-
2
-
-
0034718472
-
Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease
-
Zerr I, Pocchiari M, Collins S, et al. Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology 2000;55:811-815.
-
(2000)
Neurology
, vol.55
, pp. 811-815
-
-
Zerr, I.1
Pocchiari, M.2
Collins, S.3
-
3
-
-
3543061153
-
Advances in diagnosing Creutzfeldt-Jakob disease with MRI and CSF 14-3-3 analysis
-
Zeidler M, Green A. Advances in diagnosing Creutzfeldt-Jakob disease with MRI and CSF 14-3-3 analysis. Neurology 2004;63:410-411.
-
(2004)
Neurology
, vol.63
, pp. 410-411
-
-
Zeidler, M.1
Green, A.2
-
4
-
-
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;335:924-930.
-
(1996)
N Engl J Med
, vol.335
, pp. 924-930
-
-
Hsich, G.1
Kenney, K.2
Gibbs, C.J.3
Lee, K.H.4
Harrington, M.G.5
-
5
-
-
0030968350
-
Diffusion-weighted magnetic resonance imaging in Creutzfeldt-Jakob disease
-
Demaerel P, Baert AL, Vanopdenbosch L, Robberecht W, Dom R. Diffusion-weighted magnetic resonance imaging in Creutzfeldt-Jakob disease. Lancet 1997;349:847-848.
-
(1997)
Lancet
, vol.349
, pp. 847-848
-
-
Demaerel, P.1
Baert, A.L.2
Vanopdenbosch, L.3
Robberecht, W.4
Dom, R.5
-
6
-
-
21744431731
-
High capacity and low cost detection of prion protein gene variant alleles through denaturing HPLC methodology
-
Castro RMRPS, Lamdenberger MC, Waltz R, et al. High capacity and low cost detection of prion protein gene variant alleles through denaturing HPLC methodology. J Neurosc Meth 2004;62:751-755.
-
(2004)
J Neurosc Meth
, vol.62
, pp. 751-755
-
-
Rmrps, C.1
Lamdenberger, M.C.2
Waltz, R.3
-
7
-
-
0031914675
-
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease
-
Zerr I, Bodemer M, Gefeller O, et al. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol 1998;43:32-40.
-
(1998)
Ann Neurol
, vol.43
, pp. 32-40
-
-
Zerr, I.1
Bodemer, M.2
Gefeller, O.3
-
8
-
-
3543049532
-
Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease
-
Castellani, RJ, Colucci M, Xie Z, et al. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology 2004;63:436-442.
-
(2004)
Neurology
, vol.63
, pp. 436-442
-
-
Castellani, R.J.1
Colucci, M.2
Xie, Z.3
-
9
-
-
3543144260
-
Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease
-
Shiga Y, Miyazawa K, Sato S, et al. Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease. Neurology 2004;63:443-449.
-
(2004)
Neurology
, vol.63
, pp. 443-449
-
-
Shiga, Y.1
Miyazawa, K.2
Sato, S.3
-
10
-
-
0033594504
-
Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease
-
Yee AS, Simon JH, Anderson CA, Sze CI, Filley CM, Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease. Neurology 1999;52:1514-1515.
-
(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
-
11
-
-
0036935168
-
Sequential MRI in a case of Creutzfeldt-Jakob disease
-
Tribl GG, Strasser G, Zeitlhofer J, et al. Sequential MRI in a case of Creutzfeldt-Jakob disease. Neuroradiology 2002;44:223-226.
-
(2002)
Neuroradiology
, vol.44
, pp. 223-226
-
-
Tribl, G.G.1
Strasser, G.2
Zeitlhofer, J.3
-
12
-
-
0041423598
-
Lateralized and focal clinical, EEG, and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease
-
Cambier DM, Kantarci K, Worrell GA, Westmoreland BF, Aksamit AJ. Lateralized and focal clinical, EEG, and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease. Clin Neurophysiol 2003;114:1724-1728.
-
(2003)
Clin Neurophysiol
, vol.114
, pp. 1724-1728
-
-
Cambier, D.M.1
Kantarci, K.2
Worrell, G.A.3
Westmoreland, B.F.4
Aksamit, A.J.5
-
14
-
-
0036120116
-
Emerging patterns of diffusion-weighted MR imaging in Creutzfeldt-Jakob disease: Case report and review of the literature
-
Mao-Draayer Y, Braff SP, Nagle KJ, Pendlebury W, Penar PL, Shapiro RE. Emerging patterns of diffusion-weighted MR imaging in Creutzfeldt-Jakob disease: case report and review of the literature. Am J Neuroradiol 2002;23:550-556.
-
(2002)
Am J Neuroradiol
, vol.23
, pp. 550-556
-
-
Mao-Draayer, Y.1
Braff, S.P.2
Nagle, K.J.3
Pendlebury, W.4
Penar, P.L.5
Shapiro, R.E.6
-
15
-
-
10744224601
-
Heidenhain variant of Creutzfeldt-Jakob disease: Diffusion-weighted MRI and PET characteristics
-
Tsuji Y, Kanamori H, Murakami G, et al. Heidenhain variant of Creutzfeldt-Jakob disease: diffusion-weighted MRI and PET characteristics. J Neuroimaging 2004;14:63-66.
-
(2004)
J Neuroimaging
, vol.14
, pp. 63-66
-
-
Tsuji, Y.1
Kanamori, H.2
Murakami, G.3
-
16
-
-
8944259890
-
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease
-
Parchi P, Castellani R, Capellari S, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996; 39:767-778.
-
(1996)
Ann Neurol
, vol.39
, pp. 767-778
-
-
Parchi, P.1
Castellani, R.2
Capellari, S.3
-
17
-
-
0032816292
-
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotype analysis of 300 subjects
-
Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotype analysis of 300 subjects. Ann Neurol 1999;46:224-233..
-
(1999)
Ann Neurol
, vol.46
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
-
18
-
-
3543061151
-
Sporadic Creutzfeldt-Jakob disease: Magnetic resonance imaging and clinical findings
-
Meissner B, Köhler K, Körtner K, et al. Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings. Neurology 2004; 63:450-456.
-
(2004)
Neurology
, vol.63
, pp. 450-456
-
-
Meissner, B.1
Köhler, K.2
Körtner, K.3
-
19
-
-
0032863045
-
Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2
-
Samman I, Schulz-Schaeffer WJ, Wohrle JC, Sommer A, Kretzschmar HA, Hennerici M. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2. J Neurol Neurosurg Psychiatry 1999;67:678-681.
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.67
, pp. 678-681
-
-
Samman, I.1
Schulz-Schaeffer, W.J.2
Wohrle, J.C.3
Sommer, A.4
Kretzschmar, H.A.5
Hennerici, M.6
-
20
-
-
1542407288
-
MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan
-
Fukushima R, Shiga Y, Nakamura M, Fujimori J, Kitamoto T, Yoshida Y. MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan. J Neurol Neurosurg Psychiatry 2004;75:485-487.
-
(2004)
J Neurol Neurosurg Psychiatry
, vol.75
, pp. 485-487
-
-
Fukushima, R.1
Shiga, Y.2
Nakamura, M.3
Fujimori, J.4
Kitamoto, T.5
Yoshida, Y.6
-
21
-
-
0141520597
-
Diagnosing variant Creutzfeldt-Jakob disease with the pulvinar sign: MR imaging findings in 86 neuropathologically confirmed cases
-
Collie DA, Summers DM, Sellar RJ, et al. Diagnosing variant Creutzfeldt-Jakob disease with the pulvinar sign: MR imaging findings in 86 neuropathologically confirmed cases. Am J Neuroradiology 2003;24:1560-1569
-
(2003)
Am J Neuroradiology
, vol.24
, pp. 1560-1569
-
-
Collie, D.A.1
Summers, D.M.2
Sellar, R.J.3
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