-
1
-
-
0025083424
-
Pre-mortem diagnosis of Creutzfeldt-Jakob disease by detection of abnormal cerebrospinal fluid proteins
-
Blisard KS, Davis LE, Harrington MG, Lovell JK, Kornfeld M, Berger ML: Pre-mortem diagnosis of Creutzfeldt-Jakob disease by detection of abnormal cerebrospinal fluid proteins. J Neurol Sci 1990;99:75-81.
-
(1990)
J Neurol Sci
, vol.99
, pp. 75-81
-
-
Blisard, K.S.1
Davis, L.E.2
Harrington, M.G.3
Lovell, J.K.4
Kornfeld, M.5
Berger, M.L.6
-
2
-
-
0028876473
-
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)
-
Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Gullotta F, Hallia M, Hauw JJ, Ironside JW, Jellinger K, Kretzschmar HA, Lantos PL, Masullo C, Schlote W, Tateishi J, Weller RO: Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995;5:459-466.
-
(1995)
Brain Pathol
, vol.5
, pp. 459-466
-
-
Budka, H.1
Aguzzi, A.2
Brown, P.3
Brucher, J.M.4
Bugiani, O.5
Gullotta, F.6
Hallia, M.7
Hauw, J.J.8
Ironside, J.W.9
Jellinger, K.10
Kretzschmar, H.A.11
Lantos, P.L.12
Masullo, C.13
Schlote, W.14
Tateishi, J.15
Weller, R.O.16
-
3
-
-
0029240512
-
Hot numbers in signal transduction
-
Burbelo PD, Hall A: Hot numbers in signal transduction. Curr Biol 1995;5:95-96.
-
(1995)
Curr Biol
, vol.5
, pp. 95-96
-
-
Burbelo, P.D.1
Hall, A.2
-
4
-
-
0031080867
-
Prion protein and the transmissible spongiform encephalopathies
-
Caughey B, Chesebro B: Prion protein and the transmissible spongiform encephalopathies. Trends Cell Biol 1997;7:56-62.
-
(1997)
Trends Cell Biol
, vol.7
, pp. 56-62
-
-
Caughey, B.1
Chesebro, B.2
-
5
-
-
0030978055
-
Human TSE disease - Viral or protein only?
-
Chescbro B: Human TSE disease - viral or protein only? Nature Med 1997;3:491-492.
-
(1997)
Nature Med
, vol.3
, pp. 491-492
-
-
Chescbro, B.1
-
6
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge J, Whittington MA, Sidle KCL, Smith CJ, Palmer MS, Clarke AR, Jefferys JGR: Prion protein is necessary for normal synaptic function. Nature 1994;370:295-297.
-
(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
Jefferys, J.G.R.7
-
7
-
-
0029831213
-
Molecular analysis of prion strain variation and the aetiology of "new variant" CJD
-
Collinge J, Sidle KCL, Meads J, Ironside J, Hill AF: Molecular analysis of prion strain variation and the aetiology of "new variant" CJD. Nature 1996;383:685-690.
-
(1996)
Nature
, vol.383
, pp. 685-690
-
-
Collinge, J.1
Sidle, K.C.L.2
Meads, J.3
Ironside, J.4
Hill, A.F.5
-
8
-
-
0022606619
-
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
-
9
-
-
0030011664
-
MR imaging of Creutzfeldt-Jakob disease
-
Finkenstaedt M, Szudra A, Zerr I, Poser S, Hise JH, Stoebner JM, Weber T: MR imaging of Creutzfeldt-Jakob disease. Radiology 1996;199:793-798.
-
(1996)
Radiology
, vol.199
, pp. 793-798
-
-
Finkenstaedt, M.1
Szudra, A.2
Zerr, I.3
Poser, S.4
Hise, J.H.5
Stoebner, J.M.6
Weber, T.7
-
10
-
-
0031015906
-
Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy
-
Hill AF, Zeidler 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
Zeidler, M.2
Ironside, J.3
Collinge, J.4
-
11
-
-
0029840653
-
The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
-
Hsich G, Kenney K, Gibbs CJ, 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;355:924-980.
-
(1996)
N Engl J Med
, vol.355
, pp. 924-980
-
-
Hsich, G.1
Kenney, K.2
Gibbs, C.J.3
Lee, K.H.4
Harrington, M.G.5
-
12
-
-
0026482458
-
High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease
-
Jimi T, Wakayama Y, Shibuya S, Nakata H, Tomaru T, Takahashi Y, Kosaka K, Asano T, Kato K: 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
Nakata, H.4
Tomaru, T.5
Takahashi, Y.6
Kosaka, K.7
Asano, T.8
Kato, K.9
-
13
-
-
16044366851
-
Premortem diagnosis of Creutzfeldt-Jakob disease by cerebrospinal fluid analysis
-
Lee KH, Harringlon MG: Premortem diagnosis of Creutzfeldt-Jakob disease by cerebrospinal fluid analysis. Lancet 1996;348:887.
-
(1996)
Lancet
, vol.348
, pp. 887
-
-
Lee, K.H.1
Harringlon, M.G.2
-
14
-
-
0027043161
-
Abnormal proteins in the cerebrospinal fluid of a patient with Creutzfeldt-Jakob disease following administration of human pituitary growth hormone
-
Macário ME, Moura-Neto V, Vaisman M, Araujo HMM, Buescu A, Cordeiro JGH, Chagas C: Abnormal proteins in the cerebrospinal fluid of a patient with Creutzfeldt-Jakob disease following administration of human pituitary growth hormone. Brazilian J Med Biol Res 1992;25:1127-1130.
-
(1992)
Brazilian J Med Biol Res
, vol.25
, pp. 1127-1130
-
-
Macário, M.E.1
Moura-Neto, V.2
Vaisman, M.3
Araujo, H.M.M.4
Buescu, A.5
Cordeiro, J.G.H.6
Chagas, C.7
-
15
-
-
0018360851
-
Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
-
Masters CL, Harris JO, Gajdusek DC, Gibbs CJ, 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, C.J.4
Bernoulli, C.5
Asher, D.M.6
-
16
-
-
0030870357
-
Die Creutzteldt-Jakob-Krankheit. Eine Sphinx der heutigen Neurobiologie
-
Poser S, Zerr I, Schulz-Schaeffer WJ, Kretzschmar HA, Felgenhauer K: Die Creutzteldt-Jakob-Krankheit. Eine Sphinx der heutigen Neurobiologie. Dtsch Med Wschr 1997;122:1099-1105.
-
(1997)
Dtsch Med Wschr
, vol.122
, pp. 1099-1105
-
-
Poser, S.1
Zerr, I.2
Schulz-Schaeffer, W.J.3
Kretzschmar, H.A.4
Felgenhauer, K.5
-
17
-
-
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
-
18
-
-
0030766643
-
Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt-Jakob disease
-
Rosenmann H, Meiner Z, Kahana E, Halimi M, Lenetsky E, Abramsky O, Gabizon R: Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt-Jakob disease. Neurology 1997;49:693-695.
-
(1997)
Neurology
, vol.49
, pp. 693-695
-
-
Rosenmann, H.1
Meiner, Z.2
Kahana, E.3
Halimi, M.4
Lenetsky, E.5
Abramsky, O.6
Gabizon, R.7
-
19
-
-
0025062357
-
Detection of neuron specific enolase concentrations in cerebrospinal fluid from patients with neurological disorders by means of a sensitive enzyme immunoassay
-
Vermuyten K, Lowenthal A, Karcher D: Detection of neuron specific enolase concentrations in cerebrospinal fluid from patients with neurological disorders by means of a sensitive enzyme immunoassay. Clin Chim Acta 1990;187:69-78.
-
(1990)
Clin Chim Acta
, vol.187
, pp. 69-78
-
-
Vermuyten, K.1
Lowenthal, A.2
Karcher, D.3
-
20
-
-
0023243715
-
High neuron-specific enolase levels of cerebrospinal fluid in the early stage of Creutzfeldt-Jakob disease
-
Wakayama Y, Shibuya S, Kawasc J, Sagawa F, Hashizume Y: High neuron-specific enolase levels of cerebrospinal fluid in the early stage of Creutzfeldt-Jakob disease. Klin Wschr 1987;65:798-801.
-
(1987)
Klin Wschr
, vol.65
, pp. 798-801
-
-
Wakayama, Y.1
Shibuya, S.2
Kawasc, J.3
Sagawa, F.4
Hashizume, Y.5
-
21
-
-
0342951746
-
A new variant of Creutzfeldt-Jakob disease in the UK
-
Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch L, Poser S, Pocchiari M, Hofman A, Smith PG: 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
Cousens, S.N.4
Estibeiro, K.5
Alperovitch, L.6
Poser, S.7
Pocchiari, M.8
Hofman, A.9
Smith, P.G.10
-
22
-
-
0006921410
-
Cerebrospinal-fluid test for new-variant Creulzfeldt-Jakob disease
-
Will RG, Zeidler M, Brown P, Harrington M, Lee KH, Kenney KL: Cerebrospinal-fluid test for new-variant Creulzfeldt-Jakob disease. Lancet 1996;348:955.
-
(1996)
Lancet
, vol.348
, pp. 955
-
-
Will, R.G.1
Zeidler, M.2
Brown, P.3
Harrington, M.4
Lee, K.H.5
Kenney, K.L.6
-
23
-
-
0029078348
-
Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease
-
Zerr I, Bodemer M, Räcker S, Grosche S, Poser S, Kretzschmar HA, Weber T: 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
Grosche, S.4
Poser, S.5
Kretzschmar, H.A.6
Weber, T.7
-
24
-
-
0030604908
-
Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid
-
Zerr I, Bodemer M, Otto M, Poser S, Windl O, Kretzschmar HA, Gefeller O, Weber T: Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid. Lancet 1996;348:846-849.
-
(1996)
Lancet
, vol.348
, pp. 846-849
-
-
Zerr, I.1
Bodemer, M.2
Otto, M.3
Poser, S.4
Windl, O.5
Kretzschmar, H.A.6
Gefeller, O.7
Weber, T.8
-
25
-
-
0000561330
-
The 14-3-3 protein and transmissible spongiform encephalopathy. Letter to the Editor
-
Zerr I, Bodemer M, Weber T: The 14-3-3 protein and transmissible spongiform encephalopathy. Letter to the Editor. N Engl J Med 1997;336:874.
-
(1997)
N Engl J Med
, vol.336
, pp. 874
-
-
Zerr, I.1
Bodemer, M.2
Weber, T.3
|