-
3
-
-
0342951746
-
A new variant of Creutzfeldt-Jakob disease
-
Will R. G., Ironside J. W., Zeidler M. A new variant of Creutzfeldt-Jakob disease. Lancet. 347:1996;921-925.
-
(1996)
Lancet
, vol.347
, pp. 921-925
-
-
Will, R.G.1
Ironside, J.W.2
Zeidler, M.3
-
4
-
-
0032816292
-
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
-
Parchi P., Giese A., Capellari S. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol. 46:1999;224-233.
-
(1999)
Ann Neurol
, vol.46
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
-
5
-
-
15144348474
-
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995
-
Will R. G., Alperovitch A., Poser S. Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. Ann Neurol. 43:1998;763-767.
-
(1998)
Ann Neurol
, vol.43
, pp. 763-767
-
-
Will, R.G.1
Alperovitch, A.2
Poser, S.3
-
6
-
-
2442735162
-
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: A systematic analysis of predisposing mutations and allelic variation in the PRNP gene
-
Windl O., Dempster M., Estibeiro J. P. Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Hum Genet. 98:1996;259-264.
-
(1996)
Hum Genet
, vol.98
, pp. 259-264
-
-
Windl, O.1
Dempster, M.2
Estibeiro, J.P.3
-
7
-
-
0028270007
-
Human prion diseases
-
Prusiner S., Hsiao K. Human prion diseases. Ann Neurol. 35:1994;385-395.
-
(1994)
Ann Neurol
, vol.35
, pp. 385-395
-
-
Prusiner, S.1
Hsiao, K.2
-
9
-
-
0018360851
-
Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
-
Masters C. L., Harris J. O., Gajdusek D. C., Gibbs, Bernoulli C., Asher D. M. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol. 5:1979;177-188.
-
(1979)
Ann Neurol
, vol.5
, pp. 177-188
-
-
Masters, C.L.1
Harris, J.O.2
Gajdusek, D.C.3
Gibbs4
Bernoulli, C.5
Asher, D.M.6
-
10
-
-
0033608367
-
Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: A case-control study
-
Collins S., Law M. G., Fletcher A., Boyd A., Kaldor J., Masters C. L. Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study. Lancet. 353:1999;693-697.
-
(1999)
Lancet
, vol.353
, pp. 693-697
-
-
Collins, S.1
Law, M.G.2
Fletcher, A.3
Boyd, A.4
Kaldor, J.5
Masters, C.L.6
-
11
-
-
0033585851
-
Routine tonsil biopsy for diagnosis of new variant Creutzfeldt-Jkob disease is not justified
-
Zeidler M., Knight R., Stewart G. Routine tonsil biopsy for diagnosis of new variant Creutzfeldt-Jkob disease is not justified. BMJ. 318:1999;538.
-
(1999)
BMJ
, vol.318
, pp. 538
-
-
Zeidler, M.1
Knight, R.2
Stewart, G.3
-
12
-
-
0030056269
-
Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease
-
Steinhoff B. J., Rächer S., Herrendorf G. Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch Neurol. 53:1996;162-166.
-
(1996)
Arch Neurol
, vol.53
, pp. 162-166
-
-
Steinhoff, B.J.1
Rächer, S.2
Herrendorf, G.3
-
13
-
-
0030011664
-
MR imaging of Creutzfeldt-Jakob disease
-
Finkenstaedt M., Szudra A., Zerr I. MR imaging of Creutzfeldt-Jakob disease. Radiology. 199:1996;793-798.
-
(1996)
Radiology
, vol.199
, pp. 793-798
-
-
Finkenstaedt, M.1
Szudra, A.2
Zerr, I.3
-
14
-
-
0032916599
-
Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease
-
Bahn M. M., Parchi P. Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease. Arch Neurol. 56:1999;577-583.
-
(1999)
Arch Neurol
, vol.56
, pp. 577-583
-
-
Bahn, M.M.1
Parchi, P.2
-
15
-
-
0032947307
-
Diffusion-weighted MRI in sporadic Creutzfeldt-Jakob disease
-
Demaerel P., Heiner L., Robberecht W., Sciot R., Wilms G. Diffusion-weighted MRI in sporadic Creutzfeldt-Jakob disease. Neurology. 52:1999;205-208.
-
(1999)
Neurology
, vol.52
, pp. 205-208
-
-
Demaerel, P.1
Heiner, L.2
Robberecht, W.3
Sciot, R.4
Wilms, G.5
-
16
-
-
0033594504
-
Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease
-
Yee A. S., Simon J. H., Anderson C. A., Sze C-I., Filley C. M. Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease. Neurology. 52:1999;1514-1515.
-
(1999)
Neurology
, vol.52
, pp. 1514-1515
-
-
Yee, A.S.1
Simon, J.H.2
Anderson, C.A.3
Sze, C.-I.4
Filley, C.M.5
-
17
-
-
0029078348
-
Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease
-
Zerr I., Bodemer M., Räcker S. Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease. Lancet. 345:1995;1609-1610.
-
(1995)
Lancet
, vol.345
, pp. 1609-1610
-
-
Zerr, I.1
Bodemer, M.2
Räcker, S.3
-
18
-
-
0022606619
-
Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
-
Harrington M., Merril C. R., Asher D. M., Gajdusek D. C. Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. N Engl J Med. 315:1986;279-283.
-
(1986)
N Engl J Med
, vol.315
, pp. 279-283
-
-
Harrington, M.1
Merril, C.R.2
Asher, D.M.3
Gajdusek, D.C.4
-
19
-
-
0026482458
-
High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzefeldt-Jakob disease
-
Jimi T., Wakayama Y., Shibuya S. High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzefeldt-Jakob disease. Clinica Chimica Acta. 211:1992;37-46.
-
(1992)
Clinica Chimica Acta
, vol.211
, pp. 37-46
-
-
Jimi, T.1
Wakayama, Y.2
Shibuya, S.3
-
20
-
-
0032889062
-
14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
-
Beaudry P., Cohen P., Brandel J. P. 14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Dement Geriatr Cogn Disord. 10:1999;40-46.
-
(1999)
Dement Geriatr Cogn Disord
, vol.10
, pp. 40-46
-
-
Beaudry, P.1
Cohen, P.2
Brandel, J.P.3
-
21
-
-
9844234269
-
S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
-
Otto M., Stein H., Szudra A. S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. J Neurol. 244:1997;566-570.
-
(1997)
J Neurol
, vol.244
, pp. 566-570
-
-
Otto, M.1
Stein, H.2
Szudra, A.3
-
22
-
-
0030934518
-
Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
-
Otto M., Wiltfang J., Tumani H. Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Neurosci Lett. 225:1997;210-212.
-
(1997)
Neurosci Lett
, vol.225
, pp. 210-212
-
-
Otto, M.1
Wiltfang, J.2
Tumani, H.3
-
23
-
-
0029840653
-
Creutzfeldt-Jakob disease. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
-
Hsich G., Kenney K., Gibbs, Lee K. H., Harrington M. G. Creutzfeldt-Jakob disease. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med. 335:1996;924-930.
-
(1996)
N Engl J Med
, vol.335
, pp. 924-930
-
-
Hsich, G.1
Kenney, K.2
Gibbs3
Lee, K.H.4
Harrington, M.G.5
-
24
-
-
0000561330
-
The 14-3-3 brain protein and transmissible spongiform encephalopathy
-
Zerr I., Bodemer M., Weber T. The 14-3-3 brain protein and transmissible spongiform encephalopathy. N Engl J Med. 336:1997.
-
(1997)
N Engl J Med
, vol.336
-
-
Zerr, I.1
Bodemer, M.2
Weber, T.3
-
25
-
-
0031914675
-
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease
-
Zerr I., Bodemer M., Gefeller O. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol. 43:1998;32-40.
-
(1998)
Ann Neurol
, vol.43
, pp. 32-40
-
-
Zerr, I.1
Bodemer, M.2
Gefeller, O.3
-
26
-
-
0026590687
-
Marked increase in cerebrospinal fluid ubiquitin in Creutzfeldt-Jakob disease
-
Manaka H., Kato T., Kurita K. Marked increase in cerebrospinal fluid ubiquitin in Creutzfeldt-Jakob disease. Neurosci Lett. 139:1992;47-49.
-
(1992)
Neurosci Lett
, vol.139
, pp. 47-49
-
-
Manaka, H.1
Kato, T.2
Kurita, K.3
-
27
-
-
0033012826
-
The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture
-
Satoh J-I., Kuohara K., Yukitake M., Kuroda Y. The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture. Eur Neurol. 41:1999;216-225.
-
(1999)
Eur Neurol
, vol.41
, pp. 216-225
-
-
Satoh, J.-I.1
Kuohara, K.2
Yukitake, M.3
Kuroda, Y.4
-
28
-
-
0029240512
-
14-3-3 proteins: Hot numbers in signal transduction
-
Burbelo P. D., Hall A. 14-3-3 proteins: hot numbers in signal transduction. Curr Biol. 5:1995;95-96.
-
(1995)
Curr Biol
, vol.5
, pp. 95-96
-
-
Burbelo, P.D.1
Hall, A.2
-
29
-
-
0026494876
-
14-3-3 proteins: A highly conserved, widespread family of eukaryotic proteins
-
Aitken A., Collinge D. B., van Heusden B. P. H. 14-3-3 proteins: a highly conserved, widespread family of eukaryotic proteins. Trends Biochem Sci. 17:1992;498-501.
-
(1992)
Trends Biochem Sci
, vol.17
, pp. 498-501
-
-
Aitken, A.1
Collinge, D.B.2
Van Heusden, B.P.H.3
-
30
-
-
0030766643
-
Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt-Jakob disease
-
Rosenmann H., Meiner Z., Kahana E. Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt-Jakob disease. Neurology. 49:1997;593-595.
-
(1997)
Neurology
, vol.49
, pp. 593-595
-
-
Rosenmann, H.1
Meiner, Z.2
Kahana, E.3
-
31
-
-
0006921410
-
Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob disease
-
Will R. G., Zeidler M., Brown P., Harrington M., Lee K. H., Kenney K. L. Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob disease. Lancet. 348:1996;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
-
32
-
-
0031588178
-
New variant Creutzfeldt-Jakob disease: Neurological features and diagnostic tests
-
Zeidler M., Stewart G. E., Barraclough C. R. New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests. Lancet. 350:1997;903-907.
-
(1997)
Lancet
, vol.350
, pp. 903-907
-
-
Zeidler, M.1
Stewart, G.E.2
Barraclough, C.R.3
-
33
-
-
0343778282
-
Creutzfeldt-Jakob disease in Australia
-
L. Court, & B. Dodet. Paris: Elsevier
-
Collins S., Fletcher A., de Luise T., Boyd A., Masters C. L. Creutzfeldt-Jakob disease in Australia. Court L., Dodet B. Transmissible Subacute Spongiform Encephalopathies: Prion Diseases. 1996;405-415 Elsevier, Paris.
-
(1996)
Transmissible Subacute Spongiform Encephalopathies: Prion Diseases
, pp. 405-415
-
-
Collins, S.1
Fletcher, A.2
De Luise, T.3
Boyd, A.4
Masters, C.L.5
-
34
-
-
0024519771
-
Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome
-
Hsiao K., Baker H., Crow T. Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Nature. 338:1989;342-345.
-
(1989)
Nature
, vol.338
, pp. 342-345
-
-
Hsiao, K.1
Baker, H.2
Crow, T.3
-
35
-
-
0342907533
-
Predictive testing for Creutzfeldt-Jakob Disease (CJD) with a novel mutation in the prion protein gene
-
Freckman M. L., Masters C., Collins S., Boyd A., Byron K., Campbell R., Darveniza P. Predictive testing for Creutzfeldt-Jakob Disease (CJD) with a novel mutation in the prion protein gene. Human Genetics Society of Australasia. 11:1998;26.
-
(1998)
Human Genetics Society of Australasia
, vol.11
, pp. 26
-
-
Freckman, M.L.1
Masters, C.2
Collins, S.3
Boyd, A.4
Byron, K.5
Campbell, R.6
Darveniza, P.7
-
36
-
-
85002479088
-
Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease
-
in press
-
Collins, S. Boyd, A. Fletcher, A. Byron, K. Harper, C. McLean, C. Masters, C. Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease. Arch Neurol (in press).
-
Arch Neurol
-
-
Collins, S.1
Boyd, A.2
Fletcher, A.3
Byron, K.4
Harper, C.5
McLean, C.6
Masters, C.7
-
37
-
-
0032768236
-
Use of capillary electrophoresis and fluorescent labeled peptides to detect the abnormal prion protein in the blood of animals that are infected with a transmissible spongiform encephalopathy
-
Schmerr M. J., Jenny A. L., Bulgin M. S. Use of capillary electrophoresis and fluorescent labeled peptides to detect the abnormal prion protein in the blood of animals that are infected with a transmissible spongiform encephalopathy. J Chromatogr. 853:1999;207-214.
-
(1999)
J Chromatogr
, vol.853
, pp. 207-214
-
-
Schmerr, M.J.1
Jenny, A.L.2
Bulgin, M.S.3
-
38
-
-
0031720905
-
scmolecules with different conformations
-
scmolecules with different conformations. Nat Med. 4:1998;1157-1165.
-
(1998)
Nat Med
, vol.4
, pp. 1157-1165
-
-
Safar, J.1
Willie, H.2
Itri, V.3
|