-
1
-
-
0011157250
-
New variant Creutzfeldt-Jakob disease
-
1 Department of Health. New variant Creutzfeldt-Jakob disease. CMO's Update 1997; 13: 4.
-
(1997)
CMO's Update
, vol.13
, pp. 4
-
-
-
2
-
-
0344342110
-
New variant of Creutzfeldt-Jakob disease in a 26-year-old French man
-
2 Chazot G, Broussolle E, Lapras Cl, et al. 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, Cl.3
-
3
-
-
0342951746
-
A new variant of Creutzfeldt-Jakob disease in the UK
-
3 Will RG, Ironside JW, Zeidler M, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 1996; 347: 921-25.
-
(1996)
Lancet
, vol.347
, pp. 921-925
-
-
Will, R.G.1
Ironside, J.W.2
Zeidler, M.3
-
4
-
-
0018360851
-
Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
-
4 Masters CL, Harris JO, Gajdusek DC, et al. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol 1979; 5: 177-88.
-
(1979)
Ann Neurol
, vol.5
, pp. 177-188
-
-
Masters, C.L.1
Harris, J.O.2
Gajdusek, D.C.3
-
5
-
-
0021333827
-
A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. 1: Clinical features
-
5 Will RG, Matthews WB. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. 1: Clinical features. J Neurol Neurosurg Psychiatry 1984; 47: 134-40.
-
(1984)
J Neurol Neurosurg Psychiatry
, vol.47
, pp. 134-140
-
-
Will, R.G.1
Matthews, W.B.2
-
6
-
-
0018599223
-
Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968-1977
-
6 Brown P, Cathala F, Gajdusek DC. Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968-1977. Ann Neurol 1979; 6: 438-46.
-
(1979)
Ann Neurol
, vol.6
, pp. 438-446
-
-
Brown, P.1
Cathala, F.2
Gajdusek, D.C.3
-
7
-
-
0018574744
-
Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977
-
7 Brown P, Cathala F, Sadowsky D, et al. Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977. Ann Neurol 1979; 6: 430-37.
-
(1979)
Ann Neurol
, vol.6
, pp. 430-437
-
-
Brown, P.1
Cathala, F.2
Sadowsky, D.3
-
8
-
-
0028876473
-
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)
-
8 Budka H, Aguzzi A, Brown P, et al. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995; 5: 459-66.
-
(1995)
Brain Pathol
, vol.5
, pp. 459-466
-
-
Budka, H.1
Aguzzi, A.2
Brown, P.3
-
9
-
-
0023778944
-
Clinical neurology and epidemiology of Creutzfeldt-Jakob disease, with special reference to iatrogenic cases
-
Bock G, Marsh J, eds. Chichester: Wiley
-
9 Brown P. Clinical neurology and epidemiology of Creutzfeldt-Jakob disease, with special reference to iatrogenic cases. In: Bock G, Marsh J, eds. Novel infectious agents of the central nervous system, Chichester: Wiley, 1988: 3-23.
-
(1988)
Novel Infectious Agents of the Central Nervous System
, pp. 3-23
-
-
Brown, P.1
-
10
-
-
0029840653
-
The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
-
10 Hsich G, Kenney K, Gibbs CJ, et al. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 1996; 335: 924-30.
-
(1996)
N Engl J Med
, vol.335
, pp. 924-930
-
-
Hsich, G.1
Kenney, K.2
Gibbs, C.J.3
-
12
-
-
0018824163
-
Creutzfeldt-Jakob disease in a 20-year-old woman
-
12 Packer RJ, Cornblath DR, Gonatas NK, et al. Creutzfeldt-Jakob disease in a 20-year-old woman. Neurology 1980; 30: 492-96.
-
(1980)
Neurology
, vol.30
, pp. 492-496
-
-
Packer, R.J.1
Cornblath, D.R.2
Gonatas, N.K.3
-
14
-
-
0020532066
-
Creutzfeldt-Jakob disease of 34 month's development in a 26-year-old woman
-
14 Raverdy P, Hauw JJ, Cathala F, et al. Creutzfeldt-Jakob disease of 34 month's development in a 26-year-old woman. Revue Neurologique 1983; 139: 381-83.
-
(1983)
Revue Neurologique
, vol.139
, pp. 381-383
-
-
Raverdy, P.1
Hauw, J.J.2
Cathala, F.3
-
15
-
-
0022405270
-
Epidemiologic implications of Creutzfeldt-Jakob disease in a 19-year-old girl
-
15 Brown P, Cathala F, Labauge R, et al. Epidemiologic implications of Creutzfeldt-Jakob disease in a 19-year-old girl. European J Epid 1985; 1: 42-47.
-
(1985)
European J Epid
, vol.1
, pp. 42-47
-
-
Brown, P.1
Cathala, F.2
Labauge, R.3
-
17
-
-
0024223734
-
Progressive neurological deterioration in a 14-year-old girl
-
17 Berman P, Davidson GS, Becker LE. Progressive neurological deterioration in a 14-year-old girl. Pediatr Neurosci 1988; 14: 42-49.
-
(1988)
Pediatr Neurosci
, vol.14
, pp. 42-49
-
-
Berman, P.1
Davidson, G.S.2
Becker, L.E.3
-
18
-
-
0031588170
-
New variant Creutzfeldt disease: Psychiatric feature
-
18 Zeidler M, Johnstone EC, Bomber RWK, et al. New variant Creutzfeldt disease: psychiatric feature. Lancet 1997; 350: 908-10.
-
(1997)
Lancet
, vol.350
, pp. 908-910
-
-
Zeidler, M.1
Johnstone, E.C.2
Bomber, R.W.K.3
-
19
-
-
0028235176
-
Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
-
19 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: 513-29.
-
(1994)
Ann Neurol
, vol.35
, pp. 513-529
-
-
Brown, P.1
Gibbs C.J., Jr.2
Rodgers-Johnson, P.3
-
20
-
-
85030305043
-
HMPAO-SPECT in the identification of new variant CJD
-
in press
-
20 de Silva RN, Patterson J, Russell A, et al. HMPAO-SPECT in the identification of new variant CJD. BMJ (in press).
-
BMJ
-
-
De Silva, R.N.1
Patterson, J.2
Russell, A.3
-
22
-
-
0029831213
-
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
-
22 Collinge J, Sidle KCL, Meads J, et al. 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
Sidle, K.C.L.2
Meads, J.3
-
23
-
-
0025069425
-
Transmissible encephalopathies in animals
-
23 Kimberlin RH. Transmissible encephalopathies in animals. Can J Vet Res 1990; 54: 30-37.
-
(1990)
Can J Vet Res
, vol.54
, pp. 30-37
-
-
Kimberlin, R.H.1
-
25
-
-
0026496257
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism
-
25 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: 806-08.
-
(1992)
Science
, vol.258
, pp. 806-808
-
-
Goldfarb, L.G.1
Petersen, R.B.2
Tabaton, M.3
-
26
-
-
0011213693
-
Growth hormone-related Creutzfeldt-Jakob disease: Genetic susceptibility and molecular pathogenesis
-
Court L, Dodet B, eds. Paris: Elsevier
-
26 Deslys JP, Lasmezas CI, Jaegly A, et al. Growth hormone-related Creutzfeldt-Jakob disease: genetic susceptibility and molecular pathogenesis. In: Court L, Dodet B, eds. Transmissible subacute spongiform encephalopathies: prion diseases. Paris: Elsevier, 1996: 465-70.
-
(1996)
Transmissible Subacute Spongiform Encephalopathies: Prion Diseases
, pp. 465-470
-
-
Deslys, J.P.1
Lasmezas, C.I.2
Jaegly, A.3
-
27
-
-
0021171932
-
Creutzfeldt-Jakob disease of long duration: Clinicopathological characteristics, transmissibility, and differential diagnosis
-
27 Brown P, Rodgers-Johnson P, Cathala F, et al. Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis. Ann Neurol 1984; 16: 295-304.
-
(1984)
Ann Neurol
, vol.16
, pp. 295-304
-
-
Brown, P.1
Rodgers-Johnson, P.2
Cathala, F.3
-
28
-
-
0001699149
-
Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France
-
28 Billette de Villemeur T, Deslys JP, Pradel A, et al. Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France. Neurology 1996; 47: 690-95.
-
(1996)
Neurology
, vol.47
, pp. 690-695
-
-
Billette De Villemeur, T.1
Deslys, J.P.2
Pradel, A.3
-
29
-
-
0026168460
-
Creutzfeldt-Jakob disease in Venezuela. A case report
-
29 Caraballo AJ. Creutzfeldt-Jakob disease in Venezuela. A case report. Arquivos de Neuro-Psiquiatria 1991; 49: 218-21.
-
(1991)
Arquivos de Neuro-Psiquiatria
, vol.49
, pp. 218-221
-
-
Caraballo, A.J.1
-
31
-
-
0011220891
-
Depression and psychosis in neurological practice
-
Bradley WG, Daroff RB, Fenichel GM, Marsden CD, eds. Boston: Butterworth-Heinemann
-
31 Trimble ME. Depression and psychosis in neurological practice. In: Bradley WG, Daroff RB, Fenichel GM, Marsden CD, eds. Neurology in clinical practice. Boston: Butterworth-Heinemann, 1996; 1: 107-18.
-
(1996)
Neurology in Clinical Practice
, vol.1
, pp. 107-118
-
-
Trimble, M.E.1
-
32
-
-
0001645432
-
Surveillance of prion diseases in humans
-
Baker HF, Ridley RM, eds. New Jersey: Humana Press
-
32 Will RG. Surveillance of prion diseases in humans. In: Baker HF, Ridley RM, eds. Prion diseases. New Jersey: Humana Press, 1996: 119-37.
-
(1996)
Prion Diseases
, pp. 119-137
-
-
Will, R.G.1
-
33
-
-
0006921410
-
Cerebrospinal fluid test for new-variant Creutzfeldt-Jakob disease
-
33 Will RG, Zeidler M, Brown P, et al. Cerebrospinal fluid test for new-variant Creutzfeldt-Jakob disease. Lancet 1997; 348: 955.
-
(1997)
Lancet
, vol.348
, pp. 955
-
-
Will, R.G.1
Zeidler, M.2
Brown, P.3
-
34
-
-
0030606390
-
Magnetic resonance imaging is not a sensitive test for Creutzfeldt-Jakob disease
-
34 Zeidler M, Will RG, Ironside JW, et al. Magnetic resonance imaging is not a sensitive test for Creutzfeldt-Jakob disease. BMJ 1996; 312: 844.
-
(1996)
BMJ
, vol.312
, pp. 844
-
-
Zeidler, M.1
Will, R.G.2
Ironside, J.W.3
-
35
-
-
0030011664
-
MR imaging of Creutzfeldt-Jakob disease
-
35 Finkenstaedt M, Szudra A, Zerr I, et al. MR imaging of Creutzfeldt-Jakob disease. Radiology 1996; 199: 793-98.
-
(1996)
Radiology
, vol.199
, pp. 793-798
-
-
Finkenstaedt, M.1
Szudra, A.2
Zerr, I.3
-
36
-
-
0025820942
-
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
-
36 Palmer MS, Dryden AJ, Hughes JT, et al. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 1991; 352: 340-42.
-
(1991)
Nature
, vol.352
, pp. 340-342
-
-
Palmer, M.S.1
Dryden, A.J.2
Hughes, J.T.3
-
38
-
-
0028778780
-
Frequencies of PrP gene variants in healthy cattle and cattle with BSE in Scotland
-
38 Hunter N, Goldmann W, Smith G, et al. Frequencies of PrP gene variants in healthy cattle and cattle with BSE in Scotland. Vet Record 1994; 135: 400-03.
-
(1994)
Vet Record
, vol.135
, pp. 400-403
-
-
Hunter, N.1
Goldmann, W.2
Smith, G.3
|