJ, Mobley WC, DeMott DL, Barry RA, Beckstead JH, Prusiner SB. Changes in the localization of brain prion proteins during scrapie infection. Neurology 1987; 37: 1271-80.
-
(1987)
Neurology
, vol.37
, pp. 1271-1280
-
-
DeArmond, S.J.1
Mobley, W.C.2
DeMott, D.L.3
Barry, R.A.4
Beckstead, J.H.5
Prusiner, S.B.6
-
7
-
-
0024827258
-
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: 145-50.
-
(1989)
Arch Virol
, vol.108
, pp. 145-150
-
-
Casaccia, P.1
Ladogana, A.2
Xi, Y.G.3
Pocchiari, M.4
-
9
-
-
8044239656
-
Prion protein immunocytochemistry-UK five centre consensus report
-
Bell JE, Gentleman SM, Ironside JW, McCardle L, Lantos PL, Doey L, et al. Prion protein immunocytochemistry-UK five centre consensus report. Neuropathol Appl Neurobiol 1997; 23: 26-35.
-
(1997)
Neuropathol Appl Neurobiol
, vol.23
, pp. 26-35
-
-
Bell, J.E.1
Gentleman, S.M.2
Ironside, J.W.3
McCardle, L.4
Lantos, P.L.5
Doey, L.6
-
10
-
-
0028040838
-
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: 375-83.
-
(1994)
Neuropathol Appl Neurobiol
, vol.20
, pp. 375-383
-
-
Hayward, P.A.R.1
Bell, J.E.2
Ironside, J.W.3
-
11
-
-
0025826175
-
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 Neuropathol 1991; 82: 260-5.
-
(1991)
Acta Neuropathol
, vol.82
, pp. 260-265
-
-
Doi-Yi, R.1
Kitamoto, T.2
Tateishi, J.3
-
12
-
-
0025997111
-
Concomitant Creutzfeldt-Jakob and Alzheimer diseases
-
Powers JM, Liu Y, Hair LS, Kascsack RJ, Lewis LD, Levy LA. Concomitant Creutzfeldt-Jakob and Alzheimer diseases. Acta Neuropathol 1991; 83: 95-8.
-
(1991)
Acta Neuropathol
, vol.83
, pp. 95-98
-
-
Powers, J.M.1
Liu, Y.2
Hair, L.S.3
Kascsack, R.J.4
Lewis, L.D.5
Levy, L.A.6
-
13
-
-
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: 686-9.
-
(1992)
Acta Neuropathol
, vol.84
, pp. 686-689
-
-
Muramoto, T.1
Kitamoto, T.2
Koga, H.3
Tateishi, J.4
-
14
-
-
0024406472
-
A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change
-
Hansen LA, Masliah E, Terry RD, Mirra SS. A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change. Acta Neuropathol 1989; 78: 194-201.
-
(1989)
Acta Neuropathol
, vol.78
, pp. 194-201
-
-
Hansen, L.A.1
Masliah, E.2
Terry, R.D.3
Mirra, S.S.4
-
16
-
-
0343952698
-
Creutzfeldt-Jakob disease
-
Adams JH, Duchen LW, eds. London: Edward Arnold
-
Tomlinson BE. Creutzfeldt-Jakob disease. In Adams JH, Duchen LW, eds. Greenfield's neuropathology. 5 ed. London: Edward Arnold; 1992. p. 1366-75.
-
(1992)
Greenfield's Neuropathology. 5 Ed.
, pp. 1366-1375
-
-
Tomlinson, B.E.1
-
17
-
-
0027731067
-
Neuropathology of spongiform encephalopathies in humans
-
Bell JE, Ironside JW. Neuropathology of spongiform encephalopathies in humans. Br Med Bull 1993; 49: 738-77.
-
(1993)
Br Med Bull
, vol.49
, pp. 738-777
-
-
Bell, J.E.1
Ironside, J.W.2
-
18
-
-
0028814065
-
Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-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 Creutzfeldt-Jakob disease. Neurosci Lett 1995; 183: 127-30.
-
(1995)
Neurosci Lett
, vol.183
, pp. 127-130
-
-
Goodbrand, I.A.1
Ironside, J.W.2
Nicolson, D.3
Bell, J.E.4
-
19
-
-
0025983158
-
Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease
-
Kitamoto T, Muramoto T, Mohri S, Doh-ura K, Tateishi J. Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease. J Virol 1991; 65: 6292-5.
-
(1991)
J Virol
, vol.65
, pp. 6292-6295
-
-
Kitamoto, T.1
Muramoto, T.2
Mohri, S.3
Doh-ura, K.4
Tateishi, J.5
-
20
-
-
0026695045
-
Light and electron microscopic localisation of B-amyloid protein in muscle biopsies of patients with inclusion-body myositis
-
Askanas V, King EW, Alvarez RB. Light and electron microscopic localisation of B-amyloid protein in muscle biopsies of patients with inclusion-body myositis. Am J Pathol 1992; 141: 31-6.
-
(1992)
Am J Pathol
, vol.141
, pp. 31-36
-
-
Askanas, V.1
King, E.W.2
Alvarez, R.B.3
-
21
-
-
0027433773
-
Prion protein is abnormally accumulated in inclusion-body myositis
-
Askanas V, Bilak M, Engel WK, Alvarez RB, Tome F, Leclerc A. Prion protein is abnormally accumulated in inclusion-body myositis. Neuroreport 1993; 5: 25-8.
-
(1993)
Neuroreport
, vol.5
, pp. 25-28
-
-
Askanas, V.1
Bilak, M.2
Engel, W.K.3
Alvarez, R.B.4
Tome, F.5
Leclerc, A.6
-
23
-
-
0001917671
-
Pathology of prions disease
-
Collinge J, Palmer MS, eds. New York: Oxford University Press
-
Ironside JW, Bell JE. Pathology of prions disease. In Collinge J, Palmer MS, eds. Prion Diseases. 1 ed. New York: Oxford University Press; 1997. p. 57-87.
-
(1997)
Prion Diseases. 1 Ed.
, pp. 57-87
-
-
Ironside, J.W.1
Bell, J.E.2
-
24
-
-
0001238110
-
Prion diseases
-
Graham DI, Lantos PL, eds. New York: Oxford University Press
-
DeArmond SJ, Prusiner SB. Prion diseases. In Graham DI, Lantos PL, eds. Greenfield's neuropathology. 6 ed. New York: Oxford University Press; 1997. p. 235-71.
-
(1997)
Greenfield's Neuropathology. 6 Ed.
, pp. 235-271
-
-
DeArmond, S.J.1
Prusiner, S.B.2
-
25
-
-
0026730281
-
The primary structure of the prion protein influences the distribution of abnormal prion protein in central nervous system
-
Kitamoto T, Doh-ura K, Muramoti T, Miyazono M, Tateishi J. The primary structure of the prion protein influences the distribution of abnormal prion protein in central nervous system. Am J Pathol 1992; 141: 271-7.
-
(1992)
Am J Pathol
, vol.141
, pp. 271-277
-
-
Kitamoto, T.1
Doh-ura, K.2
Muramoti, T.3
Miyazono, M.4
Tateishi, J.5
-
26
-
-
0026751775
-
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
-
Kitamoto T, Shin RW, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J. 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: 1285-94.
-
(1992)
Am J Pathol
, vol.140
, pp. 1285-1294
-
-
Kitamoto, T.1
Shin, R.W.2
Doh-ura, K.3
Tomokane, N.4
Miyazono, M.5
Muramoto, T.6
Tateishi, J.7
-
27
-
-
0025967257
-
Scrapie-associated prion protein accumulates in astrocytes during scrapie infection
-
Diedrich JF, Bendheim PE, Kim YS, Carp RI, Haase AT. Scrapie-associated prion protein accumulates in astrocytes during scrapie infection. Proc Nat Acad Sci U S A 1991; 88: 375-9.
-
(1991)
Proc Nat Acad Sci U S A
, vol.88
, pp. 375-379
-
-
Diedrich, J.F.1
Bendheim, P.E.2
Kim, Y.S.3
Carp, R.I.4
Haase, A.T.5
-
29
-
-
0026692758
-
Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides
-
Hashimoto K, Mannen T, Nukina N. Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides. Acta Neuropathol 1992; 83: 613-7.
-
(1992)
Acta Neuropathol
, vol.83
, pp. 613-617
-
-
Hashimoto, K.1
Mannen, T.2
Nukina, N.3
-
30
-
-
0031053453
-
Pathology and immunocytochemistry of a Kuru brain
-
Hainfellner JA, Liberski PP, Guiroy DC, Cervenakova L, Brown P, Gajdusek DC, et al. Pathology and immunocytochemistry of a Kuru brain. Brain Pathol 1997; 7: 547-53.
-
(1997)
Brain Pathol
, vol.7
, pp. 547-553
-
-
Hainfellner, J.A.1
Liberski, P.P.2
Guiroy, D.C.3
Cervenakova, L.4
Brown, P.5
Gajdusek, D.C.6
-
31
-
-
0026453980
-
Gerstmann-Sträusler syndrome- A variant type: Amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex
-
Amano N, Yagishita S, Yokio S, Itoh Y, Kinoshita J, Mizutani T, et al. Gerstmann-Sträusler syndrome- a variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex. Acta Neuropathol 1992; 84: 15-23.
-
(1992)
Acta Neuropathol
, vol.84
, pp. 15-23
-
-
Amano, N.1
Yagishita, S.2
Yokio, S.3
Itoh, Y.4
Kinoshita, J.5
Mizutani, T.6
-
32
-
-
0024856333
-
Gerstmann-Sträusler-Scheinker disease. II neurofibrillary tangles and plaques with PrP-amyloid coexists in an affected family
-
Ghetti B, Tagliavini F, Masters CL, Beyreuther K, Giaccone G, Verga L, et al. Gerstmann-Sträusler-Scheinker disease. II neurofibrillary tangles and plaques with PrP-amyloid coexists in an affected family. Neurology 1989; 39: 1453-61.
-
(1989)
Neurology
, vol.39
, pp. 1453-1461
-
-
Ghetti, B.1
Tagliavini, F.2
Masters, C.L.3
Beyreuther, K.4
Giaccone, G.5
Verga, L.6
-
33
-
-
0024324177
-
Familial dementia with PrP-positive amyloid plaques: A variant of Gerstmann-Sträusler syndrome
-
Nochlin D, Sumi SM, Bird TD, Snow AD, Leventhal CM, Beyreuther K, et al. Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträusler syndrome. Neurology 1989; 39: 910-8.
-
(1989)
Neurology
, vol.39
, pp. 910-918
-
-
Nochlin, D.1
Sumi, S.M.2
Bird, T.D.3
Snow, A.D.4
Leventhal, C.M.5
Beyreuther, K.6
-
35
-
-
0025802164
-
CT appearance of panencephalopathic and ataxic type of Creutzfeldt-Jakob disease
-
Berciano J, Díez C, Polo JM, Pacual J, Figols J. CT appearance of panencephalopathic and ataxic type of Creutzfeldt-Jakob disease. J Comput Assis Tomogr 1991; 15: 332-4.
-
(1991)
J Comput Assis Tomogr
, vol.15
, pp. 332-334
-
-
Berciano, J.1
Díez, C.2
Polo, J.M.3
Pacual, J.4
Figols, J.5
-
36
-
-
0023679125
-
Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease
-
Kitamoto T, Tateishi J, Sato Y. Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease. Ann Neurol 1988; 24: 537-42.
-
(1988)
Ann Neurol
, vol.24
, pp. 537-542
-
-
Kitamoto, T.1
Tateishi, J.2
Sato, Y.3
-
37
-
-
0029774050
-
'Neuritic conglomerates' in the cerebral cortex of a patient with Creutzfeldt-Jakob disease
-
Shintaku M, Ogura J, Terashima A. 'Neuritic conglomerates' in the cerebral cortex of a patient with Creutzfeldt-Jakob disease. Acta Neuropathol 1996; 92: 319-23.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 319-323
-
-
Shintaku, M.1
Ogura, J.2
Terashima, A.3
-
38
-
-
0023928966
-
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: 435-43.
-
(1988)
Am J Pathol
, vol.131
, pp. 435-443
-
-
Kitamoto, T.1
Tateishi, J.2
-
39
-
-
0026487234
-
Prion protein immunocytochemistry helps to establish the true incidence of prions diseases
-
Lantos PL, McGill IS, Janota I, Doey LJ, Collinge J, Bruce MT, et al. Prion protein immunocytochemistry helps to establish the true incidence of prions diseases. Neurosci Lett 1992; 147: 67-71.
-
(1992)
Neurosci Lett
, vol.147
, pp. 67-71
-
-
Lantos, P.L.1
McGill, I.S.2
Janota, I.3
Doey, L.J.4
Collinge, J.5
Bruce, M.T.6
-
40
-
-
0026002459
-
Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease
-
Kretzschmar HA, Kitamoto T, Doerr-Schott J, Mehraein P, Tateishi J. Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease. Acta Neuropathol 1991; 82: 536-40.
-
(1991)
Acta Neuropathol
, vol.82
, pp. 536-540
-
-
Kretzschmar, H.A.1
Kitamoto, T.2
Doerr-Schott, J.3
Mehraein, P.4
Tateishi, J.5
-
41
-
-
0029908149
-
Mutation in the prion protein gene at codon 232 in japanese patients with Creutzfeldt-Jakob disease: A clinicopathological, immunohistochemical and transmission study
-
Hoque MZ, Kitamoto T, Furukawa H, Muramoto T, Tateishi J. Mutation in the prion protein gene at codon 232 in japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study. Acta Neuropathol 1996; 92: 441-6.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 441-446
-
-
Hoque, M.Z.1
Kitamoto, T.2
Furukawa, H.3
Muramoto, T.4
Tateishi, J.5
-
42
-
-
0022530547
-
Pathology of Creutzfeldt-Jakob disease associated with pituitary-derived human growth hormone administration
-
Weller RO, Steart PV, Powell-Jackson JD. Pathology of Creutzfeldt-Jakob disease associated with pituitary-derived human growth hormone administration. Neuropathol Appl Neurobiol 1986; 12: 117-29.
-
(1986)
Neuropathol Appl Neurobiol
, vol.12
, pp. 117-129
-
-
Weller, R.O.1
Steart, P.V.2
Powell-Jackson, J.D.3
-
43
-
-
0001699149
-
Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France
-
Billet de Villemeur TB, Deslys JP, Pradel A, Soubrie C, Alperovitch A, Tardieu M, et al. Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France. Neurology 1995; 47: 690-5
-
(1995)
Neurology
, vol.47
, pp. 690-695
-
-
Billet De Villemeur, T.B.1
Deslys, J.P.2
Pradel, A.3
Soubrie, C.4
Alperovitch, A.5
Tardieu, M.6
-
44
-
-
0026667331
-
'Friendly fire' in medicine: Hormones, homografts, and Creutzfeldt-Jakob disease
-
Brown P, Preece MA, Will RG. 'Friendly fire' in medicine: hormones, homografts, and Creutzfeldt-Jakob disease. Lancet 1992; 340: 24-7.
-
(1992)
Lancet
, vol.340
, pp. 24-27
-
-
Brown, P.1
Preece, M.A.2
Will, R.G.3
-
45
-
-
0342951746
-
A new variant of Creutzfeldt-Jakob disease in the UK
-
Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 1996; 347: 921-5.
-
(1996)
Lancet
, vol.347
, pp. 921-925
-
-
Will, R.G.1
Ironside, J.W.2
Zeidler, M.3
Cousens, S.N.4
Estibeiro, K.5
Alperovitch, A.6
-
46
-
-
0028835989
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Clinical, pathological and molecular features
-
Gambrtti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. Brain Pathol 1995; 5: 43-51.
-
(1995)
Brain Pathol
, vol.5
, pp. 43-51
-
-
Gambrtti, P.1
Parchi, P.2
Petersen, R.B.3
Chen, S.G.4
Lugaresi, E.5
-
47
-
-
0026563279
-
Fatal familial insomnia: Clinical and pathologic study of five new cases
-
Manetto V, Medori R, Cortelli P, Montagna P, Tinuper P, Baruzzi A, et al. Fatal familial insomnia: clinical and pathologic study of five new cases. Neurology 1992; 42: 312-9.
-
(1992)
Neurology
, vol.42
, pp. 312-319
-
-
Manetto, V.1
Medori, R.2
Cortelli, P.3
Montagna, P.4
Tinuper, P.5
Baruzzi, A.6
-
48
-
-
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
-
49
-
-
0027763639
-
Fatal familial insomnia and the widening spectrum of prion diseases
-
Gambetti P, Peterson R, Monari L, Tabaton M, Autillo-Gambetti L, Cortelli P, et al. Fatal familial insomnia and the widening spectrum of prion diseases. Br Med Bull 1993; 49: 980-94.
-
(1993)
Br Med Bull
, vol.49
, pp. 980-994
-
-
Gambetti, P.1
Peterson, R.2
Monari, L.3
Tabaton, M.4
Autillo-Gambetti, L.5
Cortelli, P.6
-
51
-
-
0029938123
-
Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: Study of brain biopsies
-
Castellani R, Parchi P, Stahl J, Capellari S, Cohen M, Gambetti. Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies. Neurology 1996; 46: 1690-93.
-
(1996)
Neurology
, vol.46
, pp. 1690-1693
-
-
Castellani, R.1
Parchi, P.2
Stahl, J.3
Capellari, S.4
Cohen, M.5
Gambetti6
-
52
-
-
0029782193
-
Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease
-
MacDonald T, Sutherland K, Ironside JW. Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease. Neuropathol Appl Neurobiol 1996; 22: 285-92.
-
(1996)
Neuropathol Appl Neurobiol
, vol.22
, pp. 285-292
-
-
MacDonald, T.1
Sutherland, K.2
Ironside, J.W.3
-
55
-
-
24344450647
-
-
Brown P, Cervenakova L, Goldfarb LG, McCombie WR, Rubestein R, Will RG, et al. Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine.
-
Iatrogenic Creutzfeldt-Jakob Disease: An Example of the Interplay between Ancient Genes and Modern Medicine
-
-
Brown, P.1
Cervenakova, L.2
Goldfarb, L.G.3
McCombie, W.R.4
Rubestein, R.5
Will, R.G.6
-
56
-
-
0025859996
-
Genetic Predisposition to iatrogenic Creutzfeldt-Jakob disease
-
Collinge J, Palmer MS, Dryden AJ. Genetic Predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 1991; 337: 1441-2
-
(1991)
Lancet
, vol.337
, pp. 1441-1442
-
-
Collinge, J.1
Palmer, M.S.2
Dryden, A.J.3
-
57
-
-
0029824332
-
Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease
-
Schulz-Schaeffer WJ, Giese A Windl O, Kretzschmar HA. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease. Clin Neuropathol 1996; 15: 353-5.
-
(1996)
Clin Neuropathol
, vol.15
, pp. 353-355
-
-
Schulz-Schaeffer, W.J.1
Giese, A.2
Windl, O.3
Kretzschmar, H.A.4
-
58
-
-
0028108709
-
Neuropathological phenotype and prion protein genotype correlation in sporadic Creutzfeldt-Jakob disease
-
De Silva R, Ironside JW, McCardle L, Esmonde T, Bell J, Will R, et al. Neuropathological phenotype and prion protein genotype correlation in sporadic Creutzfeldt-Jakob disease. Neurosci Lett 1994; 179: 50-2.
-
(1994)
Neurosci Lett
, vol.179
, pp. 50-52
-
-
De Silva, R.1
Ironside, J.W.2
McCardle, L.3
Esmonde, T.4
Bell, J.5
Will, R.6
-
59
-
-
0029831213
-
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
-
Collinge J, Slide KCL, Meads J, Ironside J, Hill FA. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature 1996; 383: 685-90.
-
(1996)
Nature
, vol.383
, pp. 685-690
-
-
Collinge, J.1
Slide, K.C.L.2
Meads, J.3
Ironside, J.4
Hill, F.A.5
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